<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Job openings at biotechjobs]]></title><description><![CDATA[The latest job openings at biotechjobs]]></description><link>http://biotechroles.com</link><image><url>http://biotechroles.com/images/logo.png</url><title>Job openings at biotechjobs</title><link>http://biotechroles.com</link></image><generator>RSS for Node</generator><lastBuildDate>Thu, 09 Apr 2026 00:06:36 GMT</lastBuildDate><atom:link href="http://biotechroles.com/rss" rel="self" type="application/rss+xml"/><item><title><![CDATA[Tax Manager]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b>The Opportunity</b></p><p></p><p>This position manages activities related to the preparation and filing of federal, state and local tax returns of the company and its US and Puerto Rico diagnostics affiliates. Manages a team of professional and support staff in planning, researching, reviewing and preparing company, affiliates and subsidiary tax filings. This position serves as a technical expert in US tax compliance, income tax provision, and tax regulations and their application to the organization’s business, and is responsible for providing sound, practical tax  advice to management on all tax matters in a complex, multi-entity environment.</p><p></p><p>Key Responsibilities:</p><ul><li><p>Assist the Vice President with the implementation of the department’s annual strategic operating plan.  Assists with planning within assigned area and directs and coordinates the ongoing activities to meet established objectives and timeliness in a fast-paced, multi-subsidiary environment.</p></li><li><p>Effectively manages assigned staff in a manner consistent with organizational policies and values. Is responsible for managing the annual performance review feedback process to enhance work processes and employee understanding. Motivate, mentor, and develop high-performing personnel to achieve effective and efficient department operations.</p></li><li><p>Oversee the planning, research, review and preparation of the company, affiliate and subsidiaries income, sales and use, and property tax returns, and Annual Report tax filings. Supervises the review prior to submission to relevant taxing authorities. Ensures timely compliance while identifying opportunities to optimize tax positions and minimize tax liabilities through the consistent application of federal and state laws and regulations.</p></li><li><p>Coordinates tax matters related to audits, notices, controversies, and litigation support.</p></li><li><p>Responsible for the preparation and review of the interim and year-end financial statement tax provisions and the oversight and monitoring of the transfer pricing calculation and documentation.  </p></li><li><p>Serves as principal contact for negotiations with state and local revenue auditors.</p></li><li><p>Prepares and reviews refund claims, protests, and administrative appeals. Leads  planning initiatives to identify tax efficiencies and manage risk across entities and jurisdictions.</p></li><li><p>Maintains supporting accounts and records, ensuring strong internal controls and audit readiness.</p></li><li><p>Collaborates cross-functionally with other departments and subsidiaries.</p></li></ul><p></p><p><b>Who You Are</b></p><ul><li><p>Bachelor’s degree in Accounting</p></li><li><p>MBA or CPA certification preferred</p></li><li><p>7&#43; years of progressive tax experience with a major public accounting firm and/or with the tax department of a large company, or similar job-related experience</p></li><li><p>Strong knowledge of US federal, state, and local tax regulations, as well as income tax provision</p></li><li><p>High level of competency in application of tax research software, tax preparation software, and Excel</p></li><li><p>3&#43; years previous supervisory or management experience, with demonstrated ability to lead teams in a deadline-driven environment</p></li><li><p>Proven ability to plan, prioritize, and manage multiple projects and resources effectively in a fast-paced environment</p></li></ul><p></p><p>This p<span>osition is based in Indianapolis, IN and has a weekly requirement of 3 days/wk on-site.</span></p><p></p><p>The expected salary range for this position based on the primary location of Indiana is $97,100 - $180,300.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><i><b>Benefits</b></i></a></p><p><br /><b>Relocation benefits are not available for this job posting.</b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/tax-manager-roche/69d67da3c8e81216cd0cafe7</link><guid isPermaLink="true">http://biotechroles.com/tax-manager-roche/69d67da3c8e81216cd0cafe7</guid><pubDate>Wed, 08 Apr 2026 16:09:07 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Ingeniero de Soporte a Soluciones Diagnósticas]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Un futuro más saludable. </span><span><span>Es lo que nos impulsa a innovar, a avanzar continuamente en la ciencia y a asegurar que todos tengan acceso a la atención médica que necesitan hoy y para las generaciones venideras</span></span><span>. </span><span><span>Crear un mundo donde todos tengamos más tiempo con las personas que amamos: eso es lo que nos hace ser Roche.</span></span></p><p></p><p><span>En Roche </span>Diagnóstica <span>nos encontramos en búsqueda del siguiente </span><b>Ingeniero/a de Soporte a Soluciones Diagnósticas</b><span> en </span><b>Barranquilla, Colombia</b><span><b> </b>quien se encargará de </span>garantizar el correcto funcionamiento de las máquinas de RD<span> (Excepto Unidad de negocios PoC).</span></p><p></p><p><b><span>La Oportunidad: </span></b></p><ul><li><p><span>Ejecutar los protocolos de mantenimientos preventivos para los instrumentos acorde con cronogramas</span></p></li><li><p><span>Ejecutar los mantenimientos correctivos que se presenten en los instrumentos instalados donde los clientes  (Especialmente casos de mediana y alta complejidad)</span></p></li><li><p><span>Realizar el correcto manejo de stock de repuestos asignados.</span></p></li><li><p><span>Realizar la completa y oportuna documentación y cierre de casos asignados</span></p></li><li><p><span>Escalamiento de casos e incidentes, acorde a los protocolos internos de la compañía*</span></p></li><li><p><span>Ser responsable activo del proceso de formación para el mejoramiento continuo en aspectos técnicos de los analizadores instalados en su zona</span></p></li><li><p><span>Atención Remota y Soporte en sitio (Especialmente para mediana y alta complejidad)</span></p></li><li><p><span>Planear y apoyar la implementación de proyectos de mediana y baja complejidad</span></p></li><li><p><span>Alinear y priorizar dentro del equipo de trabajo la atención del servicio ante la simultaneidad de eventos</span></p></li><li><p><span>Detectar y escalar situaciones que afecten indicadores de desempeño</span></p></li><li><p><span>Apoyar en la gestión de proveedores. Ser punto de contacto directo con los proveedores (UPS, Agua, obra civil) para solicitudes de servicio que permitan garantizar la operación de nuestros analizadores</span></p></li><li><p><span>Apoyar en la gestión de acciones diseñadas para el sostenimiento o mejora de los indicadores de CSAT del Capítulo de Experiencia del cliente}</span></p></li><li><p><span>Dar conceptos técnicos sobre el funcionamiento de los instrumentos con el fin de cotizar mantenimientos preventivos y/o correctivos</span></p></li><li><p><span>Responsable de hacer la gestión de servicio en las cuentas del modelo celular a su cargo generando un impacto memorable incluyendo: indicadores de CSAT, resolución de conflicto, Gestión de requerimientos dentro de los tiempos establecidos en los ANS (Acuerdos de Nivel de Servicio), entendimiento y respuesta a necesidades y solicitudes</span></p></li><li><p><span>Otras funciones que el líder estime convenientes.</span></p></li></ul><p></p><p><b><span>Quien eres: </span></b></p><ul><li><p><span>Ingeniería Electrónica y/o Eléctrica, Electromedicina o Biomédico es requerido. Estudios en mantenimiento en equipos biomédicos es deseable. </span></p></li><li><p><span>Nivel Intermedio de inglés. </span></p></li><li><p><span>Experiencia de 2 años en mantenimiento de equipos biomédicos. </span></p></li><li><p><span>Orientación al Cliente</span></p></li></ul><ul><li><p><span>Conseguir resultados</span></p></li><li><p><span>Colaborador relacionado: El colaborador mide el grado en que involucra a otros de una manera que permite a las partes involucradas descubrir puntos en común</span></p></li><li><p><span>70% de la  posición será en campo. </span></p></li></ul><p></p><p><span>Note: Relocation benefits are not available. </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/ingeniero-de-soporte-a-soluciones-diagnosticas-roche/69d67da2c8e81216cd0cafe6</link><guid isPermaLink="true">http://biotechroles.com/ingeniero-de-soporte-a-soluciones-diagnosticas-roche/69d67da2c8e81216cd0cafe6</guid><pubDate>Wed, 08 Apr 2026 16:09:06 GMT</pubDate><company>Roche</company><location>Barranquilla</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Customer & Marketing Manager (Fixed-Term)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>As our </span><b>Customer &amp; Marketing Manager</b><span>, you will take the lead in crafting seamless, high-impact experiences that bridge the gap between innovative medicine and patient needs. By blending data-driven insights with creative storytelling, you will ensure our mission resonates across every digital and physical touchpoint. Join us to drive meaningful outcomes in a role where your entrepreneurial spirit and strategic expertise truly matter.</span></p><p></p><p><b><b>The Opportunity</b></b></p><ul><li><p><span>You will design and execute the strategic portfolio for your assigned Disease Area, taking full accountability for local outcomes and work packages.</span></p></li><li><p><span>You will spearhead the development and implementation of our national customer engagement strategy to ensure a unified brand presence.</span></p></li><li><p><span>You will integrate digital and traditional channels - from email and web to in-person visits - to create a seamless journey for every customer.</span></p></li><li><p><span>You will create and optimize high-quality marketing messages and campaigns that align with brand goals and speak directly to customer needs.</span></p></li><li><p><span>You will regularly shape the customer experience by leveraging direct feedback and data to ensure every initiative is relevant and impactful.</span></p></li><li><p><span>You will use real-time data insights to review and pivot your plans, ensuring all activities consistently deliver on their intended business outcomes.</span></p></li><li><p><span>You will define clear KPIs and track marketing effectiveness, maintaining a relentless focus on initiatives that drive the highest value.</span></p></li></ul><p></p><p><b>Who You Are</b></p><p></p><ul><li><p><span>You possess expertise in crafting forward-thinking marketing strategies and have the confidence to make the necessary trade-offs to deliver the right content to the right person.</span></p></li><li><p><span>You are skilled at translating complex data into actionable plans, using analytics to detect trends and optimize performance against forecasts.</span></p></li><li><p><span>You excel at storytelling and consultative persuasion, with a unique ability to engage diverse audiences ranging from healthcare professionals to internal partners.</span></p></li><li><p><span>You bring a technology-first mindset, eager to leverage AI and digital platforms to maximize both patient outcomes and operational efficiency.</span></p></li><li><p><span>You balance a growth mindset with an entrepreneurial spirit, proactively sharing knowledge across teams and aligning your work with the broader goals of the organization.</span></p></li><li><p><span>You have a Bachelor&#39;s degree in Business Administration, Marketing, Health Sciences or similar.</span></p></li><li><p><span>You are fluent in Finnish and English.</span><span> </span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/customer-and-marketing-manager-fixed-term-roche/69d67da2c8e81216cd0cafe5</link><guid isPermaLink="true">http://biotechroles.com/customer-and-marketing-manager-fixed-term-roche/69d67da2c8e81216cd0cafe5</guid><pubDate>Wed, 08 Apr 2026 16:09:06 GMT</pubDate><company>Roche</company><location>Espoo</location><salary>$85000-115000</salary><type>Full time</type></item><item><title><![CDATA[Practicante de Soporte Técnico - TI]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>Funciones principales y responsabilidades</b></p><p></p><p>-Mejora de Procesos y Automatizacion: Identificar &#34;cuellos de botella&#34;y proponer soluciones tecnologicas. Mapear flujos de procesos, colaborar con el equipo de desarrollo o herramientas para implementar workflows o Chatboots.</p><p>-Documentación y Mapeo de Procesos: Apoyar en el diseño, la preparación y la creación de la documentación detallada de los procesos clave de la organización.</p><p>-Soporte al Plan de Continuidad del Negocio (BCP): Colaborar en la recopilación de información y el análisis de riesgos para el diseño e implementación del Plan de Continuidad del Negocio, asegurando que los procesos críticos estén protegidos.</p><p>-Análisis y Mejora de Flujos de Trabajo: Participar activamente en el análisis de los procesos existentes para identificar cuellos de botella e ineficiencias, proponiendo soluciones de optimización alineadas con los principios de Ingeniería.</p><p>-Soporte al anaisis de datos y calidad: Realizar auditorias ciegas sobre tickets cerrados para verificar el cumplimiento de las politicas de comunicacion.</p><p>Identificar tendencias de problemas emergentes, antes de que se conviertan en crisis.</p><p></p><p><b>Requerimientos Profesionales y Técnicos</b></p><p></p><p><b>Formación Académica:</b></p><p></p><p><u><b>-Estudiante activo de las carreras de Ingeniería en Sistemas, Tecnologías de la Información, Ingeniería Industrial o Administración de Empresas, buscando experiencia profesional en la optimización de procesos.</b></u></p><p>-Interés y/o conocimiento en metodologías de Gestión de Proyectos, con enfoque en la documentación y mejora continua de procesos. Visión de Negocio y Enfoque en el Valor.</p><p>-Capacidad para trabajar en la creación y organización de documentación técnica detallada (diagramas de flujo, procedimientos operativos, etc.).</p><p>-Excelentes habilidades de comunicación y colaboración para interactuar con diferentes áreas de la organización.</p><p></p><p><b>Nivel Educativo:</b></p><p></p><p>-Estudiante activo cursando el tercer o cuarto año de la carrera universitaria, para asegurar que posea la base teórica en gestión de proyectos, análisis de sistemas o ingeniería de procesos necesaria para el rol.</p><p>Requerimientos Básicos:</p><p>-Dominio de Herramientas de Documentación: Manejo intermedio de suites de productividad (ej. Microsoft Office, Google Workspace)</p><p>-Competencia en Inglés (Deseable/Intermedio): Nivel de inglés que le permita comprender documentación técnica y, potencialmente, participar en reuniones con equipos o stakeholders internacionales.</p><p>-Disponibilidad y Compromiso: Disponibilidad para cumplir un horario de práctica (tiempo parcial o según el programa universitario) y un fuerte compromiso con la duración del proyecto</p><p>Idioma: Español e Inglés intermedio (preferiblemente avanzado)</p><p></p><p><b>Competencias Profesionales</b></p><p></p><p>Gestión y Optimización de Procesos</p><p>Organización y Gestión de la Documentación</p><p>Análisis Estratégico y Planificación</p><p>Comunicación Técnica y Documentación</p><p>Colaboración Interfuncional y Enfoque al Cliente</p><p>Adaptabilidad y Aprendizaje Continuo</p><p>Buen nivel de redacción y ortografía.</p><p>Capacidad para trabajar en equipo y adaptarse a entornos dinámicos.</p><p>Organización, proactividad y atención al detalle.</p><p>Sensibilidad para temas de salud, sostenibilidad y cultura corporativa.</p><p>Experiencia previa en áreas de comunicaciones (prácticas, voluntariados o trabajos universitarios).</p><p></p><p><b>Perfil Ideal del Estudiante</b></p><p></p><p>Entusiasta de la Tecnología: Gran pasión por las computadoras, el software y la resolución de acertijos digitales.</p><p>Habilidades de Comunicación: Excelentes capacidades verbales y escritas; te sientes cómodo hablando con personas nuevas y trabajando en equipo.</p><p>Atención al detalle: Notas las &#34;pequeñas cosas&#34; y te enorgullece organizar tu trabajo y seguir instrucciones con precisión.</p><p>Deseo de Aprender: Alta aptitud para adquirir nuevas habilidades rápidamente y una actitud proactiva ante tareas desconocidas.</p><p>Fiable y Disciplinado: Capacidad para cumplir con un horario, gestionar las prioridades de la universidad y la pasantía, y mantener la compostura profesional.</p><p>Espíritu Colaborativo: Disfrutas ayudando a los demás y te emociona contribuir en un entorno global orientado al trabajo en equipo.</p><p></p><p><b>Habilidades Blandas (Soft Skills)</b></p><p></p><p>Estas habilidades determinan cómo el estudiante se integra al equipo y trata a los usuarios.</p><p>Escucha Activa y Empatía: Capacidad para escuchar con atención el problema del usuario sin interrumpir, validando sus sentimientos de frustración y demostrando una actitud de servicio genuina.</p><p>Pensamiento Analítico y Curiosidad: Habilidad para desglosar un problema complejo en pasos pequeños y lógicos. El estudiante no solo busca &#34;arreglar&#34; algo, sino entender el porqué falló.</p><p>Adaptabilidad y Resiliencia: Capacidad para mantener la calma en un entorno de TI que cambia rápidamente y recibir retroalimentación constructiva de sus mentores para mejorar continuamente.</p><p>Comunicación Asertiva: Habilidad para explicar conceptos técnicos de forma sencilla (sin usar tecnicismos innecesarios) para que cualquier usuario, sin importar su nivel de conocimiento, pueda entender la solución.</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/practicante-de-soporte-tecnico-ti-roche/69d67da2c8e81216cd0cafe4</link><guid isPermaLink="true">http://biotechroles.com/practicante-de-soporte-tecnico-ti-roche/69d67da2c8e81216cd0cafe4</guid><pubDate>Wed, 08 Apr 2026 16:09:06 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Business Intelligence Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span><b>Un futuro más saludable. Es lo que nos impulsa a innovar.</b> Para hacer avanzar la ciencia continuamente y garantizar que todos tengan acceso a la atención médica que necesitan hoy y para las generaciones venideras. Crear un mundo donde todos tengamos más tiempo con las personas que amamos. Eso es lo que nos hace Roche.</span><br /> </p><p><span>En la posición de <span><b>Business Intelligence Specialist</b></span>, te unirás a nuestro equipo de <span>Business Insights and Data Analytics</span> para transformar datos complejos en conocimientos accionables. Liderarás la gobernanza de datos y la inteligencia de mercado, asegurando que la información de alta calidad impulse la toma de decisiones ágil y estratégica en toda la afiliada.</span></p><p></p><p><br /><span><b>La Oportunidad</b></span></p><ul><li><span>Lideras la recepción y consolidación de fuentes de ventas (Sell-in / Sell-out) y auditorías de mercado para toda la compañía.</span></li><li><span>Garantizas la excelencia operativa mediante el diseño de controles de validación rigurosos y el mantenimiento de bases de datos.</span></li><li><span>Impulsas estrategias de Inteligencia Competitiva cruzando múltiples fuentes de información para anticipar tendencias del mercado.</span></li><li><span>Actúas como el orquestador principal frente a proveedores de datos, asegurando el cumplimiento de niveles de servicio e integridad de la información.</span></li><li><span>Estructuras la información con la granularidad requerida para facilitar el análisis por unidad de negocio, territorio o cliente.</span></li><li><span>Colaboras en el cálculo de métricas de desempeño territorial analizando datos históricos y comportamiento del mercado.</span></li><li><span>Brindas consultoría estratégica a los equipos de Marketing y Ventas para asegurar la correcta interpretación y adopción de los datos.</span></li><li><span>Lideras el entrenamiento de colegas en el uso de herramientas analíticas, reportes y tableros de control.</span></li></ul><p><span><b>Quién eres</b></span></p><ul><li><span>Cuentas con una licenciatura en Actuaría, Matemáticas, Administración, Finanzas, Ingeniería o áreas afines.</span></li><li><span>Tienes más de 5 años de experiencia en Inteligencia de Negocios, Efectividad de Fuerza de Ventas u Operaciones Comerciales en la industria farmacéutica o de investigación de mercados.</span></li><li><span>Posees un nivel experto en Excel (Power Query, modelado) y experiencia sólida en SQL para el manejo de bases de datos.</span></li><li><span>Tienes dominio en <span>el diseño de tableros interactivos</span> y la narrativa de datos (<i>storytelling</i>) utilizando herramientas de visualización como Tableau, Power BI, <span>Qlik, Looker</span>.</span></li><li><span>Posees un conocimiento profundo de auditorías de mercado (ej. IQVIA, DDD, <span>ATV, Non-Retail Channel, PMM, INEFAM, GOB360</span>) y del modelo comercial de la industria.</span></li><li><span>Dominas el español y cuentas con un nivel de inglés intermedio-avanzado para la colaboración con equipos regionales o globales.</span></li></ul><p><span><b>Preferencias</b></span></p><ul><li><span>Maestría o MBA en Ciencia de Datos, Inteligencia de Negocios o Administración.</span></li><li><span><span>Tableau – Black Belt or Green Belt</span></span></li><li><span>Experiencia con programación en Python/R o automatización de procesos (Alteryx, UiPath, Power Automate).</span></li><li><span>Conocimiento de plataformas CRM como Salesforce o Veeva.</span></li></ul><p></p><p><span>Relocation benefits are not available for this posting.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/business-intelligence-specialist-roche/69d67da1c8e81216cd0cafe3</link><guid isPermaLink="true">http://biotechroles.com/business-intelligence-specialist-roche/69d67da1c8e81216cd0cafe3</guid><pubDate>Wed, 08 Apr 2026 16:09:05 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$35000-60000</salary><type>Full time</type></item><item><title><![CDATA[Cash Applications Accounts Receivable Accountant (Trilingual English/Spanish/Portuguese)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>The Opportunity:</b></p><p></p><p>As a <b>Cash Applications &amp; Accounts Receivable Accountant</b> based in San José, Costa Rica, you will be a key driver of financial accuracy within the Roche Services Americas team. This center provides critical Finance and Procurement services to various countries across the Americas region. Your primary mission is to ensure that all incoming payments are identified, matched, and applied to customer accounts with precision, effectively &#34;closing the loop&#34; on the Invoice-to-Cash cycle.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p><b>Cash Application:</b> Execute daily posting of incoming payments (Wire, ACH, Checks) and accurately match remittances to customer invoices.</p></li><li><p><b>Reconciliation:</b> Manage bank account reconciliations and clear AR/bank suspense accounts to ensure zero unexplained variances.</p></li><li><p><b>Operational AR:</b> Handle manual invoicing, corrections, and customer credit analysis to support regional financial health.</p></li><li><p><b>Dispute Management:</b> Identify and code payment discrepancies (short-pays/over-payments) and resolve inquiries from affiliates and customers.</p></li><li><p><b>Process Improvement:</b> Propose automation and system enhancements (SAP/BlackLine) to improve &#34;auto-match&#34; rates and SSC efficiency.</p></li></ul><h3></h3><p><b>Who You Are:</b></p><p>You are a detail-oriented professional with a strong understanding of accounting flows and a commitment to high-integrity financial reporting.</p><p></p><p><b>Qualifications:</b></p><ul><li><p><b>Education:</b> Bachelor’s degree in <b>Accounting, Finance, Business Administration or related field</b>.</p></li><li><p><b>Experience:</b> <b>3&#43; years</b> in Finance/Accounting; Shared Services experience is a plus.</p></li><li><p><b>Technical Skills:</b> Proficiency in <b>SAP, BlackLine</b>, or similar ERPs, and advanced <b>Excel/G-Suite</b> skills.</p></li><li><p><b>Languages:</b> Fluency in <b>English and Spanish</b> is required. <b>Intermediate Portuguese</b> is strongly preferred</p></li><li><p><b>Competencies:</b> Strong ability to prioritize under tight deadlines and a focus on proactive problem-solving.</p></li></ul><p></p><p><b><i>Relocation benefits are not available for this posting.</i></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/cash-applications-accounts-receivable-accountant-trilingual-englishspanishportuguese-roche/69d67da1c8e81216cd0cafe2</link><guid isPermaLink="true">http://biotechroles.com/cash-applications-accounts-receivable-accountant-trilingual-englishspanishportuguese-roche/69d67da1c8e81216cd0cafe2</guid><pubDate>Wed, 08 Apr 2026 16:09:05 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Account Manager]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><u><b>职位概述:</b></u><br />负责区域内的客户管理</p><p><br /><u><b>主要工作职责 :</b></u></p><ul><li>完成地区经理制定的该区域及客户业务目标及预算内开支</li><li>管理负责的客户团队&#xff0c;调动协调各支持部门资源&#xff0c;以全力支持客户管理的相关活动</li><li>与市场部紧密合作并提供建议方案&#xff0c;以全面开拓市场机会</li><li>加强负责区域内的大客户管理系统的执行力度</li><li>协助制定年度计划</li><li>协助做出产品预测以适应市场需要</li><li>确保客户整体满意度&#xff0c;对客户有效管理</li><li>主管指派的其他任务</li></ul><p></p><p><u><b>基本任职资格:</b></u></p><ul><li>本科以上学历&#xff0c;检验相关专业或商业管理专业</li><li>英语说写能力俱佳</li><li>熟练应用微软办公软件</li><li>产品和应用的专业知识</li><li>具有医院诊断实验室工作检验或相关行业5年销售经验</li></ul><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/account-manager-roche/69d67da0c8e81216cd0cafe1</link><guid isPermaLink="true">http://biotechroles.com/account-manager-roche/69d67da0c8e81216cd0cafe1</guid><pubDate>Wed, 08 Apr 2026 16:09:04 GMT</pubDate><company>Roche</company><location>Hohhot</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[治疗领域专员_ GI]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>主要职责</p><p>规范诊疗</p><p><span>1.基于公司相关产品策略&#xff0c;介绍罗氏产品的关键信息&#xff0c;使医生及专家认知并了解罗氏的产品知识</span></p><p><span>2.基于公司疾病领域相关策略&#xff0c;传递相应疾病领域产品相关医学信息&#xff0c;促进医生制定规范治疗方案运用专业知识&#xff0c;助力生态圈内诊断准确度的提升</span></p><p>学科建设</p><p><span>1.访问临床及病理医生&#xff0c;按时按质的完成相关客户(尤其重点专家)对于疾病领域洞见的收集进行总结、分析和反馈</span></p><p><span>2.组织、协调并整合各类治疗领域学术会议&#xff0c;推动建立治疗领域治疗规范</span></p><p>疾病全程管理</p><p><span>支持协助患者解决方案经理&#xff0c;关注疾病领域全程管理和治疗方案优化</span></p><p><span> </span></p><p>能力与经验</p><p>岗位所需胜任力</p><p><span>● 具备相关疾病领域的基础知识&#xff1b;3年以上医药行业工作经验</span></p><p><span>● 良好学习能力&#xff0c;业务敏锐度&#xff1b;较高的沟通能力和高效的执行能力</span></p><p><span>● 正确的思维和行为 (使命驱动&#xff0c;合作共赢&#xff0c;成长性思维)</span></p><p><span>● 既往有销售/市场/医学经验&#xff0c;跨职能工作经验为佳</span></p><p>教育程度/所获资格证书</p><p><span>● 医学或药学相关本科及以上学历</span></p><p><span>● 在试用期内通过RDPAC考试&#xff1b;在试用期内完成罗氏所有必修课程</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/gi-roche/69d67d9fc8e81216cd0cafe0</link><guid isPermaLink="true">http://biotechroles.com/gi-roche/69d67d9fc8e81216cd0cafe0</guid><pubDate>Wed, 08 Apr 2026 16:09:03 GMT</pubDate><company>Roche</company><location>Yancheng</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Account Manager - BB]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span><span><b><u><span>Job Summary:</span></u></b></span></span></p><p><span><span><span>Responsible for Blood Bank account management and achieved the assigned business quota. </span></span></span></p><p></p><p><span><span><b><u><span>Main  Tasks &amp; Responsibilities :</span></u></b></span></span></p><ul><li><span><span><span>Achieve sales objective and expense budget set by Area Manager in the assigned area </span></span></span></li><li><span><span><span>Manage sales team and in coordination with Service and Application support team in order to support sales effort</span></span></span></li><li><span><span><span>Work closely with marketing team so as to exploit full marketing intelligence</span></span></span></li><li><span><span><span>Reinforces implementation of Key Account Management system in the assigned area</span></span></span></li><li><span><span><span>Assist in the appointment of suitable distributors, set sales target for appointed distributors and monitor performance of Distributors to ensure yearly target is achieved</span></span></span></li><li><span><span><span>Assist in yearly budgeting exercise</span></span></span></li><li><span><span><span>Assist in working out forecasting for products required by market</span></span></span></li><li><span><span><span>Ensure overall customer satisfaction and be responsible for VIP account management.</span></span></span></li><li><span><span><span>Prepare monthly report</span></span></span></li><li><span><span><span>Establish after-sales service system and ensure service quality</span></span></span></li><li><span><span><span>Other projects or tasks assigned by line manager</span></span></span></li><li><span><span><span>Conduct business in full compliance including but not limited to Roche Secure, Roche Behavior in Business, Roche Competition Law Interactive Dialogues, Roche Safety, Security Health and Environmental Protection  </span></span></span></li><li><span><span><span>Understand and fulfill the responsibility of line manager&#39;s SHE tasks and duties (as defined in SHE handbook)</span></span></span></li></ul><p></p><p><u><span><span><span><b>Basic Requirements of the Job:</b></span></span></span></u></p><ul><li>At least Bachelor Degree in Health/Clinical Diagnostics/Science disciplines</li><li>Good command of English in both spoken and written</li><li>Good command of MS office software application</li><li>Product &amp;amp; Application Expertise</li><li>At least 5 years’ experience in Sales and /or similar experience in the industry<br /> </li></ul><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/account-manager-bb-roche/69d67d9fc8e81216cd0cafdf</link><guid isPermaLink="true">http://biotechroles.com/account-manager-bb-roche/69d67d9fc8e81216cd0cafdf</guid><pubDate>Wed, 08 Apr 2026 16:09:03 GMT</pubDate><company>Roche</company><location>Shenyang</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Cluster Section Lead - E2E Finance]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><i>The Opportunity</i></b></p><p></p><p>As a <b>Cluster Section Lead</b> in the Global Finance Support organization, you will be responsible for establishing and leading day-to-day Finance Technical support, working with the respective Global Cluster Lead. The role has a strong focus on people management, compliance and operational excellence. In this position you will drive operational excellence to achieve the objectives of the Global Product Line, leading a team of Finance Business and System Analysts.</p><p>As a people manager you will inspire and help to shape the future of our organization.</p><p>You will actively coach and foster the development of the team members, help remove siloes and support your team to evolve with the organic development of the business.</p><p>You will lead the collaboration across clusters, as well as, across Global Product Lines, and Global teams.</p><p></p><ul><li><p><span>Strategic Talent Management: Lead the full employee lifecycle by managing recruitment with P&amp;C, overseeing onboarding/integration, and ensuring comprehensive training through various learning channels.</span></p></li><li><p><span>Performance &amp; Development: Motivate and develop team members by setting clear goals, documenting performance, and providing proactive coaching and feedback.</span></p></li><li><p><span>Operational Excellence: Drive service quality in Finance Business Support by meeting KPI targets, ensuring high end-user satisfaction, and maintaining a deep understanding of end-to-end finance processes.</span></p></li><li><p><span>Collaboration &amp; Communication: Foster a culture of teamwork and transparency by proactively sharing information, project roadmaps, and business knowledge across global and functional boundaries.</span></p></li><li><p><span>Continuous Improvement: Partner with enabling functions to implement best practices and identify system/process enhancements that drive automation, efficiency, and customer satisfaction.</span></p></li><li><p><span>Stakeholder &amp; Risk Management: Manage key business relationships and collaborate with leadership to set performance targets, manage team workloads, and mitigate operational risks.</span></p></li><li><p><span>Values-Driven Leadership: Serve as a role model by embodying Roche values and Leadership Commitments while promoting Agile, LEAN, and ITIL methodologies.</span></p></li></ul><p></p><p><b><i>Who you are</i></b></p><ul><li><p><span>Strategic Leadership &amp; Change Management: Proven ability to lead projects in complex matrix organizations, drive organizational change, and mentor/coach team members to success.</span></p></li><li><p><span>Operational Excellence &amp; Metrics: Extensive experience in customer support (preferably Finance) with a focus on meeting department KPIs, managing escalations, and utilizing reporting tools for data-driven decisions.</span></p></li><li><p><span>Stakeholder &amp; Account Management: Expert in demand and relationship management, possessing exceptional negotiation, facilitation, and communication skills to navigate a dynamic international environment.</span></p></li><li><p><span>Agile &amp; Structured Methodologies: Proficient in implementing support processes through modern ways of working, such as Agile, ITIL, and LEAN, while maintaining a strong sense of urgency.</span></p></li><li><p><span>Results-Oriented Professionalism: Highly accountable and resourceful problem-solver with a university degree and the ability to manage multiple priorities with composure and integrity.</span></p></li></ul><p></p><p><b><i>In exchange we provide you with</i></b></p><ul><li><p><span>Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; training, the possibility of international assignments, internal position changes and the chance to shape your own career. </span></p></li><li><p><span>Excellent benefits: Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party.</span></p></li><li><p><span>Flexibility: We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</span></p></li><li><p><span>A global inclusive community, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion. </span></p></li></ul><p></p><p><i>Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:</i><a href="https://go.roche.com/budapest-data-privacy-notice-candidate" target="_blank"><i> </i><u>https://go.roche.com/budapest-data-privacy-notice-candidate</u></a></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/cluster-section-lead-e2e-finance-roche/69d67d9ec8e81216cd0cafde</link><guid isPermaLink="true">http://biotechroles.com/cluster-section-lead-e2e-finance-roche/69d67d9ec8e81216cd0cafde</guid><pubDate>Wed, 08 Apr 2026 16:09:02 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Learning Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>The Global Learning Services teams focus on executing system data maintenance and administrative activities in Cornerstone and all relevant Learning management systems, as well as providing all necessary non-systems related Learning process support. Global Learning Services provides customer service and advisory support to the Learning Community and business partners on global Learning systems and processes and ensuring end-to-end process completion in line with customer focused principles to ensure the Roche People Practices work for the business.</p><p></p><p>As a Learning Specialist, you are responsible for executing Learning system data maintenance and administrative activities in a timely and accurate manner in support of Learning business processes.  You are also contributing to the continuous improvement of the People Support Solutions delivery through analysis of the interactions and collaboration with other HR functions within and outside of People Support Solutions. You need a broad understanding across global Learning processes and tools, as well as local and global downstream impacts on compliance, audits and right-to-operate, as well as finance, IT, etc. This is coupled with strong customer focus, communication skills and solution orientation.</p><p></p><p><b>The opportunity:</b></p><p></p><ul><li><p>Service Delivery</p></li></ul><ul><li><p>Execute system data maintenance and administrative activities in Cornerstone and all relevant Learning management systems, as well as providing all necessary non-systems related Learning process support.</p></li><li><p>Provide customer service support on Learning related activities, such as NEO, NMO, External Training, Professional Training, Leadership Training, Program Training and other training events request management and troubleshooting.</p></li><li><p>Supports the Global Learning Center of Excellence and our business customers with system maintenance and project activities.</p></li><li><p>Cooperate effectively with team members with daily work and projects.</p></li><li><p>Provide optional and standard Cornerstone admin service based on local end-to-end process and support the embedding of the new ways of learning.</p></li><li><p>Actively participate in the development and implementation of Roche Learning continuous improvement initiatives</p></li><li><p>Actively participate in workshops, meetings and work-related team events</p></li><li><p>To be the focal point for HR learning experts providing integrated learning solutions tailored to customers’ demand, and manage HR training matrix, training records as well as training data analytics. </p></li><li><p>Be up-to-date on processes, own the knowledge development on processes, and contribute to the update of relevant documentations (SWIs, SOP, GWIs).</p></li><li><p>Update SWIs and local SOP documentation</p></li></ul><ul><li><p>Participating in project activities as required</p></li><li><p>Display high integrity on the job and comply with the Roche guidelines, including data privacy rules and regulations.</p></li></ul><ul><li><p>Ensure consistent and reliable service delivery for customers serviced.</p></li><li><p>Implement processes and initiatives to ensure continuous improvement as well as service enhancement.</p></li><li><p>Align service delivery and quality with overarching objectives of the global People Support Solutions organization. Manage service quality expectations and address customer concerns</p></li><li><p>Ensure end to end ownership of resolution</p></li><li><p>Ensure operations according to defined KPIs and SLAs.</p></li><li><p>Ensure regulatory compliance in line with the countries, customers, and regulations.</p></li><li><p>Develop and manage key stakeholder relationships and communications to partner in a proactive and customer outcomes focused way.</p></li><li><p><b>Cross-Functional Collaboration</b></p><ul><li><p> Build relationships with HR colleagues within the People Support Solutions organization as well as with customers to ensure ongoing service delivery effectiveness.</p></li><li><p>Collaborate with peers within region and globally to ensure the People Support Solutions network provides consistent and effective services to our customers.</p></li><li><p>Achieve our People Support Solutions vision by driving global consistency through collaboration.</p></li></ul></li><li><p><b>Outputs &amp; Deliverables</b></p><ul><li><p>Continuous contribution to the improvement of the performance of the Shared Service Centre </p></li><li><p>Reaching high customer satisfaction through consistent, high quality delivery and application of customer care principles (measured by defined stakeholder feedback)</p></li><li><p>Provide feedback, coaching and advice for contacts in both HR and the business (measured by defined stakeholder feedback)</p></li></ul></li></ul><p><br /> </p><p><b>Who you are:</b></p><p></p><p>In this role, you will be working within a team of Learning Specialists focusing on a customer group or key Learning process and across various functions and levels within the organization.</p><p></p><p><b>Minimum requirements:</b></p><ul><li><p>We are seeking an individual with a degree and 1–3 years of related experience in a Learning/HR area and/or working experience in a team and service delivery or customer care environment. </p></li><li><p>Experienced and efficient handling of standard IT-applications, preferably Google suite</p></li><li><p>You bring the following qualifications: </p><ul><li><p>University degree, HR preferred </p></li></ul></li></ul><ul><li><p>Fluent in English required, additional languages a plus, based on region (i.e. German, French, Italian, Spanish, Portuguese, Hungarian, Chinese)</p></li></ul><p></p><p><b>You bring the following skills and competencies:</b></p><ul><li><p>Experience in a shared service center, preferably in a Learning/HR services environment. </p></li><li><p>Experience with Cornerstone or other cloud-based learning management solutions preferred</p></li><li><p>Learning and development know-how.</p></li><li><p>Knowledge of Learning processes an advantage</p></li><li><p>Strong customer service &amp; interpersonal skills</p></li><li><p>Excellent communication skills &amp; team player</p></li><li><p>Excellent problem-solving/analytical abilities</p></li><li><p>Proven track record of being able to deliver in a matrix organization.</p></li><li><p>Ability to work independently in a fast-paced environment and to handle multiple, competing priorities.</p></li><li><p>Ability to thrive in an ambiguous and multicultural environment, working across borders. </p></li><li><p>Experience of effectively working in a matrix organization across geographies and divisions. </p></li><li><p>Ability to navigate complex Learning data structure</p></li><li><p>Core capabilities include:</p><ul><li><p>Living customer centricity through your day-to-day interactions (incl. needs anticipation, cultural awareness, managing one’s response)</p></li><li><p>Demonstrating end-to-end accountability (incl. big picture and impact understanding, engaging others to ensure a successful outcome) </p></li><li><p>Demonstrating problem-solving (incl. active listening, critical thinking, process improvements)</p></li><li><p>Having a growth mindset (incl. taking risks and experimenting, seeking new learning opportunities, asking and giving feedback)</p></li></ul></li></ul><p></p><p><b>SHE requirements</b></p><p></p><p>Employees are responsible for performing their duties in line with the SHE (Safety, Security, Health and Environmental Protection) Guidelines and the applicable law. It is required to complete the mandatory training courses and follow procedures and instructions accordingly.</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/learning-specialist-roche/69d67d9ec8e81216cd0cafdd</link><guid isPermaLink="true">http://biotechroles.com/learning-specialist-roche/69d67d9ec8e81216cd0cafdd</guid><pubDate>Wed, 08 Apr 2026 16:09:02 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Data Scientist - Product Sustainability]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>The Opportunity </b></p><p></p><p><span>At Roche, we believe that sustainability is a fundamental part of our strategy to deliver long-term value for patients, society, and the environment.</span></p><p><span>As a </span>Data Scientist for Product Sustainability<span>, you will be the key architect of data-driven transparency for our environmental footprint. Your mission is to translate high-level ambitions—such as Net Zero emissions and waste reduction—into measurable, automated, and scalable data products. Reporting to the Chapter Lead Compliance Operations, you will bridge the gap between Global Sustainability Experts and our IT/ERP backbone, ensuring that product-level environmental data is &#34;fit-for-purpose&#34; and actionable for Senior Management, R&amp;D, and Manufacturing.</span></p><p></p><p>Your Impact &amp; Responsibilities</p><ul><li><p>Data Discovery &amp; Exploration:<span> Proactively identify and map required data points across the Roche ERP backbone (SAP) and global systems. This includes transforming unstructured information into structured relational data to ensure data integrity for sustainability modeling.</span></p></li><li><p>Infrastructure Design:<span> Design and build robust integrated databases and automated pipelines, establishing logical schemas that enable consistent global reporting and decision-making.</span></p></li><li><p>Environmental Modeling:<span> Develop advanced methods to consolidate diverse data sources to measure CO2 emissions, energy usage, and waste metrics at a global product level.</span></p></li><li><p>Technical Leadership:<span> Act as the technical lead for Sustainability Tooling . Automate product &#34;scoring&#34; and creatively merge sustainability with compliance data to enable Lifecycle Assessments (LCAs).</span></p></li><li><p>Strategic Collaboration:<span> Partner with Global IT, the Data Office, and Manufacturing to align sustainability data products with Roche’s broader digital architecture using an Agile framework.</span></p></li></ul><p></p><p>Who You Are<span> </span></p><p></p><p><span>We are looking for someone who is passionate about using data to drive environmental change and who thrives in complex, collaborative environments.</span></p><ul><li><p>Experience:<span> 5&#43; years of experience in data-heavy roles. You have a proven ability to influence stakeholders and translate complex business needs into technical specifications.</span></p></li><li><p>Technical Expertise:<span> Expert proficiency in </span>SQL and Python/R<span>, with hands-on experience in </span>Cloud Data Warehousing (Snowflake/AWS)<span> and building ETL/ELT pipelines.</span></p></li><li><p>Data Storytelling:<span> Skilled in </span>Tableau<span> (or similar visualization tools) with the ability to transform complex metrics into compelling narratives that drive action.</span></p></li><li><p>Mindset:<span> You have a strong “Data Scout” mindest and excel at navigating complex corporate data landscapes and act as a bridge between Sustainability Experts and Data Engineers. You are comfortable working in </span>Agile<span> environments.</span></p></li><li><p>Academic Background:<span> University degree (Master’s or PhD) in a quantitative field (Data Science, Engineering, Mathematics, or similar).</span></p></li></ul><p><b> </b></p><p><b> </b></p>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Sant Cugat del Vallès. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/data-scientist-product-sustainability-roche/69d67d9cc8e81216cd0cafdb</link><guid isPermaLink="true">http://biotechroles.com/data-scientist-product-sustainability-roche/69d67d9cc8e81216cd0cafdb</guid><pubDate>Wed, 08 Apr 2026 16:09:00 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Be Our Future 2026]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Are you a </span><b>talented student or recent graduate</b><span> with a true passion for </span><b>Healthcare and innovation</b><span>?</span></p><p></p><p><b>Don’t miss the chance to join the world’s largest Biotech Group</b>!<span> Roche is waiting for you for an </span><b>international challenge</b> <span>that will kick-start your career!</span></p><p></p><p><span>You will live a unique competitive and educational experience where you will:</span></p><ul><li><b>Challenge Yourself</b><span>: Working intensively and collaborating with students from major Italian Universities with Roche Managers.</span></li><li><b>Make a Difference</b><span>: The most successful participants will have the opportunity to start a reimbursed 6-month internship (from July / September 2026) at our Italian Headquarters, where you will have the chance to become an integral part of product teams, working on key initiatives and business activities, immediately experiencing an agile and innovative mindset and way of working.</span></li></ul><p></p><p><b>We offer 8 internship positions</b> <span>in crucial areas such as Marketing, Digital, Finance, Controlling, Supply Chain &amp; Customer Care, Access.</span></p><p></p><p></p><p><b>Who Are We Looking for?</b></p><p><span>You are the right fit if you:</span></p><ul><li><span>Have a solid University background </span><i>(Bachelor’s already achieved and Master’s ongoing) </i><span>in: Economics and Management, Finance, Marketing, Natural Sciences, Management Engineering, Mathematics and Statistics, Data &amp; AI Analytics</span><i>;</i></li><li><span>Are fluent in both Italian (B2 level) and English (C1 level), both written and spoken;</span></li><li><span>Have an international spirit (an experience abroad like Erasmus or an internship will be considered a plus);</span></li><li><span>Already have previous internship experience (another plus);</span></li><li><span>Are curious, with a strong attraction to the Biotech sector and a multinational environment;</span></li><li><span>Are an excellent team player, have a digital attitude, and an open mind with a passion for continuous learning in agile contexts.</span></li></ul><p><br /><b>Your Selection Journey</b></p><ul><li><b>Online Challenge (Beginning of May)</b>:<span> if your application receives positive feedback, you will be invited to an individual online challenge. We will ask you to record a short video to answer a set of questions;</span></li><li><b>Recruiting Event (June 4th)</b>:<span> Finalists will be invited to our Monza Campus! This will be the perfect opportunity to meet Roche leaders and people, participate in the Assessment Center and have individual interviews on the same day*;</span></li><li><b>Internship Start (July 1st or September 1st)</b>:<span> Start dates will be defined based on personal and organizational needs. </span></li></ul><p></p><p><span>Want to find out more about our Culture and Early in Careers at Roche Italy? <a href="http://www.roche.it/storie/be-our-future-2025-il-programma-di-stage-roche" target="_blank">Discover our stories</a>!</span></p><p></p><p><span>We look forward to meeting you!</span></p><p></p><p><i>*Roche will not support travel expenses to reach the site of the event.</i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/be-our-future-2026-roche/69d67d9bc8e81216cd0cafda</link><guid isPermaLink="true">http://biotechroles.com/be-our-future-2026-roche/69d67d9bc8e81216cd0cafda</guid><pubDate>Wed, 08 Apr 2026 16:08:59 GMT</pubDate><company>Roche</company><location>Monza</location><salary>$1000-3000</salary><type>Full time</type></item><item><title><![CDATA[Internship in Innovation & Sustainability - For students in the field of Data Science, Business Analytics, Health Economics, or Digital Transformation]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Our Global Internship Programme in Innovation &amp; Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.</span></p><p></p><p><span>Are you ready to join a global network spanning 20&#43; countries, where bright minds collaborate to tackle real-world challenges in Innovation &amp; Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within?</span></p><p></p><p><span>You will contribute to the development of an AI-powered framework that automates the creation of personalized business cases for private and public diagnostics labs in Spain. The project aims to reduce a highly manual consulting process from weeks to minutes by combining market intelligence, ROI modeling, and generative AI to produce strategic narratives and financial cases tailored to individual lab profiles. Within your first 6 months, you are expected to help deliver a segmentation taxonomy of the lab ecosystem, a structured data model linking lab profiles to value dimensions, an AI-assisted prototype, validation with real-world Spanish lab profiles, and a replication guide for broader EMEA use. Your work will support Roche’s Access to Innovation and Equitable Health Outcomes priorities by helping labs adopt precision diagnostics more effectively and by quantifying the health equity impact of earlier and more accurate diagnosis. This internship offers a unique opportunity to bridge AI, healthcare consulting, and sustainability while shaping the future of precision medicine in Spain.</span></p><p></p><h3>The Opportunity</h3><p></p><ul><li><p><span>Map the Spanish private and public lab ecosystem and identify key high-volume laboratory profiles relevant for strategic engagement</span></p></li><li><p><span>Shadow the Spanish Consulting team to understand current manual workflows, data bottlenecks, and improvement opportunities</span></p></li><li><p><span>Define ROI dimensions tailored to the Spanish market, including clinical, financial, and operational value drivers</span></p></li><li><p><span>Develop AI prompts and framework logic to transform structured data into high-quality strategic narratives and business cases</span></p></li><li><p><span>Quantify health equity metrics and integrate them into the value proposition of the tool</span></p></li><li><p><span>Build and test an AI-assisted prototype for business case generation using relevant low-code or technical tools</span></p></li><li><p><span>Validate the prototype with 3–5 real-world Spanish lab profiles in collaboration with the local consulting team</span></p></li><li><p><span>Create a technical playbook to support scaling the framework across other Roche EMEA markets</span></p></li></ul><p></p><h3>Who You Are</h3><p></p><p><span>You are enrolled or have completed your Master’s or MBA studies at a university, preferably in the field of Data Science, Business Analytics, Health Economics, or Digital Transformation within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 6 months.</span></p><p></p><p>Furthermore you are</p><p></p><ul><li><p><span>Experienced or strongly interested in Generative AI and LLMs, including prompt engineering and the use of AI tools to generate professional narratives from structured data</span></p></li><li><p><span>Knowledgeable in business and ROI modeling, with an understanding of financial and operational KPIs in healthcare or laboratory settings</span></p></li><li><p><span>Proficient in data analytics and visualization tools such as PowerBI or Tableau; familiarity with Python, Streamlit, or Microsoft Power Apps is an advantage</span></p></li><li><p><span>A structured thinker with an entrepreneurial mindset who is comfortable working in ambiguity and turning complex inputs into practical solutions</span></p></li><li><p><span>A collaborative and resilient communicator who speaks Spanish fluently or at a native level and has advanced English skills</span></p></li></ul><p></p><p><span>If you meet most but not all qualifications, we still encourage you to apply.</span></p><p></p><h3>Additional information</h3><p></p><p><span>The internship is expected to start between 1 and 16 July 2026 and will last at least 6 months.</span></p><p></p><p><span>For more information about IP2TIS and to explore other opportunities within the programme, please visit go.roche.com/ip2tis_26.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-data-science-business-analytics-health-economics-or-digital-transformation-roche/69d67d9ac8e81216cd0cafd9</link><guid isPermaLink="true">http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-data-science-business-analytics-health-economics-or-digital-transformation-roche/69d67d9ac8e81216cd0cafd9</guid><pubDate>Wed, 08 Apr 2026 16:08:58 GMT</pubDate><company>Roche</company><location>Spain</location><salary>$1000-3000</salary><type>Full time</type></item><item><title><![CDATA[Internship in Innovation & Sustainability - For students in the field of Digital Health, Health Informatics, Biomedical Engineering, Healthcare IT, or Computer Science]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Our Global Internship Programme in Innovation &amp; Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.</span></p><p></p><p><span>Are you ready to join a global network spanning 20&#43; countries, where bright minds collaborate to tackle real-world challenges in Innovation &amp; Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within?</span></p><p></p><p><span>As an intern, you will contribute to a project focused on improving safety and adherence for unattended chronic anticoagulated patients through AI-driven virtual care. The project aims to design a practical integration framework that connects conversational AI with TAONET Pro, Roche’s established patient management platform, to enable structured remote follow-up and earlier intervention without disrupting existing hospital workflows. Within your first 6 months, you are expected to support the mapping of the anticoagulation monitoring workflow, assess technical and clinical integration requirements, help identify a suitable pilot healthcare center, and contribute to a 12-month strategic roadmap with relevant KPIs and partnership goals. Your work will help bridge an important care gap for patients who are at risk due to limited continuous monitoring and poor adherence. This internship offers a unique opportunity to shape how conversational AI can be embedded into routine chronic care in a clinically meaningful way.</span></p><p></p><h3>The Opportunity</h3><p></p><ul><li><p><span>Map clinical decision trees and structured workflows for remote anticoagulation monitoring using conversational AI</span></p></li><li><p><span>Define how conversational responses can be translated into structured clinical data within TAONET Pro</span></p></li><li><p><span>Assess the technical and clinical integration requirements between TAONET, external conversational AI solutions, and hospital systems</span></p></li><li><p><span>Analyze existing healthcare data flows and interoperability needs to support a feasible integration approach</span></p></li><li><p><span>Develop a strategic roadmap including implementation phases, KPIs, and partnership goals for an integrated pilot</span></p></li><li><p><span>Prepare presentation materials and pitch decks to support stakeholder discussions and pilot alignment</span></p></li><li><p><span>Conduct market research and support the selection of a candidate healthcare center for pilot testing</span></p></li><li><p><span>Facilitate collaboration between Roche teams, clinical stakeholders, and external AI partners to support pilot preparation</span></p></li></ul><p></p><h3>Who You Are</h3><p></p><p><span>You are enrolled or have completed your Master’s studies at a university, preferably in the field of Digital Health, Health Informatics, Biomedical Engineering, Healthcare IT, or Computer Science with a strong interest in the healthcare sector within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 6 months.</span></p><p></p><p>Furthermore you are</p><p></p><ul><li><p><span>Experienced or strongly interested in strategic planning, KPI design, and the development of pilot roadmaps in healthcare or digital health settings</span></p></li><li><p><span>Knowledgeable about the healthcare ecosystem, including hospital workflows, clinical stakeholders, and the digital health or AI landscape</span></p></li><li><p><span>Comfortable with healthcare IT concepts such as EHR or HIS systems, APIs, and interoperability, and able to act as a bridge between technical and clinical stakeholders</span></p></li><li><p><span>Skilled in creating impactful presentations and communicating complex ideas clearly and persuasively</span></p></li><li><p><span>Fluent or native in Spanish and have advanced English skills</span></p></li></ul><p></p><p><span>If you meet most but not all qualifications, we still encourage you to apply.</span></p><p></p><h3>Additional information</h3><p></p><p><span>The internship is expected to start between 1 and 16 July 2026 and will last at least 6 months.</span></p><p></p><p><span>For more information about IP2TIS and to explore other opportunities within the programme, please visit go.roche.com/ip2tis_26.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-digital-health-health-informatics-biomedical-engineering-healthcare-it-or-computer-science-roche/69d67d9ac8e81216cd0cafd8</link><guid isPermaLink="true">http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-digital-health-health-informatics-biomedical-engineering-healthcare-it-or-computer-science-roche/69d67d9ac8e81216cd0cafd8</guid><pubDate>Wed, 08 Apr 2026 16:08:58 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Procurement Analytics and Insights Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>This role is based in the Global Procurement function, which supports Roche’s goal of bringing innovative solutions to patients through business and supplier partnerships. We act as the bridge between Roche business functions and our suppliers, delivering value through productivity, speed, risk management, sustainability, innovative solutions, and streamlined buying experiences. </p><p></p><p><b>What is Analytics, Governance &amp; Enablement?</b></p><p>Our team is focused on enabling a best-in-class procurement organization through co-creating, delivering, and owning such topics and data insights, procurement governance, performance, and capability building. Within the analytics area, we strive to connect and work across GP to unlock the power of data to drive insights and decision-making for procurement and our customers.</p><p></p><h3><b>The Opportunity:</b></h3><p>We are seeking a highly skilled and motivated business analyst to join our Analytics &amp; Insights team within Global Procurement. The successful candidate will manage a diverse group of stakeholders, ensuring the delivery of high-quality ad-hoc analytics and insights related to procurement operations data and performance reporting. The role demands strong, soft skills, advanced data analytics capabilities, and extensive experience in stakeholder and project management.</p><p></p><h3><b>Your Key Responsabilities:</b></h3><ul><li><h3>Manage and coordinate analytics projects and deliverables, ensuring timely delivery and adherence to project objectives.</h3></li><li><p>Document and prioritize requests, implement, and manage project plans, including timelines, deliverables, risk management, issues escalation, and resource allocation.</p></li><li><p>Serve as the primary liaison between the Analytics team and internal stakeholders, understanding and addressing their needs for procurement operations and performance data.</p></li><li><p>Develop and maintain strong stakeholder relationships, manage expectations, and communicate clearly.</p></li><li><p>Act as a domain knowledge and subject matter expert in procurement data, providing input, advice, and know-how on data availability, analytics, visualization, data analysis, usage approaches, and best practices.</p></li><li><p>Analyze complex procurement operations data, developing, overseeing, and improving analytics deliverables and generating actionable insights to support GP and Roche in understanding and improving operational effectiveness and uptake.</p></li><li><p>Ensure all analytics outputs are accurate, reliable, and delivered in a user-friendly format.</p></li><li><p>Foster a collaborative team environment, promoting knowledge sharing and continuous improvement.</p></li></ul><h3></h3><h3><b>Who you are:</b></h3><p></p><p>You are a passionate, experienced professional in analytics and data insights with a focus on project management and a background in agile environments. </p><ul><li><p>You hold a Master&#39;s degree in business management, data science/analytics, finance, or a related field and at least 7 years of progressive experience in analytics, data science, or a related field.</p></li><li><p>You have proven experience as an analyst within a procurement operations or supply chain analytics environment.</p></li></ul><ul><li><p>You have advanced proficiency in analytical software, techniques, and tools (e.g., SAS, R, Python, SQL, Tableau, Power BI).</p></li></ul><ul><li><p>You have demonstrated experience translating business problems into analytical solutions using data modeling techniques, with high attention to detail and commitment to quality.</p></li></ul><ul><li><p>You have strong influencing and presentation skills, can translate data into actionable insights, and have the ability to convey complex information and meaningful messages to both technical and non-technical stakeholders.</p></li></ul><ul><li><p>You have exceptional organizational and prioritization skills, with the ability to manage multiple tasks and projects simultaneously.</p></li><li><p>You have proven ability to collaborate effectively, deliver outcomes, and have agility in adapting to changing priorities in a fast-paced environment.</p></li><li><p>You have excellent business-level fluency in English and demonstrated proficiency in communication, negotiation, and resolving conflicts in a global environment. </p></li></ul><p></p><p>Preferred:</p><ul><li><p>Exceptionally qualified applicants with relevant experience but without a Master&#39;s degree are also encouraged to apply. </p></li></ul><ul><li><p>You have a deep understanding of core procurement activities and have practical experience with processes, data,  and systems  (e.g., SAP Ariba, Coupa), especially those related to data and advanced analytics.</p></li><li><p>You have an understanding of data management and systems (e.g. Snowflake).</p></li></ul><ul><li><p>You have an understanding of data governance and compliance considerations.</p></li><li><p>You have certifications related to project management (e.g., PMP, PMI-ACP)</p></li></ul><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/procurement-analytics-and-insights-specialist-roche/69d67d9ac8e81216cd0cafd7</link><guid isPermaLink="true">http://biotechroles.com/procurement-analytics-and-insights-specialist-roche/69d67d9ac8e81216cd0cafd7</guid><pubDate>Wed, 08 Apr 2026 16:08:58 GMT</pubDate><company>Roche</company><location>Madrid</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Global Head of Strategic Planning and Business Operations (SPBO)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Who We Are:</b> </p><p><span>At Roche, we are passionate about transforming patients’ lives, and we are bold in both decision and action - we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Roche is strongly committed to a diverse and inclusive workplace. We strive to build teams that represent a range of backgrounds, perspectives, and skills. Embracing diversity enables us to create a great place to work and to innovate for patients. </span></p><p><span>At Roche Diagnostics Global Operations, our employees produce reagents and instruments that help diagnose disease and impact the lives of people all over the world. Across our global manufacturing network and our supply chain hubs, more than 9,000 employees are working to ensure the timely delivery of world-leading,  high-quality products for all Diagnostics Business Areas, fulfilling the Roche purpose of “doing now what patients need next”. </span></p><p></p><p><b><span>Position Summary:</span></b></p><p><span>As the Global Head of Strategic Planning and Business Operations (SPBO), you serve as a high-impact architect of the Global Operations division, shaping long-term strategic direction and driving operational excellence. This role is the cornerstone for delivering innovative solutions and cultivating a high-performing, collaborative culture aligned with the organization’s broader diagnostics strategy. As a member of the Global Operations Leadership Team (GOLT), you will oversee critical functions and ensure seamless daily execution while steering the long-term roadmap. Crucially, this role centralizes key resources and strategic capabilities requiring you to deliver at a global scale with high accountability.</span></p><p></p><p></p><h1><span>Your main responsibilities:</span></h1><p></p><p><u><b><span>Leadership:</span></b></u></p><ul><li><p>Visionary and Strategic Leadership:<span> You combine a bold long-term vision with an entrepreneurial mindset, prioritizing sustainable global impact over short-term gains while focusing on innovation and the broader competitive landscape.</span></p></li><li><p>Authenticity and Integrity:<span> You build trust and organizational credibility through transparent communication, genuine engagement, and unwavering ethical principles.</span></p></li><li><p>High-Performance Culture and Talent Development:<span> You empower global teams to thrive by unlocking potential and building a diverse, cross-functional talent pipeline for manufacturing excellence. You are a master of interpersonal dynamics, using these skills to shape influence and drive performance across the network.</span></p></li><li><p>Transformational Leadership in Ambiguity:<span> You navigate complexity with resilience and strategic problem-solving. You are expected to navigate extreme organizational complexity, using your influence to drive growth even when the path forward is not yet defined.</span></p></li><li><p>Courageous Servant Leadership:<span> You demonstrate tenacity by constructively challenging the status quo. You are able to push back when required and have the courage to communicate clear priorities, even when those decisions are difficult or unpopular.</span></p></li><li><p>Collaboration and Operational Excellence:<span> You dismantle functional silos to standardize processes across manufacturing and enabling functions, ensuring seamless integration with Supply Chain, Procurement, and External Manufacturing.</span></p></li><li><p>Systems Thinker:<span> You analyze complex global challenges with strong analytical skills, crafting integrated solutions that drive efficiency and future-readiness.</span></p></li></ul><p></p><p><u><b><span>Business &amp; Strategy:</span></b></u></p><ul><li><p>Investment Oversight:<span> As a member of the Diagnostic Investment Committee, you contribute to capital and strategic investment decisions for the entire global organization.</span></p></li><li><p>Strategic Roadmapping:<span> You develop and operationalize the 10-year strategic plan for Global Operations, including procurement, manufacturing, supply network strategies, and asset allocation. Because you hold the resources previously managed at the site level, you are responsible for ensuring these global assets meet the needs of the entire enterprise.</span></p></li><li><p>Global Representation:<span> You represent Global Operations in divisional investment committees, regulatory bodies, and overarching sustainability committees.</span></p></li><li><p>Strategic Integration:<span> You ensure that cross-functional requirements from regulatory or decision boards are seamlessly integrated into global operational workflows.</span></p></li><li><p>Digital Architecture:<span> You design and implement a robust digital strategy, including Cybersecurity, IT/OT Management, Master Data Governance, and Business Process Management.</span></p></li><li><p>Future Capability Building:<span> You are accountable for identifying and embedding critical functions such as Risk Management, Long-Term Capacity Planning, Business Continuity, and Sustainability.</span></p></li><li><p>Global Strategy Execution:<span> You lead the long-term &#34;One Network&#34; footprint, aligning business plans across the global manufacturing landscape.</span></p></li><li><p>Leadership Accountability:<span> You co-own the Global Operations strategy, acting as a key decision-maker within the executive leadership team.</span></p></li><li><p>Compliance &amp; Safety:<span> You ensure strict adherence to Safety, Health &amp; Environment (SHE) requirements and legal standards.</span></p></li><li><p>Executive Presence:<span> You represent the organization effectively to high-level internal and external stakeholders. Your ability to negotiate and influence at the executive level is a key differentiator for success in this role.</span></p></li><li><p>Innovation and Improvement:<span> You leverage healthcare trends to drive innovation, balancing cost efficiency with a culture of continuous improvement.</span></p></li><li><p>Workforce Oversight:<span> You provide strategic leadership for a global workforce of approximately 250–300 professionals.</span></p></li></ul><p></p><p><u><b><span>Continuous Improvement and Innovation:</span></b></u></p><ul><li><p>Efficiency Gains:<span> You identify and manage opportunities for cost savings and innovation across both core and enabling functions.</span></p></li><li><p>Manufacturing Technology:<span> You champion innovative practices to elevate manufacturing performance, capitalizing on the collective capabilities of the global network.</span></p></li><li><p>Data-Driven Decision Making:<span> You lead the integration of advanced analytics and digital tools to optimize processes and enhance predictive capabilities across the manufacturing network.</span></p></li></ul><p></p><p></p><h1><span>Who you are:</span></h1><p></p><p><b><span>As the Global Head of Strategic Planning and Business Operations (SPBO), you bring:</span></b></p><ul><li><p><span>Bachelor’s degree in Engineering, Manufacturing, Operations Management, or a related field (required); MBA or advanced degree (Master’s/Ph.D.) is highly preferred.</span></p></li><li><p><span>15&#43; years of progressive experience in manufacturing, operations, or technology management, specifically within healthcare, pharmaceuticals, or highly regulated industries.</span></p></li><li><p><span>Proven senior leadership of multi-site or global operations, with a track record of implementing strategies that deliver significant enterprise value.</span></p></li><li><p><span>A strong background in production, quality assurance, operational excellence (Lean/Six Sigma), and regulatory compliance.</span></p></li><li><p><span>Proven success in financial management, cost optimization, and mitigating operational risk in complex, global environments.</span></p></li><li><p><span>The ability to negotiate, influence without authority, and collaborate across a matrixed organization. You must be comfortable being the &#34;final word&#34; on resource allocation for the global network.</span></p></li><li><p><span>Alignment with a coaching-based leadership framework, focused on collaborative decision-making and developing others.</span></p></li></ul><p></p><p><b>Mindset:</b></p><p><span>Roche Operating Principles are the mindset and culture we as Diagnostics colleagues strive to adopt to help achieve our vision and realize our strategy. The Operating Principles are:</span></p><ul><li><p><span>Put patients first</span></p></li><li><p><span>Follow the science</span></p></li><li><p><span>Act as one team</span></p></li><li><p><span>Embrace differences</span></p></li><li><p><span>Accelerate learning</span></p></li><li><p><span>Simplify radically</span></p></li><li><p><span>Make impact now</span></p></li><li><p><span>Think long term</span></p></li></ul><p></p><p></p><p><i>Travel Requirements </i></p><p>As this position is a global role, high flexibility and frequent international business travel will be required</p><p><b> </b></p><p><b> </b></p>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Rotkreuz. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/global-head-of-strategic-planning-and-business-operations-spbo-roche/69d67d99c8e81216cd0cafd6</link><guid isPermaLink="true">http://biotechroles.com/global-head-of-strategic-planning-and-business-operations-spbo-roche/69d67d99c8e81216cd0cafd6</guid><pubDate>Wed, 08 Apr 2026 16:08:57 GMT</pubDate><company>Roche</company><location>Rotkreuz</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Junior Talent Acquisition Partner - German Speaker]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Are you passionate about people, communication, and making a real difference in a global organization? If you excel at coaching, building relationships, and solving complex problems, we want you! Join our People Support Solutions team as a </span><b>Junior Talent Acquisition Partner</b><span><b> </b>and leverage your expertise in human interaction to launch a career in global talent acquisition.</span></p><h2></h2><h2>The Opportunity:</h2><ul><li><p><span>Launch your career in Talent Acquisition by learning to manage the full recruiting lifecycle within a supportive global team.</span></p></li><li><p><span>Act as a key communication partner for hiring managers and senior leaders, applying your coaching and interpersonal skills to guide them through the hiring process.</span></p></li><li><p><span>Learn to conduct in-depth candidate assessments, focusing on evaluating core competencies and fit.</span></p></li><li><p><span>Manage and optimize the candidate experience, ensuring clear, consistent communication from application to offer.</span></p></li><li><p><span>Utilize advanced HR technology (Workday) to streamline recruiting activities and support crucial data management.</span></p></li><li><p><span>Collaborate closely on internal talent management efforts, including succession planning and internal mobility, applying a strategic lens to organizational needs.</span></p></li><li><p><span>Contribute to process innovation, helping us challenge the status quo and continuously improve our talent search strategies.</span></p></li></ul><p></p><p><b><span>Who You Are:</span></b></p><ul><li><p><span>Advanced language skills in<b> German and English </b>(both written and spoken) are mandatory.</span></p></li><li><p><span>Ideally 1-2  years of experience in recruitment</span></p></li><li><p><span>Bachelor’s degree in Human Resources, Business, Life Science or equivalent work experience is required.</span></p></li><li><p><span>You possess a strong customer-centric, growth, and agile mindset, thriving in ambiguous and multicultural environments.</span></p></li><li><p><span>You demonstrate proven stakeholder management and influencing skills, with the ability to manage expectations and build trust with diverse partners.</span></p></li><li><p><span>You are capable of working independently, effectively managing multiple, competing priorities, and driving toward results with a positive attitude.</span></p></li></ul><p></p><p><b><i>In exchange we provide you with:</i></b></p><ul><li><p><span>Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; training, the possibility of international assignments, internal position changes and the chance to shape your own career. </span></p></li><li><p><span>Excellent benefits: Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. </span></p></li><li><p><span>Flexibility: We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</span></p></li><li><p><span>A global inclusive community, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</span></p></li></ul><p></p><p><b><i>Please note that the position official name is</i> Talent Acquisition Partner.</b></p><p></p><p><i>Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:</i><a href="https://go.roche.com/dpn4candidates" target="_blank"><u> https://go.roche.com/dpn4candidates</u></a><span> </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/junior-talent-acquisition-partner-german-speaker-roche/69d67d99c8e81216cd0cafd5</link><guid isPermaLink="true">http://biotechroles.com/junior-talent-acquisition-partner-german-speaker-roche/69d67d99c8e81216cd0cafd5</guid><pubDate>Wed, 08 Apr 2026 16:08:57 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$32000-45000</salary><type>Full time</type></item><item><title><![CDATA[Senior Group Director, PV Quality Management]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p>At Roche, our Global Product Development Safety &amp; Risk Management (PDS) department aims to enhance healthcare for patients by elucidating and communicating the safety profile of Roche medicines to optimise their benefit-risk profile.</p><p></p><h3>The Opportunity</h3><p></p><p><span>The Senior Group Director of Pharmacovigilance Quality Management (PVQM)  provides strategic leadership, expertise and oversight for the implementation of the QMS within the global PV system and the Pharma Development Safety function.</span></p><p></p><p><span>As a member of the PVSD Leadership Team, the Senior Group Director leads the global PVQM function across Welwyn and Basel. This role integrates GxP safety knowledge with QMS expertise to support process experts across GVP, GCP, and medical device safety and is a vital enabler for GxP compliance and continued license to operate.</span></p><p></p><p><span>The Senior Group Director is responsible for providing systematic oversight of the QMS for the Roche enterprise-wide PV system, working in strategic partnership with the PD Quality function and the EU QPPV to ensure that all elements of a fully functioning QMS are in place and identifying gaps, driving strategies to close any gaps within the PDS Function.</span></p><p></p><p><span>The Senior Group Director leverages the strengths of a diverse global team and creates an inspiring environment where the PVQM team members feel empowered to take ownership of deliverables, build knowledge and deploy resources effectively, always striving for continuous improvement. </span></p><p><span>They are accountable for the implementation and functioning of defined global and/or functional process(es), including associated systems/tools, for the areas of the team&#39;s remit.</span></p><p></p><p><u>The PVQM team&#39;s remit spans the following main areas:</u></p><ul><li><p><span>The definition, collection, review and actioning of critical QMS and PV system-wide quality and compliance performance measures; </span></p></li><li><p><span>The global PV System Master File process and EU PSMF delivery; </span></p></li><li><p><span>End-to-end CAPA management of quality events within PDS (deviations/findings) </span></p></li><li><p><span>Leadership of inspection activities at the PDS level, providing strategic support and direction and managing documentation requests before and during inspections</span></p></li><li><p><span>PDS functional processes and training framework, strategy and execution</span></p></li><li><p><span>PV Business Continuity Management and for compliance risk management at the PDS level. </span></p></li></ul><p></p><p><u>Primary Responsibilities and Accountabilities:</u></p><ul><li><p><span>Leadership: Provides line-leadership for the global PVQM sub-function; coaches members to maximise potential and well-being while sustaining a climate of purpose and urgency</span></p></li><li><p><span>Strategic Direction: Responsible for defining and articulating vision and strategy for PVQM, in alignment with the overarching PVSD, PDS and wider enterprise strategies</span></p></li><li><p><span>Partners closely with the PD Quality function and EU QPPV to ensure alignment on QMS strategy, oversight of compliance and management of enterprise compliance issues and risks</span></p></li><li><p><span>Accountable for ensuring effective, timely and accurate production of the EU PMSF on a regular and ad hoc basis. Also, for ensuring there is an effective process in place for the EU and any required national PSMFs.</span></p></li><li><p><span>May be personally responsible for assuming a formal role as PDS/PVSD representative on compliance governance bodies (e.g. GXP Council representation) or deputising for the formal representative.</span></p></li><li><p><span>Resource Management: Oversees recruitment, onboarding, and deployment of PVQM resources across multiple locations based on strategic value</span></p></li><li><p><span>Stakeholder &amp; Strategy: Partners and maintains relationships with key stakeholders; anticipates future opportunities via internal/external networks. Contributes to PVSD leadership in scenario planning, prioritisation, and budget management</span></p></li></ul><p></p><p></p><h3>Who you are</h3><p></p><ul><li><p><span>You hold an advanced degree in a relevant discipline, or are a qualified health professional, with strong established experience in PV/safety, and/or Quality</span></p></li><li><p><span>A post-graduate qualification in an area relevant to PV (e.g. PV Diploma or MSc); quality management and/or business performance management/analysis (e.g. MBA; Lean Sigma certification; Quality or Project Management certification) would be highly desirable.</span></p></li><li><p><span>You are a highly developed, senior leader, with the proven ability to lead global line- or matrix- teams </span></p></li><li><p><span>You have significant business experience in areas directly relevant to PV, clinical quality management, business performance management, business analysis, process management and/or closely related disciplines, and essentially, you have a detailed understanding of QMS and associated approaches</span></p></li><li><p><span>You can apply analytical thinking to the design, implementation, review and/or delivery of complex, cross-functional processes, measures, metrics, key performance indicators and/or management information system design.</span></p></li><li><p><span>You utilise highly developed communication and influencing skills to build global collaborations and drive decisions</span></p></li></ul><p></p><p></p><h3>Location &amp; Travel Requirements</h3><p></p><ul><li><p><span>This position must be based in either Welwyn Garden City in the United Kingdom (preferably) or Basel, Switzerland. Although this can be a hybrid role, with an expectation of ongoing and sustained site presence, in compliance with local company site requirements</span></p></li><li><p><span>International business travel may be required. Typically, this will be required around 10% of the time, depending upon the site location of the jobholder and/or the requirements of the role for ongoing leadership or business project-related activities</span></p></li></ul><p></p><p>Scientific rigour and creativity, inclusive teamwork and exceptional delivery are key behaviours that drive our mission of doing now what patients need next. Together, we can be transformative.</p><p><b> </b></p><p><b> </b></p>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Welwyn. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.</span></p>]]></description><link>http://biotechroles.com/senior-group-director-pv-quality-management-roche/69d67d98c8e81216cd0cafd4</link><guid isPermaLink="true">http://biotechroles.com/senior-group-director-pv-quality-management-roche/69d67d98c8e81216cd0cafd4</guid><pubDate>Wed, 08 Apr 2026 16:08:56 GMT</pubDate><company>Roche</company><location>Welwyn</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Talent Acquisition Partner - German speaking]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Are you passionate about people, communication, and making a real difference in a global organization? If you excel at coaching, building relationships, and solving complex problems, we want you! Join our People Support Solutions team as a <b>Talent Acquisition Partner</b> and leverage your expertise in human interaction to launch a career in global talent acquisition.</p><p></p><h2>The Opportunity:</h2><ul><li><p><b>Launch your career in Talent Acquisition</b> by learning to manage the full recruiting lifecycle within a supportive global team.</p></li><li><p>Act as a <b>key communication partner</b> for hiring managers and senior leaders, applying your coaching and interpersonal skills to guide them through the hiring process.</p></li><li><p>Learn to conduct <b>in-depth candidate assessments</b>, focusing on evaluating core competencies and fit.</p></li><li><p><b>Manage and optimize the candidate experience</b>, ensuring clear, consistent communication from application to offer.</p></li><li><p><b>Utilize advanced HR technology (Workday)</b> to streamline recruiting activities and support crucial data management.</p></li><li><p>Collaborate closely on <b>internal talent management</b> efforts, including succession planning and internal mobility, applying a strategic lens to organizational needs.</p></li><li><p>Contribute to <b>process innovation</b>, helping us challenge the status quo and continuously improve our talent search strategies.</p></li></ul><p></p><p><b>Who You Are:</b></p><ul><li><p><b>Advanced language skills in German and English</b> (both written and spoken) are mandatory.</p></li><li><p><b>2-3 years</b> of experience in <b>end-to-end recruitment</b></p></li><li><p>Bachelor’s degree in Human Resources, Business, Life Science or equivalent work experience is required</p></li><li><p>You possess a <b>strong customer-centric, growth, and agile mindset</b>, thriving in ambiguous and multicultural environments.</p></li><li><p>You demonstrate proven <b>stakeholder management and influencing skills</b>, with the ability to manage expectations and build trust with diverse partners.</p></li><li><p>You are capable of working <b>independently</b>, effectively managing multiple, competing priorities, and driving toward results with a positive attitude.</p></li></ul><p></p><p><i><b>In exchange we provide you with:</b></i></p><ul><li><p><b>Development opportunities:</b> Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; training, the possibility of international assignments, internal position changes and the chance to shape your own career. </p></li><li><p><b>Excellent benefits: </b>Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. </p></li><li><p><b>Flexibility:</b> We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</p></li><li><p><b>A global inclusive community</b>, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</p></li></ul><p></p><p><i>Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:</i><a href="https://go.roche.com/budapest-data-privacy-notice-candidate" target="_blank"><u> </u></a><a href="https://go.roche.com/dpn4candidates" target="_blank"><u>https://go.roche.com/dpn4candidates</u></a> </p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/talent-acquisition-partner-german-speaking-roche/69d67d98c8e81216cd0cafd3</link><guid isPermaLink="true">http://biotechroles.com/talent-acquisition-partner-german-speaking-roche/69d67d98c8e81216cd0cafd3</guid><pubDate>Wed, 08 Apr 2026 16:08:56 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Payroll & Time Senior Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>The Payroll, Time &amp; Benefits Team is dedicated to delivering payroll, benefits, absence management, customer service, and advisory support to employees, managers, and business partners.</p><p>This team ensures end-to-end process completion, adhering to customer-focused principles and enabling Roche People Practices to support the business effectively.</p><p>As a Payroll&amp;Time Senior Specialist at Roche Italy, you will be part of the People &amp; Culture (P&amp;C) department and will join a team dedicated to end-to-end process excellence, providing advisory support to employees. You will be in charge of executing HR system data maintenance and administrative activities in a timely and accurate manner, supporting processes related to payroll, tax, social insurance, time, and local/global benefits. You will also drive continuous improvement by analyzing interactions and collaborating with other P&amp;C functions across the organization. This role requires a deep understanding of the Italian HR processes, tools, and their downstream impacts on employee lifecycle management, finance, procurement, IT, and more. Strong customer focus, communication skills, and solution orientation are crucial.</p><p></p><p><b>Your Key Responsibilities</b><br />- Expert Service Delivery: Execute complex data maintenance and administrative tasks across payroll, tax, social insurance, time, and benefits processes (local and global). you will be the “go-to” expert for troubleshooting and resolving pay and time inquiries. Troubleshoot and resolve payroll/time/benefits issues while identifying root causes.<br />- Stakeholder Partnership: Act as a bridge between P&amp;C and employees. Handle union negotiations specific to Payroll, Time &amp; Benefits activities, ensuring timely resolutions. Collaborate cross-functionally with other departments<br />- Process Orchestration: Manage and reconcile  mass upload files across all pay frequencing. Monitor and manage Workday data flows to vendors, ensuring timely processing and errors resolution.<br />- Ensure regulatory compliance with country-specific requirements.<br />- Continuous Improvement: Lead and participate in continuous improvement initiatives to optimize workflows, using ServiceNow data and KPIs to drive quality. Maintain up-to-date process knowledge and contribute to updating relevant documentation.<br />- Global Collaboration: Partner with peers across the global People Support Solutions network to ensure consistency, while coaching and onboarding more junior specialists to foster a culture of growth.</p><p><br /><b>Who You Are</b><br />You will work alongside a team that supports a diverse customer base across various functions and organizational levels.</p><p></p><p><i>Experience Required:</i><br />- 5&#43; years of payroll services experience, preferably in a Shared Service Center environment or local affiliate of a multinational company.<br />- Expertise in payroll cycles, processes, and benefits operations. Mandatory knowledge of Italian payroll context. Strong grasp of local tax and social insurance regulations. Knowledge of Workday P&amp;C processes.<br />- Proven ability to navigate matrix organizations and manage competing priorities. Excellent attention to detail and analytical skills. End-to-end accountability, understanding the big picture, as well as problem-solving and growth mindset.<br />- Advanced proficiency in Excel (e.g., pivot tables and v-lookups).<br />- Fluency in English (spoken and written); mandatory fluent knowledge of Italian language (both written and spoken)<br />- Ability to excel in ambiguous, multicultural environments while working across borders.<br /> </p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/payroll-and-time-senior-specialist-roche/69d67d97c8e81216cd0cafd2</link><guid isPermaLink="true">http://biotechroles.com/payroll-and-time-senior-specialist-roche/69d67d97c8e81216cd0cafd2</guid><pubDate>Wed, 08 Apr 2026 16:08:55 GMT</pubDate><company>Roche</company><location>Monza</location><salary></salary><type>Full time</type></item><item><title><![CDATA[People Strategy Intern]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Are you ready to dive into an immersive learning experience where you don&#39;t just observe but actively contribute to and implement vital Strategic People Initiatives? Join us in shaping the future of our organization—together!<br /><br /><b>The Opportunity</b><br />Embark on a journey to understand and contribute to transformative Strategic People Initiatives, with opportunities to support areas such as:</p><div><div><div><div><div><div><div><div><div><p><b>Employee Engagement &amp; Change Communications</b>: Co-create compelling communications and presentations that drive awareness, engagement, and alignment across initiatives.</p><ul><li><p><b>Key Talent &amp; Learning Initiatives</b>: Assist in shaping and implementing impactful programs like the Key Talent Program and RSS learning experiences, helping us build a future-ready and empowered workforce.</p></li><li><p><b>Employee Voice &amp; Experience</b>: Help us better understand how people feel and what they need through initiatives like Employee Circles and engagement survey insights.</p></li><li><p><b>Collaborate &amp; Innovate</b>: Bring your tech-savviness or creative mindset to co-design innovative, people-centered solutions. Experience with G-Suite, design tools, or automation platforms is a plus.</p></li><li><p><b>Additional Support</b>: Pitch in on a variety of initiatives and support tasks to keep our momentum going—your contributions will help shape real outcomes.</p></li></ul><p><br />We’re Looking for Someone Who:</p><ul><li><p><b>Is enrolled to a Hungarian University </b>and<b> </b>able to work at least<b> 20 hours/week</b></p></li><li><p><b>Is Curious:</b> You enjoy exploring new ideas, rethinking how things are done, and turning creativity into action.</p></li><li><p><b>Thrives on Creativity</b>: Whether you’re a wordsmith, social media enthusiast, digital design talent, or video creator, we value your flair for making ideas come alive.</p></li><li><p><b>Values Collaboration</b>: You love working in a team, value diverse perspectives, and take ownership of your contributions.</p></li><li><p><b>Communicates with Impact</b>: You express yourself clearly and confidently in English—both in writing and in conversation.</p></li><li><p><b>Is Driven and Proactive:</b> You’re self-motivated, take initiative, and approach challenges with a solutions-focused mindset.</p></li><li><p><b>Has PR or Event Management Savvy</b>: Experience or interest in public relations or event planning is a big plus.</p></li><li><p><b>Is Ready to Commit:</b> We’re looking for someone available for <b>at least 6 months, ideally a year,</b> to make the most of this experience and contribute meaningfully.<span> </span></p></li></ul></div></div></div></div></div></div></div></div></div><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/people-strategy-intern-roche/69d67d97c8e81216cd0cafd1</link><guid isPermaLink="true">http://biotechroles.com/people-strategy-intern-roche/69d67d97c8e81216cd0cafd1</guid><pubDate>Wed, 08 Apr 2026 16:08:55 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$1000-2000</salary><type>Part time</type></item><item><title><![CDATA[Internship in Innovation & Sustainability - For students in the field of Business Administration, Management, or Communications]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Our Global Internship Programme in Innovation &amp; Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.</span></p><p></p><p><span>Are you ready to join a global network spanning 20&#43; countries, where bright minds collaborate to tackle real-world challenges in Innovation &amp; Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within?</span></p><p></p><p><span>As an intern, you will contribute to a project focused on scaling sustainability expertise across Roche’s Global Operations network by transforming a static information repository into an activating digital ecosystem. The project aims to make sustainability knowledge easier to find, understand, and replicate across supply, manufacturing, and distribution by organizing community expertise into actionable tools and communication formats. Within your first 6 months, you are expected to help create an operational dashboard, develop a structured library of replicable blueprints, translate complex content into clear visual assets, and support a communication roadmap that encourages wider adoption across sites. Your work will help accelerate the shift from isolated local pilots to scalable global standards and support Roche’s broader sustainability goals across the value chain. This internship offers a unique opportunity to work at the intersection of communications, knowledge management, and sustainability transformation in a global operations environment.</span></p><p></p><h3>The Opportunity</h3><p></p><ul><li><p><span>Create an operational dashboard that visualizes key North Star goals such as SBTi progress and tender wins across sites</span></p></li><li><p><span>Develop a structured library of replicable sustainability blueprints that include validation data and cost-benefit templates</span></p></li><li><p><span>Translate fragmented documents and expert input into high-impact visual assets and interactive navigation pathways</span></p></li><li><p><span>Support the design of a communication roadmap that shifts the community of practice from information sharing to movement building</span></p></li><li><p><span>Help make site-specific sustainability pilots more discoverable, understandable, and scalable across Global Operations</span></p></li><li><p><span>Work with digital tools such as Google Sites and internal communication platforms to organize and activate content</span></p></li><li><p><span>Support project management activities that help structure community deliverables and maintain momentum</span></p></li><li><p><span>Collaborate with stakeholders across the community of practice to connect expert knowledge with practical implementation needs</span></p></li></ul><p></p><h3>Who You Are</h3><p></p><p><span>You are enrolled or have completed your studies at a university, preferably in the field of Business Administration, Communications, or a related field within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 6 months.</span></p><p></p><p>Furthermore you are</p><p></p><ul><li><p><span>Fluent in the use of digital tools such as Google Sites and internal communication media</span></p></li><li><p><span>Interested in experimenting with Roche digital tools and able to structure content in a clear and practical way</span></p></li><li><p><span>Experienced or comfortable with project management and coordinating structured deliverables</span></p></li><li><p><span>Able to translate complex information into engaging visuals and accessible communication formats</span></p></li><li><p><span>A collaborative and proactive communicator with strong English skills; additional languages are an advantage</span></p></li></ul><p></p><p><span>If you meet most but not all qualifications, we still encourage you to apply.</span></p><p></p><h3>Additional information</h3><p></p><p><span>The internship is expected to start between 1 and 16 July 2026 and will last at least 6 months.</span></p><p></p><p><span>For more information about IP2TIS and to explore other opportunities within the programme, please visit go.roche.com/ip2tis_26.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-business-administration-management-or-communications-roche/69d67d96c8e81216cd0cafd0</link><guid isPermaLink="true">http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-business-administration-management-or-communications-roche/69d67d96c8e81216cd0cafd0</guid><pubDate>Wed, 08 Apr 2026 16:08:54 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Supply Chain Quality Technical Lead - Europe & LATAM]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span> </span></p><p><span>At Roche, we are passionate about transforming patients’ lives and we are fearless in both decision and action - we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow.</span></p><p></p><p><span>Quality is a competitive advantage for Roche. It allows us to deliver high-quality products to patients, ensures our right to operate, and helps us create value through process excellence and continual improvement efforts. Quality is every patient’s right and every employee’s responsibility.  </span></p><p></p><p>As the Supply Chain Quality Technical Lead, you will be a key Quality, Affiliate and Operations interface who works to enable business ambitions.  You will facilitate solving challenging and strategic issues that have an impact on the Supply Chain network, functions, or chapters by supporting or leading global and functional, overarching initiatives. You translate operational insights into systemic improvements and strategic initiatives, leveraging your profound, cross-functional knowledge. You will be the leading technical expert providing guidance on process and key initiatives. You will work closely with Operations and Quality Leaders to collaborate across Networks, Chapters and Affiliates to deliver comprehensive and successful customer solutions. You champion our Quality Management System to innovate and improve end-to-end functionality.</p><p></p><p><span>You are a strong, visionary and catalyst leader who is ready to collaborate across the  network to deliver high quality products to customers and patients, ensures our right to operate and helps us create value through leveraging analytics, process excellence, Lean Manufacturing and continual improvement efforts.</span></p><p></p><p><span>You are someone who is ready to create an environment of innovation and collaboration.  You support the operational activities of the organization by promoting and developing a strong connectivity across the network s to ensure the organization is cohesively delivering overarching product quality strategies that leverage the chapters, networks, process excellence, and our continual improvement efforts. </span></p><p></p><p><b>You will be responsible to …</b></p><p><b>Drive business results and customer value</b></p><ul><li><p><span>Support the organization and network with a customer and patient centric mindset</span></p></li><li><p><span>Support Chapter lead  as Point of Contact &amp; ensure alignment with Technical and Sub-Chapter Leads</span></p></li><li><p><span>Responsible for  defining key objectives/ KPIs/ OKRs and ensure alignment thereof with the organization’s business strategy</span></p></li><li><p><span>Responsible for  developing a long term vision and backlog to deliver E2E value across Chapters, networks and its Squads</span></p></li></ul><p></p><p><b>Advance the work of the organization, making tradeoffs and breaking silos</b></p><ul><li><p><span>Partner with Global Operations on strategic business direction and decisions. Break down silos and improve working effectiveness as an ‘integrator’ across the organization as needed; in particular through collaboration  across the organization to resolve escalated bottlenecks and dependencies, as well as rebalance work &amp; help in line with greater strategic priorities </span></p></li></ul><p></p><p><b>Empower and enable the Network</b></p><ul><li><p><span>Decide if Squad within the network is needed; lead and moderate Squads, accountable for Squad deliverables across the organization </span></p></li><li><p><span>Enable team to take decisions in area of expertise through strong facilitation skills</span></p></li><li><p><span>Negotiate with Senior Leadership across the organization to influence decision-making.</span></p></li><li><p><span>Be the champion and advocate for Engrained Quality across the organization.</span></p></li><li><p><span>Build a culture of continuous improvement, proactively seeking and integrating feedback to refine strategies and improve processes, and model lean leadership principles.</span></p></li><li><p><span>Act as organizational change agent delivering results focused on digitization of business processes</span></p></li></ul><p></p><p><b>Enable the organization’s New Ways of Working</b></p><ul><li><p><span>Act as role-model for Agile Leadership behaviors, as well as for our culture, mindset &amp; behaviors as defined in We&#64;RocheDiagnostics</span></p></li><li><p><span>Model behaviors to support the organization’s transformation to new, more Agile Ways of Working – e.g. new decision making/governance practices, collaboration, etc.</span></p></li><li><p><span>Everything you do should contribute directly to the achievement of our Roche Ten Year ambitions, including:</span></p></li><li><p><span>a. Double patient access to novel, high-medical-value diagnostics solutions</span></p></li><li><p><span>b. Build the leading, profitable insights business</span></p></li><li><p><span>c. Improve patients’ lives via ‘OneRoche Approach’ to ecosystem in every country</span></p></li></ul><p></p><p><b>Specific job accountabilities</b></p><ul><li><p><span>Interface for escalated issues, may act as a proxy for the Chapter Lead</span></p></li><li><p><span>Can represent the Chapter in audits and inspections, contract negotiations etc by ensuring we are compliant and conform to established quality processes, standards, and regulations.</span></p></li><li><p><span>Is involved in solving unique and unprecedented problems that have an impact on the network, functions, or chapters, ensuring systemic root cause analysis and implementing robust preventive actions across the organization.</span></p></li><li><p><span>Solves challenging and strategic issues; leads global and functional overarching project teams and Squads, anticipates challenges for the organization; adds with innovative and conceptual thinking to the strategy of the E2E organization.</span></p></li><li><p><span>Acts as a coach for colleagues with less experience and helps them to develop their skills/expertise, with a focus on fostering self-reflection and connecting operational challenges to personal/professional growth.</span></p></li><li><p><span>Provides guidance and feedback across the organization k on processes and product technical knowledge.</span></p></li><li><p><span>Deliver and support implementation of reliable and efficient end- to- end business process solutions, i. e. enable faster decision making using digital solutions</span></p></li></ul><p><br /> </p><p><b>As a Chapter Technical Lead you:</b></p><ul><li><p><span>Possess profound knowledge of own area of expertise and broad knowledge of proximate areas. </span></p></li><li><p><span>Possess a highly  interdisciplinary mindset and coordination ability, a systemic, cross-functional approach to problem-solving activities and customer orientation</span></p></li><li><p><span>Bring a mix of passion, functional knowledge and customer-focus to your work to inspire, motivate and lead Squads within the network</span></p></li><li><p><span>Are committed to cross-functional collaboration  and breaking down silos to achieve the best results for the organization</span></p></li><li><p><span>Have the ability to navigate within a changing organization, maintaining objectivity, respect for differences of opinion, fairness, open communication and consensus building skill</span></p></li><li><p><span>Deliver against the GQ&amp;R North Star</span></p></li></ul><p></p><p><b>What else do you have in your toolbox: </b></p><ul><li><p><span> </span>High degree of subject matter expertise:<span>.</span></p><ul><li><p><span>Demonstrated experience and knowledge of Supply Chain Quality processes.</span></p></li><li><p><span>At least years (5) years in the Medical Device/Pharma/Biopharmaceutical industry with 3 years working in Quality, Compliance, Regulatory and/or Validation, preferred or equivalent experience. </span></p></li><li><p><span>Bachelor’s / Master degree in Life Science, Pharmacy or related subject. Advanced degree is considered an advantage.</span></p></li><li><p><span>Excellent knowledge of the European, US, China and International cGMP regulations and demonstrated ability to adequately interpret and implement quality standards.</span></p></li><li><p><span>Demonstrated experience in European, US and other relevant Health Authority inspections.</span></p></li><li><p><span>Spanish Language skills preferred.</span></p></li></ul></li></ul><p></p><p><span>As this position is part of a global organization, international business travel will be required depending upon the business location of the successful candidate and ongoing business project activities.</span></p><p></p><p><b><b>Interested? </b></b><span>Great. We’d like to hear from you! Just click that “Apply Now” button and send us your CV in English …. and anything else that you think might impress us.</span></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/supply-chain-quality-technical-lead-europe-and-latam-roche/69d67d96c8e81216cd0cafcf</link><guid isPermaLink="true">http://biotechroles.com/supply-chain-quality-technical-lead-europe-and-latam-roche/69d67d96c8e81216cd0cafcf</guid><pubDate>Wed, 08 Apr 2026 16:08:54 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Head of Marketing - Dia Affiliate]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Crafting a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>As the Head of Marketing you are responsible for shaping and leading both our organizational and marketing strategy for Roche Diagnostics in Denmark. The role focuses on driving organizational strategy, aligning it with global objectives, and ensuring sustainable business growth through effective decision-making and leading and developing a high performing marketing organization. The Head of Marketing also serves as a critical bridge between global marketing organizations and local teams, ensuring alignment and advancing Roche’s impact within the Danish healthcare market.</span></p><p></p><p><i><b><span><span><span>Key Accountabilities:</span></span></span></b></i></p><ul><li><p><span><span>Establish and implement organizational and marketing strategies that achieve our short and long term priorities and objectives.</span></span></p></li><li><p><span><span>Ensure the organization is equipped to address current and future market demands.</span></span></p></li><li><p><span><span>Represent the Danish affiliate as a member of the Affiliate Leadership Team (LT), advocating for strategic alignment at both local, subregional, regional and global levels.</span></span></p></li><li><p><span><span>Champion global brand alignment and oversee product positioning, branding, and messaging to enhance market capture.</span></span></p></li><li><p><span><span>Drive innovation through strategic experimentation while maintaining focus on sustainability and system-wide perspective.</span></span></p></li></ul><ul><li><p><span><span>Inspire and align teams toward a common vision, fostering accountability, collaboration, diversity, inclusion, and trust.</span></span></p></li><li><p><span><span>Lead with an entrepreneurial growth mindset, balancing short-term objectives with long-term outcomes.</span></span></p></li><li><p><span><span>Partner with the Head of Sales to set short-, mid-, and long-term commercial goals and cascade objectives across the organization.</span></span></p></li><li><p><span><span>Be an active member of and collaborate effectively with the Affiliate Leadership Team to ensure the affiliate’s sustainability and success.</span></span></p></li><li><p><span><span>Serve as a liaison between the global marketing organization and local teams, enabling collaboration across geographies and promoting best practices.</span></span></p></li><li><p><span><span>Evaluate and enhance local capabilities, linking initiatives to Global Academy programs.</span></span></p></li><li><p><span><span>Act as a change agent, driving the rollout of new ways of working and continuous process improvements in alignment with global standards.</span></span></p></li><li><p><span><span>Upskill, coach, and mentor individuals and teams in strategic thinking, marketing expertise, and Roche core competencies.</span></span></p></li></ul><p></p><p><i><b><span><span><span>Who you are:</span></span></span></b></i></p><ul><li><p><span><span>You hold a bachelor&#39;s degree in either business or life sciences is required; a master’s degree or higher is preferred.</span></span></p></li><li><p><span><span>You have proven experience in a marketing or strategy role within the healthcare or diagnostics industry.</span></span></p></li><li><p><span><span>You are a visionary leadership with the ability to architect strategies and catalyze teams toward shared goals.</span></span></p></li><li><p><span><span>You have strong collaboration and relationship management skills across local and international teams.</span></span></p></li><li><p><span><span>You demonstrated experience leading and developing teams (leading leaders), with strong leadership and coaching skills.</span></span></p></li><li><p><span><span>You have a strong background in developing and executing dynamic marketing strategies and operational plans.</span></span></p></li><li><p><span><span>You demonstrated the ability to influence, inspire, and foster collaboration across diverse teams.</span></span></p></li><li><p><span><span>You have a track record of identifying and driving innovative business opportunities while navigating complex organizational priorities.</span></span></p></li><li><p><span><span>You act with urgency and curiosity to take smart risks and continuously improve outcomes.</span></span></p></li><li><p><span><span>You display enterprise portfolio thinking, understanding how global strategies interplay with Danish market dynamics.</span></span></p></li><li><p><span><span>You maintain a commitment to Roche’s mission and values, championing sustainable innovations for the healthcare system.</span></span></p></li></ul><p></p><p><span><span>Join Roche to be at the forefront of innovation in healthcare and make a true difference in people&#39;s lives. Together, let’s create a healthier future.</span></span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/head-of-marketing-dia-affiliate-roche/69d67d95c8e81216cd0cafce</link><guid isPermaLink="true">http://biotechroles.com/head-of-marketing-dia-affiliate-roche/69d67d95c8e81216cd0cafce</guid><pubDate>Wed, 08 Apr 2026 16:08:53 GMT</pubDate><company>Roche</company><location>Copenhagen</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Praktikum in Quality Compliance (m/w/d) - Standort Mannheim]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p><b>Deine Abteilung</b></p><p><span>Als Pharmazeut/in im Praktikum hast Du im Rahmen des 6-monatigen Praktikantenprogramms für angehende Apotheker die Möglichkeit, einen spannenden Einblick in die pharmazeutische Industrie zu erhalten. Hierbei lernst Du die Arbeit eines Apothekers in der pharmazeutischen Industrie umfassend kennen. Außerdem wird Dir während des gesamten Praktikums ein kompetenter Ansprechpartner zur Seite stehen. </span></p><p><span>Wir sind das Team der Quality Compliance in Sterile Drug Product Manufacturing in Mannheim und treiben mit viel Engagement und Leidenschaft alle Quality Compliance Themen (u.a. Lokale Quality Management System Implementierungen und Inspektionen) voran. Wir sind aktuell 8 Quality Compliance Manager  und 1 Quality Compliance Lead und möchten Dir als Praktikant (m/w/d) einen Einblick in die lokale Umsetzung des Quality Management Systems (QMS) und das „Daily business“ eines Inspection Managements geben.</span></p><p></p><p><b>Deine Aufgaben</b></p><ul><li><p><span>Du unterstützt den German Translation Coordinator bei der Umsetzung von globalen QMS Änderungen in die deutsch sprachigen Versionen </span></p></li><li><p><span>Du unterstützt bei der Vorbereitung und Durchführung von Behörden Inspektionen und Kunden Audits  </span></p></li><li><p><span>Du bist in die Routine Arbeit des Quality Compliance Teams involviert und lernst dabei typische Aufgabengebiete eines Apothekers (gemäß AMG und AMWHV) kennen</span></p></li></ul><p></p><p><b>Dein Profil</b></p><ul><li><p><span>Du hast den zweiten Abschnitt der Pharmazeutischen Prüfung (zweites Staatsexamen) erfolgreich abgelegt und kannst gute Studienleistungen vorweisen</span></p></li><li><p><span>Entsprechend der Approbationsordnung für Apotheker möchtest Du nun die Hälfte Deines praktischen Jahrs dazu nutzen, die pharmazeutische Industrie im Bereich Qualitäts Sicherung und Compliance näher kennenzulernen</span></p></li><li><p><span>Idealerweise hast Du bereits erste praktische Erfahrungen in der Industrie gesammelt</span></p></li><li><p><span>Durch Deine strukturierte, lösungsorientierte und selbstständige Arbeitsweise begeisterst Du ebenso wie durch Dein analytisches Denken</span></p></li><li><p><span>Du hast eine schnelle Auffassungsgabe, freust Dich auf die Arbeit im Team und bringst Engagement und Eigeninitiative mit</span></p></li><li><p><span>You are proficient in English and not afraid of talking to international clients </span></p></li></ul><p></p><p><b>Deine Vorteile</b></p><ul><li><p><span>Flexible Arbeitszeiten (37,5 Stundenwoche)</span></p></li><li><p><span>2.268 € Vergütung im Monat für ein Vollzeitpraktikum &gt; 3 Monate</span></p></li><li><p><span>Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine</span></p></li><li><p><span>Fitnesszentrum auf dem Roche-Campus</span></p></li><li><p><span>Weiterbildungsmöglichkeiten und spannende Gastvorträge</span></p></li><li><p><span>Vernetzung mit anderen Praktikanten</span></p></li></ul><p></p><p><b>Deine Bewerbung</b></p><p><span>Für eine vollständige Bewerbung bitten wir Dich, einen aktuellen Lebenslauf und ein für die Stelle passendes Anschreiben hochzuladen</span>.</p><p></p><p><b>Zeitraum</b><span><b>:</b> ab sofort oder nach Vereinbarung für die Dauer von 6 Monaten</span></p><p></p><p><b><span>Wir freuen uns auf Deine Bewerbung!</span></b></p><p><b> </b></p><p><b> </b></p><h3></h3><h1>Your contact to us! With people. For people.</h1><p style="text-align:left">Do you need further support?</p><p style="text-align:left">Please have a look at our FAQs, you will find them via <a href="https://careers.roche.com/global/en/faq" target="_blank"><span><span><span><span class="WCO0">https://careers.roche.com/global/en/faq</span></span></span></span></a>.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b><span>Roche is an Equal Opportunity Employer.</span></b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/praktikum-in-quality-compliance-mwd-standort-mannheim-roche/69d67d95c8e81216cd0cafcd</link><guid isPermaLink="true">http://biotechroles.com/praktikum-in-quality-compliance-mwd-standort-mannheim-roche/69d67d95c8e81216cd0cafcd</guid><pubDate>Wed, 08 Apr 2026 16:08:53 GMT</pubDate><company>Roche</company><location>Mannheim</location><salary>$2000-2000</salary><type>Full time</type></item><item><title><![CDATA[Customer Success Specialist (Account Specialist / Account Executive / Sales Specialist) - North Luzon]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p>We advance science so that we all have more time with the people we love.</p><div><div><div><div><div><div><div><div><div><p></p></div></div></div></div></div></div></div></div></div><p><b>The Opportunity: </b></p><ul><li><p>Execute effective sales strategies and initiatives in order to achieve or exceed sales targets within your assigned territory</p></li><li><p><span>Builds a deep understanding of each customer account – its structure, organizational dynamics, influential stakeholders inside and outside the account, and their priorities, decision-makers, and product preferences</span></p></li><li><p><span><span>Oversee and ensure that statistical information such as census and pricing are provided to finance accordingly before the final proposal.</span></span></p></li><li><p><span><span>Build long-term value-based relationships by continuously uncovering customers’ changing needs, improving customer experience, anticipating new opportunities for their business in the future, and adding value through creative solutions/products</span></span></p></li><li><p><span><span>Build credibility with customers and stakeholders at different levels by demonstrating business acumen, professional expertise, confidence, and effective communication.</span></span></p></li><li><p><span><span>Identify and develop business opportunities within the area of responsibility and collaborate across teams to ensure attainment.</span></span></p></li><li><p><span><span>Present and sell products to key decision-makers and stakeholders by analyzing customer needs and proposing solutions where applicable.</span></span></p></li></ul><p></p><p><b><span><span>Others: </span></span></b></p><ul><li><p><span><span>Collaborates with team and cross-functional groups to create exceptional customer experiences. </span></span></p></li><li><p><span><span>Ensure timely implementation and execution of all business activities, which align with company policies and SOPs and follow the highest compliance standard.</span></span></p></li></ul><p></p><p><b>Who you are:</b></p><ul><li><p><span><span>Bachelor’s Degree</span></span></p></li><li><p><span><span>Medical Technologist or related fields is an added advantage.</span></span></p></li><li><p><span><span>3&#43; years of sales-related experience, preferably in IVD, medical devices, or related fields.</span></span></p></li><li><p><span><span>Relevant and proven complex sales experience is preferred</span></span></p></li><li><p><span><span>Preferably with IVD market knowledge coupled with an entrepreneurial flair, resilience and a growth mindset.</span></span></p></li></ul><p></p><p><b><span><span>Location: </span></span></b></p><ul><li><p><span><span><b>This position is based in North Luzon</b>.</span></span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/customer-success-specialist-account-specialist-account-executive-sales-specialist-north-luzon-roche/69d67d94c8e81216cd0cafcc</link><guid isPermaLink="true">http://biotechroles.com/customer-success-specialist-account-specialist-account-executive-sales-specialist-north-luzon-roche/69d67d94c8e81216cd0cafcc</guid><pubDate>Wed, 08 Apr 2026 16:08:52 GMT</pubDate><company>Roche</company><location>Philippines</location><salary>$12000-25000</salary><type>Full time</type></item><item><title><![CDATA[Internship in Innovation & Sustainability - For students in the field of Computer Science, Software Engineering, Data Science, or Data Analytics]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Our Global Internship Programme in Innovation &amp; Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.</span></p><p></p><p><span>Are you ready to join a global network spanning 20&#43; countries, where bright minds collaborate to tackle real-world challenges in Innovation &amp; Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within?</span></p><p></p><p><span>As an intern, you will contribute to GreenCoding, a project focused on scaling sustainable software engineering practices across Roche’s developer community. The project aims to implement a practical framework to measure, monitor, and optimize the carbon footprint of software development by embedding energy awareness into engineering workflows. Within your first 3 months, you are expected to help evaluate open-source green coding tools, benchmark the environmental impact of selected Roche applications, support the development of a proof of concept integrated into CI/CD pipelines, and contribute to a developer-focused toolkit with energy-efficient coding guidance. Your work will provide actionable data to support the decarbonization of Roche’s software assets and help demonstrate that digital innovation and environmental responsibility can go hand in hand. This internship offers a unique opportunity to work at the intersection of software engineering, cloud technologies, and sustainability for supporting Roche’s Net Zero ambition</span></p><p></p><p><b>The Opportunity</b></p><ul><li><p><span>Conduct a landscape analysis of open-source green coding tools such as CodeCarbon, Scaphandre, Kepler, or Carbon Aware SDKs</span></p></li><li><p><span>Perform initial carbon benchmarking of selected Roche applications to establish a baseline of digital environmental impact</span></p></li><li><p><span>Develop and implement a proof of concept integrated into CI/CD pipelines to track the energy consumption of code execution</span></p></li><li><p><span>Enable real-time visibility of energy and carbon impact for developers during software development workflows</span></p></li><li><p><span>Support the creation of a developer-centric toolkit such as an SDK or CLI with practical sustainable coding guidance</span></p></li><li><p><span>Translate complex energy and carbon metrics into actionable refactoring patterns for engineers (eg. Iteration vs. Recursion)</span></p></li><li><p><span>Help promote sustainable software engineering practices across the developer community</span></p></li></ul><p></p><p><b>Who You Are</b></p><p></p><p><span>You are enrolled or have completed your studies at a university, preferably in the field of Computer Science, Software Engineering, Data Science, or Data Analytics within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 6 months.</span></p><p></p><p><b>Furthermore you are</b></p><ul><li><p><span>Strong in modern programming languages such as Python, Java, or Go and familiar with CI/CD orchestration tools such as GitHub Actions, GitLab CI, or Jenkins</span></p></li><li><p><span>Knowledgeable about cloud resource consumption and containerized environments, for example AWS, Azure, Kubernetes, or Docker</span></p></li><li><p><span>Interested in Green IT principles such as hardware utilization, carbon intensity, and energy-aware engineering</span></p></li><li><p><span>Able to translate technical findings into practical guidance that helps others improve software efficiency</span></p></li><li><p><span>A proactive communicator with a strong sustainability mindset and fluent English skills</span></p></li></ul><p><span>If you meet most but not all qualifications, we still encourage you to apply.</span></p><p></p><p><b>Additional information</b></p><p></p><p><span>The internship is expected to start between 1 and 16 July 2026 and will last at least 6 months.</span></p><p></p><p><span> For more information about IP2TIS and to explore other opportunities within the programme, please visit go.roche.com/ip2tis_26.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-computer-science-software-engineering-data-science-or-data-analytics-roche/69d67d93c8e81216cd0cafcb</link><guid isPermaLink="true">http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-computer-science-software-engineering-data-science-or-data-analytics-roche/69d67d93c8e81216cd0cafcb</guid><pubDate>Wed, 08 Apr 2026 16:08:51 GMT</pubDate><company>Roche</company><location>Madrid</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Internship in Innovation & Sustainability - For students in the field of Data Science, Machine Learning, Business Analytics, Data Engineering, Digital Marketing Technology, or Computer Science]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Our Global Internship Programme in Innovation &amp; Sustainability (#IP2TIS) offers a unique opportunity for passionate individuals to gain hands-on experience in the pharmaceutical industry while making a positive impact on the world.</span></p><p></p><p><span>Are you ready to join a global network spanning 20&#43; countries, where bright minds collaborate to tackle real-world challenges in Innovation &amp; Sustainability? Do you want to work on impactful projects, shape the future, and drive change from within?</span></p><p></p><p><span>As an intern, you will contribute to a project that aims to transform Roche Diagnostics Spain’s digital marketing approach from reactive campaign management to a predictive, data-driven strategy. The project focuses on consolidating fragmented marketing data, identifying high-performing patterns across channels and audiences, and building an AI-powered framework that recommends more effective messaging and campaign decisions. Within your first 3 months, you are expected to support the centralization and cleaning of key marketing datasets, deliver an AI analysis report, help develop a smart campaign framework, and create scalable data and dashboarding foundations for future use. Your work will help improve commercial effectiveness, reduce digital noise, and support more relevant communication with healthcare professionals. This internship offers an exciting opportunity to combine advanced data science with real business impact in digital marketing.</span></p><p></p><p><b>The Opportunity</b></p><ul><li><p><span>Consolidate and clean marketing performance data from multiple platforms, including CRM, analytics, social media, and marketing automation tools</span></p></li><li><p><span>Analyze historical campaign performance to identify patterns across themes, target audiences, channels, and conversion KPIs</span></p></li><li><p><span>Develop a smart campaign framework using AI or machine learning to predict effective channel and messaging combinations</span></p></li><li><p><span>Document the model logic and data architecture to support scalability and long-term use within the department</span></p></li><li><p><span>Design and implement automated dashboards that visualize campaign performance, ROI, and key insights for stakeholders</span></p></li><li><p><span>Incorporate user feedback and voice-of-the-customer inputs into the predictive analysis</span></p></li><li><p><span>Build a feedback loop that captures actual campaign results and user responses to continuously improve model performance</span></p></li><li><p><span>Collaborate with marketing stakeholders to translate analytical findings into actionable recommendations for future campaigns</span></p></li></ul><p></p><p><b>Who You Are</b></p><p></p><p><span>You are enrolled or have completed your Master’s studies at a university, preferably in the field of Data Science, Machine Learning, Business Analytics, Data Engineering, Digital Marketing Technology, or Computer Science within the last 12 months and are interested in applying your knowledge in a modern working environment as part of an internship of at least 6 months.</span></p><p></p><p><b>Furthermore you are</b></p><ul><li><p><span>Experienced in collaborative data science environments and in building end-to-end data pipelines, ideally with platforms such as Dataiku</span></p></li><li><p><span>Proficient in Python or R and SQL, with experience in marketing performance analytics, CRM or marketing data ecosystems, and data extraction from platforms such as Salesforce or Adobe</span></p></li><li><p><span>Familiar with NLP approaches, data visualization tools such as PowerBI or Tableau, and basic MLOps concepts for model monitoring and retraining</span></p></li><li><p><span>A structured and proactive problem solver who can connect with existing solutions, work independently, and translate technical insights into business recommendations</span></p></li><li><p><span>Fluent in Spanish and have advanced English skills</span></p></li></ul><p></p><p><span>If you meet most but not all qualifications, we still encourage you to apply.</span></p><p></p><p><b>Additional information</b></p><p></p><p><span>The internship is expected to start between 1 and 16 July 2026 and will last at least 6 months.</span></p><p></p><p><span> For more information about IP2TIS and to explore other opportunities within the programme, please visit go.roche.com/ip2tis_26.</span></p><p><span> </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-data-science-machine-learning-business-analytics-data-engineering-digital-marketing-technology-or-computer-science-roche/69d67d93c8e81216cd0cafca</link><guid isPermaLink="true">http://biotechroles.com/internship-in-innovation-and-sustainability-for-students-in-the-field-of-data-science-machine-learning-business-analytics-data-engineering-digital-marketing-technology-or-computer-science-roche/69d67d93c8e81216cd0cafca</guid><pubDate>Wed, 08 Apr 2026 16:08:51 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Projektmanager (m/w/d) für große Automatisierungsprojekte -  Region Bayreuth, Bamberg, Nürnberg & Erlangen]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p></p><p><span>Stell Dir vor, Du bist der Architekt hinter den Kulissen, der die Vision einer vollautomatisierten Gesundheitsversorgung Realität werden lässt. Bei Roche Diagnostics treiben wir die Wissenschaft voran, damit jeder Mensch die bestmögliche Behandlung erhält. Als Projektmanager bist Du die treibende Kraft, die komplexe Laborsysteme zum Leben erweckt und so einen direkten Einfluss auf die Schnelligkeit und Präzision von Diagnosen für Millionen von Patient:innen weltweit nimmt.</span></p><h2></h2><h2>Dein neues Team:</h2><p><span>Du wirst Teil unseres Teams Field Force Workflow Solutions im Customer Service Außendienst. Wir sind eine dynamische Gemeinschaft aus Spezialist:innen, die technische Exzellenz,  Erfahrung mit Laborprozessen mit einer großen Portion Teamgeist verbindet. </span></p><h2></h2><h2>Verantwortlichkeiten | Das erwartet Dich</h2><p><span>In dieser Rolle gestaltest Du die Zukunft der Labordiagnostik durch professionelles Projektmanagement und Workflow-Optimierung:</span></p><ul><li><span>Du leitest überregionale Implementierungsprojekte für Automatisierungslösungen und behältst dabei Planung, Steuerung und Kontrolle fest im Griff.</span></li><li><span>Du koordinierst Teilprojektleiter:innen sowie externe Partner, um Projektziele termingerecht und in höchster Qualität zu erreichen.</span></li><li><span>Du steuerst die Kommunikation zu unseren Kunden und internen Stakeholdern und begleitest Veränderungsprozesse durch aktives Change Management.</span></li><li><span>Du wirkst bei technischen Installationen mit, führst Testläufe durch und trainierst Kunden, um ihre Workflows perfekt auf ihre Bedürfnisse abzustimmen.</span></li><li><span>Du analysierst abgeschlossene Projekte (&#34;Lessons Learned&#34;), optimierst unsere Prozesse und berätst Kunden als Spezialist:in für Prozessoptimierung.</span></li><li><span>Du unterstützt internationale Länderorganisationen bei der Weiterentwicklung interner Standards und Best Practices.</span></li></ul><h2></h2><h2>Qualifikationen | Das bringst Du mit</h2><p><span>Du verstehst es, Menschen für technische Innovationen zu begeistern und behältst auch in komplexen Situationen den Überblick:</span></p><ul><li><span>Du verfügst über ein abgeschlossenes Studium im Bereich Ingenieurwesen (z. B. Medizintechnik, Automatisierungstechnik, Elektrotechnik), Biologie, IT oder eine vergleichbare Qualifikation.</span></li><li><span>Du bringst fundierte Erfahrung in der Leitung komplexer Projekte sowie sichere Kenntnisse in modernen Projektmanagement-Methoden und -Tools mit.</span></li><li><span>Umfangreiche  Führungserfahrungen  in Matrix-Organisationen helfen Dir dabei, Teams zu motivieren und gemeinsam Erfolge zu feiern.</span></li><li><span>Du hast ein Verständnis für Abläufe in medizinischen Laboren und begeisterst Dich für Software- sowie Netzwerktechnik.</span></li><li><span>Du kommunizierst sicher auf Deutsch und Englisch, auch auf Management-Ebene (C-Level), und überzeugst durch ein souveränes Auftreten.</span></li><li><span>Ein Führerschein Klasse B sowie die Bereitschaft zu (internationalen) Dienstreisen und gelegentlichen Rufbereitschaften sind für Dich selbstverständlich.</span></li></ul><p></p><p><b>Soweit so gut? Es geht noch besser.</b></p><p></p><p><span>Wir bieten dir vielfältige Top-Benefits an unseren Standorten. Nur mit dir zusammen können wir das Leben von Patient:innen verbessern. Du machst Roche mit Deinem Beitrag einzigartig. Deswegen bieten wir außergewöhnliche Benefits, die Dich unterstützen, Dein Leben, Deine Finanzen und Deine Gesundheit so zu gestalten, wie Du es möchtest. Finde hier mehr heraus:</span><a href="https://go.roche.com/Kandidaten-Benefits-DE" target="_blank"><span> </span></a><a href="https://go.roche.com/Kandidaten-Benefits-DE" target="_blank"><u>https://go.roche.com/Kandidaten-Benefits-DE</u></a></p><p></p><p>Bewerbungszeitraum bis mindestens:<span> 21.04.2026</span></p><p><span>(Bewerbung möglich, solange die Stelle ausgeschrieben ist)</span></p><p></p><p><b>Deine Bewerbung</b></p><p><span>Wir bitten Dich um folgende Dokumente:</span></p><ul><li><span>Aktueller Lebenslauf oder Workday-Profil</span></li><li><span>Deine offiziellen (Bildungs-) Zeugnisse &amp; Nachweise</span></li></ul><p></p><p><span>Weitere Dokumente werden derzeit nicht zwingend benötigt. Bitte beachte vor Absendung der Bewerbung, dass im Nachgang keine weiteren Dokumente hinzugefügt werden können.</span></p><p></p><p><b>Bewirb Dich jetzt – wir freuen uns!</b></p><p></p><p><b> </b></p><p><b> </b></p><h3></h3><h1>Your contact to us! With people. For people.</h1><p style="text-align:left">Do you need further support?</p><p style="text-align:left">Please have a look at our FAQs, you will find them via <a href="https://careers.roche.com/global/en/faq" target="_blank"><span><span><span><span class="WCO0">https://careers.roche.com/global/en/faq</span></span></span></span></a>.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b><span>Roche is an Equal Opportunity Employer.</span></b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/projektmanager-mwd-fur-grosse-automatisierungsprojekte-region-bayreuth-bamberg-nurnberg-and-erlangen-roche/69d67d92c8e81216cd0cafc9</link><guid isPermaLink="true">http://biotechroles.com/projektmanager-mwd-fur-grosse-automatisierungsprojekte-region-bayreuth-bamberg-nurnberg-and-erlangen-roche/69d67d92c8e81216cd0cafc9</guid><pubDate>Wed, 08 Apr 2026 16:08:50 GMT</pubDate><company>Roche</company><location>Bavaria</location><salary>$85000-110000</salary><type>Full time</type></item><item><title><![CDATA[Supply Chain Excellence Lead]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><h3>The Opportunity</h3><p><span>The Global Supply Chain and Product Strategy Organization (PTS) seamlessly connects markets to the global manufacturing network by managing inventory, supply and replenishment planning. We orchestrate the value streams between sites and affiliates by balancing demand and supply, and ensure right first time order fulfillment and delivery of medicines across the global network. In addition, we are also accountable for product strategies, leading in the design of products and supply chain in line with go to market strategies and ensuring the health of our products.</span></p><p><span>We are an agile organization with clear accountabilities and a purpose driven culture that is built on trust and collaboration, where people are inspired to co-create solutions and develop the capabilities required to deliver our mission. The Supply Chain Insights and Performance team is newly set up within PTS with the following objectives:</span></p><ul><li><p><span>Benchmark and embed best practices in </span>E2E supply chain processes <span>through stronger orchestration across the enterprise, further accelerated by a strong focus on continuous improvement and performance management, and building capabilities where required</span></p></li><li><p><span>Accelerate </span>performance improvement<span> by actively seeking opportunities to optimize operations and eliminate inefficiencies. This is enabled by identifying challenges and opportunities from insights, proposing solutions, and supporting the change deployment across the supply chain</span></p></li><li><p><span>Establish a supply chain </span>performance management office<span> equipped with a strong Business Insights &amp; Analytics engine that defines a clear and unified vision of what good performance is, while offering insights on our opportunities to do better</span></p></li></ul><p></p><p><span>The SC Excellence Lead is a key member of this new team reporting to the </span>Head of Supply Chain Insights and Performance<span>. The role is responsible for spearheading continuous improvement initiatives and driving operational efficiency across the E2E supply chain processes.<span> </span>The successful candidate achieves this through the ability to leverage LEAN and SIX SIGMA methodologies, fostering a culture of operational excellence, innovation, and data-driven decision-making to enhance overall performance. </span></p><p></p><p><span>Your general accountability is defined by the Roche corporate directives, guidelines, and operating principles, as well as by the company’s core values and behaviors. In the particular role you will be accountable to:</span></p><ul><li><p><span>Act as an ambassador of OE/LEAN/SIX SIGMA principles to foster a culture of continuous improvement and learning, and orchestrate OE capability building across the supply chain for performance improvement</span></p></li><li><p><span>Identify and prioritize improvement opportunities, lead business performance initiatives using Lean and Six Sigma methodologies, and embed improvements in supply chain processes and systems</span></p></li><li><p><span>Develop and implement supply chain KPIs to measure and control performance across various reporting levels, defining accountability and tracking performance improvement in collaboration with Business Capability Owners</span></p></li><li><p><span>Establish strong relationships and manage conflict across the business to ensure success as an agent of change, ensuring effective cross-functional collaboration</span></p></li></ul><p></p><h3>Who you are</h3><p><span>Both skills and mindset will be critical to success in this role. Experience and expertise form an important foundation for success, but your mindset will make the difference. The successful candidate will be able to balance competing priorities across various stakeholders, identify a route of action that best serves E2E supply chain processes, and influence others to follow the desired route of action. In this role you need to balance functional priorities (yours, and those of others) with the broader enterprise priorities, and influence others to change in the service of the enterprise. A growth mindset and curiosity will be keys to success. For this position we are looking for someone with:  </span></p><ul><li><p><span>Over 10 years of professional experience in biotechnology, pharmaceutical, or related industries, with an MBA, M.Sc., or Bachelor&#39;s degree in supply chain or related field, and certifications such as APICS or Lean Six Sigma (Black belt)</span></p></li><li><p><span>Solid track record of achieving results through continuous improvement and OE/LEAN/SIX SIGMA methodologies, with the ability to apply process and system thinking to optimize operations and organizational efficiency</span></p></li><li><p><span>Proven ability to navigate cross-cultural matrix environments, negotiate and influence outcomes, and excel in both face-to-face and virtual interactions. Excellent English communication skills, with German being a plus</span></p></li><li><p><span>Goal-directed and persistent in achieving key results, holding oneself and the team accountable for commitments. Links responsibilities with the organization&#39;s mission, adapts to changing circumstances, and focuses on high-value activities</span></p></li><li><p><span>Establishes strong collaborative relationships, addresses and resolves conflicts by fostering openness and trust, and inspires others through support and encouragement. Recognizes the contributions of teammates and peers</span></p></li><li><p><span>Develop and implement business rules, procedures, and policies to ensure consistent operational performance and proactively manage risks. Define and sustain resiliency measures to maintain high service levels and anticipate, mitigate, and monitor supply chain risks</span></p></li><li><p><span>Utilize end-to-end system thinking to capture, integrate, and analyze data for process and performance optimization. Continuously assess and interpret internal and external variables impacting supply chain performance. Identify and deploy appropriate systems and technologies to achieve desired performance goals</span></p></li></ul><p></p><p><i>Are you ready to apply? We want someone who thinks beyond the job offered - someone who knows that this position can be an outstanding opportunity to craft the future of Roche.</i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/supply-chain-excellence-lead-roche/69d67d92c8e81216cd0cafc8</link><guid isPermaLink="true">http://biotechroles.com/supply-chain-excellence-lead-roche/69d67d92c8e81216cd0cafc8</guid><pubDate>Wed, 08 Apr 2026 16:08:50 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Business Digitalization Lead - Clinical Supply Chain]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche</p><p><span>You will be the architect of the Clinical Supply Chain’s digital future and the Lead of the PTDS Digital  Community. Your goal is to ensure our 2030 Strategy isn&#39;t just a document, but a lived reality powered by AI, Analytics, and Automation. You will orchestrate a community of digital enthusiasts to solve supply chain bottlenecks and manage a high-impact portfolio of ideas from inception to scale.</span></p><p></p><p><b>The Opportunity</b></p><ul><li><p>Oversee the &#34;Idea-to-Impact&#34; funnel by managing the intake, scoring, and prioritization of digital initiatives to focus on impactful projects.</p></li><li><p>Maintain a &#34;Digital Ledger&#34; that tracks project ROI and Value Realization for AI/Automation tools across the supply chain.</p></li><li><p>Collaborate with IT and business leads to ensure balanced resource allocation between quick wins and transformative projects.</p></li><li><p>Leverage deep knowledge of end-to-end clinical supply chains to identify unique opportunities beyond typical IT perspectives.</p></li><li><p>Serve as a critical liaison between business stakeholders and IT, translating supply chain needs into actionable technical requirements.</p></li><li><p>Lead the &#34;3A&#34; (AI, Analytics, Automation) community by facilitating knowledge sharing, organizing events, and scaling impactful ideas globally.</p></li><li><p>Address digital skill gaps and create learning pathways to enhance digital fluency within the organization.</p></li><li><p>Promote frontline innovation through crowdsourcing and convey the value of digital transformation using success stories to drive organizational buy-in.</p></li></ul><p></p><p></p><p><b>Who you are</b>​</p><ul><li><p>Bachelor degree in Supply Chain, Business, or technical fields (MBA/Master’s preferred).</p></li><li><p>Proven record in digital transformation or portfolio management within Life Sciences/Supply Chain</p></li><li><p>7&#43; years of experience in Clinical Supply Chain operations, including planning, manufacturing, distribution, GxP requirements, and patient delivery processes.</p></li><li><p>Skilled storyteller who can translate complex technical concepts into clear business value and engage diverse audiences effectively.</p></li><li><p>Solid knowledge of Cloud, Data Analytics, Machine Learning, and digital feasibility, ensuring focus on impactful initiatives.</p></li><li><p>Strong networking and leadership skills to inspire and engage communities, drive collaboration, and influence without formal authority.</p></li><li><p>Expertise in managing digital project lifecycles using structured methodologies like Agile or Kanban and prioritizing initiatives by business impact.</p></li></ul><p></p><p><b>Relocation benefits are not available for this posting</b>.</p>The expected salary range for this position based on the primary location of Mississauga is 136,936.00 and 179,728.50 of hiring range.  Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/business-digitalization-lead-clinical-supply-chain-roche/69d67d91c8e81216cd0cafc7</link><guid isPermaLink="true">http://biotechroles.com/business-digitalization-lead-clinical-supply-chain-roche/69d67d91c8e81216cd0cafc7</guid><pubDate>Wed, 08 Apr 2026 16:08:49 GMT</pubDate><company>Roche</company><location>Mississauga</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[IMPQ Quality Systems and Quality Strategy Implementation Lead]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>At Roche, we believe every employee can make a real difference. We are a global leader in healthcare, combining our strengths in Pharmaceuticals and Diagnostics to improve lives and advance the frontiers of science. With a history of innovation spanning over 125 years, our mission is to deliver better outcomes for more patients, faster. We foster an environment of belonging, where diverse perspectives are celebrated and where our commitment to sustainability and ethics drives everything we do. Join us in our pursuit to transform the future of medicine.</b></p><p></p><h2><u><b>The Opportunity</b></u></h2><p></p><p>As the IMPQ Quality Systems and Quality Strategy Implementation Lead, you will play a pivotal role in shaping the quality landscape of our Investigational Medicinal Products (IMP) and Cell &amp; Gene Therapy (CGT) networks.</p><ul><li><p>You will provide strategic functional leadership for the successful deployment and integration of the PT Quality Management System (QMS) across the global IMP and CGT networks.</p></li><li><p>You will act as the Quality Process Owner (QPO) for specific QMS processes, ensuring that product development and clinical supply operations remain in a constant state of inspection readiness.</p></li><li><p>You will drive the execution of the IMP Quality Strategy, overseeing high-impact strategic initiatives including compliance improvement programs and organizational transformation.</p></li><li><p>You will harmonize and standardize quality processes and systems across PTD, PTC, and REDs to ensure a consistent application of global standards across all operational touchpoints.</p></li><li><p>You will proactively identify, communicate, and manage quality and compliance risks, representing IMP Quality in the PTQ Risk Roll-Up process to safeguard our license to operate.</p></li><li><p>You will collaborate as a member of the Global IMPQ Leadership Team and an extended PTQ Leadership member to align site and functional operations with overarching corporate objectives.</p></li><li><p>You will build and maintain strong partnerships with cross-functional stakeholders to facilitate expert interpretation of QMS requirements and support the management of routine and complex quality audits.</p></li></ul><p></p><h2><u><b>Who you are</b></u></h2><p></p><p>We are looking for a visionary leader with a deep technical foundation in quality systems and the ability to influence global healthcare standards.</p><ul><li><p>You possess a Bachelor’s degree in Life Sciences, Pharmacy, or a related field, with a PhD considered a distinct advantage for this strategic level.</p></li><li><p>You bring at least 15 years of experience in the Pharmaceutical or Biopharmaceutical industry, with a minimum of ten years specifically focused on Quality, Compliance, Regulatory, or Validation.</p></li><li><p>You have demonstrated leadership excellence with at least eight years of experience in a management capacity, ideally within a complex matrix environment.</p></li><li><p>You are an expert in US, European, and International cGMP regulations, with the specialized ability to interpret and implement quality standards in early to late-stage technical development.</p></li><li><p>You possess a proven track record of managing Quality Systems and successfully leading organizations through US, European, and other relevant Health Authority inspections.</p></li><li><p>You are skilled at driving positive change and continuous improvement, utilizing your strong collaboration and influencing skills to solve complex problems across a global network.</p></li><li><p>You exhibit the professional maturity to notify Senior Management of critical regulatory issues and the accountability to deliver results that align with Roche’s core competencies.</p></li></ul><p></p><p><b>**This role is not eligible for relocation**</b></p><p></p>The expected salary range for this position based on the primary location of Mississauga is 148,568.00 and 194,995.50 of hiring range.  Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/impq-quality-systems-and-quality-strategy-implementation-lead-roche/69d67d91c8e81216cd0cafc6</link><guid isPermaLink="true">http://biotechroles.com/impq-quality-systems-and-quality-strategy-implementation-lead-roche/69d67d91c8e81216cd0cafc6</guid><pubDate>Wed, 08 Apr 2026 16:08:49 GMT</pubDate><company>Roche</company><location>Mississauga</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[PI Automation Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span> </span><span>Als PI Automation Engineer bist du im Bereich „Business Solutions“ im Circle „Pharma Engineering Solutions Drug Product“ des Standortes Basel / Kaiseraugst tätig. Die Rolle ist im Kreis Verpackung Lager Logistik angesiedelt.</span><span> </span><span> </span></p><p><span>Der Bereich „Business Solutions“ ist am Standort Basel/ Kaiseraugst verantwortlich für das Gebäude- und Betriebsingenieurwesen, das technische Qualitätsmanagement und für eine zuverlässige Störungsbehebung und Instandhaltung, inklusive dem Betreiben der erforderlichen Infrastruktur.  Des Weiteren liegt innovatives, kostengünstiges und GMP-gerechtes Planen und Umsetzen von Investitionsprojekten in unserer Verantwortung. Wir unterstützen unser Management und unsere Business Partner bei biotechnologischen, chemischen und galenischen Produktions-/ Verpackungsanlagen, Laborbauten und Administrationsbauten. </span></p><p><span>Wir bieten internen Kunden / Anlagenbetreibern in den Bereichen Forschung, Entwicklung, Launch und Marktproduktion sowie Verpackung, Lager, Logistik und professionelle Ingenieurdienstleistungen an.  </span></p><p><span>Als </span>PI Automation Engineer (w/m/d) <span>obligen dir verschiedene Aufgabengebiete, diese umfassen die Planung, Realisierung und das Betriebsengineering des Reinraum-Monitoring Systems und Anlagenanbinudngen an das PI Data Historian System von Aveva am Standort Kaiseraugst. Darüber hinaus unterstützt du unsere Business Partner bei der Ideenfindung und Konzepterstellung von neuen, innovativen Lösungen zur Gestaltung von effizienten Produktions- und Monitoringprozessen. Im Rahmen des Betriebsengineerings werden in direkter Zusammenarbeit mit den Business Partnern Umbaumassnahmen, Problemlösungen und Effizienzsteigerungen umgesetzt.</span></p><p><span>Aufträge und Projekte werden ohne Hierarchien in selbstorganisierten Fachteams mit einem rollenbasierten Arbeitsmodell abgewickelt. Dies erfordert von dir ein hohes Maß an Selbstorganisation, Weitblick und Teamspirit sowie ausgeprägte Kommunikationseigenschaften und bietet dir die Möglichkeit, sich in die Gestaltung des Arbeitsumfeldes direkt einzubringen.</span></p><p><span>Als </span>PI Automation Engineer <span>im Kreis Verpackung Lager Logistik bist du </span><span>für das Betriebsengineering und für Investitionsprojekte zuständig, welche das Implementieren und Anbinden von Reinraummonitoring und Prozessanlagen in die Roche Infrastruktur umfassen. Die zu betreuenden Anlagen verfügen über einen sehr hohen Automatisierungsgrad und sind stark untereinander bzw. mit übergeordneten IT Systemen vernetzt.</span></p><p></p><h3>Die Möglichkeit</h3><p></p><ul><li><p><span>Betriebsengineering mit dem Ziel, die Aufrechterhaltung der Produktion und des Reinraum-Monitoring Systems jederzeit zu gewährleisten (80%) Betreuung und durchführung von Konfigurationen in PI Monitoringsystemen der Firma OSIsoft (Aveva)</span></p></li><li><p><span>Kontinuierliche Optimierung der Prozessanlagen und Evaluieren, Prüfen und Empfehlen neuer Technologien</span></p></li><li><p><span>Leitung und Abwicklung von Automationsprojekten in allen Projektphasen wie Initiierung, Design und Realisierung (selbständig und mit Unterstützung von internen und externen Spezialisten) sowie proaktives Unterstützen der Kunden bei der Definition und Initiierung von Investitionsvorhaben</span></p></li><li><p><span>Zusammenarbeit mit internen Business Partnern bei Projekten, Changes und Deviations inkl. Root-Cause Analysen</span></p></li><li><p><span>Implementierung von Reinraummonitoring und Prozessanlagen in die Roche Infrastruktur</span></p></li><li><p><span>Erstellung und Abarbeitung von Testplänen für die Qualifizierung</span></p></li><li><p><span>Vertikale Anbindungen der Automationssysteme an den PI Data Historian und MES Systeme </span></p></li><li><p><span>Strategie und Aufrechterhaltung des Lifecycles von PC basierten AutomationssystemenUnterstützung unserer internen Kunden bei technischen Fragen sowie bei Behördeninspektionen</span></p></li></ul><p></p><h3><span>Wer du bist</span></h3><p></p><p><span>Du besitzt eine fundierte Grundausbildung mit abgeschlossenem Studium (FH/TU) in Automation</span><br /><span>oder Informatik oder die entsprechenden Kenntnisse sowie mind. 5 Jahre Berufserfahrung in der</span><br /><span>Automation oder Informatik, im besten Fall im Pharmaumfeld.</span><br /><span>Du bist vertraut mit der Abwicklung von Investitionsprojekten und bringst Erfahrung im Projektmanagement und Betriebsengineering im Pharmaumfeld mit.</span></p><ul><li><p><span>Du hast eine vertiefte technische Expertise von Netzwerktechnik und PI Anbindungen von Reinraummonitoring bzw. Prozessanlagen mit AVEVA PI, Rotronic Hard-und Softwarelösungen</span></p></li><li><p><span>Du bringst mehrjährige Erfahrung als Betriebsingenieur mit</span></p></li><li><p><span>Du hast Erfahrungen im Projektumfeld oder idealerweise erste Erfahrungen in der Projektleitung sowie fundierte Erfahrung im GMP- und GAMP- Umfeld</span><span><span><span> </span></span>Idealerweise kennst du dich zusätzlich auch mit EMSR-Planung und Hardware aus </span></p></li><li><p><span>Du hast Erfahrung mit Lieferantenbetreuung und scheust dich nicht, auch hier, wenn nötig, die Fachbauleitung zu übernehmen</span></p></li><li><p><span>Teamfähigkeit und sehr gute Kommunikations- und Koordinationsfähigkeiten innerhalb der Organisation sowie ein angemessener Umgang mit Stakeholdern auf allen Ebenen zeichnen dich aus</span></p></li><li><p><span>Du zeigst Bereitschaft im agilen, selbstorganisierten Arbeitsumfeld zu arbeiten und bringst die Bereitschaft zum Pikettdienst 24/7 mit </span></p></li><li><p><span>Du verfügst über sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift</span></p></li></ul><p></p><p> </p><p><span> </span><span> </span><span> </span></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/pi-automation-engineer-roche/69d67d91c8e81216cd0cafc5</link><guid isPermaLink="true">http://biotechroles.com/pi-automation-engineer-roche/69d67d91c8e81216cd0cafc5</guid><pubDate>Wed, 08 Apr 2026 16:08:49 GMT</pubDate><company>Roche</company><location>Kaiseraugst</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Talent Acquisition Associate - German speaking]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Are you passionate about people, communication, and making a real difference in a global organization? If you excel at coaching, building relationships, and solving complex problems, we want you! Join our People Support Solutions team as a </span><b>Talent Acquisition Associate</b><span> and leverage your expertise in human interaction to launch a career in global talent acquisition.</span></p><p></p><h2><b><b>The Opportunity:</b></b></h2><ul><li><p><span>Launch your career in Talent Acquisition by learning to manage the full recruiting lifecycle within a supportive global team.</span></p></li><li><p><span>Act as a key communication partner for hiring managers and senior leaders, applying your coaching and interpersonal skills to guide them through the hiring process.</span></p></li><li><p><span>Learn to conduct in-depth candidate assessments, focusing on evaluating core competencies and fit.</span></p></li><li><p><span>Manage and optimize the candidate experience, ensuring clear, consistent communication from application to offer.</span></p></li><li><p><span>Utilize advanced HR technology (Workday) to streamline recruiting activities and support crucial data management.</span></p></li><li><p><span>Collaborate closely on internal talent management efforts, including succession planning and internal mobility, applying a strategic lens to organizational needs.</span></p></li><li><p><span>Contribute to process innovation, helping us challenge the status quo and continuously improve our talent search strategies.</span></p></li></ul><p></p><p><b><span>Who You Are:</span></b></p><ul><li><p><span>Advanced language skills in<b> German and English </b>(both written and spoken) are mandatory.</span></p></li><li><p><span>You bring 2&#43; years of senior experience in a people-focused field (e.g., teaching, therapy, counseling, psychology, advanced customer relationship management, or translation etc.) where strong communication and coaching were central</span></p></li><li><p><span>Bachelor’s degree in Human Resources, Business, Life Science or equivalent work experience is required.</span></p></li><li><p><span>You possess a strong customer-centric, growth, and agile mindset, thriving in ambiguous and multicultural environments.</span></p></li><li><p><span>You demonstrate proven stakeholder management and influencing skills, with the ability to manage expectations and build trust with diverse partners.</span></p></li><li><p><span>You are capable of working independently, effectively managing multiple, competing priorities, and driving toward results with a positive attitude.</span></p></li></ul><p></p><p><b><i>In exchange we provide you with:</i></b></p><ul><li><p><b><span>Development opportunities: </span></b><span>Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; training, the possibility of international assignments, internal position changes and the chance to shape your own career. </span></p></li><li><p><b><span>Excellent benefits:</span></b><span> Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. </span></p></li><li><p><b><span>Flexibility: </span></b><span>We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</span></p></li><li><p><b><span>A global inclusive community, </span></b><span>where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</span></p></li></ul><p></p><p><b><i>Please note that the position official name is</i><b> Talent Acquisition Partner.</b></b></p><p></p><p><b><i>Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:</i><a href="https://go.roche.com/dpn4candidates" target="_blank"><u> https://go.roche.com/dpn4candidates</u></a><span> </span></b></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/talent-acquisition-associate-german-speaking-roche/69d67d90c8e81216cd0cafc4</link><guid isPermaLink="true">http://biotechroles.com/talent-acquisition-associate-german-speaking-roche/69d67d90c8e81216cd0cafc4</guid><pubDate>Wed, 08 Apr 2026 16:08:48 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$22000-32000</salary><type>Full time</type></item><item><title><![CDATA[Corporate Affairs & Access Assistant]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>La Oportunidad:</b></p><p><span>Funciones y Responsabilidades principales</span></p><ul><li><span>Coordinar la participación, realización de Simposios, workshops, eventos propios locales y regionales.</span></li><li><span>Dentro de las normas regulatorias y de compliance vigentes, coordinar la logística relacionada con los participantes y con el evento mismo (tales como: contacto con disertantes, traslados, alojamiento, contrato, pago de honorarios, etc.)</span></li><li><span>Organizar eventos internos del área, tanto dentro como fuera de las oficinas.</span></li><li><span>Dar soporte en la planificación de la alocación de las principales inversiones.</span></li><li><span>Dar seguimiento a los presupuestos de las áreas de Policy, Corporate Affairs. Monitorear los desvíos en el acumulado trimestral/anual e informar a las gerencias.</span></li><li><span>Realizar el control/análisis de gastos en SAP, generar reportes e informes. Enviar las provisiones mensuales al departamento de Finanzas. Controlar el WBS (work breakdown structure: seguimiento de gastos imputados a cada uno de los productos).</span></li><li><span>Seleccionar gimmicks (obsequios), materiales promocionales y no promocionales.</span></li><li><span>Dar Soporte en la adaptación del branding internacional a los requisitos nacionales, slogan y frases promocionales acordes al mercado argentino.</span></li><li><span>Recibir solicitudes de becas y donaciones (G&amp;D), seguimiento de la aprobación de las mismas, evaluación de presupuestos relacionados, confección de carta de aceptación, carga en el sistema SAP y control de ejecución del pedido.</span></li><li><span>Participar en el armado y la validación de Contratos para diferentes actividades en conjunto con Depto. de Legales, para que puedan ser firmados en tiempo y forma, dentro de los lineamientos regulatorios y de compliance vigentes.</span></li><li><span>Evaluar y tramitar alta de Proveedores, según los procedimientos establecidos por el departamento de compras de la compañía.</span></li><li><span>Cargar requerimientos en SAP, realizar el seguimiento de la aprobación correspondiente y el posterior control del cumplimiento de la compra.</span></li><li><span>Recibir facturas y recibos, verificar los datos de los mismos, ingresar los documentos en SAP y realizar el seguimiento del circuito de pago de dichas facturas para evitar demoras.</span></li><li><span>Cargar materiales y eventos en las plataformas Veeva, Rome, Epicx.</span></li></ul><p></p><p><b>Quien Eres:</b></p><p><br /><b><span>Requerimientos del Puesto:</span></b></p><ul><li><span>Experiencia: 2 - 3 años experiencia en puestos similares</span></li><li><span>Formación: Nivel Terciario o Universitario completo o en curso (pref. Comunicación, Ciencias Políticas, Marketing, Administración o Publicidad)</span></li><li><span>Idiomas: Inglés (Nivel Avanzado)</span></li><li><span>Herramientas Informáticas: Manejo de Office (Word, Excel y Power Point), Google, SAP</span></li><li><span>Otros: Comunicación fluida y transparente, Capacidad de organización, Capacidad de trabajo en equipo, Flexibilidad (en horarios y disponibilidad para viajar), Autonomía, Proactividad, Apertura a los cambios constantes, sentido de la urgencia, Capacidad para cumplir con deadlines en tiempo y forma.</span></li></ul><p><span>#LI-DNI</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/corporate-affairs-and-access-assistant-roche/69d67d90c8e81216cd0cafc3</link><guid isPermaLink="true">http://biotechroles.com/corporate-affairs-and-access-assistant-roche/69d67d90c8e81216cd0cafc3</guid><pubDate>Wed, 08 Apr 2026 16:08:48 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$18000-28000</salary><type>Full time</type></item><item><title><![CDATA[Senior Director/Chapter Lead, Software Development]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><span>The Pathology Lab Development consists of four key capabilities:  Assay and Reagent Development, System Development and Integration, Hardware and Software Development.   </span></p><p></p><p><span>The Senior Director/Chapter Lead, Software Development will lead the software Chapter and its Subchapters for key business areas within the Pathology Customer Area and acts as a functional leader for Software Engineering. Leads people, development tools/technology, and processes for Software Development, Test &amp; Validation, and Release Management of Roche&#39;s Pathology Lab Software products. Successfully operates within a matrix organization and provides functional expertise to project teams, technology development teams, and software product care teams (legacy software products). Ensures the timely development of superior-quality products in a highly disciplined and design-controlled environment.</span></p><p></p><p><b><b>The Opportunity </b></b></p><ul><li><p><span>Provides vision, expertise, and leadership to lead the Software Chapter tactically and strategically.</span></p></li><li><p><span>Develops and maintains skills and technical expertise required to support Roche’s new product development initiatives; builds, mentors, and develops employees across teams.</span></p></li><li><p><span>Acts as a critical functional leader partnering with Lifecycle Team (LCT) leadership on forecasting, budgeting, and prioritizing the right employees on the right project to maximize the overall effectiveness.</span></p></li><li><p><span>Acts as a key leader of the Product Development senior leadership team and is a crucial contributor in strategic planning meetings with all LCTs.</span></p></li><li><p><span>Owns relationships with and directs the activity of external software development service providers within Roche and with external consulting groups to build the breadth and depth of software skill sets needed to be world-class.</span></p></li><li><p><span>Monitors work to ensure quality and continuously promote Quality First Time.</span></p></li><li><p><span>Manages staff; provides staff with coaching, training, and opportunities to develop skills. And gives ongoing, constructive, timely feedback on performance and progress toward goals and expectations.</span></p></li></ul><p><b><span>​</span></b></p><p><b><b>Who You Are:  </b></b></p><ul><li><p><span>You have a BS in Software Engineering or a relevant engineering discipline. </span></p></li><li><p><span>You have 15 years of experience in relevant development experience  </span></p></li><li><p><span>You have 7 years of leadership experience. </span></p></li><li><p><span>You have prior leadership experience in a software development function.</span></p></li><li><p><span>You have a proven ability to work on extremely complex problems where analysis of situations or data requires an evaluation of intangible variables. Uses innovation where little or no precedence exists.</span></p></li><li><p><span>You have demonstrated best practices in software development principles, practices, and methodology.</span></p></li><li><p><span>You have leadership skills in managing multidisciplinary teams in a matrix environment.</span></p></li><li><p><span>You are effective at developing and building effective teams and driving results.</span></p></li><li><p><span>You have the ability to resolve conflicts and adapt to change.</span></p></li><li><p><span>You have the ability to make/execute authoritative decisions and account for the results.</span></p></li><li><p><span>You have experience with projects that required activity/milestone achievement to launch the product.</span></p></li><li><p><span>You have a proven ability to present and discuss data, present alternative action plans (and consequences), and clearly communicate recommendations to any level of the organization while challenging senior management as required.</span></p></li><li><p><span>You have expertise in Information Security and Data Privacy Fundamentals.</span></p></li><li><p><span>You have experience using the Scaled Agile Framework (SAFe) or similar Agile development approaches.</span></p></li></ul><p></p><p><b><b>Preferred Qualifications: </b></b></p><ul><li><p><span>You have an MS degree in Software Engineering or a relevant discipline</span></p></li></ul><p></p><p><span>The expected salary range for this position is 192,900-358,300 based on the primary location of Tucson, AZ. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. </span></p><p></p><p><span>This position also qualifies for the benefits detailed here:</span><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u> Benefits</u></a></p><p></p><p><span>Relocation benefits are available for this position</span></p><p></p><p><b><b> </b></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/senior-directorchapter-lead-software-development-roche/69d67d8fc8e81216cd0cafc2</link><guid isPermaLink="true">http://biotechroles.com/senior-directorchapter-lead-software-development-roche/69d67d8fc8e81216cd0cafc2</guid><pubDate>Wed, 08 Apr 2026 16:08:47 GMT</pubDate><company>Roche</company><location>Tucson</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Account Executive - Near Patient Care]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b>Account Executive - Near Patient Care</b></p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p><b>The Opportunity</b></p><p>As an Account Executive - Near Patient Care, you will be responsible for total account management and selling the full Roche Point of Care portfolio. Specifically focused on Respiratory, Sexually Transmitted Disease and Women’s Health molecular point of care testing as well as hospital-based glucose testing throughout the Integrated Health Network continuum of care. This includes a range of selling skills in multiple segments of care such as the Hospital Laboratory environment, Urgent Care, Emergency Department and associated physician office labs. As part of the Roche Point of Care portfolio you will also be positioning IT solutions that will connect instruments across the IHN continuum of care in both inpatient and outpatient settings. This position requires conducting presentations and business reviews to potential customers thereby demonstrating in-depth knowledge of our product line, as well as relevant healthcare/industry trends including related products or services.</p><p></p><p><b>​</b><b>This is a field based role - the territory is Northern New Jersey. You must live within 50 miles of the territory.</b></p><p></p><p><b>Job Facts</b></p><ul><li><p>Generates new customer demand and expansion within the IHN segment across the full portfolio of Near Patient Care products. Penetrates large, complex IHN accounts to gain access to and favor with all buying influences and key decision makers.</p></li><li><p>Demonstrates strong clinical and financial acumen with ability to listen and understand customer needs and align Roche products within the IHN segment.</p></li><li><p>Translates customers’ defined business/technical and personal goals into internal action while balancing key business priorities and goals.</p></li><li><p>Balances the need to advocate for customers while also demonstrating the drive and ability to negotiate and achieve strong business results for Roche</p></li><li><p>Develops territory-specific executional strategies to consistently meet and exceed sales targets.</p></li><li><p>Works cross functionally with internal colleagues and peers to share information and best practices while remaining actively involved in industry/customer organizations that impact business.</p></li><li><p>Conducts system demonstrations &amp; presentations where applicable; POC Committee Meetings, Trade Shows, VIPS, etc.</p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p>Bachelor’s degree or equivalent experience</p></li><li><p>3&#43; years relevant sales or equivalent experience</p></li><li><p>Participation in an approved accelerated development, fellowship or rotational program may be considered in lieu of experience</p></li><li><p>Demonstrates strong oral and written communication skills including making impactful presentations.</p></li></ul><p></p><p><b>Preferred Qualifications</b></p><p>• Preferred experience in the Point of Care diagnostic and Integrated Health Network space.</p><p></p><p><i>Relocation is not available for this position.</i></p><p></p><p><i>The expected salary range for this position based on the primary location of New Jersey is $91,000-169,000.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.</i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/account-executive-near-patient-care-roche/69d67d8fc8e81216cd0cafc1</link><guid isPermaLink="true">http://biotechroles.com/account-executive-near-patient-care-roche/69d67d8fc8e81216cd0cafc1</guid><pubDate>Wed, 08 Apr 2026 16:08:47 GMT</pubDate><company>Roche</company><location>New Jersey</location><salary>$110000-160000</salary><type>Full time</type></item><item><title><![CDATA[Patient Journey Partner, Ophthalmology (GTA)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p></p><p><b>Patient Journey Partner, Ophthalmology</b></p><p><b>Location:</b> This is an Ontario-based position covering the Greater Toronto Area (GTA). Frequent travel is a core requirement of this position.</p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p></p><p><b>Join Our Mission in Ophthalmology!</b></p><p>At Roche, we don’t just build networks; we build bridges to better patient outcomes. As a Patient Journey Partner, you will embody our core values of Integrity, Courage, and Passion to reshape the Ophthalmology landscape. </p><p>We are looking for a visionary who has the courage to challenge the status quo and the integrity to build deep, trust-based partnerships with our stakeholders.</p><p>Your relentless passion for networking won&#39;t just open doors, it will fuel your curiosity to uncover the &#34;why&#34; behind customer needs. By fostering authentic connections, you will be the catalyst that unlocks innovative collaborations, ensuring that every partnership we forge translates into a meaningful impact on patients&#39; lives.</p><p></p><p></p><p><b>The Opportunity</b></p><ul><li><p>You are acting as the key liaison between stakeholders and Roche, leveraging your influence to foster impactful relationships, trust, and collaboration within the Ophthalmology sector, thereby driving meaningful connections and mutual growth. </p></li><li><p>You are ensuring appropriate use of Roche&#39;s products, sharing benefits and risks with Health Care Practitioners in a truthful and balanced manner</p></li><li><p>You are collaborating with cross-functional colleagues to prioritize and plan account activities based on team priorities</p></li><li><p>You are partnering across functions to address stakeholder needs, prioritize solutions, and evaluate progress</p></li><li><p>You are implementing an omnichannel approach to engage stakeholders with Roche&#39;s offerings</p></li><li><p>You are participating in a peer-to-peer coaching and mentorship model within self-organizing teams</p></li><li><p>You are embracing self-directed learning and experiential growth as part of the working culture</p></li></ul><p></p><p></p><p><b>Who you are</b></p><ul><li><p>You hold an University degree in scientific, economic, or business field</p></li><li><p>You bring 7&#43; years&#39; of experience in life sciences or healthcare sector</p></li><li><p>You have the ability to build strong relationships with external stakeholders and deliver tailored solutions</p></li><li><p>You demonstrate an understanding of fast-paced, competitive market dynamics and the Canadian healthcare system</p></li><li><p>You prove expertise in stakeholder engagement and partnering, including leading cross-functional teams and leveraging digital tools for improved stakeholder experience.</p></li><li><p>You have the ability to travel depending on the business need</p></li></ul><p></p><p></p><p><b>Preferred</b></p><ul><li><p>Advanced degree</p></li><li><p>You have 3&#43; years experience in pharmaceutical sales or key account management, Ophthalmology preferred</p></li></ul><p></p><p></p><p>Relocation benefits are not available for this posting.</p>The expected salary range for this position based on the primary location of Mississauga is 136,936.00 and 179,728.50 of hiring range.  Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.<p></p><p>We use artificial intelligence to screen, assess or select applicants for this role.</p><p></p><p>This posting is for an existing vacancy at Hoffmann-La Roche Ltd.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/patient-journey-partner-ophthalmology-gta-roche/69d67d8fc8e81216cd0cafc0</link><guid isPermaLink="true">http://biotechroles.com/patient-journey-partner-ophthalmology-gta-roche/69d67d8fc8e81216cd0cafc0</guid><pubDate>Wed, 08 Apr 2026 16:08:47 GMT</pubDate><company>Roche</company><location>Mississauga</location><salary>$85000-110000</salary><type>Full time</type></item><item><title><![CDATA[Pasante de Patient Services]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Buscamos un estudiante con una fuerte vocación de servicio para formarse en nuestra área de Patient Services. El objetivo es que el pasante aprenda a acompañar a las personas en su tratamiento, funcionando como un facilitador entre el paciente, su médico y su cobertura de salud. Adicionalmente, aprenderás las tareas administrativas relacionadas a los servicios a pacientes.</p><p></p><p><b>La Oportunidad:</b></p><ul><li><p>Realizas el seguimiento telefónico de los pacientes, brindando escucha activa y resolviendo dudas relacionadas al área.</p></li><li><p>Explicas de forma sencilla el alcance de nuestras soluciones para educar y apoyar al paciente.</p></li><li><p>Orientas al paciente en sus trámites con obras sociales para gestionar y superar las barreras de acceso.</p></li><li><p>Colaboras en la identificación de las necesidades del paciente para asegurar su adherencia y cuidado continuo.</p></li><li><p>Coordinas el soporte al paciente integrando el trabajo de las áreas médicas, de acceso y operativas de la compañía.</p></li><li><p>Aprendes y ejecutas las tareas y circuitos administrativos vinculados a los servicios a pacientes.</p></li></ul><p></p><p><b>Quién eres:</b></p><ul><li><p>Eres estudiante de carreras de Salud (Enfermería, Farmacia, Psicología, Medicina, Nutrición) o Administración de Salud.</p></li><li><p>Te caracterizas por tu empatía, calidez y fuerte vocación de servicio.</p></li><li><p>Demuestras responsabilidad y compromiso para manejar información sensible y cuidar la continuidad del tratamiento del paciente.</p></li><li><p>Tienes ganas de aprender y un gran interés por desarrollarte en servicios que tienen al paciente como centro.</p></li><li><p>Cuentas con disponibilidad para cumplir uno de los siguientes horarios: de 9 a 13 hs o de 13 a 17 hs.</p></li></ul><p></p><p>No se ofrecen beneficios de reubicación para este puesto.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/pasante-de-patient-services-roche/69d67d8ec8e81216cd0cafbf</link><guid isPermaLink="true">http://biotechroles.com/pasante-de-patient-services-roche/69d67d8ec8e81216cd0cafbf</guid><pubDate>Wed, 08 Apr 2026 16:08:46 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$0-1000</salary><type>Part time</type></item><item><title><![CDATA[Pasante de Medical Information]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Como Pasante de Información Médica, te sumarás a un equipo dinámico enfocado en generar un impacto positivo y real en los profesionales de la salud y los pacientes.</p><p></p><p><b>La Oportunidad:</b></p><ul><li><p>Aprendes y brindas soporte operativo al área de Información Médica, colaborando en la gestión de consultas de profesionales de la salud y pacientes bajo la supervisión del equipo.</p></li><li><p>Colaboras en la recepción y derivación de consultas que ingresan por teléfono, plataforma web y correo electrónico, utilizando las guías de procedimientos globales y locales.</p></li><li><p>Asistes en la búsqueda de información científica para responder consultas externas, garantizando en todo momento la calidad y la precisión de los datos brindados.</p></li><li><p>Identificas y das curso a los reportes de eventos adversos o reclamos de calidad, asegurando el estricto cumplimiento de los tiempos regulatorios establecidos.</p></li><li><p>Participas y ofreces soporte administrativo en las tareas de reconciliación de eventos en conjunto con las áreas de seguridad y calidad.</p></li><li><p>Brindas soporte administrativo y participas activamente en el Programa de Soporte a Pacientes, marcando una diferencia en su experiencia.</p></li><li><p>Registras meticulosamente las interacciones y consultas de nuestros clientes en los sistemas globales corporativos.</p></li><li><p>Colaboras en la gestión de artículos científicos mientras te familiarizas con las normativas de derechos de autor vigentes.</p></li></ul><p></p><p><b>Quién eres:</b></p><ul><li><p>Eres estudiante de carreras de grado relacionadas con la salud, tales como Farmacia, Bioquímica, Medicina, Biotecnología, Biología o disciplinas afines.</p></li><li><p>Cuentas con excelentes habilidades de comunicación y demuestras una gran capacidad de escucha activa.</p></li><li><p>Posees una fuerte empatía para el trato con los pacientes, complementada con una estricta atención al detalle.</p></li><li><p>Tienes un nivel de inglés intermedio o avanzado que te permite leer de manera fluida las guías globales y utilizar los sistemas informáticos.</p></li></ul><p></p><p>Los beneficios de reubicación no están disponibles para esta vacante.</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/pasante-de-medical-information-roche/69d67d8ec8e81216cd0cafbe</link><guid isPermaLink="true">http://biotechroles.com/pasante-de-medical-information-roche/69d67d8ec8e81216cd0cafbe</guid><pubDate>Wed, 08 Apr 2026 16:08:46 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$0-1000</salary><type>Part time</type></item><item><title><![CDATA[Field Product Manager (focusing in CoreLab portfolio)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Join Roche Diagnostics Solutions (RDS) as a<b> </b></span><b>Field Product Manager</b><span> to drive the success of our diagnostic portfolio, specifically our CoreLab solutions. You will advance sales through our industry-leading systems, assay menus and digital solutions designed for the entire healthcare continuum.</span></p><p></p><p><span>This position balances strategic planning tasks with sales duties. You will engage customers to generate new business, map their needs using your market expertise, and adapt your competencies to new technologies as our portfolio evolves. To succeed, you must thrive in a changing environment, co-creating solutions with customers and colleagues through skillful reflection and the use of various digital tools. You will be reporting to the Roche Diagnostics Solutions (RDS) Chapter Lead. </span></p><p></p><p><b>The Opportunity</b></p><ul><li><p><b>Achieve Results</b>: <span>Deliver sales and profit targets. Contribute actively to tender shaping. Prepare and execute product launches. Drive portfolio profitability and value positioning, including contributing to local pricing strategies.</span></p></li><li><p><b>Strategy &amp; Planning</b>: <span>Create and drive local marketing strategy, planning, and execution in alignment with the global strategy for both upcoming product launches and on-the-market solutions for CoreLab portfolio. Perform accurate local customer segmentation and develop commercial strategies for CoreLab products and solutions. Define priorities and key areas of growth such as our high-medical value assays. Identify new market opportunities for CoreLab portfolio based on customer and competitive data analysis. Manage and monitor product-specific local competitor activities and develop actions to address them. Ensure effective execution and prioritization across the CoreLab portfolio while incorporating various digital solutions into the offering. <br />Maintain a long-term view to maximize the impact of the portfolio. </span></p></li><li><p><b>Promotion</b>: Use local market information to prioritize customer segments and define high-impact, multi-channel strategies and tactics that drive the adoption of our solutions. Lead local marketing efforts by prioritizing campaigns across various channels, congresses, and events. Ensure consistency in messaging and branding for all customers.</p></li><li><p><b>Collaboration</b>: Work in close collaboration with internal stakeholders, including also Medical, Regional, and Global colleagues.</p></li><li><p><b>Field Engagement</b>:Travel and engage frequently to maintain strong relationships and gain first-hand market insights from customers and stakeholders. Shape the market by utilizing your expertise and stakeholder engagement.</p></li></ul><p><br /><b>Who You Are</b></p><ul><li><p><b>Education</b>: Master’s degree or higher in a biomedical field.</p></li><li><p><b>Experience</b>: 5–10 years in sales and marketing from a regulated environment with a customer-oriented mindset. A proven track record of delivering sales and profit targets, with specific expertise in tender shaping and value positioning.</p></li><li><p><b>Marketing Expertise</b>: Proven experience in developing and executing local marketing strategies that align with global objectives, covering both new product launches and the management of existing portfolios.<br />Demonstrated ability to perform accurate customer segmentation and contribute to high-impact, multi-channel marketing tactics to drive product adoption.</p></li><li><p><b>Technical Expertise</b>: Solid background in a routine diagnostics laboratory; specific knowledge of the CoreLab portfolio (Immunochemistry, Clinical Chemistry, LabCoagulation, Mass Spectrometry) is highly valued. We prefer candidates who understand fully automated clinical laboratory environments.</p></li><li><p><b>Skills</b>: Evidence of strong strategic thinking, decisive communication, planning and organizational skills, e.g. through successfully leading strategic initiatives. </p></li><li><p><b>Ways of working</b>: Consistent record of building collaborative relationships with peers and teams, helping cross-functional teams address strategic opportunities and solve problems across the organization. </p></li><li><p><b>Communication</b>: <span>Fluent in Finnish and English; willing to travel as required.</span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/field-product-manager-focusing-in-corelab-portfolio-roche/69d67d8dc8e81216cd0cafbd</link><guid isPermaLink="true">http://biotechroles.com/field-product-manager-focusing-in-corelab-portfolio-roche/69d67d8dc8e81216cd0cafbd</guid><pubDate>Wed, 08 Apr 2026 16:08:45 GMT</pubDate><company>Roche</company><location>Finland</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Healthcare System Partner Puebla]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Healthcare System Partner (HSP)</b></p><p><span><span>Los sistemas de salud se están transformando gracias a la innovación y al empoderamiento de los pacientes</span></span><span>. </span><span><span>Como Especialista en Sistemas de Salud (HSP) en Roche, actúas como un líder que trabaja estrechamente con el ecosistema de salud local</span></span><span>. </span><span><span>Construyes relaciones estratégicas con legisladores, reguladores y pagadores para anticipar barreras de acceso y co-crear soluciones que brinden mejores resultados de salud a más pacientes, con mayor rapidez y de forma sostenible</span></span><span>.</span></p><div></div><p></p><p><b>La oportunidad:</b></p><ul><li><p><span><span>Colabora con los actores del sistema de salud para impulsar la innovación y entregar valor a la sociedad</span></span><span>.</span></p></li><li><p><span><span>Identifica, mapea y coordina a los integrantes del ecosistema, siendo el punto de contacto estratégico entre ellos y Roche</span></span><span>.</span></p></li><li><p><span><span>Gestiona y prioriza recursos para implementar soluciones que aceleren los resultados en el entorno local</span></span><span>.</span></p></li><li><p><span><span>Actúa como catalizador y guía interna y externamente, reuniendo la experiencia de diversas áreas de la red global</span></span><span>.</span></p></li><li><p><span><span>Mantiene un entendimiento profundo de las tendencias, patrones y gobernanza del sistema de salud para influir en decisiones estratégicas</span></span><span>.</span></p></li><li><p><span><span>Desafía y moldea el sistema de salud para asegurar resultados de salud sostenibles e impactantes</span></span><span>.</span></p></li><li><p><span><span>Aprovecha las herramientas digitales en beneficio de todos los actores del entorno sanitario</span></span><span>.</span></p><div></div><p></p></li></ul><p><b>Quién eres:</b></p><ul><li><p><span><span>Cuentas con un título universitario en Ciencias, Economía o Administración de Empresas</span></span><span>.</span></p></li><li><p><span><span>Posees un conocimiento profundo del Sistema de Salud, sus procesos y gobernanza</span></span><span>.</span></p></li><li><p><span><span>Tienes experiencia comprobada liderando equipos multifuncionales y gestionando proyectos complejos.</span></span></p></li><li><p><span><span>Demuestras una mentalidad emprendedora con habilidades excepcionales de escucha activa y redes estratégicas</span></span><span>.</span></p></li><li><p><span><span>Eres un profesional autogestionado, capaz de asumir riesgos y aprender rápidamente en entornos dinámicos</span></span><span>.</span></p></li><li><p><span><span>Te comunicas eficazmente en el idioma local y posees un dominio profesional del inglés</span></span><span>.</span></p><div></div><p></p></li></ul><p><b>Preferencias:</b></p><ul><li><p><span><span>Estudios avanzados (Maestría o MBA) en Ciencias de la Salud o Política de Salud</span></span><span>.</span></p></li><li><p><span><span>Entendimiento práctico de metodologías de innovación digital o certificaciones especializadas</span></span><span>.</span></p></li><li><p><span><span>Experiencia en comercialización y en la creación de experiencias excepcionales para el cliente</span></span><span>.</span></p></li><li><div><p><span>Viaje el 30% del tiempo.</span></p></div><p></p></li></ul><p><span><span>Relocation benefits are not available for this posting</span></span><span>.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/healthcare-system-partner-puebla-roche/69d67d8dc8e81216cd0cafbc</link><guid isPermaLink="true">http://biotechroles.com/healthcare-system-partner-puebla-roche/69d67d8dc8e81216cd0cafbc</guid><pubDate>Wed, 08 Apr 2026 16:08:45 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Design Lead Pathology]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b>Design Lead Pathology</b></p><p><span>At Roche, we are passionate about transforming patients’ lives, and we are bold in both decision and action - we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Roche is strongly committed to a diverse and inclusive workplace. We strive to build teams that represent a range of backgrounds, perspectives, and skills. Embracing diversity enables us to create a great place to work and to innovate for patients.</span></p><p></p><p><b><span>The Opportunity:</span></b></p><p><span>For our Global Diagnostics Customer Experience &amp; Solution Design Chapter (DIA CXSD), we are looking for a motivated Design Lead, who is experienced in managing and connecting across several design projects and is passionate to contribute to the transformation of user and customer experience in healthcare. In this exciting role, you will have the opportunity to bring in your design management, design and research expertise as well as to prove your leadership and solution/CX mindset.</span></p><p></p><p><span>Additionally, Design Leads shape and manage Design Operations capabilities, support strategic direction and evolving needs within the chapter.</span></p><p></p><p><b><span>Key Roles &amp; Responsibilities:</span></b></p><ul><li><p><span>Set project design scope, timeline, and key milestones, acting as the liaison between the business, R&amp;D and design</span></p></li><li><p><span>Supervise the delivery across multiple project teams, conducting periodic alignment meetings with the teams, and maintaining a close relationship with business and R&amp;D</span></p></li><li><p><span>Lead the team to synthesize insights and map CX/solution/product opportunities</span></p></li><li><p><span>Apply systems thinking and understand technical architectures and cross-platform data/workflow dependencies</span></p></li><li><p><span>Build rapport, emanate confidence, and inspire when advising business, R&amp;D and design teams</span></p></li><li><p><span>Incorporate business objectives alongside customer and user needs into the design process throughout the work</span></p></li></ul><p></p><p><b><span>Who You Are:</span></b></p><ul><li><p>Minimum 5&#43; years of relevant experience with a Bachelor’s degree in Design (medical background a plus)</p></li><li><p><span>Inspiring, hands-on leader with a strong track record in design delivery, operations, and team management</span></p></li><li><p><span>Proven expertise in healthcare product and service design, including research and insights analysis</span></p></li><li><p><span>Experience successfully bringing products or services to market<br />Familiar with highly regulated environments (e.g., Pharmaceuticals, Medical Devices, IVD)</span></p></li><li><p><span>Strong ability to influence within complex, matrixed organizations</span></p></li><li><p><span>Confident engaging and collaborating with diverse stakeholders</span></p></li><li><p><span>Excellent written and verbal communication skills in English</span></p></li></ul><p></p><p><b>Location:</b> This position is based in Tucson, AZ.</p><p>Relocation benefits are not available for this job posting. </p><p></p><p>The expected salary range for this position based on the primary location of Tucson, AZ is $114,400 - $212,400.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/design-lead-pathology-roche/69d67d8bc8e81216cd0cafbb</link><guid isPermaLink="true">http://biotechroles.com/design-lead-pathology-roche/69d67d8bc8e81216cd0cafbb</guid><pubDate>Wed, 08 Apr 2026 16:08:43 GMT</pubDate><company>Roche</company><location>Tucson</location><salary>$140000-190000</salary><type>Part time</type></item><item><title><![CDATA[Patient Value Partner Hematology]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>The Patient Value Partner is responsible for the engagement of all activities related to the brand assigned through different levels of their life cycle, covering all specific steps associated to patient’s journeys.</p><p></p><p><b>Your Responsibilities</b></p><ul><li><p>Provides input to the Chapter Head for strategy definition, but also its periodic adaptation, depending on the changes that have occurred in the external environment or whenever it is needed.</p></li><li><p>Takes the proper actions to implement the brand strategy in order to maximize the use of the brand, for relevant patient population, achieving the Company objectives.</p></li><li><p>Collaborates in the Chapter to ensure the relevance of his/her brand strategies and the achievement of overall goals.</p></li><li><p>Working cross-functional with other Chapters.</p></li><li><p>Initiates the budget proposals and participates in the pre-budget discussions.</p></li><li><p>Responsible for the resource allocation within the product promotion activities for assigned brands.</p></li><li><p>Identifies and recommends new channels for product promotion.</p></li><li><p>Develops and maintains high standard of product knowledge and updated information refers to all matters related to the product promotion and commercialization.</p></li><li><p>Actively supports the field force on product information, key messages and company’s strategies regarding the assigned brands.</p></li><li><p>Actively participation in allocated Squad, with higher expertise and knowledge on the brand/disease area, but also with overall perspective on all activities driven inside the squad.</p></li><li><p>Proactive market research and analysis covering trends, competitiveness, innovative tools, specific to customers promotion or/and from other agile markets.</p></li><li><p>KOL’s engagement with solid product knowledge, consultancy over the product space and interactions.</p></li><li><p>Active presence and contribution to products comities internal and external.</p></li></ul><p></p><p><b>Who You Are</b></p><ul><li><p>You hold a University degree in natural sciences, Medical, Pharmacy, Chemistry, or Biology. Business related degree would be an advantage</p></li><li><p>You built more than 5 years of work experience in marketing (product management)/or similar in the Pharmaceutical industry</p></li><li><p>You built in-depth knowledge of competitive activity in the pharmaceutical/ biotechnology industry</p></li><li><p>You built excellent product and marketing knowledge within the hematology and hemophilia therapy areas</p></li><li><p>Proven track record of effective decision-making, and proven financial analysis, planning and reporting capabilities. Moreover, advanced knowledge of Microsoft Office suite: Excel, Word, and PowerPoint</p></li><li><p>You are strategic thinker who brings analytical and problem-solving skills, scenarios and risks/opportunities mind set to growth products perspective</p></li><li><p>Advanced organisational and time management skills, and ability</p></li><li><p>You are a self-motivated team player who excels in cross-functional collaboration</p></li><li><p>You have excellent communication skills and high sensitiveness to local conditions</p></li><li><p>You are creative, curious, and flexible at adopting new methodologies and exploring new business areas</p></li><li><p>You are fluent in English and Romanian languages, both written and spoken</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/patient-value-partner-hematology-roche/69d67d8ac8e81216cd0cafba</link><guid isPermaLink="true">http://biotechroles.com/patient-value-partner-hematology-roche/69d67d8ac8e81216cd0cafba</guid><pubDate>Wed, 08 Apr 2026 16:08:42 GMT</pubDate><company>Roche</company><location>Romania</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Pharmazeutischer Assistent Robocell (m/w/d)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><h3><b>Unsere Pharma-Vision</b></h3><p><span>Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen. Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt. So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen:  20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen.  Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele Patienten große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten. Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar</span><i> </i><u>#WIRGEMEINSAM</u><i> </i><span>in SDPM! ​</span></p><p></p><h3><b>Verantwortlichkeiten | Das erwartet Dich</b></h3><p><span>Als <b><i>Pharmazeutischer Assistent Robocell (m/w/d)</i></b> unterstützt Du den Asset Lead im Rahmen der folgenden Aufgaben:</span></p><ul><li><p><span>Du unterstützt den Leiter der Herstellung (m/w/d) gemäß AMWHV und stellst die GMP-gerechte Dokumentation im Betrieb sicher.</span></p></li><li><p><span>Du verantwortest den papierbasierten und elektronischen Chargen-Review, sowie die konzeptionelle Erstellung der GMP-Dokumente in deutscher und englischer Sprache.</span></p></li><li><p><span>Du bist Ansprechperson für interne und externe Reklamationen und</span> <span>Changes, Abweichungen und CAPAs werden von Dir erstellt und bearbeitet.</span></p></li><li><p><span>Du bist für die Erstellung, Aktualisierung, Schulung und Kontrolle der ordnungsgemäßen</span> <span>Durchführung von Arbeitsanweisungen (SOPs) und Herstellanweisungen auf Papier</span> <span>(HEAs) und elektronisch (MRTs) verantwortlich.</span></p></li><li><p><span>Du nimmst eigenverantwortlich an behördlichen Inspektionen teil und stellst die nachhaltige Umsetzung von Maßnahmen sicher.</span></p></li><li><p><span>Du treibst die kontinuierliche Verbesserung voran, indem Du Projekte zur Effizienzsteigerung und Einführung innovativer Technologien leitest.</span></p></li></ul><p></p><h3><b>Qualifikationen | Das bringst Du mit</b></h3><p></p><ul><li><p><span>Du hast ein erfolgreich abgeschlossenes Studium der Pharmazie oder eine vergleichbares naturwissenschaftliches Studium und verfügst über mehrjährige Berufserfahrung in der Pharmaindustrie (idealerweise im Bereich aseptische Produktion, Qualitätskontrolle oder Qualitätssicherung).</span></p></li><li><p><span>Du hast ein sehr gutes GMP-Verständnis und sehr gute Kenntnisse der gesetzlichen Vorschriften (AMG, AMWHV) und bringst fundierte Erfahrung in der Begleitung behördlicher Inspektionen mit.</span></p></li><li><p><span>Du besitzt Erfahrungen in der Bearbeitung von (hoch) komplexen Abweichungen als Owner inkl. Durchführung von Root-Cause-Analysen (RCA), Trouble Shootings und daraus resultierenden Maßnahmen</span></p></li><li><p><span>Du hast Freude daran, Prozesse aktiv zu gestalten – sei es durch die Analyse und Implementierung von CAPAs und Changes oder die präzise Erstellung von Herstellvorschriften (HEA/MRT).</span></p></li><li><p><span>Vertiefte Kenntnisse in Lean-Methoden helfen Dir dabei, Effizienz und Qualität harmonisch zu vereinen.</span></p></li><li><p><span>Du überzeugst mit deinen verhandlungssicheren Sprachkenntnissen und einem sehr guten Ausdrucksvermögen in Deutsch und Englisch (in Wort und Schrift).</span></p></li><li><p><span>Du besitzt ein hohes Maß an Teamfähigkeit, Verantwortungsbereitschaft, Flexibilität und</span> <span>nimmst eine Vorbildfunktion wahr.</span></p></li><li><p><span>Die Fähigkeit zu interdisziplinärem Denken, Konfliktbewältigung sowie Integrations- und</span> <span>Überzeugungsfähigkeit runden dein Profil ab.</span></p></li></ul><p></p><p><b>Diese Stelle ist auf 2 Jahre befristet.</b></p><p></p><p><b><b>Soweit so gut? </b></b>Es geht noch besser. Wir bieten dir vielfältige Top-Benefits an unseren Standorten. Nur mit dir zusammen können wir das Leben von Patient:innen verbessern. Du machst Roche mit Deinem Beitrag einzigartig. Deswegen bieten wir außergewöhnliche Benefits, die Dich unterstützen, Dein Leben, Deine Finanzen und Deine Gesundheit so zu gestalten, wie Du es möchtest. Finde hier mehr heraus:</p><p><a href="https://go.roche.com/Kandidaten-Benefits-DE" target="_blank"><u>https://go.roche.com/Kandidaten-Benefits-DE</u></a></p><p></p><p><b><b>Deine Bewerbung </b></b></p><p>Wir bitten Dich um folgende Dokumente: </p><ul><li><p>Aktueller Lebenslauf oder Workday-Profil</p></li><li><p>Deine offiziellen (Bildungs-) Zeugnisse &amp; Nachweise </p></li></ul><p>Weitere Dokumente werden derzeit nicht zwingend benötigt. Bitte beachte vor Absendung der Bewerbung, dass im Nachgang keine weiteren Dokumente hinzugefügt werden können.</p><p><b><b>Bewirb Dich jetzt – wir freuen uns!</b></b></p><p><b> </b></p><p><b> </b></p><h3></h3><h1>Your contact to us! With people. For people.</h1><p style="text-align:left">Do you need further support?</p><p style="text-align:left">Please have a look at our FAQs, you will find them via <a href="https://careers.roche.com/global/en/faq" target="_blank"><span><span><span><span class="WCO0">https://careers.roche.com/global/en/faq</span></span></span></span></a>.</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b><span>Roche is an Equal Opportunity Employer.</span></b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/pharmazeutischer-assistent-robocell-mwd-roche/69d67d8ac8e81216cd0cafb9</link><guid isPermaLink="true">http://biotechroles.com/pharmazeutischer-assistent-robocell-mwd-roche/69d67d8ac8e81216cd0cafb9</guid><pubDate>Wed, 08 Apr 2026 16:08:42 GMT</pubDate><company>Roche</company><location>Mannheim</location><salary>$45000-55000</salary><type>Full time</type></item><item><title><![CDATA[Global Business Process Specialist - Travel & Expense (1 Year Fixed-Term)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>As a <b>Travel &amp; Expense GBPS</b>, you will be part of the Roche Services &amp; Solutions (RSS) Business Process Management (BPM) organization. In this role you will actively contribute to the implementation of the end-to-end BPM strategy for corporate Travel &amp; Expense (T&amp;E) management. You are responsible for the global, cross divisional, state-of-the-art process design and you work in close collaboration with stakeholders from Finance, Procurement &amp; IT, to ensure fit-for-purpose solutions.<br /><br /><i>Please note that this is a 1 year fixed-term role with a possibility to extend for another year.</i><br /><br /><b>The Opportunity</b></p><p></p><p>Your main responsibilities include:</p><ul><li><p>Actively contribute to the implementation of the E2E BPM strategy, according to guardrails set by the E2E Global Business Process Owner (GBPO) and Global Business Process Managers (GBPMs)</p></li><li><p>Deliver lean cross-divisional processes &amp; solutions, with maximum standardization and harmonization</p></li><li><p>Ensure documentation of process requirements, implementation through guidelines and Standard Operating Procedures (SOPs)</p></li><li><p>Drive efficiencies and improvements (incl. automation) across E2E business process, RSS Operations, affiliates and IT.</p></li><li><p>Manage prioritization, justification and realization of change requests and initiatives in line with the strategic roadmap, with support of the GBPMs and other Global Business Process Specialists</p></li><li><p>Contribute to partner projects, providing advice and guidance</p></li><li><p>Supporting the development of agile ways of working in teams and the organization</p></li></ul><p></p><p><b>Who you are</b></p><p></p><p>A successful candidate will have a customer orientated (agile) and design thinking mindset. Completed degree in Business, Finance or related field and a minimum 2-3 years of professional experience in Finance, Procurement or IT.</p><p>You demonstrated your ability of working in cross-functional projects (preferably transformation of nature) and cross-functional teams.</p><p></p><p>For this position, you bring the following qualifications:</p><ul><li><p>Solid background in Finance or Procurement with proven Business Process Management skills.</p></li><li><p>Excellent analytical and problem-solving abilities, leading to effective decision-making.</p></li><li><p>Strong influencing and communication skills (written and verbal in English is essential) for working with international teams and complex stakeholder networks.</p></li><li><p>Familiarity with upstream Finance &amp; Procurement processes and systems is a plus.</p></li><li><p>Good understanding of End-to-End (E2E) travel &amp; expense processes and systems, along with technical expertise in SAP ERP &amp; Concur.</p></li></ul><p></p><p><i><b>In exchange we provide you with:</b></i></p><ul><li><p>Development opportunities: Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; training, the possibility of international assignments, internal position changes and the chance to shape your own career. </p></li><li><p>Excellent benefits &amp; flexibility:  competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. We also ensure flexibility, to help you find your balance: home office is a common practice (2 office days/week on average).  We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</p></li><li><p>A global diverse community, where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</p></li></ul><p></p><p><i>Please read the Data Privacy Notice for further information about how we handle your personal data related to the recruitment process:</i><a href="https://go.roche.com/budapest-data-privacy-notice-candidate" target="_blank"><u> https://go.roche.com/budapest-data-privacy-notice-candidate</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/global-business-process-specialist-travel-and-expense-1-year-fixed-term-roche/69d67d89c8e81216cd0cafb8</link><guid isPermaLink="true">http://biotechroles.com/global-business-process-specialist-travel-and-expense-1-year-fixed-term-roche/69d67d89c8e81216cd0cafb8</guid><pubDate>Wed, 08 Apr 2026 16:08:41 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Business Support - Digital (Intern)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><h2>The Position</h2><p></p><p>Typically studying in a field related to Analytics, Data Science, or Engineering, the <b>Business Support - Digital Intern</b> will be assigned a variety of tasks relevant to site <b>Operational Excellence and Digital projects</b>. Reporting to the <b>Head of Digitalisation</b>, the objective of this assignment is for the intern to practically apply academic studies in a Roche setting while learning more about the organization&#39;s technical operations.</p><p></p><p>The intern will support site initiatives on key activities such as <b>Predictive Analytics</b>, AI-related projects, and the design of <b>End User Manufacturing applications</b>. Assignments typically involve supporting the activities of regular employees, such as entry-level data modeling, reporting, and coordinating technical troubleshooting. The length of the internship will vary according to business needs.</p><p></p><h2>Key Responsibilities</h2><ul><li><p><b>Digital Translation &amp; Project Support</b>: Act as a digital translator to drive the implementation of key digital use cases and contribute to manufacturing technology initiatives.</p><p></p></li><li><p><b>Requirements &amp; Documentation</b>: Define and manage user requirements and backlogs; author detailed <b>User Requirement Specifications (URS)</b> and design complex process or data flow maps.</p><p></p></li><li><p><b>Data Analytics</b>: Utilize existing data pipelines to create <b>Multivariate Data Analysis (MVDA)</b> models and combine raw datasets to refine data models.</p><p></p></li><li><p><b>Application Development</b>: Support the development of manufacturing prototypes (such as on the <b>Low Code platform</b>) and assist with site-specific applications like Autoclave or Manufacturing Yield tools.</p><p></p></li><li><p><b>Validation &amp; Quality</b>: Support <b>Computerised System Validation (CSV)</b> during system qualification activities and ensure high standards of data quality.</p><p></p></li><li><p><b>Stakeholder Liaison</b>: Coordinate with system owners, site Subject Matter Experts (SMEs), and global teams to resolve technical issues and support workshops across Manufacturing and Safety departments.</p><p></p></li></ul><p>Academic Requirement</p><ul><li><p><b>Educational Background</b>: Undergraduate Diploma or Bachelor’s Degree in <b>Pharmaceutical</b>, <b>Computing Engineering</b>, <b>Data Science</b>, or an equivalent field.</p><p></p></li><li><p><b>Experience</b>: 0 to 3 years of work experience; prior experience in a biotech or pharmaceutical operating environment is a significant plus.</p><p></p></li><li><p><b>Availability</b>: Available for a duration that meets business needs and internship program requirements.</p><p></p></li></ul><p></p><h2>Key Competencies Required</h2><ul><li><p><b>Technical Acumen</b>: Proficiency in data extraction, transformation, and reporting (e.g., Microsoft Excel) and interest in AI/Predictive Analytics.</p><p></p></li><li><p><b>Analytical &amp; Troubleshooting Skills</b>: Strong numerical and analytical ability to turn raw data into actionable insights and resolve complex technical challenges.</p><p></p></li><li><p><b>Communication</b>: Excellent verbal and written English skills; ability to act as a vital liaison between business process owners and technical developers.</p><p></p></li><li><p><b>Proactive Mindset</b>: A &#34;can-do&#34; attitude with a commitment to excellence, often operating beyond the defined job scope to add value.</p><p></p></li><li><p><b>Collaborative Spirit</b>: Ability to work independently while being a motivated team player in a dynamic, fast-paced environment.</p><p></p></li><li><p><b>Creative Thinking</b>: Not afraid to challenge the status quo, speak up, and share innovative ideas for process improvement</p></li></ul><p></p><p><span><span><b>Safety, Health &amp; Environment</b></span></span></p><ul><li><p><span><span>Comply with all RSTO’s Safety, Health &amp; Environmental (SHE) requirements, never put oneself and others at safety &amp; health risks, and report any workplace accidents, near misses and hazards as soon as practicable.</span></span></p></li><li><p><span><span>Observe all RSTO’s site security measures at all times, and report any suspicious characters/objects &amp; damaged security mechanisms to Site Security immediately.</span></span></p></li></ul><p></p><p><span><span><b>Lean Production System</b></span></span></p><ul><li><p><span><span>Embody PT Lean Production System (LPS), while demonstrating a continuous improvement mindset and behaviors through the use and application of LPS tools for continuous improvement initiatives.</span></span></p></li></ul><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/business-support-digital-intern-roche/69d67d89c8e81216cd0cafb7</link><guid isPermaLink="true">http://biotechroles.com/business-support-digital-intern-roche/69d67d89c8e81216cd0cafb7</guid><pubDate>Wed, 08 Apr 2026 16:08:41 GMT</pubDate><company>Roche</company><location>Central Singapore</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[Sales Representative]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>Affiliate: Roche Diagnostics Korea (한국로슈진단)</b></p><p><b>Division: Core Lab &amp; POC (진단검사 사업부)</b></p><p><b>Location: 서울</b></p><p><b>Position: Sales Representative (영업)</b></p><p></p><p></p><p><b><span>Your key responsibilities</span></b></p><p><u><b>Job Summary</b></u></p><p>한국로슈진단은 <b>고객 중심의 영업 활동</b>을 통해 진단 분야의 혁신적인 가치를 전달하며, 시장 리더십을 강화할 영업 전문가를 찾고 있습니다.</p><p></p><p><u><b>Responsibilities </b></u></p><p></p><p><b>1. 고객 관리</b></p><ul><li><p>기존 고객사를 관리하고 유지하며 매출 증대</p></li><li><p>신규 고객사 발굴 및 개발</p></li></ul><p></p><p><b>2. 대리점 관리</b></p><ul><li><p>대리점과 협력하여 매출 목표 달성</p></li><li><p>대리점 재고 모니터링 및 관리</p></li><li><p>제품 교육 실시</p></li><li><p>대리점 영업 활동 지원</p></li></ul><p></p><p><b>3. 마케팅 및 영업 활동</b></p><ul><li><p>월별/분기별 및 연간 매출 목표 달성</p></li><li><p>신규 장비 설치</p></li><li><p>기존 장비에 신규 제품 추가</p></li></ul><p></p><p><b>4. 기술 지원</b></p><ul><li><p>장비 및 시약 관련 고객 문의 및 요청사항 응대</p></li></ul><p></p><p><b>Who you are </b></p><ul><li><p>학사 학위 이상 또는 이에 준하는 학력 (신입 ~ 경력 7년 이하 선호)</p></li><li><p>체외진단(IVD)에 대한 이해 및 지식 보유 선호</p></li><li><p>고객지향적 사고 및 커뮤니케이션 능력</p></li><li><p>비지니스 영어 구사 능력</p></li></ul><p></p><p><b><b>Submission</b></b></p><p><span>자유 양식의 국/영문 이력서 및 국/영문 자기소개서 (하나의 MS Word 혹은 PDF 파일로 제출)</span></p><p><span>※ 이력서 상단에 반드시 현재 연봉과 희망 연봉을 표기하시기 바랍니다. 누락 시 이력서가 검토되지 않습니다.</span></p><p><span>※ 이력서 내 이메일 주소와 서류전형 지원 사이트의 입력하시는 이메일 주소를 반드시 동일하게 작성해주시기 바랍니다. </span></p><p><span>※ 국가보훈대상 및 장애인은 관련 서류 제출시 관련 법규에 의거 우대합니다.</span></p><p><span>※ 이력서에 개인민감정보 (신체적 조건, 출신 지역, 혼인 여부, 가족관계 등)는 기재하지 말아주십시오.</span></p><p><span>※ 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후 라도 채용이 취소될 수 있습니다.</span></p><p></p><p><b><b>Process</b></b></p><p><span>서류 전형▶ 면접 전형 ▶ 종합 심사 ▶ 최종 합격 통지</span></p><p><span>※ 면접은 서류전형 합격자에 한해 개별 통보합니다.</span></p><p><span>※ 면접 일정 안내 및 조율을 위해 해외 번호(중국)로 연락이 갈 수 있는 점 미리 안내드립니다.</span></p><p><span>※채용이 유력한 후보자에 대해서 이력 검증 및 평판 조회, 건강검진 등의 종합심사를 진행하여 최종 합격자를 선정합니다.</span></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/sales-representative-roche/69d67d88c8e81216cd0cafb6</link><guid isPermaLink="true">http://biotechroles.com/sales-representative-roche/69d67d88c8e81216cd0cafb6</guid><pubDate>Wed, 08 Apr 2026 16:08:40 GMT</pubDate><company>Roche</company><location>Seoul</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Internship in Structural Biology (9-12 months in Basel)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>We are offering a unique opportunity to join the Structural Biology team in the Roche Innovation Center in Basel.</p><p><span>The Internship is based within Lead Discovery, a part of Roche Pharma Research and Early Development, in collaboration with Antibody and Protein Technologies of Roche Diagnostics. The Structural Biology team delivers cutting-edge structural insights for all research and development across Roche, including small and large molecule research, genomic medicine and diagnostic solution. We are a diverse group of individuals with a broad range of deep expertise in X-ray crystallography, cryo electron microscopy (cryo-EM), protein purification and biophysical methods. We are looking for a talented master or bachelor student to support the structural biology team in delivering high quality protein structures and insights for our Diagnostics colleagues. The student will have access to world-class X-ray crystallography and cryo-EM facilities. This is a fantastic opportunity for someone who wants to further their practical knowledge in cryo-EM and X-ray crystallography methods while obtaining insights into how these methods are applied in the diagnostics and pharmaceutical industry.</span></p><p></p><h3><span>The Opportunity</span></h3><ul><li><p><span>Be integrated into the Structural Biology team within Lead Discovery.</span></p></li><li><p><span>Work closely in a highly collaborative spirit with Diagnostics colleagues in Germany and USA.</span></p></li><li><p><span>Perform and learn wet-lab experiments on proteins, such as high-throughput crystallisation screening, cryo-EM grid preparation and SPS-PAGE analysis, with the ultimate aim of generating 3D protein structures.</span></p></li><li><p><span>Use and learn IT tools to solve and build protein structures by X-ray crystallography and/or cryo-EM.</span></p></li><li><p><span>Plan experiments independently and present your results to stakeholders and within group seminars.</span></p></li><li><p><span>Learn how structural biology is a key tool in drug discovery and diagnostics research.</span></p></li></ul><p></p><h3><span>Who You Are</span></h3><ul><li><p><span>You should be enrolled in a Master’s program or be a recent graduate (within 12 months of the start date) in biochemistry, biology, biophysics or a related scientific field with a background in structural biology.</span></p></li><li><p><span>You are dedicated and willing to learn on-the-go, take ownership of projects and have excellent organisational skills.</span></p></li><li><p><span>You have excellent communication skills and are able to communicate with multiple stakeholders and multi-task projects.</span></p></li><li><p><span>You have professional fluency in English, both written and verbal.</span></p></li><li><p><span>You have some prior hands-on experience in either X-ray crystallography or cryo-EM (other biophysical methods, protein expression/purification and/or Linux fluency is a plus).</span></p></li></ul><p></p><h3><span>Application Process</span></h3><ul><li><p><span>Please upload your CV, a motivation letter with your application, and a certificate of enrolment (if you are currently studying). </span></p></li><li><p><span>Non-EU/Non-EFTA citizens must attach a confirmation from the university to the application documents, stating that a mandatory internship is part of the education.</span></p></li></ul><p></p><h3><span>Additional Information</span></h3><ul><li><p><span>This position is based in Basel, Switzerland.</span></p></li><li><p><span>The earliest start date for this internship is September 2026, with a minimum duration of 9 months.</span></p></li></ul><p></p><p>If you are passionate about collaboration and innovation, Roche is the place for you! Every role at Roche plays a part in making a difference in patients’ lives. Apply now and join us in making an impact!</p><p><span> </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/internship-in-structural-biology-9-12-months-in-basel-roche/69d67d88c8e81216cd0cafb5</link><guid isPermaLink="true">http://biotechroles.com/internship-in-structural-biology-9-12-months-in-basel-roche/69d67d88c8e81216cd0cafb5</guid><pubDate>Wed, 08 Apr 2026 16:08:40 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$35000-50000</salary><type>Full time</type></item><item><title><![CDATA[Intern - Capability Development Partner]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. </p><p><span>Join Roche, where every voice matters.</span></p><p> </p><p><b>The Position</b></p><ul><li><p><span>Are you ready to dive into an immersive learning experience where you don&#39;t just observe, but actively contribute and implement vital Organization Enablement initiatives?  Join us in shaping the future of our organizations together!</span></p></li></ul><p> </p><p><b>Key Responsibilities</b></p><ul><li><p><span>Embark on a journey to understand and contribute to transformative Organization Enablement initiatives, focusing on areas such as:</span></p><ul><li><p>Capability Framework:<span> Bring your passion to enhance the efficiency of our Capability Framework, supporting our organization&#39;s future workforce needs and driving efficiencies.</span></p></li><li><p>Learning and Development: <span>Dive into the essence of our RSS Academy, supporting its mission to empower our workforce through continuous learning and development opportunities. </span></p></li><li><p>Employee Engagement and Change Communications:<span> Creatively designing, crafting communications and presentations supporting our initiatives</span></p></li><li><p>Collaborate and Innovate:<span> Bring your tech-savvy or creative mindset to co-create innovative solutions with diverse teams for the key initiatives you spearhead. It will be an added advantage if you know tools like g-suite &amp; other automation tools</span></p></li><li><p>Additional Support<span>: Be prepared to lend a hand in various other support activities and initiatives as needed to keep the momentum going.</span></p></li></ul></li></ul><p> </p><p><b>We&#39;re Seeking Someone Who:</b></p><ul><li><p><span><b>Embodies Curiosity:</b> Whether you&#39;re an undergraduate or a recent graduate from a renowned university, we&#39;re looking for individuals with insatiable curiosity and a knack for reimagining the status quo.</span></p></li><li><p><span><b>Thrives in Creativity: </b>Are you a wordsmith? Social media enthusiast? Digital marketing whiz? Do you excel in creating engaging slideshow presentations? Can you develop captivating videos? These skills are considered a significant advantage in our dynamic environment.</span></p></li><li><p><span><b>Values Collaboration:</b> Join a team that values collaboration above all else. We&#39;re seeking individuals who thrive in diverse environments and carry a strong sense of ownership for their contributions.</span></p></li><li><p><span><b>Communicates with Impact:</b> From verbal discussions to written reports, your English communication skills should be top-notch. </span></p></li><li><p><span><b>Driven Individuals: </b>We seek candidates who are self-motivated, willing to take initiative, and possess a solution-oriented mindset.</span></p></li><li><p><span><b>PR and Event Management Savvy:</b> Strong skills in public relations and event management are highly valued in this role.</span></p></li><li><p><span><b>Commits to Growth: </b>Ready to embark on a journey? We&#39;re seeking interns who can commit to a minimum of 6 months, preferably a year, to truly immerse themselves in this transformative experience.</span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/intern-capability-development-partner-roche/69d67d88c8e81216cd0cafb4</link><guid isPermaLink="true">http://biotechroles.com/intern-capability-development-partner-roche/69d67d88c8e81216cd0cafb4</guid><pubDate>Wed, 08 Apr 2026 16:08:40 GMT</pubDate><company>Roche</company><location>Petaling Jaya</location><salary>$1000-2000</salary><type>Full time</type></item><item><title><![CDATA[PI Engineer]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Die Organisation “Site Network Basel/Kaiseraugst”, Teil der globalen Group Function “Corporate Strategy, Sustainability &amp; Sites”, stellt die Infrastruktur und Services  für den gesamten Standort bereit und entwickelt diese kontinuierlich und auf innovative Art weiter. Wir arbeiten mit allen Anspruchsgruppen entlang der gesamten Wertschöpfungskette zusammen, von der frühen Forschung bis zur Versorgung der Patient:innen. Bei uns kannst du dich auf ein modernes Organisationsmodell freuen, in welchem du in Eigenverantwortung deine Talente in sinnhafter Arbeit einbringen kannst. Wir garantieren Gestaltungsspielraum und Entscheidungsfreiheit in unserer Organisation. Klassische Vorgesetzte suchst du bei uns vergebens.</p><p></p><h3><span>Die Möglichkeit</span></h3><p><span>Als PI Engineer (d/f/m) bist du Teil des Kreises „Pharma Engineering Drug Product“ am Standort Basel / Kaiseraugst. Wir sind verantwortlich für das innovative, GMP-gerechte Engineering sowie den zuverlässigen Betrieb komplexer Produktionsanlagen in der Galenik und Verpackung. In einem modernen Arbeitsumfeld unterstützen wir unsere Businesspartner von der ersten Idee über die Projektumsetzung bis hin zum Life-Cycle-Management der Systeme.</span></p><p></p><p><span>In dieser Rolle bist du die zentrale Schnittstelle zwischen Produktion, Pharma Engineering und ITOT. Du gestaltest die digitale Landschaft unseres Produktionsstandorts aktiv mit, indem du nicht nur bestehende Systeme wartest, sondern die Datenstruktur der Zukunft aufbaust.</span></p><p></p><p><span>Deine Kernaufgaben sind:</span></p><ul><li><p><span>System-Architekt:<span> </span></span>Du verantwortest die Anbindung von Automationssystemen an unseren Data Historian (AVEVA PI) inkl. der Konfiguration der entsprechenden Schnittstellen und die kontinuierliche Pflege über den Lifecycle dieser Systeme.</p></li><li><p><span>Lösungsdesign: Du analysierst gemeinsam mit internen Businesspartnern Anforderungen an das PI-System und implementierst optimale, GMP-konforme Lösungen.</span></p></li><li><p><span>Projektleitung: Du planst und leitest Projekte mit Fokus auf PI-Historian – von der Spezifikation bis zur Übergabe an den Betrieb.</span></p></li><li><p><span>Betrieb &amp; Support: Zusammen mit dem Team stellst du die Administration und den reibungslosen Betrieb sicher (inkl. Fehleranalyse, Root-Cause-Analysen und Deviation Handling).</span></p></li><li><p><span>Compliance: Du steuerst Change-Control-Prozesse sowie Qualifizierungs- und Validierungsaktivitäten gemäss Roche-Richtlinien.</span></p></li><li><p><span>Wissenstransfer: Du schulst Mitarbeitende und unterstützt unsere Kunden bei technischen Fragestellungen sowie Behördeninspektionen.</span></p></li></ul><p></p><p><span>Wir arbeiten in selbstorganisierten Fachteams ohne klassische Hierarchien. Dies erfordert ein hohes Mass an Eigenverantwortung, Teamspirit und ausgeprägte Kommunikationsfähigkeiten.</span></p><p></p><h3><span>Wer du bist</span></h3><p><span>Du bist eine integre Persönlichkeit, die gerne konventionelle Denkmuster hinterfragt und eine hohe Dienstleistungsmentalität mitbringt.</span></p><ul><li><p><span>Ausbildung: Studium oder Ausbildung in Informatik, Elektrotechnik, Automatisierungstechnik oder einer vergleichbaren Fachrichtung.</span></p></li><li><p><span>Expertise: Vertiefte Kenntnisse in AVEVA PI</span><span><span> </span>sowie Erfahrung in der Anbindung von Automationssystem und der Pflege dieser Anbindungen über den Lifecycle.</span></p></li><li><p><span>IT-Architektur: Breites Verständnis von Netzwerktechnik und Systemintegration im industriellen Umfeld.</span></p></li><li><p><span>Erfahrung: Mehrjährige Praxis als System Engineer oder Projektleiter, idealerweise im GMP-regulierten Umfeld.</span></p></li><li><p><span>Sprachen: Verhandlungssicheres Deutsch und Englisch.</span></p></li><li><p><span>Know-how in der automatisierten Herstellung pharmazeutischer Produkte.</span></p></li><li><p><span>Routine in der Administration komplexer IT-Infrastrukturen für die Produktion.</span></p></li></ul><p></p><p><span>Werde jetzt Teil von Roche, setze Dein technisches Know-how ein und gestalte den Bereich &#39;Pharma Engineering Drug Product&#39; am Standort Basel mit. Bewirb Dich jetzt!</span></p><p></p><p></p><p></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/pi-engineer-roche/69d67d87c8e81216cd0cafb3</link><guid isPermaLink="true">http://biotechroles.com/pi-engineer-roche/69d67d87c8e81216cd0cafb3</guid><pubDate>Wed, 08 Apr 2026 16:08:39 GMT</pubDate><company>Roche</company><location>Kaiseraugst</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Systemverantwortliche/-r Infrastruktur]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Die Organisation “Site Network Basel/Kaiseraugst”, Teil der globalen Group Function “Corporate Strategy, Sustainability &amp; Sites”, stellt die Infrastruktur und Services für den gesamten Standort bereit und entwickelt diese kontinuierlich und auf innovative Art weiter. Wir arbeiten mit allen Anspruchsgruppen entlang der gesamten Wertschöpfungskette zusammen, von der frühen Forschung bis zur Versorgung der Patient:innen. Bei uns kannst du dich auf ein modernes Organisationsmodell freuen, in welchem du in Eigenverantwortung deine Talente in sinnhafter Arbeit einbringen kannst. Wir garantieren Gestaltungsspielraum und Entscheidungsfreiheit in unserer Organisation. Klassische Vorgesetzte suchst du bei uns vergebens.</span></p><p></p><p><span>Der Circle “Energieversorgung” stellt den zuverlässigen, behördenkonformen und kostenbewussten Betrieb der Heiz-, Kühl- und Prozessmedien, inklusive der Ver- und Entsorgung sicher.</span></p><p></p><h3>Die Möglichkeit</h3><p><span>Du bist verantwortlich für den Betrieb, Störungsbehebung, Instandhaltung und kontinuierliche Optimierungen (Energie, Kosten). </span></p><p><span> </span></p><p><span>Als Systemverantwortliche/-r Infrastruktur umfasst Dein Aufgabengebiet die folgenden Tätigkeiten:</span></p><ul><li><p><span>Betreiben von Energieverbundsystemen, industriellen Kälteanlagen/ Wärmepumpen  und der Wasserversorgunganlagen (zB. Grundwasserbrunnen, Rheinwasserfassung)</span></p></li><li><p><span>Instandhaltungs- und Störungsbehebung inkl. Pikettdienst </span></p></li><li><p><span>kontinuierliche Optimierungen</span></p></li><li><p><span>Betreuung und Koordination von Fremdfirmen</span></p></li><li><p><span>Durchführung von Kontrollgängen und Datenerfassung</span></p></li><li><p><span>Logbücher führen SAP</span></p></li><li><p><span>Analyse und Interpretation von Energieverbräuchen sowie Ableitung von Optimierungsmassnahmen</span></p></li><li><p><span>Mitarbeit in Projekten</span></p></li></ul><p></p><p><span>Des Weiteren bist Du verantwortlich für die<span> Gestaltung Deiner persönlichen und fachlichen Weiterentwicklung, das <span>aktive Einbringen und die Mitarbeit im Interesse des OneRoche Gedanken und für die a<span>ktive Mitarbeit im selbstorganisierenden Teams. </span></span></span></span></p><p></p><h3><span>Wer Du bist</span></h3><p><span>Du schätzt es, in einer leistungsorientierten und agilen Umgebung zu arbeiten, die von gegenseitigem Respekt, Diskussion und Zusammenarbeit getragen wird. Dann ist Roche für Dich der Ausgangspunkt für ein internationales Arbeitsumfeld mit vielfältigen Entwicklungschancen. Du bist eine positiv denkende, integere und selbstreflektierende Persönlichkeit mit guten kommunikativen Fähigkeiten.</span></p><p></p><p><span>Als erfolgreicher Systemverantwortliche/-r Infrastruktur bringst Du Folgendes mit:</span></p><ul><li><p><span>eine abgeschlossene technische Berufsausbildung (z.B. Kältesystem-Monteur EFZ oder vergleichbar) und idealerweise eine Weiterbildung als Instandhaltungsfachmann oder einer Höheren Fachschule HF. </span></p></li><li><p><span>Mindestens fünf Jahre Berufserfahrung im Betrieb und der Instandhaltung von NH3 Kälteanlagen, Grundwasseranlagen und Energiesystemen ist von Vorteil</span></p></li><li><p><span>Praktische Erfahrung in einem GMP-Umfeld sowie p</span><span>raktische Erfahrung in der Energieversorgung ist von Vorteil. </span></p></li><li><p><span>In der Bedienung von Prozessleitsystemen der genannten Systeme bist Du geübt. </span></p></li><li><p><span>Gute IT-Kenntnisse (SAP, Google Workspace, MS365) </span></p></li><li><p><span>Fliessende Deutschkenntnisse in Wort und Schrift, idealerweise Englischkenntnisse runden Dein Profil ab.</span></p></li></ul><h3></h3><p>Darüber hinaus bist du ein guter Teamplayer und hast eine selbständige und selbstorganisierte Arbeitsweise. Du bringst das Verständnis und gute Orientierungsfähigkeit innerhalb einer Matrix-Organisation mit.</p><p></p><p>Setze dein Know-how ein und gestalte den Bereich &#39;Energieversorgung&#39; am Standort Basel mit. Bewirb dich jetzt !</p><p></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/systemverantwortliche-r-infrastruktur-roche/69d67d87c8e81216cd0cafb2</link><guid isPermaLink="true">http://biotechroles.com/systemverantwortliche-r-infrastruktur-roche/69d67d87c8e81216cd0cafb2</guid><pubDate>Wed, 08 Apr 2026 16:08:39 GMT</pubDate><company>Roche</company><location>Basel</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Order Process Team Lead (Spanish, Italian or French is an advantage)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p>As an Order Process Team Leader you are responsible for high quality services to Roche suppliers and internal partners.</p><p>The Buyer team is responsible for approving and maintaining Purchase Orders. We also reconcile price and quantity discrepancies between orders and invoices, and help ensuring timely vendor payments.</p><p></p><p><b>The opportunity: </b>  </p><ul><li><p>Building, leading, coaching and managing a strong and collaborative Order Processing team </p></li><li><p>Creating a safe and positive team environment and ensuring that the team demonstrates the right mindset and attitude</p></li><li><p>Setting up clear and challenging expectations and goals for team members and role modelling these</p></li><li><p>Through frequent check-ins, ensuring that ongoing dialog occurs on the topics of Career, Capabilities, Connections and Contributions; and developing the team members’ knowledge, skills and competency in order to retain and develop talented staff as well as building a team talent pipeline. Setting and monitoring team working plan and resource allocations</p></li><li><p>Developing and managing key stakeholder relationships, working with peers to develop future service portfolio in the area of D2P Services &amp; Solutions</p></li><li><p>Ensuring high quality knowledge transfers and smooth transitions in case of transferring work to own area</p></li><li><p>Liaising with other Service teams for cross-functional end-to-end service delivery and process improvement</p></li></ul><p></p><p><b>Who you are:</b></p><ul><li><p>University degree in Economics or relevant professional experience</p></li><li><p>General understanding of finance or procurement processes and standards. Procurement experience is an advantage.</p></li><li><p>2-5 years of experience in a shared service center, with a proven track record of leading regional or global service delivery teams</p></li><li><p>Proficiency in <b>English. Spanish, Italian or French </b>knowledge is an advantage.</p></li><li><p>A growth &amp; continuous improvement mindset, coupled with strong business acumen and an understanding of servicing impact</p></li><li><p>Customer centricity &amp; accountability as well as excellent communication &amp; problem-solving skills</p></li><li><p>Strong leadership competencies and demonstrated success in cross-cultural collaboration, change &amp; stakeholder management</p></li><li><p>You bring a creative leadership style and a coaching mindset (empowering, facilitating accountability, collaboration, experimentation &amp; continuous learning)</p></li></ul><p></p><p><i><b>In exchange we provide you with:</b></i></p><ul><li><p><b>Development opportunities: </b>Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; trainings, the possibility of international assignments, internal position changes and the chance to shape your own career. </p></li><li><p><b>Excellent benefits: </b>Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. </p></li><li><p><b>Flexibility:</b> We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</p></li><li><p><b>A global inclusive community, </b>where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</p></li></ul><p></p><p><i>Please read the </i><a href="http://assets.roche.com/f/174885/x/ff2c6695a6/20221220_data-privacy-notice-for-candidates.pdf" target="_blank">Data Privacy Notice </a><i>for further information about how we handle your personal data related to the recruitment process.</i></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/order-process-team-lead-spanish-italian-or-french-is-an-advantage-roche/69d67d86c8e81216cd0cafb1</link><guid isPermaLink="true">http://biotechroles.com/order-process-team-lead-spanish-italian-or-french-is-an-advantage-roche/69d67d86c8e81216cd0cafb1</guid><pubDate>Wed, 08 Apr 2026 16:08:38 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$35000-50000</salary><type>Full time</type></item><item><title><![CDATA[Accounts Payable Accountant - German speaking]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><i><b>The Opportunity: </b></i></p><p>As an Accounts Payable Accountant you are responsible for high quality services to Roche suppliers and internal partners. You will be responsible for booking complex invoices in accordance with Roche and local standards so that the supplier receives the funds in time for the goods supplied and the services rendered. You will have the possibility to have full responsibility for the end-to-end AP process and handling both internal and supplier queries received by phone or mail in local language.</p><ul><li><p>Process and validate PO based and direct invoices and payment requests, manage and run payments</p></li><li><p>Manage vendor accounts</p></li><li><p>Audit, report and support AP invoice resolution</p></li><li><p>Handle affiliate’s internal invoice queries</p></li><li><p>Act as a point of contact, promoting strong collaborative relationships between the affiliate’s finance teams and all other internal SSC teams</p></li><li><p>Participate in process improvement and ongoing projects, opportunity to take part in knowledge transfer</p></li></ul><p></p><p><i><b>Who you are:</b></i></p><ul><li><p>University degree in Finance or relevant professional experience</p></li><li><p>General understanding of finance processes and standards. Broad experience in accounts payable processes (or related field) and using SAP is an advantage</p></li><li><p>Strong communication and advisory skills and you are able to deal with complex issues</p></li><li><p>Customer centricity through your day-to-day interactions</p></li><li><p>End-to-end accountability, problem-solving skills, growth &amp; agile mindset in ambiguous situations</p></li><li><p>Multi-cultural acceptance, ability to work in a fast-paced and changing environment</p></li><li><p>Proficiency in <b>English and German</b></p></li></ul><p></p><p><i><b>In exchange we provide you with:</b></i></p><ul><li><p><b>Development opportunities: </b>Roche is rich in learning resources. We provide constant development opportunities, free language courses &amp; trainings, the possibility of international assignments, internal position changes and the chance to shape your own career. </p></li><li><p><b>Excellent benefits: </b>Competitive salary and cafeteria package, annual bonus, Private Medical Services, Employee Assistance Program, All You Can Move Sportpass, coaching / mentoring opportunity, buddy program, team buildings, holiday party. </p></li><li><p><b>Flexibility:</b> We also support flexibility to help you find your balance. Home office is commonly available (typically 2 office days/week on average). We create the opportunity for freedom in working, where your corporate and private life coexist in harmony.</p></li><li><p><b>A global inclusive community, </b>where we learn from each other. At Roche, we cooperate, debate, make decisions, celebrate successes and have fun as a team. Our leadership is very focused on people, creating a strong, inclusive culture, so you always have the chance to share your opinion.</p></li></ul><p></p><p><i>Please read the </i><a href="http://assets.roche.com/f/174885/x/ff2c6695a6/20221220_data-privacy-notice-for-candidates.pdf" target="_blank">Data Privacy Notice </a><i>for further information about how we handle your personal data related to the recruitment process.</i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/accounts-payable-accountant-german-speaking-roche/69d67d86c8e81216cd0cafb0</link><guid isPermaLink="true">http://biotechroles.com/accounts-payable-accountant-german-speaking-roche/69d67d86c8e81216cd0cafb0</guid><pubDate>Wed, 08 Apr 2026 16:08:38 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Learning Coordinator]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>The Opportunity:</b></p><p></p><p>As a <b>Learning Coordinator</b>, you are a vital member of the Global Learning Services team. You are responsible for executing system data maintenance and administrative activities within Cornerstone and other relevant Learning Management Systems (LMS).</p><p><b>Your key responsibilities will include:</b></p><ul><li><p><b>LMS Administration &amp; Data Integrity:</b> Record and control training information in Cornerstone to ensure accurate learning plans, histories, and availability of current materials. You will perform data entry, report on data to support audits/inspections, and provide front-line technical support to managers and learners.</p></li><li><p><b>Advisory &amp; Customer Support:</b> Provide expert consultation to the learning community and business partners on global learning systems and processes. You will ensure end-to-end process completion aligned with customer-focused principles and PSS Core Capabilities.</p></li><li><p><b>Operational Coordination:</b> Manage complex administrative, financial, and procurement tasks associated with the Learning and Development scope. This includes coordinating session logistics, managing vendor relationships, and ensuring compliance with Roche standards.</p></li><li><p><b>Event &amp; Project Management:</b> Plan and conduct event management activities, including organizing site-related onboarding and learning programs. You will support learning projects through meeting facilitation, project plan execution, and cross-functional collaboration.</p></li><li><p><b>Continuous Improvement:</b> Identify solutions for known learning issues, advocate for system improvements, and participate in global initiatives to optimize learning performance. You will contribute to the update of relevant documentation (SOPs, SWIs) and share best practices for complex issue resolution.</p></li><li><p><b>Compliance &amp; Audit Support:</b> Provide learning expertise during audits, ensuring all data maintenance aligns with company policies, legal constraints, and data privacy rules.</p></li></ul><h3></h3><p><b>Who you are:</b></p><p>You are a result-oriented professional with an agile mindset, capable of navigating complex data structures and performing with high precision in a fast-paced, matrixed environment.</p><p><b>Requirements and Qualifications:</b></p><ul><li><p><b>Education:</b> High School Diploma required; Bachelor’s degree in HR, Learning and Development, or a related field is preferred.</p></li><li><p><b>Experience:</b> 3-5 years of relevant experience in learning administration or HR shared services.</p></li><li><p><b>Technical Skills:</b> * Expertise in <b>Cornerstone</b> or similar Learning Management Systems (LMS).</p><ul><li><p>Proficiency in <b>ServiceNow</b> and digital collaboration tools (G-Suite, Microsoft Office).</p></li><li><p>Strong understanding of administrative processes related to finance, procurement, and audit compliance.</p></li></ul></li><li><p><b>Languages:</b> <b>English is mandatory</b>; additional languages are a plus.</p></li><li><p><b>Core Competencies:</b> * <b>Customer Centricity:</b> Ability to anticipate needs and manage diverse stakeholder responses.</p><ul><li><p><b>End-to-End Accountability:</b> Understanding the &#34;big picture&#34; impact and engaging others for successful outcomes.</p></li><li><p><b>Problem Solving:</b> Active listening, critical thinking, and a drive for process improvement.</p></li><li><p><b>Growth Mindset:</b> A desire to experiment, learn from feedback, and seek new learning opportunities.</p></li></ul></li></ul><p></p><p><b><i>Relocation benefits are not available for this job posting.</i></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/learning-coordinator-roche/69d67d86c8e81216cd0cafaf</link><guid isPermaLink="true">http://biotechroles.com/learning-coordinator-roche/69d67d86c8e81216cd0cafaf</guid><pubDate>Wed, 08 Apr 2026 16:08:38 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$28000-42000</salary><type>Full time</type></item><item><title><![CDATA[Medical Science Partner - Neurologie (m/w/d)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><h2></h2><p><span>Bei Roche Pharma Schweiz treibt uns der Grundsatz „<i>Doing now what patients need next</i>“ an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die sie benötigen, und schaffen eine Welt, in der Menschen mehr Zeit mit ihren Liebsten verbringen können. In unserem Team erwartet dich ein spannendes und internationales Arbeitsumfeld, das von gegenseitigem Respekt, Diskussion und Zusammenarbeit geprägt ist.</span></p><p></p><p><span>Wir suchen aktuell eine:n <b>Medical Science Partner (MSP) </b>für den Bereich <b>Neuroscience</b>. In dieser medizinischen, nicht-promotionellen Aussendienst-Funktion agierst du auf hohem wissenschaftlichen Niveau als wichtiges Bindeglied zwischen medizinischen Expert:innen in Spitälern sowie Praxen und Roche Pharma Schweiz. Die Position ist mit einer nationalen und internationalen Reisetätigkeit von ca. 60% verbunden.</span></p><p></p><h3><span><b>Die Möglichkeit</b></span></h3><ul><li><p><span>Medizinische Expertise: Externer und interner medizinisch-wissenschaftlicher Experte:in für das Portfolio über den gesamten Produktlebenszyklus hinweg. Medizinischer Input und Review von Zulassungsanträgen, HTAs sowie weiteren wissenschaftlichen Dokumenten.</span></p></li><li><p><span>Strategiegestaltung: Maßgebliche Mitgestaltung der Indikationsstrategie  und Entwicklung relevanter Medical Taktiken zur Erreichung gemeinsamer Geschäftsziele.</span></p></li><li><p><span>Kundenengagement: Aufbau effektiver Peer-to-Peer-Beziehungen zu externen Stakeholdern und Identifizierung/Entwicklung wissenschaftlich fundierter Kooperationen mit Therapieexperten (TAEs). Interaktion mit Ärztinnen und Ärzten zur Identifikation von Bedürfnissen und potenziellen Bereichen für wissenschaftliche Zusammenarbeit.</span></p></li><li><p><span>Medizinische Information &amp; Weiterbildung: Präsentation medizinisch-wissenschaftlicher Daten sowie Durchführung von Schulungen für externes Publikum und Roche-Mitarbeitende.</span></p></li><li><p><span>Insights Generation &amp; Strategische Beratung: Durchführung von Landscaping und Profiling bei neuen Indikationen. Einbringen von Erkenntnissen aus dem Feld und Einordnung strategisch umsetzbarer Empfehlungen für das Indikationsteam.</span></p></li><li><p><span>Klinische Studien: Primäre:r Ansprechpartner:in für TAEs und medizinische Fachpersonen zum wissenschaftlichen Austausch und im Rahmen von klinischen Roche-sponsored  oder Investigator Initiated (IIS) Studien. Strategische Priorisierung von Studien für den Schweizer Markt im Rahmen der Gesamtstrategie und Positionierung an Klinischen Zentren. </span></p></li></ul><p><br /> </p><h3><span><b>Wer du bist</b></span></h3><ul><li><p><span>Hochschulabschluss in Medizin, Pharmazie oder Naturwissenschaften (bevorzugt PhD oder MD).</span></p></li><li><p><span>Erfahrung als Medical Science Liaison oder Medical Manager </span></p></li><li><p><span>Fundierte Kenntnisse im Bereich Neuroscience/MS </span></p></li><li><p><span>Bestehendes Netzwerk im Bereich Neurologie im Schweizer Markt von Vorteil.</span></p></li><li><p><span>Versiertheit in der Interpretation und Präsentation klinischer Daten sowie exzellente Kommunikationsfähigkeiten.</span></p></li><li><p><span>Starke Eigeninitiative, Strategisches Denken und Handeln</span></p></li><li><p><span>Kundenzentriertes Denken und die Fähigkeit, Prioritäten in einem dynamischen Umfeld flexibel auszurichten.</span></p></li><li><p><span>Verhandlungssicher in Deutsch und Englisch; Französischkenntnisse sind ein zusätzlicher Vorteil.</span></p></li></ul><h2></h2><h3><span><b>Call to Action</b></span></h3><p><span>Bereit für den nächsten Schritt? Wir freuen uns darauf, von dir zu hören. Bewerbe dich jetzt, um diese spannende Möglichkeit zu entdecken!</span></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/medical-science-partner-neurologie-mwd-roche/69d67d85c8e81216cd0cafae</link><guid isPermaLink="true">http://biotechroles.com/medical-science-partner-neurologie-mwd-roche/69d67d85c8e81216cd0cafae</guid><pubDate>Wed, 08 Apr 2026 16:08:37 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Computational Biology - Oncology]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p> In Roche’s <a href="https://www.roche.com/innovation/structure/pred/" target="_blank"><u>Pharmaceutical Research and Early Development organization (pRED</u></a><span>)</span> ​, we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.</p><p></p><p><span>The Computational Sciences Centre of Excellence is a global organisation enabling Roche’s Research and Early Development units to become more data-driven, more digitally adept and better prepared for the challenges of the future. Within the <i>Computational Sciences Centre of Excellence</i>, the Computational Biology department focuses on furthering our understanding of disease, patient populations, and target biology by having access to the largest Pharma R&amp;D datasets in the world. In partnership with our scientists across pRED, we create better medicines by augmenting every part of R&amp;D through our data-driven culture. </span></p><p></p><h3>The Opportunity</h3><p><span>We are seeking a highly motivated computational scientist to join our Research Oncology sub-unit of Computational Biology. You will be a member of a team of world-leading computational scientists with the express aim of developing a competitive advantage for pRED through the application of computational biology in the Oncology space.  You will also be part of the wider Computational Biology and Medicine unit within the <i> Computational Sciences Centre of Excellence</i> drawing on the shared experience and expertise of colleagues globally.  </span></p><p><span>To ensure successful delivery for the portfolio, you collaborate with other subunits in Computation Biology and/or Computational Medicine where needed. Our collective success in the Oncology sub-unit and our contribution to pRED/Pharma goals will be the measure of your impact.</span></p><p><span>In this role, you will: </span></p><ul><li><p><span>Drive and execute the data and analytics strategy for your area, working closely with stakeholders to focus on the highest-impact opportunities.</span></p></li><li><p><span>Generate clear, high-value insights from complex data to support decision-making and help advance projects toward meaningful patient impact.</span></p></li><li><p><span>Act as a trusted partner to scientists and cross-functional teams, collaborating to shape priorities and deliver on shared goals.</span></p></li><li><p><span>Contribute to a collaborative and inclusive team environment by sharing expertise, supporting peers, and actively engaging in a feedback-rich culture.</span></p></li><li><p><span>Contribute to continuously improving how we work, helping to strengthen Computational Biology as a key driver of innovation and impact within pRED</span></p></li></ul><p></p><h3>Who you are</h3><ul><li><p><span>You hold a PhD in Bioinformatics, Biostatistics, or a related quantitative field, with a strong foundation in data-driven problem solving, statistical modeling, and machine learning.</span></p></li><li><p><span>You bring a solid understanding of cancer biology and are motivated to apply data science to drive impact in drug discovery and decision-making.</span></p></li><li><p><span>You have strong expertise in AI/ML and modern AI-driven workflows, ideally including hands-on experience with LLMs, AI-assisted coding, or agentic workflows applied to biological problems.</span></p></li><li><p><span>You are proficient in R and/or Python and comfortable working in Linux/Unix environments, including processing data on HPC/cloud platforms.</span></p></li><li><p><span>You have experience working with large-scale biological datasets (e.g., genomics, transcriptomics, spatial omics/imaging), ideally including cancer cell dependency, perturbation, or drug-response data, and enjoy integrating diverse data types.</span></p></li><li><p><span>You communicate clearly and effectively, create impactful visualizations, and thrive in collaborative, multidisciplinary environments where you take ownership and work closely with experimental scientists.</span></p></li></ul><p></p><p><span>Ready to take the next step? We&#39;d love to hear from you. Apply now to explore this exciting opportunity!</span></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/computational-biology-oncology-roche/69d67d85c8e81216cd0cafad</link><guid isPermaLink="true">http://biotechroles.com/computational-biology-oncology-roche/69d67d85c8e81216cd0cafad</guid><pubDate>Wed, 08 Apr 2026 16:08:37 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$110000-160000</salary><type>Full time</type></item><item><title><![CDATA[Marketing Enabler]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>Roche Philippines is looking for a </span><b>Marketing Enable</b>r to join<span> our commercial</span> <span>team. We&#39;re moving beyond just offering world-class medicines to becoming true partners in the healthcare ecosystem, leading innovation and generating disruption to deliver better outcomes for patients, the system, and our organization, faster. </span></p><p></p><p><span>As a Marketing Enabler, you will serve as a visionary leader and strategic expert, empowering our disease area teams to lead generative disruption in the healthcare space. Your purpose is to bridge the gap between world-class medicines and transformative partnerships, ensuring that every customer interaction is personalized, insightful, and orchestrated to address the real-world needs of patients. You will co-define our portfolio strategy and take ownership of the customer engagement tactics that differentiate Roche in the market.</span></p><p></p><p><b><span>What You Will Be Working On</span></b></p><p><span>In this role, you will be a powerful lever for change, blending traditional and digital activities into a unified experience. You will:</span></p><ul><li><p><b>Co-create the vision:</b> <span>Work closely with cross-functional disease area teams and medical enablers to make customer experience an integral part of our local strategy.</span></p></li><li><p><b>Architect omnichannel campaigns: </b><span>Design and execute integrated campaigns that balance speed, cost-effectiveness, and customer satisfaction across all touchpoints.</span></p></li><li><p><b>Lead with insights: </b><span>Transform qualitative and quantitative data into actionable suggestions that directly contribute to desired disease area outcomes.</span></p></li><li><p><b>Drive segmentation strategy: </b><span>Define and implement customer segmentation based on local needs and global frameworks to address key pain points in the patient journey.</span></p></li><li><p><b>Collaborate across networks:</b> <span>Partner with the APAC Customer Experience (Cx) Network to tailor global strategies for our local affiliate.</span></p></li><li><p><b>Champion content excellence: </b><span>Work with stakeholders and agencies to create, localize, and deploy high-quality content across all communication channels.</span></p></li><li><p><b>Own the learning loop: </b><span>Lead the closed-loop process to ensure continuous improvement based on the &#34;Voice of the Customer&#34; and performance analytics.</span></p></li><li><p><b>Ensure ethical standards:</b><span><b> </b>Oversee the review and approval of promotional materials, ensuring all activities meet the highest ethical and compliance standards.</span></p></li><li><p><b>Partner in event management:</b><span><b> </b>Collaborate with teams and external partners to deliver impactful events that engage our community.</span></p></li><li><p><b>Foster innovation:</b><span><b> </b>Use an &#34;outcomes-based&#34; planning approach to identify new priorities and establish leadership in prioritized disease areas.</span></p></li></ul><p></p><p><b>Who you are:</b></p><p><span>You are a passionate and experienced professional with a desire to create a significant impact. As the Marketing enabler, you will actively participate in our network and provide guidance to customer-facing teams. </span></p><p></p><p><span>You have:</span></p><ul><li><p><b>Education:</b><span> A degree in Health/Medical Sciences and/or Business/Marketing or equivalent</span></p></li><li><p><b>Significant experience </b>(5&#43; years)<span> in a commercial setting within the pharmaceutical or a related industry, with a strong understanding of the relevant codes of conduct.</span></p></li><li><p><b>Hands-on experience</b> in digital marketing<span> and are skilled at creating engaging omnichannel customer journeys.</span></p></li><li><p><b>Omnichannel Expertise:</b><span><b> </b>You have demonstrated experience in planning and delivering complex campaigns that seamlessly integrate digital and face-to-face engagement.</span></p></li><li><p><b>VACC Leadership:</b><span><b> </b>You naturally embody the roles of Visionary, Architect, Catalyst, and Coach to navigate structures and drive personalized engagement.</span></p></li><li><p><b>Collaborative Spirit:</b><span><b> </b>You excel at leading cross-functional projects and have a &#34;steal with pride&#34; attitude toward adopting global best practices.</span><br />Analytical Depth:<span> You are skilled at turning complex data into clear insights and owning the success signals for omnichannel plans.</span></p></li><li><p><b>A Customer-Centric Heart:</b><span><b> </b>You prioritize the needs of customers and patients in every decision, demonstrating a willingness to experiment and take calculated risks to improve their experience</span></p></li><li><p><b>Excellent project management skills</b><span><b> </b>and are comfortable managing multiple priorities in a dynamic environment.</span></p></li><li><p><b>Proficiency in English</b><span><b> </b>including oral &amp; written communication</span></p></li></ul><p></p><p><span>You will demonstrate the Roche values of Integrity, Courage, and Passion in every interaction, ensuring all activities are of the highest ethical standard and comply with company policies and regulations.</span></p><p></p><p><span>This <b>field-based role</b> is exclusively available to candidates who possess <b>full eligibility to live and work in the Philippines.</b></span></p><p></p><p><span>We do not accept any unsolicited resumes or enquiries from recruitment agencies. Roche has a dedicated in-house Talent Acquisition team.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/marketing-enabler-roche/69d67d84c8e81216cd0cafac</link><guid isPermaLink="true">http://biotechroles.com/marketing-enabler-roche/69d67d84c8e81216cd0cafac</guid><pubDate>Wed, 08 Apr 2026 16:08:36 GMT</pubDate><company>Roche</company><location>Taguig City</location><salary>$28000-45000</salary><type>Full time</type></item><item><title><![CDATA[Order Handling Agent]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span style="color:#000000"><b><u>Customer Excellence &amp; Digital Transformation Partner</u></b></span></p><p><br /></p><p><span style="color:#000000">A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Doing now what patients need next.</span></p><p><br /></p><p><span style="color:#000000"><b><u>The Role</u></b>:</span></p><p><br /></p><p><span style="color:#000000">As a “Customer Excellence &amp; Digital Transformation Partner” within our Supply Chain team in Spain, you will be at the heart of our evolution. This is not just an order management role; it is also a consultative position designed to bridge the gap between traditional operations and a digital-first future.</span></p><p><br /></p><p><span style="color:#000000">You will be responsible for the end-to-end &#34;Order to Cash&#34; journey, ensuring that every interaction adds value to our clinicians and patients. You will act as a Catalyst for change, moving from reactive processing to proactive customer consultancy, helping our partners optimize their ordering patterns and embrace digital ecosystems.</span></p><p><br /></p><p><span style="color:#000000">The role provides an end-to-end visibility and responsibility in terms of order lifecycle, from the moment the orders are captured in our systems, pricing topics, logistics fulfillment as well as billing &amp; collecting. </span></p><p><br /></p><p><span style="color:#000000">Offering a unique challenge combining operative responsibility and digitalization projects.</span></p><p><br /></p><p><span style="color:#000000"><b><u>Your Key Challenges &amp; Responsibilities</u></b>:</span></p><p><br /></p><p><span style="color:#000000">-Strategic Order Management: Execute the daily management of customer orders within SAP with precision, acting as the primary point of contact to ensure a seamless experience.</span></p><p><br /></p><p><span style="color:#000000">-Digital Onboarding &amp; Transformation: Drive the continuous development of the customer journey by migrating clients to automated solutions (EDI, Webshop/Online Ordering, Track and Trace). You will represent the Spanish affiliate in regional forums to align on global digital strategies.</span></p><p><br /></p><p><span style="color:#000000">-Consultative Logistics: Analyze customer ordering patterns to identify inefficiencies. Act as an Architect to influence and advise clients on better planning, safety stocks, and consolidated ordering to improve operational flow for both the client and Roche.</span></p><p><br /></p><p><span style="color:#000000">-Agile Collaboration: Work within cross-functional &#34;Squads&#34; to break down silos. Contribute to strategic projects that radically simplify current processes and shorten the &#34;Order to Cash&#34; cycle.</span></p><p><br /></p><p><span style="color:#000000">-Ownership of Customer Experience: Manage and resolve customer claims and enquiries using CRM tools (Rexis), ensuring high-quality resolution and redirecting non-logistic issues to the appropriate experts. Detecting and analyzing repetitive claims - reduce long term customer claims through root cause analysis with respective solutions. </span></p><p><br /></p><p><span style="color:#000000">-Change Management: Act as a Visionary by communicating and accompanying our customers through the transition from manual email-based ordering to digital-first interactions.</span></p><p><span style="color:#000000">-Digital Solution Testing &amp; Deployment: Participation in the user acceptance testing (UAT) and deployment of new digital tools or AI solutions that streamline O2C processes.</span></p><p><br /></p><p><span style="color:#000000"><b><u>Who You Are</u></b>:</span></p><p><br /></p><p><span style="color:#000000">-A Proactive Mindset: You are energized by a fast-paced, demanding environment and possess the &#34;courageous&#34; spirit needed to navigate uncertainty.</span></p><p><br /></p><p><span style="color:#000000">-Experienced Professional: You have a solid background in Customer Service,Supply Chain, Billing, Accounts Receivable or Pricing Administration (SAP experience is a must). You understand that the &#34;What&#34; (results) is just as important as the &#34;How&#34; (mindset and collaboration).</span></p><p><br /></p><p><span style="color:#000000">-Effective Communicator: You possess excellent phone etiquette and the assertive communication skills required to influence stakeholders and &#34;burn&#34; old habits in favor of new, agile ways of working.</span></p><p><br /></p><p><span style="color:#000000">-Analytical &amp; Creative: You don&#39;t just enter data; you see the story behind the numbers. You identify patterns and propose creative solutions to improve efficiency and customer satisfaction.</span></p><p><br /></p><p><span style="color:#000000">-Agile &amp; Adaptable: You are familiar with AGILE methodologies and are committed to continuous learning and fast iteration.</span></p><p><br /></p><p><span style="color:#000000">-Digital skills: You enjoy seeing new digital &amp; automated tools deployed which make the lives of our customer and us easier and more efficient allowing us to focus on tasks that really add value. You see innovation and AI deployment as an opportunity. Proven track record in deploying or supporting the implementation of automation technologies (e.g., RPA, workflow automation, AI applications) within a Supply Chain or Finance environment</span></p><p><br /></p><p><span style="color:#000000">-Sensibility for accuracy: Specific experience ensuring data quality and governance standards for critical O2C elements (customer master, material master, pricing condition records) to ensure reliable automation and AI outcomes.</span></p><p><br /></p><p><span style="color:#000000">-Language Skills: You are fluent in Spanish and have a professional command of English, enabling you to collaborate with regional colleagues. A good command of Catalan is very welcome.</span><br /></p><p><span style="color:#000000"><b><u>What We Offer</u></b>:</span></p><p><br /></p><p><span style="color:#000000">At Roche, we offer more than just a job. We offer the opportunity to contribute to a collective leadership culture where every individual contributor is empowered to be a leader. You will have a clear framework for development, where your contributions are recognized and rewarded based on the impact you create for our patients.</span></p><p><br /></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/order-handling-agent-roche/69d67d84c8e81216cd0cafab</link><guid isPermaLink="true">http://biotechroles.com/order-handling-agent-roche/69d67d84c8e81216cd0cafab</guid><pubDate>Wed, 08 Apr 2026 16:08:36 GMT</pubDate><company>Roche</company><location>Sant Cugat del Vallès</location><salary>$32000-45000</salary><type>Full time</type></item><item><title><![CDATA[Credit Analyst- Accounts Receivable]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p></p><p><b>The Opportunity:</b></p><p></p><p>As a <b>Credit Analyst - Accounts Receivable </b>based in our Americas Shared Service Center (SSC) in Costa Rica, you will play a critical role in safeguarding the company’s financial assets while enabling business growth. Your primary focus will be on <b>advanced credit risk assessment and order management</b>, ensuring that our commercial activities are backed by sound financial analysis.</p><p><b>Your key responsibilities will include:</b></p><ul><li><p><b>Financial Credit Analysis:</b> Perform evaluations of customer financial statements to assess creditworthiness. You will determine appropriate credit limits and risk categories, ensuring that Roche’s exposure is aligned with global credit policies.</p></li><li><p><b>Strategic Order Management:</b> Lead the Customer Order Release process, making critical decisions on held orders based on real-time credit data and payment history. <i>(Note: On-call availability outside working hours at least once a month may be required for urgent business needs).</i></p></li><li><p><b>Master Data Governance:</b> Maintain and optimize customer credit master data to ensure accurate system-driven controls and reporting.</p></li><li><p><b>Financial Operations:</b> Coordinate stringent financial tasks including manual corrections, posting and reconciling AR transactions, and maintaining a strong working knowledge of cash application and suspense account clearing.</p></li><li><p><b>Continuous Improvement:</b> Proactively propose system and process enhancements to streamline credit workflows and improve the overall performance and risk-mitigation capabilities of the SSC.</p></li><li><p><b>Collaboration &amp; Communication:</b> Handle complex inquiries from stakeholders in a timely manner. Provide guidance to team members, foster a collaborative environment, and support cross-functional projects as the business evolves.</p></li></ul><h3></h3><p><b>Who you are:</b></p><ul><li><p><b>Education:</b> University or College degree with a concentration in <b>Finance or Accounting </b>or related field.</p></li><li><p><b>Experience:</b> <b>3–5 years</b> of experience in Finance and Accounting, with a proven track record in <b>Credit Analysis or Risk Management</b>.</p></li><li><p><b>Technical Skills:</b> * Advanced ability to interpret financial statements (Balance Sheets, P&amp;L, Cash Flow).</p><ul><li><p>Solid understanding of operational accounting and Finance Shared Services workflows.</p></li><li><p>Experience with <b>SAP and BlackLine</b> is highly desirable.</p></li></ul></li><li><p><b>Languages:</b> Fluency in <b>English and Spanish</b> is required; Portuguese is preferred.</p></li><li><p><b>Core Competencies:</b> * Strong presentation and analytical skills with high attention to detail.</p><ul><li><p>Ability to work independently, manage tight deadlines, and &#34;manage up&#34; effectively.</p></li><li><p>Excellent customer service focus and stakeholder management abilities.</p></li></ul></li></ul><p></p><p><b><i>Relocation benefits are not available for this job posting.</i></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/credit-analyst-accounts-receivable-roche/69d67d83c8e81216cd0cafaa</link><guid isPermaLink="true">http://biotechroles.com/credit-analyst-accounts-receivable-roche/69d67d83c8e81216cd0cafaa</guid><pubDate>Wed, 08 Apr 2026 16:08:35 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Medical Copywriter]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>As a <b>Medical Copywriter</b>, you will support the growing medical writing team within Roche Services &amp; Solutions Centre, developing medical writing and digital content solutions for our business partners. You will play a key role in formulating and identifying current and future content needs while supporting various content creation initiatives.</p><div></div><p>Working alongside senior medical writers, you will help ensure the effective deployment of resources and tools to support efficient, cost-effective writing activities aligned with business needs. As part of the medical copy and content team within our Global Digital Hub, you will contribute to generating high-quality commercial content for diverse digital formats—including emails, videos, banners, infographics, and websites—that supports Roche&#39;s global communication strategies.</p><p></p><div></div><h2><b>The Opportunity</b></h2><p></p><p>In this role, you will:</p><p></p><div></div><ul><li>Develop your expertise through continuous learning, mentorship programs, and training to build comprehensive knowledge of Roche&#39;s therapeutic areas and enhance your medical writing capabilities</li><li>Create medical content across multiple formats and digital channels, including patient information, HCP educational materials (slides, posters, speaker briefs), conference presentations, newsletters, medical reports, and public relations materials</li><li>Master content briefs by identifying key components, asking probing questions, and proactively flagging potential issues that could affect delivery</li><li>Deliver publication-ready quality through high-level self-editing, accurate referencing, and marked-up packs that maintain source authenticity and authority</li><li>Manage concurrent projects across diverse therapeutic areas, adhering to regulatory frameworks while meeting agreed timelines and deadlines</li><li>Collaborate creatively with internal teams, clients, and stakeholders to develop compelling content and contribute innovative ideas that add measurable value</li><li>Prepare content for approval in VVPM, including comprehensive referencing</li><li>Demonstrate excellence in communication through professional liaison with team members, healthcare professionals, and key stakeholders</li></ul><div></div><h2></h2><h2><b>Who You Are</b></h2><p></p><p>Required Experience &amp; Profile:</p><p></p><div></div><ul><li>Bachelor&#39;s degree in medical sciences or a related field</li><li>0–2 years of experience in medical writing, communications, or a similar role (internships and academic projects are valued)</li><li>Native-level written and spoken English; fluency in Spanish, Italian, German, or French is a significant advantage</li><li>Exceptional attention to detail with a commitment to scientific rigor, consistency, and clarity</li><li>Strong time management and organizational skills, with the ability to prioritize tasks in a fast-paced environment</li><li>Excellent written and verbal communication skills</li><li>Proven ability to interpret data and understand complex scientific information</li><li>Proficiency with standard IT applications, including Google Suite</li><li>Collaborative mindset with the ability to work effectively across diverse teams and business stakeholders</li><li>Natural communicator and relationship builder with strong interpersonal skills</li><li>Customer-service mentality with a can-do attitude</li><li>Growth-oriented mindset with a passion for continuous improvement and emerging technologies</li><li>Accountable, focused, and precise in your approach to work</li><li>Quick learner with adaptability to changing priorities and environments</li></ul><div></div><h2></h2><h2><b>Ready to Join Our Team?</b></h2><p></p><p>If you&#39;re a motivated professional eager to launch your career in medical copywriting and make an impact at a global healthcare leader, we&#39;d love to hear from you.</p><p></p><p>Relocation benefits are not available for this job posting.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/medical-copywriter-roche/69d67d82c8e81216cd0cafa9</link><guid isPermaLink="true">http://biotechroles.com/medical-copywriter-roche/69d67d82c8e81216cd0cafa9</guid><pubDate>Wed, 08 Apr 2026 16:08:34 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$28000-45000</salary><type>Full time</type></item><item><title><![CDATA[Scientist, Patient-Centered Outcomes Research]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>This role is based in the Digital Endpoints and Patient-Centered Solutions (DEPCS) team, the innovative digital, AI, and tech function within Roche Product Development Data Sciences (PDD). DEPCS is responsible for embedding patient-centered and AI-enabled digital solutions into the fabric of clinical research.</span></p><p></p><h3><b><span>The Opportunity: </span></b></h3><p></p><ul><li><p><b><span>Lead Patient-Centered Measurement Strategy:</span></b><span><span> </span>Support the full lifecycle—design, validation, and deployment—of patient-centered outcome measures (PCOMs) across diverse clinical development programs within DEPCS.</span></p></li><li><p><b><span>Drive Data-Driven Development:</span></b><span><span> </span>Actively contribute to and implement quantitative drug development strategies, leveraging data science to enable critical, evidence-based decisions across our product pipeline.</span></p></li><li><p><b><span>Ensure Patient Voice Integrity:</span></b><span><span> </span>Collaborate with therapeutic area teams to ensure the patient voice and experience are robustly captured using evidence-based tools, modern methodologies, and a focus on both COAs and digital health measures.</span></p></li><li><p><b><span>Influence Strategy and Leadership:</span></b><span><span> </span>Depending on level, take the lead on measurement strategies for a specific molecule, indication, or multiple studies, supporting cross-functional development initiatives and potentially guiding a smaller franchise area.</span></p></li><li><p><b><span>Advance Scientific and Technical Knowledge:</span></b><span><span> </span>Apply expertise to develop or refine fit-for-purpose PCOM strategies, assisting with strategic and analytical activities for novel molecules and digital medical devices.</span></p></li><li><p><b><span>Execute Rigorous Research and Documentation:</span></b><span><span> </span>Execute detailed research plans, contributing to key validation studies, literature reviews, and the preparation of comprehensive health authority documentation and regulatory packages.</span></p></li><li><p><b><span>Modernize Measurement:</span></b><span><span> </span>Support the continuous improvement of PCOR methodologies, processes, and tools across DEPCS, exploring new innovative tools and technologies to modernize insight generation.</span></p></li><li><p><b><span>Expand Expertise and Collaboration:</span></b><span><span> </span>Build deep expertise in novel data types, statistical methods, advanced analytics, and data handling methods, while contributing to broader scientific advancement through authorship and participation in industry consortia.</span></p></li></ul><h3><b><span>Who you are:</span></b></h3><ul><li><p><b><span>Educational Foundation:</span></b><span><span> </span>You hold a Master’s or PhD in Psychology, Public Health, Biomedical Sciences, or a closely related field.</span></p></li><li><p><b><span>Core Experience:</span></b><span><span> </span>You bring a minimum of 2-4 years of experience (or 0-2 years with an advanced degree) supporting outcomes research, clinical trials, or digital endpoint development, ideally within the pharmaceutical/biotech industry.</span></p></li><li><p><b><span>PCOR &amp; Measurement Skills:</span></b><span><span> </span>You are familiar with psychometric validation, eCOA system implementation, or the data-driven design of Clinical Outcome Assessment (COA) instruments.</span></p></li><li><p><b><span>Regulatory &amp; Lifecycle Knowledge:</span></b><span><span> </span>You possess a growing understanding of the end-to-end drug development lifecycle and evolving regulatory science, particularly as it relates to PCOR and digital endpoints.</span></p></li><li><p><b><span>Collaboration &amp; Communication:</span></b><span><span> </span>You demonstrate strong collaboration skills and proven experience working effectively in cross-functional settings with clinical, regulatory, data science, and access teams.</span></p></li><li><p><b><span>Independent Contribution:</span></b><span><span> </span>You are able to independently contribute to critical study documents and evidence packages, demonstrating a capacity for independent, sound decision-making and problem-solving.</span></p></li><li><p><b><span>Strategic Agility:</span></b><span><span> </span>You possess excellent strategic agility, critical thinking skills, and a global mindset, demonstrating respect for cultural differences when interacting with colleagues worldwide.</span></p></li></ul><div></div><p><span>Ready to bring your unique qualities to Roche and make an impact? Apply now and join us in our mission to shape the future of healthcare.</span></p><p><b> </b></p><p><b> </b></p>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/scientist-patient-centered-outcomes-research-roche/69d67d82c8e81216cd0cafa8</link><guid isPermaLink="true">http://biotechroles.com/scientist-patient-centered-outcomes-research-roche/69d67d82c8e81216cd0cafa8</guid><pubDate>Wed, 08 Apr 2026 16:08:34 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$110000-160000</salary><type>Full time</type></item><item><title><![CDATA[Strategy Lead]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><div><p><b><u>Strategy Lead</u></b></p></div><div><div><div><div><div><div><div><div><div><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p><b>The Opportunity:</b></p></div></div></div></div></div></div></div></div></div><p><span>Customers are more empowered than ever, with more data to support their decision making, and lower barriers to switching loyalties. This has created an imperative for us to structure and build our organization around our customers to ensure we listen and understand their needs and respond at speed. As part of this new focus, we are searching for a Head of Strategy and Business Operations (Molecular Lab Customer Area) to support the Head of Molecular Lab Customer Area in the daily operations and shaping the strategic direction together with the Molecular Lab Leadership team.</span></p><p><span>This role offers a unique perspective with exposure to a broad range of topics, functions and senior management. This is a highly visible position that requires executive presence, exceptional leadership, strategic thinking, analytic detail and rigor, and ability to operate at most senior levels of the company. </span></p><p></p><p><b>Key Roles &amp; Responsibilities:</b></p><ul><li><p><span>Act as a strategic advisor to the Head of Molecular Lab Customer Area in collaboration with the senior leadership team </span></p></li><li><p><span>Drives the strategic planning for this team together with the Molecular Lab leadership Team and in conjunction with the RDS strategy leader </span></p></li><li><p><span>Ensures clear responsibilities for defined actions of the Molecular Lab strategic plan and tracks implementation</span></p></li><li><p><span>Collaborates effectively with the Strategy &amp; Transformation Office </span></p></li><li><p><span>Drive the Molecular Lab leadership meetings and plan the agenda and support the team in timely, well-informed decision making</span></p></li><li><p><span>Design and facilitate effective meetings by selecting relevant topics, balancing content review with discussion, and moderating dialogue.</span></p></li><li><p><span>Increase LT effectiveness and cohesiveness.</span></p></li><li><p><span>Track and monitor LT decisions and actions; hold LT members accountable to decisions and actions</span></p></li><li><p><span>Lead, supported by Molecular Lab administrative staff, on all aspects of logistics and planning of LT meetings</span></p></li><li><p><span>Collaborate with Head of RDS and subject matter experts to develop strategic communications and presentation materials for various speaking engagement</span></p></li><li><p><span>Lead high impact strategic initiatives relevant to Molecular Lab in partnership with the other Customer Area </span></p></li><li><p><span>Work with Customer Area Head and LCLs on Investor Relations Strategy and Slide Decks</span></p></li><li><p><span>Work to enable better cross Customer Area relations and strategy heads and Functions as well as with RDS, RIS, Function and the Strategy &amp; Transformation Office</span></p></li><li><p><span>Strengthen communication flows from the leadership team to the employees and vice versa</span></p></li></ul><p></p><p><b>Who you are:  </b></p><p>Professional and Technical Requirements:</p><ul><li><p>Education: Master&#39;s degree or higher in Bioengineering, Biomedical Engineering, or a related field.</p></li><li><p><span>5&#43; years of experience in the life science sector that may be directly comparable to Diagnostics and/or Pharmaceuticals is an advantage</span></p></li><li><p><span>Strategy consulting background and skill set would be desirable </span></p></li><li><p><span>Strong leadership experience, preferably with experience leading diverse team and/or highly complex matrix leadership of enterprise-level projects </span></p></li><li><p><span>Strong business sense with a solid understanding of the healthcare industry and experience operating in a regulated environment</span></p></li></ul><p></p><p>Experience, Skills, Knowledge:</p><ul><li><p><span>Translate divisional strategy into clear BA priorities and initiatives</span></p></li><li><p><span>Strong project management and ability to operate across functions and global teams</span></p></li><li><p><span>Excellent communication and presentation skills; able to simplify complex topics</span></p></li><li><p><span>Strategic thinker with strong problem-solving skills and ability to connect cross-functional impacts</span></p></li><li><p><span>Highly organized, detail-oriented, and able to manage multiple priorities effectively</span></p></li><li><p><span>Self-starter with strong stakeholder management skills; builds trust and influences senior leadership</span></p></li></ul><p></p><p><b><i>As this position is a global role, international business travel maybe required depending upon the business location of the successful candidate.</i></b></p><p></p><p><b><i>Relocation Benefits Are Not Available For This Job Posting.</i></b></p><p></p><p>The expected salary range for this position based on the primary location of Pleasanton, CA is $186,300 - $346,100. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/strategy-lead-roche/69d67d81c8e81216cd0cafa7</link><guid isPermaLink="true">http://biotechroles.com/strategy-lead-roche/69d67d81c8e81216cd0cafa7</guid><pubDate>Wed, 08 Apr 2026 16:08:33 GMT</pubDate><company>Roche</company><location>Pleasanton</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Technical Assessor & Service Excellence Support]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><i>Beneficios de relocalización <b>están</b> disponibles para esta posición.</i></p><p></p><p><b>Objetivo del Puesto:</b> <span>Soporte técnico, instalación, configuración, modificación y reparación de equipamientos Roche.</span></p><p><span>Co-crear el diseño de soluciones con clientes e identificar y dar solución a problemas asociados al uso de los equipos en todos los clientes.</span></p><p><span>Apoyo en taller y coordinación de mantenimientos preventivos.</span></p><p></p><p><b>Sobre Nuestra Oportunidad:</b></p><ul><li><p><span>Ejecutar la instalación, configuración y mantenimiento de equipos, asegurando el cumplimiento de estándares de calidad del fabricante y coordinando con áreas de aplicaciones e IT.</span></p></li><li><p><span>Gestionar y ejecutar mantenimientos preventivos y correctivos, incluyendo la planificación, monitoreo de cumplimiento, registro y cierre oportuno de casos, así como la adecuada documentación en sistemas.</span></p></li><li><p><span>Asegurar la operación del taller técnico, incluyendo procesos de descontaminación, gestión de stock de repuestos y cumplimiento de protocolos establecidos.</span></p></li><li><p><span>Brindar soporte técnico y asesoría a clientes, resolviendo consultas y reclamos, participando en demostraciones, y promoviendo la co-creación de soluciones para optimizar el uso de los equipos.</span></p></li><li><p><span>Cumplir y promover normativas corporativas, calidad y seguridad, participar en entrenamientos técnicos, transferir conocimiento al equipo y dar seguimiento a acciones derivadas de notificaciones, asegurando su correcta implementación y cierre.</span></p></li></ul><p></p><p><b>Tu Perfil:</b></p><ul><li><p><span>Título Universitario o Técnico en Electrónica, Mecánica o profesionales afines.</span></p></li><li><p><span>Experiencia laboral de al menos 2 años relacionada con el puesto.</span></p></li><li><p><span>Nivel de Inglés Intermedio.</span></p></li><li><p><span>Manejo de Office nivel intermedio.</span></p></li></ul><p></p><p><span>#LI-DC1</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/technical-assessor-and-service-excellence-support-roche/69d67d81c8e81216cd0cafa6</link><guid isPermaLink="true">http://biotechroles.com/technical-assessor-and-service-excellence-support-roche/69d67d81c8e81216cd0cafa6</guid><pubDate>Wed, 08 Apr 2026 16:08:33 GMT</pubDate><company>Roche</company><location>RM- Region Metropolitana de Santiago</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Pasante de Estudios Clínicos]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Como <b>Pasante de Estudios Clínicos </b>tendrás la oportunidad de aprender y desarrollarte en un entorno dinámico, contribuyendo directamente al inicio, conducción y cierre de nuestros estudios. Únete a un equipo colaborativo donde tu trabajo diario impactará en la mejora continua de procesos y en el desarrollo de soluciones médicas para el futuro.</p><p></p><p><b>La Oportunidad:</b></p><ul><li><p>Asistes al equipo local gestionando pagos a comités, entes regulatorios, investigadores y centros de investigación.</p></li><li><p>Preparas, envías y das seguimiento a la documentación regulatoria para su presentación ante los centros y autoridades correspondientes.</p></li><li><p>Actualizas los sistemas de gestión clínica y otras herramientas para asegurar el correcto seguimiento y avance de los proyectos.</p></li><li><p>Archivas y realizas el control de calidad de los documentos generados, manteniendo los repositorios y archivos de los estudios al día.</p></li><li><p>Participas en la revisión de los procedimientos de los comités de ética y gestionas la información en nuestras bases de datos.</p></li><li><p>Das soporte operativo en la renovación anual de seguros para nuestros estudios en Argentina y coordinas la logística de materiales de investigación.</p></li><li><p>Colaboras en la elaboración de instructivos locales, enfocándote en la mejora continua de los procesos del equipo.</p></li><li><p>Gestionas la importación y realizas el seguimiento de inventario de dispositivos médicos y otros insumos clínicos.</p></li></ul><p></p><p><b>Quién eres:</b></p><ul><li><p>Eres <b>estudiante activo universitario </b>con marcado interés en desarrollarte en el área de estudios clínicos y gestión de calidad.</p></li><li><p>Manejas el idioma inglés para comunicarte eficientemente.</p></li><li><p>Tienes facilidad y experiencia en el uso de sistemas informáticos de manejo de datos.</p></li><li><p>Manejas eficientemente herramientas del entorno Office (Word, Excel, PowerPoint) y el ecosistema de Google (Mail, Calendar, Gemini, Notebook LM).</p></li><li><p>Te destacas por tu organización, prestando especial atención a los detalles en la revisión y archivo de documentación.</p></li></ul><p></p><p><b>Preferible:</b></p><ul><li><p>Cursar tu carrera universitaria en el campo de las Ciencias de la Salud o Ciencias Económicas.</p></li></ul><p></p><p>Los beneficios de reubicación no están disponibles para esta publicación.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/pasante-de-estudios-clinicos-roche/69d67d80c8e81216cd0cafa5</link><guid isPermaLink="true">http://biotechroles.com/pasante-de-estudios-clinicos-roche/69d67d80c8e81216cd0cafa5</guid><pubDate>Wed, 08 Apr 2026 16:08:32 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$0-1000</salary><type>Part time</type></item><item><title><![CDATA[Head, Quality & Regulatory Affairs, Singapore]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><b>Head of Quality &amp; Regulatory Affairs, Singapore</b></b></p><p></p><h3></h3><h3><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. </span></h3><h3></h3><h3><span>That’s what makes us </span>Roche<span>.</span></h3><h3></h3><h3><span>As the </span><b>Head of Quality &amp; Regulatory Affairs</b><span>, you are a senior leader accountable for overseeing all aspects of the Singapore affiliate business, ensuring our products and services meet the highest standards of safety and compliance throughout their lifecycle. You work as a strategic partner to business teams to ensure in depth transfer of requirements and information between internal product and regulatory teams with local stakeholders. Ensuring the translation of vital modular Quality Management System (mQMS) requirements into efficient local operations. You push the boundaries to implement smart, risk-based processes that ensure the Singapore affiliate remains a leader in the IVD industry while navigating an evolving regulatory landscape.</span></h3><h3></h3><h3><b><b>Your Opportunity</b></b></h3><ul><li><h3><b><b>Affiliate Quality Leadership:</b><span> </span></b><span>You drive business results by ensuring the successful implementation of the mQMS. You monitor internal global metrics and KPIs, coordinate local management reviews, and lead the organisation’s preparation for required certifications and audits, e.g. SS GDPMDS certification.</span></h3></li><li><h3><b><b>Regulatory Excellence:</b><span> </span></b><span>You take overall responsibility for regulatory submissions and product registrations across diverse portfolios, including Core Lab, Molecular Lab, Point of Care, Pathology Lab, and Digital Solutions. You ensure all local regulations are observed and implemented seamlessly across the company.</span></h3></li><li><h3><b><b>Strategic Liaison:</b><span> </span></b><span>You serve as the primary external contact for the Health Sciences Authority (HSA) and industry bodies. You advocate for the IVD industry and coordinate closely with internal product regulatory teams to keep the affiliate informed of emerging global issues.</span></h3></li><li><h3><b><b>Compliance &amp; Risk Mitigation:</b><span> </span></b><span>You oversee the complaint management system and drive the review of promotional materials to ensure full compliance with local laws. You communicate significant quality or regulatory risks to Executive Management in a timely manner. You also serve as the Enterprise Risk Manager for the Singapore affiliate. </span></h3></li><li><h3><b><b>Operational Oversight:</b><span> </span></b><span>You ensure all products maintain valid licensing and lead your team to develop and independently implement solutions that ensure daily work is completed without jeopardizing compliance.</span></h3></li><li><h3><b><b>Innovation &amp; Digital Readiness:</b><span> </span></b><span>At the intersection of evolving traditional diagnostics and software/AI regulations, you keep up with the trend and enable the organisation to face the latest regulatory requirements, ensuring data privacy requirements (PDPA) are integrated into our diagnostic data strategies.</span></h3></li></ul><h3></h3><h3><b><b>Who You Are</b></b></h3><ul><li><h3><b><b>Qualified Professional:</b><span> </span></b><span>You hold a Bachelor’s degree in Biomedical Science or an equivalent field; a medical laboratory background is preferred.</span></h3></li><li><h3><b><b>Subject Matter Expert:</b><span> </span></b><span>You have at least 8 years of relevant work experience, with a recognized expertise in both Regulatory and Quality Affairs within the healthcare sector.</span></h3></li><li><h3><b><b>Strategic Advocate:</b><span> </span></b><span>You have a proven track record of influencing external stakeholders and industry bodies. You possess the executive presence required to represent Roche in high-stakes quality and regulatory discussions.</span></h3></li><li><h3><b><b>Digital Navigator:</b><span> </span></b><span>You demonstrate digital fluency, with experience navigating software/AI regulations and data privacy requirements (PDPA), which is considered a significant advantage in our evolving portfolio.</span></h3></li><li><h3><b><b>Agile Leader:</b><span> </span></b><span>You are a role model for agile leadership behaviors, able to troubleshoot complex technical issues as they arise and lead a high-performing team in a fast-paced, regulated environment.</span></h3></li></ul><h3></h3><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/head-quality-and-regulatory-affairs-singapore-roche/69d67d80c8e81216cd0cafa4</link><guid isPermaLink="true">http://biotechroles.com/head-quality-and-regulatory-affairs-singapore-roche/69d67d80c8e81216cd0cafa4</guid><pubDate>Wed, 08 Apr 2026 16:08:32 GMT</pubDate><company>Roche</company><location>Singapore</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Service Engineer  - Lothian Region]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p>Field Service Engineer</p><p>Location: Lothian Region</p><p></p><h3><b><span>Are you an experienced field service engineer seeking a meaningful role in the healthcare industry? Are you excited about the prospect of joining a forward-thinking, high-tech business that is passionate about improving patients&#39; lives? If so, we have the perfect opportunity for you at Roche Diagnostics, the world&#39;s leading provider of diagnostic equipment.   Roche covers territories throughout the UK, Scotland, Ireland and Wales England</span></b></h3><h3><br /><b><b>The Role</b><br /><span>As a service engineer with experience in diagnosing and repairing electro-mechanical, fluidic, and electronic systems. Applicants with a background in biomedical engineering, industrial engineering, automation, or aerospace (to name a few) are encouraged to apply. You will be assigned to the trust within the NHS Lothian health board. If you have a strong foundation in troubleshooting at the component level and have progressed to systems-level expertise, we want to hear from you.</span></b></h3><h3><br /><b><span>In this important position within the Technical Services group, you will provide technical support for a variety of medical equipment. With exciting product launches and significant R&amp;D investment in our portfolio, you will have the chance to support the growth of key business accounts across your territory and the UK. You will report to a Regional Technical Manager and be responsible for preventative, corrective, modification, installation, and out-of-hours support for specified products ranging from large to medium-sized equipment.</span></b><br /> </h3><h3><b><b>Who You are</b><br /><span>To be considered for this role, you should have an engineering or electrical qualification and be able to confidently represent the company at client sites. You should have good previous field service experience with high-value capital equipment and be able to build productive customer relationships in a complex environment. You may be required to travel throughout the UK on occasion but will primarily be assigned to the NHS Lothian Health Board. </span><br /><span>At Roche Diagnostics, we are committed to investing in our people as well as our business. In addition to a competitive salary and benefits package, we offer a recognized product training program and continuous support to help you develop your knowledge, skills, and potential. If you are ready to take the next step in your professional development and make a positive impact in the healthcare industry, we encourage you to apply for this exciting field service engineer opportunity</span></b></h3><p> </p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.</span></p>]]></description><link>http://biotechroles.com/service-engineer-lothian-region-roche/69d67d7fc8e81216cd0cafa3</link><guid isPermaLink="true">http://biotechroles.com/service-engineer-lothian-region-roche/69d67d7fc8e81216cd0cafa3</guid><pubDate>Wed, 08 Apr 2026 16:08:31 GMT</pubDate><company>Roche</company><location>Scotland</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director, Incentive Compensation]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>This position can be based remotely anywhere in the U.S. (there may be some restrictions based on legal entity). The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 10% travel.<br><br>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible to you.<br><br>Company will not sponsor visas for this position.<br><br>The Executive Director, Incentive Compensation is an enterprise leader who shapes and delivers the next generation of incentive compensation strategy across U.S. customer facing organizations. This role is central to evolving incentive compensation from a legacy, process driven function into a modern, strategically aligned capability that motivates the right behaviors, reinforces commercial priorities, and builds trust with the field. The Executive Director owns the enterprise vision, governance, and operating model, ensuring clarity, consistency, and impact across the organization. By balancing innovation with rigor and transformation with operational excellence, this leader helps ensure incentive compensation is both meaningful and effective.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Key Responsibilities:  </span></b></p><ul><li><span>Serve as the enterprise architect for incentive compensation, shaping a future</span><span>‑</span><span>ready strategy that aligns performance measurement and rewards with evolving commercial and customer engagement priorities.</span></li><li><span>Partner closely with Sales Leadership, Therapeutic Area leaders, Finance, P&amp;O, Legal, Compliance, and Technology to ensure incentive compensation is fair, compliant, scalable, and tightly aligned to enterprise goals.</span></li><li><span>Position incentive compensation as a powerful strategic lever that drives the right behaviors and outcomes – not simply an administrative or transactional process.</span></li><li><span>Lead the design and continuous evolution of incentive frameworks, ensuring alignment with field roles, portfolio needs, and go</span><span>‑</span><span>to</span><span>‑</span><span>market models.</span></li><li><span>Own enterprise governance, including decision rights, documentation standards, change management, and escalation pathways, bringing clarity and confidence to stakeholders.</span></li><li><span>Provide executive oversight of end</span><span>‑</span><span>to</span><span>‑</span><span>end incentive compensation delivery, ensuring accurate, timely, and trusted reporting and payouts across the field.</span></li><li><span>Champion operational excellence by partnering with Sales Operations, Analytics, Finance, Data Enablement, and Technology to maintain a high</span><span>‑</span><span>quality, audit</span><span>‑</span><span>ready environment.</span></li><li><span>Drive modernization of incentive compensation tools, platforms, and processes, increasing transparency, reducing manual effort, and improving speed and insight.</span></li><li><span>Lead, develop, and inspire a high</span><span>‑</span><span>performing incentive compensation organization, fostering a culture of accountability, collaboration, and continuous learning.</span></li></ul><p></p><p><b>Essential Requirements: </b></p><ul><li>Bachelor’s degree required from 4-year college or university.</li><li>10&#43; years’ experience of analytics experience in pharmaceutical, biotech, healthcare, or similarly structured industries with large, geographically dispersed sales teams; including 6&#43; years’ experience in an Incentive Compensation role with excellent achievements. We also welcome candidates from other complex environments such as medical devices, diagnostics, life sciences services, insurance, consumer health, or B2B sectors, especially where strong leadership and customer engagement are central to success.</li><li>Demonstrated experience leading enterprise‑scale incentive compensation strategy, design, and execution in highly matrixed organizations.</li><li>Strong track record of partnering with senior commercial, finance, and functional leaders to shape strategy and deliver meaningful business outcomes.</li><li>Proven success leading teams through transformation, modernization, and operating model evolution.</li><li>Ability to attract, develop, and retain diverse talent while building high‑performing, engaged teams.</li><li>Strategic and analytical thinker with strong cross‑functional leadership skills and experience managing complex initiatives and budgets.</li><li>Executive presence and systems thinking, with comfort navigating ambiguity while creating clarity, alignment, and momentum.</li></ul><p></p><p><b>Desirable Requirements: </b></p><ul><li>Forward‑looking leader with deep expertise in incentive compensation governance, compliance, operational risk, and technology modernization, skilled at navigating complexity and creating alignment at scale.</li><li>Recognized as a trusted, collaborative change leader with strong executive presence and a passion for shaping the future of customer engagement in healthcare.</li></ul><p></p><p><b>Novartis Compensation Summary</b><b>:</b></p><p>The salary for this position is expected to range between $236,000.00 and $439,400.00 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$236,600.00 - $439,400.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Calls Handling, Customer Requirements, Customer Service, E-Learning, Employee Onboarding, Leadership, Microsoft Access, Operations, Procurement, Sales Targets, Selling Skills, Technical Skills]]></description><link>http://biotechroles.com/executive-director-incentive-compensation-novartis/69d67ccfc8e81216cd0caf8a</link><guid isPermaLink="true">http://biotechroles.com/executive-director-incentive-compensation-novartis/69d67ccfc8e81216cd0caf8a</guid><pubDate>Wed, 08 Apr 2026 16:05:35 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Director, Data Quality and Governance]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Insights and Decision Science (IDS) team is dedicated to enabling improved decision-making at Novartis by leveraging data and advanced analytics capabilities to generate actionable insights that drive business growth. We collaborate closely with the US business, bringing insights and challenging ideas to empower smarter, data-driven decision-making. The Lead, Quality Assurance and Governance is responsible to ensure operational processes adopt data governance frameworks, policies, and standards that support the organization's strategic objectives. <br><br> <br><br>By collaborating with Data Strategy and Governance pillar of IDS, this role will ensure that all relevant frameworks are implemented, governance is put in place along with escalation mechanism. The Lead will also work with cross functional IDS pillars to understand and triage data quality issues ultimately ensuring enhancement of product or business process quality. The ultimate goal of this team will be to deliver high trust in data.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><div><div><div><p><b><span>Major Accountabilities</span></b><span><span>  </span></span><span> </span></p></div></div><div><div><p><span> </span></p></div></div></div></div><div><div><p><b><span>Data Quality Management</span></b><span><span>: Overseeing the implementation of data quality initiatives to ensure that data is </span><span>accurate</span><span>, complete, and reliable. This includes monitoring data quality metrics, </span><span>identifying</span><span> data quality issues, and implementing corrective actions.</span></span><span> </span></p></div><div><p></p><p><b><span>Data Governance Framework</span></b><span><span>: Developing and </span><span>maintaining</span><span> a robust data governance framework that defines roles, responsibilities, and processes for data management. This framework ensures that data is managed as </span><span>a valuable asset</span><span> and is used in compliance with regulatory requirements.</span> Establish and enforce data governance policies, standards and procedures. </span></p></div><div><p></p><p><b><span>EDM Support</span></b><span><span>: </span><span>Supporting US EDO with quality processes and monitoring.</span> Embed DCAM and DAMA principles into data management processes, including metadata management, data lineage, data privacy, and master/reference data management.<span> </span>Conduct regular DCAM-based capability assessments to identify gaps and drive continuous improvement.</span></p><p><span> </span></p></div><div><p><b><span>Stakeholder Collaboration</span></b><span><span>: Collaborating with various stakeholders, including IT, business units, and external partners, to ensure that data governance practices are aligned with business needs and </span><span>objectives</span><span>.</span></span><span> </span></p><p></p></div><div><p><b><span>Risk Management</span></b><span><span>: </span><span>Identifying</span><span> and mitigating risks associated with data management, including data breaches, data loss, and non-compliance with regulations.</span></span><span> </span></p><p></p></div><div><p><b><span>Training and Awareness</span></b><span><span>: Promoting data governance awareness and providing training to employees on data management best practices and policies.</span></span><span> </span></p><p></p><p><b><span>Data Stewardship Oversight:</span></b><span> Establishing and managing a network of Data Stewards across business units. Defining stewardship roles and responsibilities, facilitating regular engagement, and ensuring Data Stewards are empowered to monitor, report, and resolve data quality and governance issues in alignment with Novartis Governance policies and standards</span></p><p></p></div><div><p><b><span>Continuous Improvement</span></b><span><span>: Continuously evaluating and improving data governance practices to adapt to changing business needs and technological advancements</span></span><span> </span></p><p></p></div></div><div><p><b><span>Key Performance Indicators </span></b><span> </span></p></div><div><div><p><span> </span></p></div><div><p><b><span>Data Accuracy</span></b><span><span>: Measure the percentage of data entries that are free from errors and discrepancies. High data accuracy ensures reliable decision-making.</span></span><span> </span></p></div><div><p><b><span>Data Completeness</span></b><span><span>: Track the proportion of data fields that are fully populated. Complete data sets are essential for comprehensive analysis.</span></span><span> </span></p></div><div><p><b><span>Data Consistency</span></b><span><span>: Evaluate the consistency of data across different systems and databases. Consistent data helps </span><span>maintain</span><span> integrity and reduces redundancy.</span></span><span> </span></p></div><div><p><b><span>Data Timeliness</span></b><span><span>: Assess the speed at which data is updated and made available for use. Timely data is crucial for real-time decision-making.</span></span><span> </span></p></div><div><p><b><span>Compliance Rate</span></b><span><span>: </span><span>Monitor</span><span> adherence to data governance policies and regulatory requirements. High compliance rates </span><span>indicate</span><span> effective governance practices.</span></span><span> </span></p></div><div><p><b><span>Data Quality Issue Resolution Time</span></b><span><span>: Measure the time taken to </span><span>identify</span><span> and resolve data quality issues. Faster resolution times improve data reliability.</span></span><span> </span></p></div><div><p><b><span>User Satisfaction</span></b><span><span>: Gauge the satisfaction levels of stakeholders and users with the quality and governance of data. Positive feedback reflects successful data management.</span></span><span> </span></p></div><div><p><b><span>Training and Awareness</span></b><span><span>: Track the number of employees trained </span><span>on</span><span> data governance policies and best practices. Increased awareness leads to better data handling.</span></span><span> </span></p></div><div><p><b><span>Risk Mitigation</span></b><span><span>: Evaluate the effectiveness of risk management strategies in preventing data breaches and losses. Effective risk mitigation ensures data security.</span></span><span> </span></p></div><div><p><b><span>Continuous Improvement</span></b><span><span>: Measure the progress in enhancing data governance practices over time. Continuous improvement </span><span>indicates</span><span> a proactive approach to data management.</span></span><span> </span></p><p></p><p><b>Essential Requirements:</b></p><ul><li>Extensive experience in the pharmaceutical or healthcare industry, with a deep understanding of data quality, data governance and other data dimensions. The candidate should be able to drive operational as well as process excellence. </li></ul><p></p><p><b>Educational Qualifications &amp; Minimum Work Experience </b></p><ul><li>Bachelor’s degree in data science, Information Technology, Business Administration, or a related field. Master&#39;s degree preferred.</li><li>Minimum of 10 years of experience in data quality assurance, data governance, or related roles, with at least 5 years in a leadership position.</li><li>Strong analytical skills, excellent communication and leadership abilities, proficiency in data management tools and software, and a deep understanding of data governance frameworks and best practices.</li><li>Lean Six Sigma Practitioner (Certified Lean Six Sigma Black Belt)</li><li>Experience of conducting internal audits and hands on experience of managing external certification/surveillance audits.</li></ul><p></p><p><b>Additional qualifications are as follows: </b></p><ul><li>Minimum 5 years of experience in the pharmaceutical or healthcare industry, with a strong focus on data quality assurance and governance in a healthcare setting.</li><li>Proven track record of enabling data-driven decision-making at a senior leadership level, including addressing complex business challenges.</li><li>Strong analytical background, strategic thinking and problem-solving skills, with the ability to translate complex data into actionable insights and aligning them with business priorities to drive impactful results.</li><li>Demonstrated experience implementing EDM, DCAM, and DAMA frameworks in a complex, regulated environment.</li><li>Certification in DCAM, DAMA (CDMP), or equivalent preferred.</li></ul><p></p><p><b>Why Novartis:</b><span> Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: </span><span><span>https://www.novartis.com/about/strategy/people-and-culture </span></span><br /><span> </span><br /><b>You’ll receive:</b><span> You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. </span><span><span>https://www.novartis.com/careers/benefits-rewards </span></span><br /><span> </span><br /><b>Commitment to Diversity and Inclusion:</b><span>  </span><br /><span>Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.  </span><br /><span> </span><br /><b>Join our Novartis Network:</b><span> If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: </span><span><span>https://talentnetwork.novartis.com/network.</span></span></p><p></p></div></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Brand Awareness, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Strategy, Digital Marketing, Go-To-Market Strategy, Influencing Skills, Inspirational Leadership, Marketing Strategy, Media Campaigns, People Management, Product Marketing, Product Roadmap, Return on Investment (ROI), Stakeholder Engagement, Stakeholder Management, Strategic Marketing]]></description><link>http://biotechroles.com/director-data-quality-and-governance-novartis/69d67ccfc8e81216cd0caf89</link><guid isPermaLink="true">http://biotechroles.com/director-data-quality-and-governance-novartis/69d67ccfc8e81216cd0caf89</guid><pubDate>Wed, 08 Apr 2026 16:05:35 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Egypt CFO]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>About the Role:<br><br>Lead the Finance function for a country or cluster of countries (typically large or medium revenue as per the Core grid). Typically leads a team of experienced professionals.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Requirements:</b></p><ul><li>Manage the execution of regional / global strategies and develop strategic long-term financial and business plans.</li><li>Manage the budgeting process and prepare long term financial forecasts in relation to developing future strategies for the Division/Business Unit, and prepare various high level management reports on a monthly, quarterly and/or annual basis.</li><li>Manage performance in Finance, monitor business performance against set objectives and take corrective measures, as required.</li><li>Engage proactively in external and commercial activities with the objective of driving growth, productivity and efficiency for the business.</li><li>Lead the implementation of risk management processes, financial compliance and controls (Business Process Controls [BPC], Internal and External Audits) and manage the correct and timely implementation of financial, purchasing and control processes and policies and ensure adherence thereof.</li><li>Manage and integrate services delivered to the organization (define processes, agree and track Service Level Agreements [SLAs]).</li><li>Manage market studies and financial analyses and set stretch objectives based on external / competitor benchmark.</li><li>Manage and develop teams of experienced Finance professionals and builds global talent pipeline.</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt. Distribution of marketing samples (where applicable)</li></ul><p></p><p><b>Essential Requirements:</b></p><ul><li>15&#43; years of experience</li><li>Proven International experience is a must</li><li>Prior CFO experience within a multinational pharma organization</li></ul><p></p><p><b>Desirable Requirements:</b></p><ul><li>Target Achievement of Sales, TFC and Consolidated Gross Income</li><li>Accuracy of Forecasts compared to Actuals</li><li>Working Capital ratios achieved</li><li>Compliance of financial processes with NFCM requirements and meeting statutory and internal reporting deadlines</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Ability To Influence Key Stakeholders, Coaching, Corporate Governance, Decision Support, Effective Communications, Financial And Management Reporting, Market Understanding, Pmi (Post-Merger Integration), Resource Allocation, Strategic Decision Making]]></description><link>http://biotechroles.com/egypt-cfo-novartis/69d67ccbc8e81216cd0caf88</link><guid isPermaLink="true">http://biotechroles.com/egypt-cfo-novartis/69d67ccbc8e81216cd0caf88</guid><pubDate>Wed, 08 Apr 2026 16:05:31 GMT</pubDate><company>Novartis</company><location>New Cairo</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Ekspert tehnologije izdelkov (m/ž/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Lokacija: Ljubljana, Slovenija<br>Interni naziv pozicije: Ekspert tehnologije izdelkov III (m/ž/d)<br><br>Če te motivira, da tvoja strokovnost neposredno vpliva na kakovost, zanesljivost in robustnost proizvodnih procesov, je to prava priložnost zate. Kot Ekspert tehnologije izdelkov III (m/ž/d) boš odgovoren/-na za poglobljeno poznavanje dodeljenih izdelkov skozi celoten življenjski cikel ter za ohranjanje zmogljivosti procesov, vrednotene s pomočjo statističnih analiz kritičnih parametrov. S svojim delom boš pomagal/-a zagotavljati robustne procese, stalno validiranost ter kulturo neprestanih izboljšav, hkrati pa boš ključna povezava pri prenosu znanja med funkcijami in lokacijami. V tesnem sodelovanju s proizvodnjo in strokovnimi ekipami boš zagotavljal/-a tehnično podporo skladno z zakonodajo, internimi standardi, dobrimi praksami in poslovnimi cilji. <br><br>Relokacijska podpora: Ta vloga je locirana v Ljubljani, Slovenija. Novartis ne nudi podpore pri relokaciji, zato se prijavite le, če vam je lokacija dostopna.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Vaše ključne odgovornosti:</b></p><ul><li>Skrb za poglobljeno strokovno poznavanje dodeljenih izdelkov skozi celoten življenjski cikel.</li><li>Pripravljanje, vzdrževanje in posodabljanje analiz tveganj kakovosti za posamezne izdelke.</li><li>Ocenjevanje trendov in sposobnosti procesov ter skrb za izvajanje ustreznih korektivnih ukrepov.</li><li>Zagotavljanje stalne validiranosti procesov ter podpora procesne in kontinuirne validacije izdelkov.</li><li>Sodelovanje pri tehničnih spremembah, ocenjevanje izvedljivosti in tveganj ter predlaganje obsega tehničnih serij.</li><li>Nudenje strokovne podpore proizvodnji ter omogočanje učinkovitega prenosa znanj med funkcijami in lokacijami.</li><li>Sodelovanje v projektih proizvodne odličnosti za večjo robustnost, vzdržnost in stabilnost procesov.</li><li><span>Skrb za specifikacije in skladnost primarnih materialov.</span></li></ul><p></p><p><b>Vaš doprinos k delovnem mestu:</b></p><ul><li>Univerzitetna izobrazba iz farmacije, farmacevtske tehnologije, kemije ali druge ustrezne znanstvene smeri.</li><li>Aktivno znanje angleškega jezika.</li><li>Poznavanje orodja Microsoft Office.</li><li>Obvladanje analitičnega razmišljanja ter uporabe podatkov za spremljanje procesov.</li><li>Sposobnost učinkovitega sodelovanja z različnimi funkcijami, laboratoriji in proizvodnjo.</li></ul><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>določen čas 1 leta</b> s poskusno dobo 6 mesecev. Prijavo oddajte z življenjepisom v slovenskem in angleškem jeziku.</p><p></p><p><b>Ugodnosti in nagrajevanje:</b> <span>Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika in delom od doma, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje, shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj.</span></p><p></p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a> </p><p></p><p><b>Predani smo raznolikosti in vključenosti: </b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.</p><p></p><p><b>Zakaj Novartis: </b>Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a> </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process and Cleaning Validation, Process Control, Quality Control, Regulatory Compliance, Resilience and Risk Management]]></description><link>http://biotechroles.com/ekspert-tehnologije-izdelkov-mzd-novartis/69d67ccbc8e81216cd0caf87</link><guid isPermaLink="true">http://biotechroles.com/ekspert-tehnologije-izdelkov-mzd-novartis/69d67ccbc8e81216cd0caf87</guid><pubDate>Wed, 08 Apr 2026 16:05:31 GMT</pubDate><company>Novartis</company><location>Ljubljana</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Senior Hematology Medical Science Liaison - Riyadh]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>To serve as a liaison to the medical/ scientific community and responsible for establishing, devel-oping and partnering with Health Care Providers/ Professionals (HCPs), e.g. external Medical Ex-perts, study investigators, treatment guideline experts, etc. to ensure the appropriate dissemina-tion of clinical and scientific information regarding Novartis’ compounds in a timely, ethical and stakeholder-focused manner. To implement clinical and educational strategies in collaboration with other Novartis colleagues for designated stakeholders. To pair key stakeholders’ scientific educational and research needs with available Novartis resources and provide the latest emerging data in response to specific HCP inquiries, as appropriate.<br><br>#LI-Onsite<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><h3><b>Medical Expert Engagement</b></h3><ul><li><p>Identify, map, and engage Medical Experts and study investigators in alignment with the Integrated Product Strategy (IPS).</p></li><li><p>Share medical, scientific, and health outcomes evidence on Novartis compounds, therapeutic areas, and new treatment options with HCPs and key stakeholders.</p></li></ul><h3><b>Scientific Information &amp; Requests</b></h3><ul><li><p>Respond to unsolicited HCP requests by presenting globally approved data, including compounds in development.</p></li><li><p>Involve HCPs in advisory boards, educational activities, and publications when relevant.</p></li></ul><h3><b>Clinical Research Support</b></h3><ul><li><p>Educate on Novartis clinical research programs, recommend study sites, and support trial feasibility and accrual.</p></li><li><p>Facilitate IIT submissions and material transfer agreements for independent research.</p></li></ul><h3><b>Scientific Exchange &amp; Insights</b></h3><ul><li><p>Promote scientific exchange on emerging principles and trends.</p></li><li><p>Collect and report HCP insights to inform medical strategy and IPS planning.</p></li></ul><h3><b>Internal Contributions</b></h3><ul><li><p>Act as a local medical resource for disease area and product training.</p></li><li><p>Contribute to IPS and Medical Affairs strategy design and execution.</p></li></ul><h3><b>Compliance &amp; Integrity</b></h3><ul><li><p>Ensure adherence to all compliance processes (e.g., IIT, Medical Affairs Field Interactions).</p></li><li><p>Foster a diverse, inclusive, and harassment-free environment.</p></li></ul><h3><b>Education &amp; Communication</b></h3><ul><li><p>Provide scientific and educational information to HCPs on patient-critical issues.</p></li><li><p>Support internal capability building through training and knowledge sharing.</p></li></ul><p></p><p><b>Minimum Requirements</b></p><ul><li><p>A degree in PharmD, PhD, MD (Medical Doctor) is essential.</p></li><li><p>At least 1-year experience as Medical Science Liaison, specific experience in Hematology is a plus.</p></li><li><p>Fluent in both Arabic and English languages.</p></li></ul><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Biostatistics, Clinical Practices, Clinical Research, Clinical Study Reports, Curious Mindset, Customer Relationship Management (CRM) Software, Disease Management, Drug Development, Education, Epidemiology, IT Tools, Medical Information, Medical Research, Medical Writing, Phase Iv Clinical Trial, Product Placement, Scientific Support]]></description><link>http://biotechroles.com/senior-hematology-medical-science-liaison-riyadh-novartis/69d67ccac8e81216cd0caf86</link><guid isPermaLink="true">http://biotechroles.com/senior-hematology-medical-science-liaison-riyadh-novartis/69d67ccac8e81216cd0caf86</guid><pubDate>Wed, 08 Apr 2026 16:05:30 GMT</pubDate><company>Novartis</company><location>Riyadh</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Expert Medical Information Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Are you passionate about delivering high quality medical information that truly makes a difference? As an Expert Medical Information Manager, you will play a pivotal role in shaping and leading medical information services across key disease areas, partnering closely with Medical Affairs leaders to support informed decision making. You will take ownership of both planned and reactive medical information activities, lead complex and escalated enquiries, and ensure the highest standards of quality, compliance, and scientific integrity. This is an opportunity to combine deep scientific expertise with leadership and mentoring, helping to elevate medical information capabilities while directly supporting healthcare professionals and ultimately improving patient outcomes.<br><br>Locations: Dublin, Ireland / London, UK #LI-Hybrid <br><br>Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Responsibilities:</b>                                                                                                                </p><ul><li><p>Lead planned and reactive medical information services across assigned disease areas, ensuring timely, high‑quality delivery</p></li><li><p>Own end‑to‑end delivery of medical information services, including forecasting, scoping, and accurate tiering of activities</p></li><li><p>Partner with Medical Affairs leaders to plan and optimise medical information strategies across therapy areas</p></li><li><p>Act as delivery lead for medical information congress support, covering both on‑site and remote activities</p></li><li><p>Deliver highly complex and escalated medical information responses with scientific accuracy and sound judgement</p></li><li><p>Manage and resolve escalations from external healthcare professionals in line with regulatory requirements</p></li><li><p>Ensure full compliance with regulatory, pharmacovigilance, and internal medical information standards and codes of practice</p></li><li><p>Oversee quality review, accuracy, and integrity of all assigned medical information deliverables and projects</p></li><li><p>Provide therapy area expertise and guidance across aligned franchises and multiple internal clients</p></li><li><p>Mentor and coach senior and manager‑level medical information colleagues, building capability and future leadership</p></li></ul><p></p><p><b>Essential for the role:</b></p><ul><li><p>Degree in a healthcare discipline or a related life sciences field</p></li><li><p>Minimum of five years’ experience delivering Medical Information services within the pharmaceutical industry</p></li><li><p>Proven experience delivering Medical Information activities at both global and local levels</p></li><li><p>Strong scientific knowledge and understanding of disease areas relevant to Novartis therapeutic areas</p></li><li><p>Demonstrated expertise in high‑quality Medical Information writing and content review</p></li><li><p>Strong understanding of regulatory, pharmacovigilance, and industry standards governing Medical Information</p></li><li><p>Proven ability to manage senior stakeholders with a strong client‑focused mindset</p></li><li><p>Experience mentoring, coaching, and supporting the development of Medical Information professionals</p></li></ul><p></p><p><b>Desirable for the role:</b></p><ul><li><p>Advanced degree in a life sciences or healthcare discipline, such as Doctor of Philosophy, Doctor of Pharmacy, or Doctor of Medicine</p></li><li><p>Experience leading Medical Information activities for complex therapy areas or multiple disease areas simultaneously</p></li></ul><p></p><p><b>Commitment to Diversity &amp; Inclusion:</b></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)]]></description><link>http://biotechroles.com/expert-medical-information-manager-novartis/69d67cc9c8e81216cd0caf85</link><guid isPermaLink="true">http://biotechroles.com/expert-medical-information-manager-novartis/69d67cc9c8e81216cd0caf85</guid><pubDate>Wed, 08 Apr 2026 16:05:29 GMT</pubDate><company>Novartis</company><location>Dublin (NOCC)</location><salary>$85000-115000</salary><type>Full time</type></item><item><title><![CDATA[Vodja strateških projektov (m/ž/d) / Operations Lead (m/f/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br><br>Lokacija / Location: Mengeš, Slovenija<br><br><br>Kot vodja strateških projektov boste podpirali vodjo globalnih operativnih centrov pri pretvarjanju strateških prednostnih nalog v konkretne poslovne rezultate. To boste dosegli z določanjem taktičnih in poslovnih prioritet, uvajanjem ukrepov za izboljšanje poslovne uspešnosti ter vodenjem ključnih strateških projektov, ki povečujejo vrednost poslovanja. Pri tem boste delovali skladno z zakonodajo, internimi predpisi, dobrimi praksami in zastavljenimi poslovnimi cilji.<br><br><br>_____________<br><br><br>We are seeking a Operations Lead to support the Head of Global Operations Centers in translating strategic priorities into business performances by setting tactical/operational priorities, driving measures of operational performance and leading strategic business projects to maximize the value of operations. You will help to build-up and lead the Novartis Global Service Hub and provide standard services to the NTO sites across platforms globally in accordance with legislation, internal rules, good practices and business objectives. Management and development of associates.<br><br><br>Ta vloga je locirana v Mengšu, Slovenija. Novartis za to delovno mesto ne nudi podpore pri selitvi, zato prosimo, da se prijavite le, če vam je ta lokacija dostopna.<br><br><br>This role is based in Mengeš, Slovenija. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Vaše ključne odgovornosti:</span></b></p><p></p><p>Prenos in uresničevanje strategije Tehničnih dejavnosti pri projektnih in vodenje izvajanja potrjenega portfelja projektov.</p><p>· Sodelovanje z glavnimi funkcijami v s ciljem razviti paleto/portfelj priložnosti za izboljšave, prednostna obravnava le-teh in zagotavljanje uspešne izvedbe za izpolnitev poslovnih potreb.</p><p>· Zagotoviti vodenje/podporo globalnim/strateškim projektom, ki se izvajajo v imenu globalnih OC.</p><p>· Oceniti in spremljati stanje, napredek in težave v zvezi z vsemi potrjenimi projekti, namenjenimi izboljšavami, vključno z merstvom za green belts/ za kandidate v celotni organizaciji.</p><p>· Zagotoviti okvirje in vodenje projektov, ki so potrebni za razvoj poslovne odličnosti in z njo povezanih koristi.</p><p>· Proaktivno komuniciranje z deležniki glede načrtov, napredka, odstopanj in korektivnih ukrepov za doseganje ciljev na programih. Zagotoviti neprekinjeno in pregledno komunikacijo kom.(komuniciranje?) v vseh OC in .</p><p>· Odgovornost za identifikacijo in skupno rabo najboljših praks ter njihovo vključitev v načrt za nadaljnjo uporabo v vseh funkcijah.</p><p>· Odgovornost za načrtovanje in upravljanje virov (število zaposlenih in proračun) za določene funkcije/lokacije. Pregledati in pretehtati zahteve za sredstva in izdatke za dodeljene funkcije/lokacije.</p><p>· Upravljanje zahteve po številu zaposlenih, dejavnosti na področju zaposlovanja skupaj s predstavnikom kadrov in spremljanje ciljev glede števila zaposlenih za določeno funkcijo/lokacijo.</p><p>· Odgovornost za upravljanje/vodenje finančnih zahtev in proračuna za dodeljeno funkcijo/lokacijo. Pripraviti najnovejše ocene za trenutni letni proračun in za prihodnje proračune.</p><p></p><p><b>Vaš doprinos k delovnem mestu:</b></p><p>· Visokošolska izobrazba na področju operativnega upravljanja ali druge primerne izobrazbe</p><p>· Aktivno znanje angleškega jezika.</p><p>· Poznavanje orodja Microsoft Office.</p><p>· 5 let zkušenj z upravljanjem multifunkcijskih projektov, upravljanje programov in sprememb z notranjimi in zunanjimi deležniki.</p><p></p><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>nedoločen čas</b> s poskusno dobo <b>6 mesecev</b>. Prijavo oddajte z življenjepisom v slovenskem in angleškem jeziku.</p><p></p><p></p><p><b>Ugodnosti in nagrajevanje:</b></p><p>Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika in delom od doma, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje, shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj.</p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: https://www.novartis.com/careers/benefits-rewards</p><p></p><p><b>Predani smo raznolikosti in vključenosti: </b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.</p><p></p><p></p><p><b>Zakaj Novartis: </b>Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? https://www.novartis.com/about/strategy/people-and-culture</p><p></p><p>________________________</p><p></p><p><b>Key Responsibilities:</b></p><p></p><p>· Translates TechOps strategy into business projects and lead implementation of en-dorsed project portfolio.</p><p>· Collaborate with NTO Global Functions to develop a portfolio of improvement opportunities, prioritize these and ensure successful execution to meet business needs.</p><p>· Deploy op. excellence across all functions at the operations centers in collaboration with all NTO Global Functions</p><p>· Provide leadership / support to gl./strategic projects on behalf of Global OC.</p><p>· Assess and track status, progress &amp; issues for all endorsed improvement projects including the mentorship of Green Belts/candidates throughout the organization.</p><p>· Provide framework and project mng. necessary to develop Operational Excellence benefits.</p><p>· Communicate proactively with stakeholders regarding plans, progress, deviations and corrective measures to reach targets of program projects. Ensures consistent communication across OC and across NTO.</p><p>· Responsible for identifying and sharing best practices and incorporate them into the playbook for future use across functions.</p><p>· Accountable for resource planning and management (headcount and budget) for defined functions/locations. Review and challenge resource requests and expenditures for assigned functions/locations.</p><p>· Manage headcount requests, staffing activities with P&amp;O representatives and monitor against hc targets for defined function/location.</p><p></p><p></p><p><b>Essential Requirements:</b></p><p></p><p>· University degree in operations management or other relevant degree.</p><p>· Fluent in English</p><p>· Knowledge of Microsoft Office</p><p>· &#39;5 years experience in managing multi-functional Projects, Programs &amp; change Management with internal and external stakeholders</p><p></p><p>We offer <b>permanent employment</b> with <b>6 months of probation period</b>. Submit your application with the CV in Slovenian and English language.</p><p></p><p></p><p><b>Benefits and Rewards:</b></p><p>Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, possibility of joining collective health insurance scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical and mental well-being and managing workload (Well-being), Unlimited learning and development opportunities.</p><p></p><p><b>Commitment to Diversity and Inclusion: </b>Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.</p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Data Analytics, digital skills, General Hse Knowledge  , gmp knowledge, process excellence, Resilience]]></description><link>http://biotechroles.com/vodja-strateskih-projektov-mzd-operations-lead-mfd-novartis/69d67cc9c8e81216cd0caf84</link><guid isPermaLink="true">http://biotechroles.com/vodja-strateskih-projektov-mzd-operations-lead-mfd-novartis/69d67cc9c8e81216cd0caf84</guid><pubDate>Wed, 08 Apr 2026 16:05:29 GMT</pubDate><company>Novartis</company><location>Mengeš</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Vodja oskrbe proizvodnje (m/ž/d) / Supply Chain Head (m/f/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br><br>Lokacija / Location: Mengeš, Slovenija<br><br><br>Kot vodja oskrbe proizvodnje boste odgovorni za vodenje procesa oskrbe proizvodnje in usklajevanje proizvodnih virov s potrebami trgov za zagotavljanje pravočasne oskrbe trgov in realizacije razvojnih planov. Skrbeli boste za vodenje in razvoj sodelavcev ter razvoj področja za doseganje konkurenčnosti in stroškovne učinkovitosti, skladno z zakonodajo, internimi predpisi, dobrimi praksami in poslovnimi cilji.<br><br><br>_____________<br><br><br>We are seeking a Head PCSM/Supply Chain Head to be responsible for the leadership of the production supply process, and for alignment of production resources with market needs to ensure timely supply of markets, and realization of development plans. Concern for the leadership and development of associates, and development of the domain to achieve competitiveness and cost efficiency, in accordance with the law, internal regulations, good practices and business objectives.<br><br><br>Ta vloga je locirana v Mengšu, Slovenija. Novartis za to delovno mesto ne nudi podpore pri selitvi, zato prosimo, da se prijavite le, če vam je ta lokacija dostopna.<br><br><br>This role is based in Mengeš, Slovenija. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Vaše ključne odgovornosti:</b></p><p>· Odgovoren je za vodenje področja in upravljanje z viri</p><p>· Odgovoren je za vodenje in optimizacijo procesa oskrbe proizvodnje in nabave, za zagotavljanje pravočasne oskrbe trgov</p><p>· Spremlja prejeta naročila, usklajuje prioritete za proizvodnjo</p><p>· Odgovoren je za vodenje in upravljanje zalog ter proizvodnih virov</p><p>· Skrbi za razvoj področja skladno s trendi v konkurenčnem okolju</p><p>· Odgovoren je za vodenje procesa sprememb na proizvodih (ovojnina, izdelki, postopki, procesi)</p><p>· Odgovoren je za zagotavljanje trajnostnega poslovanja (BCM/ Business Continuity Management)</p><p>· Druge naloge po navodilu nadrejenega in naloge na podlagi posebnega imenovanja</p><p>· Ostale naloge določene z letnim pogovorom o ciljih in s kazalniki uspešnosti</p><p>· Zagotavlja pogoje in nadzor nad izvajanjem nalog in zahtev zdravja, varnosti in okolja v enoti</p><p></p><p><b>Vaš doprinos k delovnem mestu:</b></p><p></p><p>· Visokošolska stopnja izobrazbe ekonomske ali druge ustrezne smeri</p><p>· Aktivno znanje angleškega jezika</p><p>· Poznavanje orodja Microsoft Office</p><p>· 3 leta ustreznih delovnih izkušenj</p><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>nedoločen čas</b> s poskusno dobo <b>6 mesecev.</b> Prijavo oddajte z življenjepisom v slovenskem in angleškem jeziku.</p><p></p><p></p><p><b>Ugodnosti in nagrajevanje:</b></p><p>Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika in delom od doma, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje, shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja), številne priložnosti za učenje in razvoj.</p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: https://www.novartis.com/careers/benefits-rewards</p><p></p><p><b>Predani smo raznolikosti in vključenosti: </b>Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.</p><p></p><p></p><p><b>Zakaj Novartis:</b> Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p>________________________</p><p></p><p></p><p><b>Key Responsibilities:</b></p><p>· Responsibility for the leadership of the respective area, and management of resources</p><p>· Responsibility for the leadership and optimization of the manufacture supply and purchasing in order to ensure timely market supply</p><p>· Follow-up of orders received, coordination of priorities for production</p><p>· Responsibility for the leadership and management of inventories and production resources</p><p>· Concern for the development of the area in accordance with the competitive environment trends</p><p>· Responsibility for the leadership of product change process (packaging, products, procedures, processes)</p><p>· Ensuring Business Continuity Management</p><p>· Other tasks as directed by the supervisor, and tasks based on a specific appointment</p><p>· Other tasks determined during the annual objectives setting process and by the key performance indicators</p><p>· Providing conditions for and control over the implementation of HSE tasks and requirements in the unit</p><p></p><p><b>Essential Requirements:</b></p><p>· University-level degree (economics or other equivalent degree)</p><p>· Knowledge of Microsoft Office</p><p>· 3 years of appropriate working experience</p><p>· Knowledge of English</p><p></p><p></p><p>We offer <b>permanent employment </b>with <b>6 months of probation period.</b> Submit your application with the CV in Slovenian and English language.</p><p></p><p></p><p><b>Benefits and Rewards:</b></p><p>Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, possibility of joining collective health insurance scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical and mental well-being and managing workload (Well-being), Unlimited learning and development opportunities.</p><p></p><p><b>Commitment to Diversity and Inclusion: </b>Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Data Analytics and Digital, Integrated Business Planning (IBP), Inventory Management, Leadership, Logistics and Transportation Management, Master Data, Operational Excellence, Project Management, Resilience and Risk Management, Sap Erp, Stakeholder Management, supply chain management, Supply Chain Planning]]></description><link>http://biotechroles.com/vodja-oskrbe-proizvodnje-mzd-supply-chain-head-mfd-novartis/69d67cc9c8e81216cd0caf83</link><guid isPermaLink="true">http://biotechroles.com/vodja-oskrbe-proizvodnje-mzd-supply-chain-head-mfd-novartis/69d67cc9c8e81216cd0caf83</guid><pubDate>Wed, 08 Apr 2026 16:05:29 GMT</pubDate><company>Novartis</company><location>Mengeš</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Quality Manager / Qualified Person]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>EU Local Distribution Qualified Person for investigational medicinal products IMPs and auxiliary medicinal products AMPs<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major Accountabilities:</b></p><ul><li><p>Batch certification / batch release of investigational medicinal products IMPs and auxiliary medicinal products AMPs in EU Local Distribution</p></li><li><p>Collaboration with local COs (SSO, Depot, NCQ) </p></li><li><p>Review and approval of quality-relevant Documentation to support batch release</p></li><li><p>Ensure compliance with local and international regulations</p></li><li><p>Continous improvement of QA system and processes</p></li><li><p>Systematic improvement of compliance and operational level</p></li><li><p>CAPA Management</p></li><li><p>Support in Complaint handling</p></li><li><p>Change Control Management</p></li><li><p>SOP preparation and review</p></li><li><p>self-reliant Project Management</p></li><li><p>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products</p></li></ul><p><br /><b>Work Experience:</b></p><ul><li><p>Audit &amp; Inspection Management</p></li><li><p>Quality Management Systems</p></li><li><p>Quality Assurance</p></li><li><p>GxP Experience</p></li><li><p>Good Manufacturing Practices (cGMP)</p></li><li><p>Quality Compliance</p></li><li><p>Drug Development</p></li><li><p>Research</p></li><li><p>Technological Expertise</p></li><li><p>Complaints Management</p></li><li><p>Good Laboratory Practice (GLP) Analytics</p></li><li><p>Incident Management</p></li><li><p>Deviation Management</p></li><li><p>Corrective and Preventive Action (CAPA) Knowledge</p></li><li><p>Third Party Management</p></li><li><p>Change Control Management</p></li><li><p>SOP (Standard Operation Procedure) Management</p></li><li><p>Patient Safety</p></li><li><p>Pharmacovigilance</p></li></ul><p><br /><b>Skills:</b></p><ul><li><p>Pharmacist</p></li><li><p>Qualification as a Qualified Person according to EU Legislation</p></li></ul><p></p><p><b>Languages:</b></p><ul><li><p>English</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Business Partnering, Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge]]></description><link>http://biotechroles.com/quality-manager-qualified-person-novartis/69d67cc8c8e81216cd0caf82</link><guid isPermaLink="true">http://biotechroles.com/quality-manager-qualified-person-novartis/69d67cc8c8e81216cd0caf82</guid><pubDate>Wed, 08 Apr 2026 16:05:28 GMT</pubDate><company>Novartis</company><location>Barcelona Gran Vía</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist - Oncology Translational Research]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Basel, Switzerland<br>Full time, onsite, #LI-Onsite<br><br>The Oncology Translational Research (OTR) group within Novartis Biomedical Research seeks a highly motivated lab head to drive the translational strategy for early clinical radioligand therapy (RLT) programs. The role involves collaborative work with various groups across the drug development spectrum, including drug discovery, data science, and early clinical development groups. The successful candidate will be responsible for leading a team and will be tasked with the design &amp; execution of preclinical translational studies and clinical biomarker plans.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>About the role:</span></b><br /><span>The Oncology Translational Research (OTR) group within Novartis Biomedical Research seeks a highly motivated lab head to drive the translational strategy for early clinical radioligand therapy (RLT) programs. The role involves collaborative work with various groups across the drug development spectrum, including drug discovery, data science, and early clinical development groups. The successful candidate will be responsible for leading a team and will be tasked with the design &amp; execution of preclinical translational studies and clinical biomarker plans. </span></p><p></p><p><b><span>Key responsibilities:</span></b></p><ul><li><p><span>Lead a research team and collaborate with groups across BR Oncology</span></p></li><li><p><span>Contribute to biomarker strategies and supervise translational experimental plans for various RLT drug discovery programs</span></p></li><li><p><span>Design and conduct translational studies, dissect the biological mechanisms driving response and resistance to RLT, and develop rational drug combinations.</span></p></li><li><p><span>Mentor and develop associates with various levels of experience</span></p></li></ul><p><span> </span></p><p><b><span>Essential Requirements:</span></b></p><ul><li><p>Ph.D. in molecular, cellular, cancer biology or related fields.</p></li><li><p>Minimum 2 years of Postdoctoral and/or industry experience in an Oncology/Cancer biology relevant field</p></li><li><p>Recognised academic publication record</p></li><li><p>Deep understanding of cancer cell biology, familiarity with innovative cell and molecular biology techniques.</p></li><li><p>Excellent creative thinking and problem-solving skills, scientific curiosity.</p></li><li><p>Proficiency in working collaboratively and flexibly on various projects</p></li><li><p>Strong communication skills, at ease with conveying complex scientific concepts</p></li></ul><p><b><span> </span></b></p><p><b><span>Desirable Requirements:</span></b></p><ul><li><p><span>Strong foundational knowledge and experience working on cell death mechanisms, experience in the field of DNA damage response and repair, radiobiology or RLT.</span></p></li><li><p><span>Expertise in prostate cancer biology</span></p></li><li><p><span>Proficiency with data mining and computational skills.</span></p></li><li><p><span>Track record in managing a research team and scientific projects</span></p></li></ul><p></p><p><b>Accessibility and accommodation</b></p><p>Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to <a href="mailto:diversity.inclusion_ch&#64;novartis.com" target="_blank">diversity.inclusion_ch&#64;novartis.com</a> and let us know the nature of your request and your contact information. Please include the job requisition number in your message</p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Biomedical Research, Cancer Biology, Cancer Cell Biology, Cancer Cells, Cell and Molecular Biology, Cell Biology, Cell Death, DNA Damage, Drug Development, Molecular Biology]]></description><link>http://biotechroles.com/principal-scientist-oncology-translational-research-novartis/69d67cc8c8e81216cd0caf81</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-oncology-translational-research-novartis/69d67cc8c8e81216cd0caf81</guid><pubDate>Wed, 08 Apr 2026 16:05:28 GMT</pubDate><company>Novartis</company><location>Basel (City)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[QA Operations Supervisor]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Help reimagine cancer care by shaping how our Radioligand Therapies (RLT) reach more patients—safely, reliably, and faster. At Novartis, we’re pioneering the future of treatment through the fusion of nuclear medicine and precision oncology.<br><br>The QA Operations Supervisor provides hands on support for shop floor quality oversight and batch release activities while acting as supervisor to the QA Operations and Batch Release Specialists of their shift.<br><br>Location: Indianapolis, IN #LI-Onsite<br><br>Shift:  Night Shift. weekend nights included<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities: </b></p><ul><li><p><span><span>Provide direct supervision of QA Operations Specialists and QA Batch Release Specialists, ensuring alignment with site quality objectives.</span></span></p></li><li><p><span><span>Coordinate daily activities, prioritize workload, and ensure timely completion of QA tasks across both functions.</span></span></p></li><li><p><span><span>Serve as the primary point of contact for quality-related issues during assigned shifts, ensuring timely escalation and resolution.</span></span></p></li><li><p><span><span>Ensure shopfloor quality oversight of production, QC, and supply chain activities, verifying adherence to cGMP, aseptic techniques, and data integrity standards.</span></span></p></li><li><p><span><span>Oversee live review of manufacturing batch records and documentation to support timely and compliant batch release.</span></span></p></li><li><p><span><span>Confirm compliance of site personnel with sterile manufacturing regulations and internal procedures.</span></span></p></li><li><p><span><span>Support the release of all manufactured, packaged and tested.</span></span></p></li><li><p><span><span>Support the Controlled issuance of batch records in preparation for manufacturing.</span></span></p></li><li><p><span><span>Perform review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately.</span></span></p></li><li><p><span><span>Support metric tracking of documentation and release data to ensure continuous improvement.</span></span></p></li><li><p><span><span>Support all QA operations as a valued business partner, with a culture of safety, quality, delivery to patients, cost, compliance, and data integrity.</span></span></p></li><li><p><span><span>Provide Quality Oversight on Deviation, Change Control, and CAPA management</span></span></p></li><li><p><span><span>Maintain batch documentation library (record check-in, check-out, follow-up, and distribution)</span></span></p></li><li><p><span><span>Provide shopfloor quality oversight of all production, quality control and supply chain departments to ensure their practice fully adheres to cGMP, including data integrity. Ensure timely escalation to management of all applicable incidents.</span></span></p></li><li><p><span><span>Perform live review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately</span></span></p></li></ul><p></p><p><b>Essential qualifications: </b></p><ul><li><p><span><span>Bachelors&#39; Degree, preferably in Life Sciences, chemistry, or related relevant degree. In lieu of degree, 5 years in a role within pharma industry that includes quality assurance and batch release experience will be considered</span></span></p></li><li><p><span><span><span>3</span></span></span><span><span>&#43; years of experience in GxP Biopharmaceutical manufacturing operations</span></span></p></li><li><p><span><span>2&#43; years of experience in a quality assurance role</span></span></p></li><li><p><span><span>Cross functional collaboration </span></span><span><span>QA and QC experience in biotech pharmaceutical biotechnology industry with environmental monitoring &amp; cleanliness zones is desired</span></span></p></li><li><p><span><span>Proven track record and practical experience with cGMP requirements</span></span></p></li><li><p><span>Knowledge of FDA and EU regulations and experience in US and international regulatory agency inspections.</span></p></li></ul><p></p><p>The salary for this position is expected to range between $89,600 and $166,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US‑based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time‑off package including vacation, personal days, holidays and other leaves.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$93,800.00 - $174,200.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence]]></description><link>http://biotechroles.com/qa-operations-supervisor-novartis/69d67cc7c8e81216cd0caf80</link><guid isPermaLink="true">http://biotechroles.com/qa-operations-supervisor-novartis/69d67cc7c8e81216cd0caf80</guid><pubDate>Wed, 08 Apr 2026 16:05:27 GMT</pubDate><company>Novartis</company><location>Indianapolis</location><salary>$95000-125000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Web Operations]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Associate Director, Web Operations will be responsible for managing and optimizing website operations as part of Studio Operations. The solution is designed as an “in-house” capability for website design and authoring operations across all US-promoted brands, ensuring full compliance on all related assets and achieving measurable operational efficiencies, quality, and cost-saving goals. This role will ensure the in-house service establishes all capabilities with consistent standards and processes that are fit for purpose.<br>The role will manage the production process, drive adoption, and enable operational and delivery excellence to meet the evolving needs of the business. It will be a key interface driving operational excellence across Integrated Marketing Operations (IMO), Holding Companies, and all related stakeholder parties.<br>The role will lead co-located teams (US, India, Mexico, Ireland, etc.) to continuously enhance and elevate web operations to ensure excellence, consistency, and efficiencies. By partnering with IMO colleagues and other functions, it will enable the MO function to operate more strategically, with agility, speed, and execution excellence.<br>As an internal organization, Studio Operations will drive value for our stakeholders, coordinating across the network to support the Novartis mission to improve patients’ lives.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key responsibilities </b></p><ul><li><b>Leadership:</b> Lead delivery, governance, and operations of the centralized Web Operations services end-to-end, including active leadership and visioning, planning, implementation, operation, stakeholder, and communication management, to ensure it meets time, cost, and quality requirements.</li><li><b>Channel Expert</b>: Utilizing your comprehensive Content management System (CMS) knowledge and expertise to lead and guide best practices in website management. You will provide strategic insights and direction to ensure the highest standards of web operations, driving continuous improvement and innovation.</li><li><b>Stakeholder Management:</b> Serve as the point of contact for business, interpreting requirements and needs to offer suitable solutions and develop partnerships and integrated solutions. Monitor and control the execution of the program through all phases to ensure timely delivery of services and outcomes, managing risks and issues.</li><li><b>Product Collaboration:</b> Partner with the Drupal platform product team to understand the roadmap and enable scaled operations for new features or releases. Coordinate with IT stakeholders to ensure compliant content deployment.</li><li><b>Team management:</b> Plan, mobilize, and manage cross-functional program teams across divisions and geographical boundaries. Manage resource phasing, solution roles, and responsibilities, and establish a high-performance team and environment to drive high-quality delivery.</li><li><b>Automation &amp; Efficiency:</b> Identify and implement automation techniques to reduce manual tasks and increase resource productivity. Design and implement a scalable operational model to address new launch requirements without increasing spend (&#34;Do more with less&#34;).</li><li><b>Functional Leadership:</b> As a functional lead for Web Operations, motivate and develop people across locations, demonstrating Novartis values and behaviors, driving positive change, and enhancing internal capabilities/skill sets.</li><li><b>Continuous Improvement:</b> Identify, contribute to, champion, and embed delivery processes and standards and continuous improvement initiatives across the team.</li><li><b>Performance Metrics:</b> Ensure operational and performance metrics and benchmarks are in place, optimized, achieved, and remediation plans are in place and adhered to, while maintaining regulatory and compliance processes.</li><li><b>Demand Management:</b> Proactively manage work volume, track progress against agreed timelines, and prioritize resources to meet overall project and solution objectives. Provide insight and input to optimize the effectiveness of brand Web Operations requests and services to drive greater agility and flexibility.</li><li><b>Financial Oversight:</b> Provide financial management and oversight of the team, including performance and productivity, bottom-line operating costs, and quality performance.</li></ul><p></p><p><b><span>Role Requirements </span></b></p><ul><li>5&#43; years’ experience Commercial experience in design/marketing/program management within creative /advertising/consulting agencies, In-House Agency or Marketing Department, including leading and managing service resource/people management/planning across multifunctional teams and complex matrix environments</li><li>Led and implemented Commercial and/or Marketing Operations and respective best practices across the pharmaceutical industry with ability to translate into commercial strategy</li><li>Preferred experience in content management in CMS platforms</li><li>Proven track record to understand regulatory guidelines and implications of brand strategy related to website development</li><li>Excellent cross-functional skills with the ability to work and lead a cross-functional team in a matrix environment. Strong process/project management skills.</li><li>Excellent presentation, interpersonal, verbal and written communication skills.</li><li>Demonstrate leadership experiences and capabilities including the ability to influence and collaborate with peers, develop, and coach others, and oversee, and guide the work of other colleagues to achieve meaningful outcomes and create business impact</li><li>Relevant program management experience in managing large enterprise programs and teams across functions and locations in a matrix structure</li><li>Past work reflects a track record of operational excellence including financial and operational metrics and accountability</li><li>Able to thrive in a complex matrix organization, acting as a voice of discipline and structure, to enable the development and deployment of operational solutions that meet the needs of the business</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Cross-Functional Collaboration, Customer Engagement, Customer Experience, Customer Insights, Data Analytics, Data Strategy, Digital Marketing, Marketing Strategy, Market Research, Media Campaigns, Product Marketing, Stakeholder Engagement, Stakeholder Management, Team Leadership, Waterfall Model]]></description><link>http://biotechroles.com/associate-director-web-operations-novartis/69d67cc7c8e81216cd0caf7f</link><guid isPermaLink="true">http://biotechroles.com/associate-director-web-operations-novartis/69d67cc7c8e81216cd0caf7f</guid><pubDate>Wed, 08 Apr 2026 16:05:27 GMT</pubDate><company>Novartis</company><location>INSURGENTES</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Director Medical Communications]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote<br><br>This position can be based remotely anywhere in the U.S. (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. <br><br>Novartis is unable to offer relocation support: please only apply if accessible.<br>Company will not sponsor visas for this position.<br><br>If you’re energized by turning complex science into clear, credible stories that move healthcare forward, this is your opportunity. As Director, Medical Communications, you’ll shape and execute the US medical communications strategy across launches and lifecycle moments for therapeutic area objectives—setting the scientific narrative, guiding publications and congress content, and ensuring every piece of medical material is accurate, consistent, and compliant. You’ll partner closely with Medical Affairs, Regulatory, Clinical Development, and Commercial teams, serving as the single point of contact to our content development partners and collaborating with external agencies and scientific experts. Your leadership will help ensure our communications earn trust, enable meaningful scientific exchange, and ultimately support better outcomes for patients.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities</b></p><ul><li><p>Design and implement the US medical communications strategy supporting product launches, lifecycle management, and scientific engagement.</p></li><li><p>Define and execute publication strategies, including manuscripts, abstracts, posters, and scientific congress presentations.</p></li><li><p>Co‑create the scientific communications platform and core scientific narratives to guide consistent, high‑impact messaging.</p></li><li><p>Oversee development of scientifically accurate medical content across education programs, digital channels, symposia, MSL tools, and congresses.</p></li><li><p>Ensure consistency and alignment of medical messaging across all communication channels and materials.</p></li><li><p>Collaborate cross-functionally with Medical Affairs, Regulatory, Clinical Development, and Commercial partners across the organization.</p></li><li><p>Serve as the US Medical Affairs single point of contact to the Novartis Corporate Center for content development.</p></li><li><p>Partner with external agencies, key opinion leaders, and scientific experts to strengthen relevance and impact.</p></li><li><p>Ensure all materials meet regulatory requirements, company policies, and industry publication guidelines (e.g., GPP, ICMJE)</p></li><li><p>Lead, mentor, and develop medical writers and communication specialists, driving quality, compliance, and timely delivery.</p></li></ul><p></p><p><b>Essential Requirements</b></p><ul><li><p>Advanced degree in life sciences, pharmacy, medicine, or a related discipline; PhD, PharmD, MD preferred.</p></li><li><p>Minimum five years of experience within the pharmaceutical industry.</p></li><li><p>At least five years of experience in medical or scientific communications, publications, or congress planning.</p></li><li><p>Strong understanding of medical affairs, clinical research, publication planning, and regulatory environments.</p></li><li><p>Excellent written and verbal communication skills, with the ability to translate complex science clearly.</p></li><li><p>Demonstrated success leading work through a matrixed organization with strong project and stakeholder management skills.</p></li></ul><p></p><p><b>Desirable Requirements</b></p><ul><li><p>Senior‑level therapeutic experience in rheumatology and/or hematology, with demonstrated influence on scientific strategy.</p></li><li><p>Proven leadership of medical or scientific communications at a strategic level, including publications and major scientific congresses.</p></li></ul><p></p><p>The salary for this position is expected to range between $185,500 and $344,500 per year.</p><p></p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p></p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p></p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p></p><p>To learn more about the culture, rewards and benefits we offer our people <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">click here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$185,500.00 - $344,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care, People Management, Pharmaceutics, Priority Disease Areas Expertise, Product Launches, Product Strategy, Real World Evidence (RWE), Regulatory Compliance, Research Methodologies {+ 4 more}]]></description><link>http://biotechroles.com/director-medical-communications-novartis/69d67cc7c8e81216cd0caf7e</link><guid isPermaLink="true">http://biotechroles.com/director-medical-communications-novartis/69d67cc7c8e81216cd0caf7e</guid><pubDate>Wed, 08 Apr 2026 16:05:27 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Ekspert tehnologije izdelkov III]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Location: Ljubljana, Slovenija<br><br>Kot Ekspert tehnologije izdelkov boste odgovorni za vsebinsko poznavanje izdelkov skozi življenjski cikel in uvajanje novih izdelkov v proizvodnjo trdnih farmacevtskih oblik. Prispevali boste k temu, da procesi ostajajo robustni, stalno validirani in usmerjeni v nenehne izboljšave. <br><br>Odprta pozicija je odlična priložnost za vse, ki bi želeli biti vpleteni v razvoj in vzpostavljanje proizvodnje novih inovativnih zdravil za izboljševanje kakovosti življenja ljudi po vsem svetu. <br><br>Če iščete priložnost, kjer lahko vaše znanje ustvarja resnično vrednost, se nam pridružite!<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Job Description</b></p><p><b>Vaše ključne odgovornosti:</b></p><ul><li><p>Odgovornost za vsebinsko poznavanje alociranih izdelkov, skrb za celoten življenjski cikel dodeljenih izdelkov.</p></li><li><p>Uvajanje novih izdelkov v proizvodnjo trdnih farmacevtskih oblik: transfer novo razvitega izdelka iz laboratorija ali obstoječega izdelka iz drugih Novartisovih proizvodnih lokacij.</p></li><li><p>Načrtovanje in izvedba tehničnih serij in poskusov v proizvodnji.</p></li><li><p>Načrtovanje in izvedba validacije procesa.</p></li><li><p>Priprava tehnološke dokumentacije za tehnične, validacijske serije ter komercialno proizvodnjo izdelka.</p></li><li><p>Odgovornost za ohranjanje optimalne zmogljivosti procesov, vrednotenih s pomočjo statističnih analiz kritičnih parametrov, procesnih podatkov itd.</p></li><li><p>Analiza laboratorijskih in procesnih podatkov z naborom statističnih orodij.</p></li><li><p>Pomoč pri prenosu znanja in informacij med funkcijami ter lokacijami ter nudenje strokovne podpore proizvodnji.</p></li><li><p>Zagotavljanje pripravljenosti na inšpekcijske preglede za vse procesne vidike dodeljenih izdelkov.</p></li></ul><p></p><p><b>Vaš doprinos k delovnem mestu: </b></p><ul><li><p>Magisterij iz farmacije, kemije, biotehnologije ali sorodnega področja.</p></li><li><p>Aktivno obvladovanje angleškega in slovenskega jezika.</p></li><li><p>Računalniška pismenost in sposobnost uporabe digitalnih orodij za analizo podatkov.</p></li><li><p>Močne komunikacijske veščine za sodelovanje med funkcijami in lokacijami.</p></li><li><p>Visoko motiviranost za delo, samostojnost in proaktivnost pri reševanju izzivov in iskanju izboljšav.</p></li><li><p>Učinkovito upravljanje s prioritetami v dinamičnem okolju.</p></li></ul><p></p><p><b>Zaželene izkušnje: </b></p><ul><li><p>Poznavanje dobre proizvodne prakse (GMP) in izkušnje s področja proizvodnje, kakovosti ali drugega sorodnega področja.</p></li><li><p>Sposobnost interpretacije statističnih podatkov in spremljanja trendov.</p></li></ul><p></p><p></p><p>Z izbranim kandidatom bomo sklenili delovno razmerje za <b>določen čas s poskusno dobo 6 mesecev</b> in možnostjo podaljšanja.</p><p></p><p>Prijavo oddajte z življenjepisom v slovenskem jeziku.</p><p></p><p><b>Ugodnosti in nagrajevanje:</b> Konkurenčen plačni paket, letni bonus, fleksibilen način dela z možnostjo prilagajanja urnika in delom od doma, pokojninska shema, možnost vključitve v kolektivno zdravstveno zavarovanje, shema nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju fizičnega in duševnega dobrega počutja ter delovne obremenitve (Polni življenja).), številne priložnosti za učenje in razvoj.</p><p></p><p>Preberite naš priročnik, da spoznate načine, s katerimi bomo spodbujali vaš osebni in profesionalni razvoj: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a> </p><p></p><p><b>Predani smo raznolikosti in vključenosti:</b> Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.</p><p></p><p><b>Zakaj Novartis:</b> Pomagati bolnikom in njihovim družinam zahteva več kot le inovativno znanost. Potrebna je skupnost zavzetih ljudi, kot ste vi. V Novartisu cenimo sodelovanje, podporo in navdihovanje drug drugega za razvoj prebojnih terapij, ki spreminjajo življenja pacientov. Ste pripravljeni ustvariti svetlejšo prihodnost skupaj z nami? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a> </p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process and Cleaning Validation, Process Control, Quality Control, Regulatory Compliance, Resilience and Risk Management]]></description><link>http://biotechroles.com/ekspert-tehnologije-izdelkov-iii-novartis/69d67cc6c8e81216cd0caf7d</link><guid isPermaLink="true">http://biotechroles.com/ekspert-tehnologije-izdelkov-iii-novartis/69d67cc6c8e81216cd0caf7d</guid><pubDate>Wed, 08 Apr 2026 16:05:26 GMT</pubDate><company>Novartis</company><location>Ljubljana</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Therapy Area Partner, Oncology- Jeddah]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Oncology Therapy Area Partner/Senior is a leading driver of our customer interactions Medical Knowledge and Key Accounts Executer to achieve KPI’s. You are the face of our customer experience approach and build deep Business and Scientific relationships that deliver value for customers and patients in order to drive sales growth in a compliant and ethical manner.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span>Major Accountabilities:</span></b></p><ul><li><h2>Meet or exceed sales targets (market share/market share growth) within agreed budgets and timescales through the skilful orchestration of positive customer experiences.</h2></li><li><h2>Identify and prioritize high-potential customers through data analysis (HCPs and stakeholders) who influence prescription decisions. Achieve agreed contact, coverage and frequency targets through face to face and meetings and deliver agreed customer centric activities within operating budget</h2></li><li><h2>Establish effective working relationships with opinion leaders and top medical influencers (at territory level) and challenge current behaviors in order to improve the patient journey (right patient, right time)</h2></li><li><h2>Engage in value-based conversations (in-person and virtually) to understand critical customer challenges, decision-drivers, pain points and opportunities</h2></li><li><h2>Personalize and orchestrate customer engagement journeys for target HCPs by reflecting customer preferences, leveraging available content and multiple engagement channels.</h2></li><li><h2>Establish effective working relationships with opinion leaders and top medical influencers (at territory level) and challenge current behaviors in order to improve the patient journey (right patient, right time)</h2></li><li><h2>Effective administration of territory business including, maintenance of high-quality record systems, daily communication with administrative systems and timely processing of territory business expenses (AV and personal). </h2></li><li><h2>Effective communication with territory colleagues and relevant members of other teams e.g. Healthcare, Hospital, in order to understand, maximize and drive territory.</h2></li></ul><h2></h2><h2><b>Requirements: </b></h2><ul><li><h2>Pharmacist/Clinical Pharmacist Degree of Education and Qualifications.</h2></li><li><h2>Proven, successful sales record with minimum 1 year in pharma specialty environment preferably in Oncology/ Breast Cancer</h2></li><li><h2>Knowledge of Pharma industry and its changing environment.</h2></li><li><h2>Experience in Building Business relationships with KOL’s and HCPs.  </h2></li><li><h2>Demonstrable high achiever mindset and translation this into actions.</h2></li></ul><p></p><p><b>Languages:</b></p><ul><li>Arabic &amp; Fluency in English is a must.</li></ul><p></p><p><b>Commitment to Diversity and Inclusion</b></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/therapy-area-partner-oncology-jeddah-novartis/69d67cc5c8e81216cd0caf7c</link><guid isPermaLink="true">http://biotechroles.com/therapy-area-partner-oncology-jeddah-novartis/69d67cc5c8e81216cd0caf7c</guid><pubDate>Wed, 08 Apr 2026 16:05:25 GMT</pubDate><company>Novartis</company><location>Jeddah</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Recruitment Solutions Pre-boarding Americas]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>As a member of our Global Talent Acquisition Team, you will join a talented group of individuals who share the singular vision of impacting the quality of patient lives by engaging the world’s most talented scientists and other professional personnel. As a Talent Acquisition (TA) Coordinator, you will be an individual contributor responsible for overseeing one of the key areas of the Global TA Coordination (TAC) team: interview scheduling, pre-boarding, or administrative excellence. Your key stakeholders will include Talent Acquisition Business Partners (TABPs), Hiring Managers and candidates.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><span>Key Responsibilities:</span></p><ul><li><span><span>Pre-boarding country specialist:  </span></span></li><li><span><span>Offer letter creation and management (in the local language) </span></span></li><li><span><span>Initiation of mobility/relocation and visa support where needed </span></span></li><li><span><span>Initiate and track employment checks including drug and medical screenings as required, and flagging discrepancies to team lead for review and completion of relevant forms to document discrepancies or offer rescinds due to background checks </span></span></li></ul><p><span> </span></p><p><span><b>Essential Requirements:</b> <b> </b> </span></p><ul><li><span><span>Education: Bachelor’s degree preferred  </span></span></li><li><span><span>Languages: Strong written and spoken English and Spanish</span></span></li><li><span><span>Required Experience: At least 1 year of experience managing coordination and/or administrative activities  </span></span></li><li><span><span>Ability to manage local / global stakeholders in a remote working environment </span></span></li><li><span><span>Proven ability to be proactive, detail-oriented, problem-solver, and adaptable to change </span></span></li><li><span><span>Advanced knowledge of the Microsoft Office suite of products (Word, Excel, PowerPoint, Teams)  </span></span></li></ul><p><span> </span></p><p><span><b>Desirable experience: </b></span></p><ul><li><span><span>Portuguese</span></span></li><li><span><span>Familiarity with systems such as Hire Right, Paradox scheduling tool, and/or Workday  </span></span></li><li><span><span>Experience in any of the focus areas preferred i.e. managing background checks, contract or HR document generation and management, global mobility or visa processing, HR management.</span></span></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/recruitment-solutions-pre-boarding-americas-novartis/69d67cc4c8e81216cd0caf7b</link><guid isPermaLink="true">http://biotechroles.com/recruitment-solutions-pre-boarding-americas-novartis/69d67cc4c8e81216cd0caf7b</guid><pubDate>Wed, 08 Apr 2026 16:05:24 GMT</pubDate><company>Novartis</company><location>INSURGENTES</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Specialist  Business Services / Solutions Delivery]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>-Entry level specialist for project delivery and/or operations in a less complex business sub capability.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><b>Major Accountabilities:</b>
<ul><li>Execute solution implementation according to technology and delivery strategy for business systems, platforms and processes for a particular service scope.</li><li>Partner with DDIT Strategic Business Partners for demand analysis solution proposal/evaluation and funding estimates.</li><li>Deliver  products according to strategy  and with  reusability. </li><li>Ensure on time within budget compliant secure and quality delivery of portfolio for responsible service scope.</li><li>Ensure services,  solutions, platforms products are fit for purpose and achieve the desired business value and impact.</li><li>Run efficient DevOps for platforms products or systems ensuring availability and optimal performance for particular  service scope.</li><li>Follow governance structure for projects operations etc. with right stakeholder representation.</li><li>Track report and deliver against agreed success factors and KPIs for various stakeholders for responsible  service area.</li><li>Follow DDIT practices to drive agility, speed efficiency and effectiveness.  </li><li>Ensure adherence to Security and Compliance policies and procedures.</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt</li><li>Distribution of marketing samples (where applicable)</li><li>Ensure a healthy and safe workplace by complying with Novartis HSE and ISEC standards, implementing measures, providing training and resources, supporting employee well-being, investigating incidents, and collaborating with HSE teams to maintain a safe environment while adhering to quality, ethical, health, safety, and environmental requirements</li></ul>
<b>Key Performance Indicators:</b>
<ul><li>Delivery on agreed KPIs including business impact</li><li>Launch of innovative technology solutions across Novartis at scale</li><li>Business impact and value generated from DDIT solutions</li><li>Adoption and development of Agile Productization and DevOps practices</li><li>Operations stability and effective risk management Feedback on customer experience</li></ul>
<b>Experience:</b>
<ul><li>Industry/ Business Exposure </li><li>Project Management </li><li>Collaborating across boundaries</li></ul>
<b>Skills and Knowledge:</b>
<ul><li>Business Acumen </li><li>stakeholder management </li><li>Project Management </li><li>Service Delivery Management </li><li>performance management </li><li>budget management </li><li>risk management </li><li>planning</li><li>Digital capabilities, Effective use of technology</li><li>Operational Excellence Projects</li></ul>
<b>Language:</b>
<ul><li>English</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Budget Management, Business Acumen, Digital capabilities, Effective use of technology, Operational Excellence Projects, Performance Management, Planning, Project Management, Risk Management, Service Delivery Management, Stakeholder Management]]></description><link>http://biotechroles.com/specialist-business-services-solutions-delivery-novartis/69d67cc4c8e81216cd0caf7a</link><guid isPermaLink="true">http://biotechroles.com/specialist-business-services-solutions-delivery-novartis/69d67cc4c8e81216cd0caf7a</guid><pubDate>Wed, 08 Apr 2026 16:05:24 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$12000-22000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Spec. DDIT ISC Identity & Access Management Priv Access mgmt]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Focused management of security operations and or technology governance and external / internal interfaces in accordance with service operations and management processes-<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Location – Hyderabad #LI Hybrid</b></p><p></p><p><b>Key Responsibilities:</b> </p><p>• 8 to 10 years of experience in Privileged Account Management using CyberArk. Implementation/Operations experience on CyberArk v12, V14.</p><p>• Responsible for privileged User account administration of various devices like Windows, UNIX DB , Networks and Security etc.</p><p>• Excellent Knowledge in managing CyberArk workflow and policies.</p><p>• Basic knowledge of MSSQL, ORACLE, UNIX, Active Directory, Windows etc.</p><p>• Experience in integrating CyberArk with SIEM systems, ticketing systems (SNOW), enterprise monitoring etc.</p><p>• Good Experience in working with AAM components.</p><p>o Support deployment, configuration and day-to-day operations of Conjur environments. (Assist in onboarding applications to Conjur including application identity creation and secrets mapping.</p><p>Experience integrating Conjur with various DevOps tools and cloud-native environments.)</p><p>• Build and maintain custom connection components using APIs and plug-ins.</p><p>Collaborate with application and DevOps teams to understand Onboarding needs and build reusable integration pattern.</p><p></p><p><b>Essential Requirements:</b></p><p>• 5&#43; years of strong PAM support experience.</p><p>• Strong oral and written communications skills</p><p>• CyberArk Certified Sentry, Or other PAM product knowledge</p><p>• Good knowledge of infrastructure management</p><p>• Strong cross functional leadership.</p><p>• Project Management.</p><p>• Interactions with senior management.</p><p></p><p>Desirable Requirements:</p><div><ul><li>5&#43; years experience in IAM/PAM, with 2–4 years hands-on CyberArk. Strong expertise in Conjur design, deployment, and new integrations</li><li>Experience integrating secrets management with CI/CD pipelines. Exposure to Connector / Plug-in development</li><li>Good understanding of LDAP and basic networking .Hands-on with standard access protocols (SSH, Telnet, RDP) and tools like PuTTY . Open to UK shift</li></ul></div><p></p><p><b>You’ll receive:</b> You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a></p><p><br /><b>Commitment to Diversity and Inclusion:</b>  <br />Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.  </p><p></p><p><b>Join our Novartis Network</b>: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: <br /><a href="https://talentnetwork.novartis.com/network" target="_blank">https://talentnetwork.novartis.com/network</a></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Change Management, Information Security Risk Management, ITIL, Operational Excellence Projects, Quality Management, Root Cause Analysis (RCA), Secops (Security Operations), Vendor Management]]></description><link>http://biotechroles.com/sr-spec-ddit-isc-identity-and-access-management-priv-access-mgmt-novartis/69d67cc3c8e81216cd0caf79</link><guid isPermaLink="true">http://biotechroles.com/sr-spec-ddit-isc-identity-and-access-management-priv-access-mgmt-novartis/69d67cc3c8e81216cd0caf79</guid><pubDate>Wed, 08 Apr 2026 16:05:23 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Customer Operations Manager - Jeddah]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Lead and manage all aspects of the Sales Administration/ Operations team within a significant country including order management team; site-to-site material purchasing process and master data maintenance to ensure uninterrupted business operations. Manage team activities including resources allocation based on workload and priorities, professional development, reporting and delivery of group objectives. Leads a key area of sales support within a significant county (Sales training, Analytics, Sales Operations). Develop an effective through training and coaching or management of key commercial programmes<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>Location : Jeddah</p><p>This role is based in Saudi Arabia. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.</p><p></p><p><b>Key responsibilities</b></p><ul><li><p>Responsible for supporting sales representatives and channel partners in processing orders / returns; providing metrics/ reports to Sales team and engaging HCPs for expense payout.</p></li><li><p>Follow up on sales orders and provide status updates; update customer lists business wise.</p></li><li><p>Research and resolve escalated problems and issues, including issues related to order management, accounting and invoicing.</p></li><li><p>Communicate status of problems and solutions to customers and other appropriate parties.</p></li><li><p>Ensure team adherence to all processes and working procedures related to customer service.</p></li><li><p>Coordination of process changes and maintenance of customer service SOP’s.</p></li><li><p>Ensuring new team members receive the required level of system support and training to efficiently and effectively perform appointed role.</p></li></ul><p></p><p><b>Requirements</b></p><ul><li><p> Bachelor’s degree in science, Business administration, or Supply chain. MBA degree is preferable.</p></li><li><p>Minimum 2 years working in multinational companies.</p></li><li><p>Experience with SAP, Power BI and Excel</p></li><li><p>Strong capability in sales operations, preferably from pharma industry</p></li><li><p>Good knowledge of supply chain and logistics    </p></li></ul><p></p><p><b>Languages: </b>English and Arabic  </p><p></p><p><span>Novartis is committed to building an outstanding, inclusive work environment and diverse team representative of the patients and communities we serve.</span> <b>         </b> </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Calls Handling, Customer Care, Customer Experience, Customer Relations, Customer Satisfaction, Customer Service, Customer-Support, E-Learning, Field Service Management, Order Management, Professional Ethics, Sales, Waterfall Model]]></description><link>http://biotechroles.com/customer-operations-manager-jeddah-novartis/69d67cc3c8e81216cd0caf78</link><guid isPermaLink="true">http://biotechroles.com/customer-operations-manager-jeddah-novartis/69d67cc3c8e81216cd0caf78</guid><pubDate>Wed, 08 Apr 2026 16:05:23 GMT</pubDate><company>Novartis</company><location>Jeddah</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Senior Analyst - Brand Analytics]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Novartis BSI Brand Analytics team is looking for Senior Analyst professionals who will provide analytics support to Novartis internal customers (CPOs &amp; Regional marketing and sales teams) on various high complexity analytical reports, dashboards and requests for International Region. Support Business Solutions International – Brand Analytics team in building practice by involving in various initiatives like performance tracking, knowledge sharing, on-boarding and training support, support team lead in all business-related tasks / activities, building process documentation and knowledge repositories.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Senior Analyst Brand Analytics</b></p><p><b>Location – Hyderabad # LI Hybrid </b> </p><p></p><p><b>Major Responsibilities:</b></p><p></p><p>•Create and deliver below customer requirements as per agreed KBQs (timeliness, accuracy, quality, etc.) and drive excellent customer service.</p><p>Market overview (brand / therapy area)</p><p>Disease area fact books</p><p>Market assessment and Situation analysis</p><p>New brand launch performance tracker</p><p>Performance report and dashboards</p><p>Country brand performance reports</p><p>Brand diagnosis</p><p>BD&amp;L support</p><p>Pricing analysis</p><p>Portfolio prioritization</p><p>Customer analysis</p><p>Brand asset maximization</p><p>Portfolio Analytics</p><p>Others ad-hoc requests based on Desk Research</p><p><b>•</b>Deliver services through structured project management approach with appropriate documentation and communication throughout the delivery of services.<br /><b>•</b>Create and maintain standard operating procedures (SOPs), quality checklists that will enable excellent quality outputs for all outputs within the function.<br /><b>•</b>Develop and maintain knowledge repositories that captures qualitative and quantitative reports of brands, disease areas, macroeconomic trends of Novartis operating markets, etc.<br /><b>•</b>Support team leaders in recruitment and on-boarding of new associates within the organization.<br /><b>•</b>Active participation in various knowledge sharing sessions that enables growth and improves quality of NOCC Hyderabad deliverables across the function.<br /><b>•</b>Comply with all internal functional operating procedures like time tracking, KPI tracking and reporting, and other internal systems and processes.</p><p><b>• </b>Comply to all Novartis operating procedures as per legal / IT / HR requirements</p><p></p><p><b>Minimum Requirements:</b> </p><ul><li>Degree level, MBA with Graduate / Postgraduate in Medicine (MD/MBBS/BDS) Pharmacy / Life Sciences</li><li>4&#43; years&#39; experience in business analytics in a market research firm or pharmaceutical company or Pharma KPO/ Consulting</li><li>MS office (Excel and PPT), Power BI, expertise is a must for this role. Seeking an adept database professional with proven expertise in desk research as well as healthcare and pharmaceutical data systems including IQVIA MIDAS and other IQVIA offerings, Evaluate Pharma, Alpha Sense, Capital IQ, Clarivate, amongst others and committed to ensuring data integrity and generating insightful analyses</li><li>High agility to work across projects, stakeholders, datasets and technologies. Hands-on experience with at least one contemporary programming language (such as Python, JavaScript, or R) to support scripting, data preparation, transformation, or system integration.</li><li>Strong analytical and troubleshooting ability, with a genuine interest in using technology to solve complex problems. Intermediate knowledge in GenAI (Prompt engineering, Data management)</li><li>Excellent presentation and stakeholder management skills. Interpersonal and strong verbal and written communication skills. Ability to operate effectively in an international matrix environment.</li><li>Strong team player who is dynamic and result oriented. Highly motivated, flexible and adaptable. Should be able self-accountable and work independently</li></ul><p></p><p><b>Why Novartis:</b> Our purpose is to reimagine medicine to improve and extend people’s lives, and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture <br /> <br /><b>You’ll receive:</b> You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards <br /> <br /><b>Commitment to Diversity and Inclusion:</b>  <br />Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.  <br /> <br /><b>Join our Novartis Network:</b> If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Advertising Campaigns, Alteryx, Analytical Thinking, Brand Awareness, Business Networking, Curiosity, Digital Marketing, Marketing Communications, Marketing Plans, Marketing Strategy, Media Campaigns, Process Documentation, Statistical Analysis, Strategic Marketing]]></description><link>http://biotechroles.com/senior-analyst-brand-analytics-novartis/69d67cc2c8e81216cd0caf77</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-brand-analytics-novartis/69d67cc2c8e81216cd0caf77</guid><pubDate>Wed, 08 Apr 2026 16:05:22 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$22000-35000</salary><type>Full time</type></item><item><title><![CDATA[Medical Scientific Liaison]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br><br>This role is based in Taipei, Taiwan. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.<br><br>As a Medical Science Liaison at Novartis, you will serve as a trusted scientific partner in the field—building peer-to-peer relationships with medical experts, key stakeholders, and members of the scientific community. Leveraging evidence-based, non-promotional materials, you will facilitate meaningful scientific exchange that informs and advances patient care.<br><br>From as early as two years before a new product launches, you will play a strategic role in preparing for and supporting product development, launch, and commercialization. By gathering external insights, you will help shape Novartis’ understanding of the therapeutic landscape. Additionally, you will respond to unsolicited scientific inquiries and provide clinical trial support.<br><br>Reporting to the Medical Scientific Liaison Manager, you will collaborate cross-functionally with Medical Affairs, Clinical, Market Access, and other teams—transforming insights into actionable strategies that accelerate access to therapeutic area.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p></p><p><b>Key Responsibilities:</b></p><ul><li>Build and maintain scientific relationships with Medical Experts, Key Stakeholders, and Healthcare professionals; respond to unsolicited scientific inquiries using approved, evidence-based materials.</li><li>Identify and map Medical Experts and key stakeholders in alignment with local strategies, document interactions and advocacy levels per Field Medical Excellence standards.</li><li>Provide accurate scientific information on Novartis products and therapeutic areas to ensure informed clinical decisions and adherence to medical guidelines.</li><li>Deliver medical support and education to external groups, promoting evidence-based understanding of Novartis products and relevant health economics data.</li><li>Support clinical research activities, including site feasibility assessments, trial recruitment education, and collaboration with internal teams to ensure compliance with protocols and regulations.</li><li>Facilitate scientific exchange and gather insights on emerging research trends, therapeutic challenges, and unmet needs; report findings to shape development plans and launch strategies.</li><li>Implement and manage scientific projects such as registries, epidemiology studies, and cross-functional initiatives aimed at improving patient diagnosis and treatment outcomes.</li><li>Collaborate cross-functionally with Medical Affairs, Clinical, Market Access, and other teams to translate insights into actionable strategies that accelerate access to Immunology therapies.<br /> </li></ul><p>​<b>Requirements:</b></p><ul><li>Proven experience in building peer-to-peer relationships with medical experts, key opinion leaders, and healthcare stakeholders</li><li>Familiarity with clinical trial processes, including site feasibility, recruitment support, and adherence to regulatory guidelines.</li><li>Strong analytical skills to collect, interpret, and report scientific insights that inform medical strategy and product lifecycle planning.</li><li>Skilled in delivering evidence-based, non-promotional scientific information to healthcare professionals.</li><li>Advanced degree in life sciences or healthcare (Pharmacy Doctorate or Degree in Medicine strongly preferred). Additional qualifications in pharmacology, clinical research, or related fields are an advantage.</li><li>Fluent in English and Mandarin</li></ul><p></p><p><span><b>Commitment to Diversity and Inclusion</b></span><br /><span>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</span></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/medical-scientific-liaison-novartis/69d67cc1c8e81216cd0caf76</link><guid isPermaLink="true">http://biotechroles.com/medical-scientific-liaison-novartis/69d67cc1c8e81216cd0caf76</guid><pubDate>Wed, 08 Apr 2026 16:05:21 GMT</pubDate><company>Novartis</company><location>Taipei</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[QC Specialist I]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Job Description Summary<br>In dieser Position werden praktischer (Re-)Qualifizierungstätigkeiten an Laborgeräten durchgeführt, und damit die Funktionalität der Laborgeräte sichergestellt.<br><br>Diese Stelle ist auf 3 Jahre befristet.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Ihr Verantwortungsbereich:</b></p><ul><li><p>Durchführung verschiedener praktischer (Re-)Qualifizierungstätigkeiten an Laborgeräten (z.B. HPLCs, pH-Meter, Pipetten, Wasserbäder) für die Freigabe derer.</p></li><li><p>Dokumentation und teilweise Review von (Re-)Qualifizierungstätigkeiten</p></li><li><p>Einhaltung und Umsetzung geltender GMP-Vorschriften und SOP‘s im Labor</p></li></ul><p></p><p><b>Was Sie für die Position mitbringen:</b></p><ul><li><p>abgeschlossene Lehre als Chemielabortechniker (oder gleichwertige technische Ausbildung wie Chemie-HTL, CTA, BTA oder MTA) oder Bachelor-Abschluss (in Biotechnologie, Bioverfahrenstechnik, Biologie, Chemie, Biochemie oder gleichwertig)</p></li><li><p>gute Deutschkenntnisse, gute Englischkenntnisse</p></li><li><p>erste Berufserfahrung in der pharmazeutischen oder vergleichbaren Industrie vorteilhaft</p></li><li><p>Erfahrung in der Qualitätskontrolle und/oder Berufserfahrung in einer GMP/GxP-Umgebung von Vorteil</p></li><li><p>EDV-Kenntnisse (Microsoft Office)</p></li><li><p>Selbstständiges Arbeiten sowie Teamfähigkeit</p></li><li><p>hohe Lernbereitschaft und Genauigkeit</p></li><li><p>großes Verantwortungsbewusstsein</p></li></ul><p></p><p><b>Warum Novartis?</b></p><p>Unser Vorsatz ist es, die Medizin neu zu gestalten, um Menschenleben zu verbessern und zu verlängern. Unsere Vision ist es, das wertvollste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie wir das erreichen werden? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns tagtäglich dazu antreiben, unsere Ziele zu erreichen. Werden Sie Teil dieser Mission und dieses großartigen Teams! Erfahren Sie hier mehr: <a target="_blank" href="https://www.novartis.com/about/strategy/people-and-culture">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p><b>Was wir bieten:</b></p><p>Neben einem marktgerechten Grundgehalt bieten wir ein attraktives Bonus/Incentive Programm, eine moderne Firmenpension, Kinderbetreuungseinrichtungen, Aus- und Weiterbildungsprogramme und weltweite Karrieremöglichkeiten innerhalb der Novartis Gruppe. Das Grundgehalt für diese Position besteht aus dem kollektivvertraglichen Mindestgehalt in Höhe von €47,532.24 im Jahr (auf Vollzeitbasis) sowie einer allfälligen Überzahlung, basierend auf Ihren bisherigen Erfahrungen, Qualifikationen und individuellen Kompetenzen. Wir sind offen für Teilzeit und Jobsharing Modelle und unterstützen wo immer möglich flexibles arbeiten und Homeoffice.</p><p></p><p><b>Engagement für Vielfalt und Inklusion:</b></p><p>Novartis setzt sich für Vielfalt, Chancengleichheit und Inklusion ein. Wir sind bestrebt, vielfältige Teams zusammenzustellen, die für die Patienten und Gemeinschaften repräsentativ sind, denen wir dienen. Wir bemühen uns um die Schaffung eines inklusiven Arbeitsplatzes, der durch Zusammenarbeit mutige Innovationen fördert und unsere Mitarbeiter in die Lage versetzt, ihr volles Potenzial zu entfalten. Unsere Einstellungsentscheidungen basieren auf Chancengleichheit und der besten Qualifikation, ungeachtet von Geschlecht, Religion, Alter, Hautfarbe, Rasse, sexueller Orientierung, Nationalität oder Behinderung.</p><p></p><p><b>Unterstützungen für BewerberInnen mit Behinderungen:</b></p><p>Wenn Sie aufgrund einer Erkrankung, einer körperlichen Behinderung oder eines neurodiversen Zustandes eine Unterstützung bei unterschiedlichen Teilen des Rekrutierungsprozesses benötigen, wenden Sie sich bitte an <a target="_blank" href="mailto:disabilities.austria&#64;novartis.com">disabilities.austria&#64;novartis.com</a> und teilen Sie uns die Art Ihrer Anfrage sowie Ihre Kontaktinformationen mit. Unsere Unterstützung umfasst die Beratung zu geeigneten Positionen sowie die Begleitung bei allen Phasen des Bewerbungsprozesses. Das österreichische Gesetz sieht die Möglichkeit vor, die örtliche Behindertenvertrauensperson (BVP) in das Bewerbungsverfahren einzubeziehen. Wenn Sie dies wünschen, teilen Sie uns dies bitte vorab als Vermerk in Ihrem Lebenslauf mit.</p><p></p><p><b>Treten Sie unserem Novartis Netzwerk bei:</b></p><p>Wenn diese Position nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber dennoch mit uns in Kontakt bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann treten Sie hier dem Novartis Netzwerk bei: <a target="_blank" href="https://talentnetwork.novartis.com/network">https://talentnetwork.novartis.com/network</a></p><p></p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Collaboration, Communication skill, Data Integrity, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Problem Solving Skills, Regulatory Requirements knowledge]]></description><link>http://biotechroles.com/qc-specialist-i-novartis/69d67cc0c8e81216cd0caf75</link><guid isPermaLink="true">http://biotechroles.com/qc-specialist-i-novartis/69d67cc0c8e81216cd0caf75</guid><pubDate>Wed, 08 Apr 2026 16:05:20 GMT</pubDate><company>Novartis</company><location>Schaftenau</location><salary>$45000-60000</salary><type>Full time</type></item><item><title><![CDATA[Mechaniker (m/f/d)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Onsite<br>Location: Schaftenau, Austria<br><br>Bei Novartis in Schaftenau gestalten Sie als Mechaniker aktiv die sichere Bereitstellung hochwertiger Arzneimittel für Patientinnen und Patienten weltweit mit. In unserem hochautomatisierten GMP-Umfeld arbeiten Sie mit modernster Anlagentechnologie, lösen abwechslungsreiche technische Herausforderungen und treiben kontinuierliche Verbesserungen voran. <br><br>Freuen Sie sich auf ein wertschätzendes, interdisziplinäres Team, klare Entwicklungsperspektiven und die Chance, mit Ihrer Expertise echten Impact zu erzielen.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b><span><span>Ihre Aufgaben sind unter anderem:  </span></span></b></p><ul><li><p><span>Vorbereitung von Werkzeugen, Ersatzteilen und Materialien für Wartungs- und Instandhaltungsarbeiten.</span></p></li><li><p><span>Identifikation passender Ersatzteile und Pflege von Auswahllisten.</span></p></li><li><p><span>Einholung erforderlicher Arbeitsgenehmigungen für Wartungs- und Reparaturtätigkeiten.</span></p></li><li><p><span>Selbstständige Ausführung von Wartungsaufträgen und Reparaturen gemäß Anweisung und geltenden Standards.</span></p></li><li><p><span>Überwachung von Wartungs- und Reparaturarbeiten auf Qualität und Sicherheit.</span></p></li><li><p><span>Lückenlose Dokumentation von Wartungen und Reparaturen gemäß Good Documentation Practice (GDP).</span></p></li><li><p><span>Umstell- und Justierarbeiter sowie laufende Überwachung eines technisch einwandfreien Produktionsablaufes mit Fokus auf Anlagenverfügbarkeit und effiziente Anlagenwartung.</span></p></li><li><p><span>Meldung technischer Beschwerden, unerwünschter Ereignisse und Sonderfälle zu Novartis-Produkten innerhalb von 24 Stunden.</span></p></li><li><p><span>Technische Betreuung von Pharma-Anlagen (sterile Abfüllung, visuelle Inspektion sowie der dazugehörigen Mediensystemen wie Dampf, Wasser, Lauge &amp; Gase) in Hinblick auf mechanische Tätigkeiten inkl. vorbeugende Instandhaltung, Reparaturen &amp; Verbesserungsmaßnahmen.</span></p></li></ul><p><span> </span></p><p><b><span><span>Was Sie für die Position mitbringen:</span></span></b></p><ul><li><p><span>Abgeschlossene Lehre in einem einschlägigen Fachbereich (z.B. Metalltechnik, Mechanik<b>, </b>Mechatronik, ...)</span></p></li><li><p><span>Technisches Verständnis von korrektiver und präventiver Wartung.</span></p></li><li><p><span>Problemlösung über Funktionsbereiche hinweg mit praxisorientierter Haltung.</span></p></li><li><p><span>Zusammenarbeit über Bereichsgrenzen hinweg mit funktionsübergreifenden Teams.</span></p></li><li><p><span>Gute Deutschkenntnisse.</span></p></li><li><p><span>Schichtbereitschaft.</span></p></li></ul><p></p><p></p><p><b>Warum Novartis?</b></p><p>Unser Vorsatz ist es, die Medizin neu zu gestalten, um Menschenleben zu verbessern und zu verlängern. Unsere Vision ist es, das wertvollste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie wir das erreichen werden? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns tagtäglich dazu antreiben, unsere Ziele zu erreichen. Werden Sie Teil dieser Mission und dieses großartigen Teams! Erfahren Sie hier mehr: https://www.novartis.com/about/strategy/people-and-culture<br /><br /><b><u>Stellen Sie sich vor, was Sie bei Novartis tun könnten!</u></b><br /><br /><b>Was wir bieten:</b><br />Neben einem marktgerechten Grundgehalt bieten wir ein attraktives Bonus/Incentive Programm, eine moderne Firmenpension, Kinderbetreuungseinrichtungen, Aus- und Weiterbildungsprogramme und weltweite Karrieremöglichkeiten innerhalb der Novartis Gruppe. Das Grundgehalt für diese Position besteht aus dem kollektivvertraglichen Mindestgehalt (für die chemische Industrie) in Höhe von € €47.543,24 im Jahr (auf Vollzeitbasis), einer allfälligen individuellen Überzahlung sowie allfälligen Zusatzzahlungen bei Schichtarbeit (z.B. bei geleisteter Nachtschicht), basierend auf Ihren bisherigen Erfahrungen, Qualifikationen und individuellen Kompetenzen.</p><p></p><p><b>Engagement für Vielfalt und Inklusion:</b></p><p>Novartis setzt sich für Vielfalt, Chancengleichheit und Inklusion ein. Wir sind bestrebt, vielfältige Teams zusammenzustellen, die für die Patienten und Gemeinschaften repräsentativ sind, denen wir dienen. Wir bemühen uns um die Schaffung eines inklusiven Arbeitsplatzes, der durch Zusammenarbeit mutige Innovationen fördert und unsere Mitarbeiter in die Lage versetzt, ihr volles Potenzial zu entfalten. Unsere Einstellungsentscheidungen basieren auf Chancengleichheit und der besten Qualifikation, ungeachtet von Geschlecht, Religion, Alter, Hautfarbe, Rasse, sexueller Orientierung, Nationalität oder Behinderung.</p><p></p><p><b>Unterstützungen für BewerberInnen mit Behinderungen:</b></p><p>Wenn Sie aufgrund einer Erkrankung, einer körperlichen Behinderung oder eines neurodiversen Zustandes eine Unterstützung bei unterschiedlichen Teilen des Rekrutierungsprozesses benötigen, wenden Sie sich bitte an <a href="mailto:disabilities.austria&#64;novartis.com" target="_blank">disabilities.austria&#64;novartis.com</a> und teilen Sie uns die Art Ihrer Anfrage sowie Ihre Kontaktinformationen mit. Unsere Unterstützung umfasst die Beratung zu geeigneten Positionen sowie die Begleitung bei allen Phasen des Bewerbungsprozesses. Das österreichische Gesetz sieht die Möglichkeit vor, die örtliche Behindertenvertrauensperson (BVP) in das Bewerbungsverfahren einzubeziehen. Wenn Sie dies wünschen, teilen Sie uns dies bitte vorab als Vermerk in Ihrem Lebenslauf mit.</p><p></p><p><b>Treten Sie unserem Novartis Netzwerk bei:</b></p><p>Wenn diese Position nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber dennoch mit uns in Kontakt bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann treten Sie hier dem Novartis Netzwerk bei: <a href="https://talentnetwork.novartis.com/network" target="_blank">https://talentnetwork.novartis.com/network</a></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Architectural Engineering, Business Networking, Cooperation, Efficiency, Employee Wellness, Equipment Testing, General Hse Knowledge  , Heat Transfers, HVAC (Heating Ventilation And Air Conditioning), Including Gdp, Job Description, Knowledge Of Gmp, Manufacturing Production, Mathematical Optimization, Microsoft Word, Outside Sales, Physics, Teamwork, Total Productive Maintenance (TPM), Troubleshooting Software]]></description><link>http://biotechroles.com/mechaniker-mfd-novartis/69d67cc0c8e81216cd0caf74</link><guid isPermaLink="true">http://biotechroles.com/mechaniker-mfd-novartis/69d67cc0c8e81216cd0caf74</guid><pubDate>Wed, 08 Apr 2026 16:05:20 GMT</pubDate><company>Novartis</company><location>Schaftenau</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Time Service Delivery Expert (German Speaker)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Location: Cairo, Egypt<br><br>Relocation Support: This role is based in Cairo, Egypt. Novartis is unable to offer relocation support: please only apply if accessible.<br><br>At Novartis, every detail matters when it comes to supporting our people—and this role sits right at the heart of that mission. As a Time Service Delivery Expert, you will be a trusted first point of contact for associates, ensuring accurate, compliant, and timely time services that directly impact employee experience and payroll outcomes. Working in a dynamic, fast‑paced environment, you will combine service excellence with strong system discipline, collaborating closely with regional partners to keep operations running smoothly and with confidence.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><h3>Key Responsibilities</h3><ul><li>Deliver first‑level time service support to associates, ensuring timely and accurate resolution of queries.</li><li>Monitor and resolve service requests through ticketing, chatbot, and telephony channels in line with service levels.</li><li>Ensure compliance with local labour laws, Novartis policies, and global time governance standards.</li><li>Maintain accurate employee time data with clear documentation of all data change requests.</li><li>Deliver scheduled time service reports with high quality, accuracy, and timeliness.</li><li>Collaborate with second‑level support teams to escalate and resolve complex cases effectively.</li><li>Support testing and continuous improvement initiatives to enhance service delivery.</li></ul><h3></h3><h3>Essential Requirements</h3><ul><li>Experience working in a customer‑focused service delivery or shared services environment.</li><li>Ability to manage employee queries accurately using case management, ticketing, or support tools.</li><li>Strong attention to detail with the ability to document data changes clearly and compliantly.</li><li>Comfort working in fast‑paced, high‑volume support environments while meeting service level expectations.</li><li>Knowledge of German language is mandatory</li><li>Fluent English communication skills, both written and spoken.</li><li>Collaborative mindset with strong communication skills and a proactive approach to problem solving.</li></ul></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/time-service-delivery-expert-german-speaker-novartis/69d67cbfc8e81216cd0caf73</link><guid isPermaLink="true">http://biotechroles.com/time-service-delivery-expert-german-speaker-novartis/69d67cbfc8e81216cd0caf73</guid><pubDate>Wed, 08 Apr 2026 16:05:19 GMT</pubDate><company>Novartis</company><location>New Cairo</location><salary>$15000-25000</salary><type>Full time</type></item><item><title><![CDATA[Performance Analytics & GenAI Manager]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Hybrid<br>Location: Mexico City, Mexico<br>Relocation Support: This role is based in Mexico City, Mexico. Novartis is unable to offer relocation support: please only apply if accessible.<br>Be at the forefront of how data, analytics, and Generative AI shape smarter decisions at Novartis. As Performance Analytics &amp; GenAI Manager, you will turn AI ambition into real‑world impact—scaling trusted, compliant, and high‑value AI solutions that accelerate insights, boost productivity, and empower teams to act with confidence and speed.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><div><h3>Key Responsibilities</h3><ul><li>Lead local execution of the AI and Generative AI roadmap from use‑case definition through pilot, scale, and adoption.</li><li>Prioritize analytics and GenAI use cases aligned with the international data, analytics, and platforms AI strategy.</li><li>Translate business needs into scalable, reusable analytics and AI products using standardized pipelines and components.</li><li>Partner with Digital and IT teams to ensure security, compliance, reliability, and lifecycle governance.</li><li>Track adoption, performance, and value realization of deployed analytics, machine learning, and GenAI solutions.</li><li>Coordinate enablement activities, including training, documentation, and stakeholder engagement.</li><li>Co‑define local AI priorities with international medical affairs, integrated insights, and value and access teams.</li></ul><h3>Essential Requirements</h3><ul><li>Proven experience delivering advanced analytics, machine learning, and Generative AI solutions in business environments.</li><li>Hands‑on experience across the full machine learning operations lifecycle, from development to monitoring and retirement.</li><li>Strong background in driving adoption and change management for data and AI solutions.</li><li>Solid understanding of responsible artificial intelligence governance, documentation, and approval processes.</li><li>Experience collaborating with technology, data platform, and architecture teams on secure and compliant solutions.</li><li>Ability to clearly communicate complex analytics and GenAI concepts to non‑technical stakeholders.</li></ul><h3>Desirable Requirements</h3><ul><li>Experience in pharmaceutical, healthcare, or other regulated industries.</li><li>Experience designing reusable analytics products and scaling solutions across teams or markets.</li></ul></div><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Analytical Thinking, Brand Awareness, Business Analytics, Cross-Functional Collaboration, Digital Marketing, Marketing Strategy, Media Campaigns, Project Management, Project Planning, Sales, Stakeholder Engagement, Stakeholder Management, Strategic Marketing, Waterfall Model]]></description><link>http://biotechroles.com/performance-analytics-and-genai-manager-novartis/69d67cbfc8e81216cd0caf72</link><guid isPermaLink="true">http://biotechroles.com/performance-analytics-and-genai-manager-novartis/69d67cbfc8e81216cd0caf72</guid><pubDate>Wed, 08 Apr 2026 16:05:19 GMT</pubDate><company>Novartis</company><location>INSURGENTES</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Sales Representative Dermatology - Base Cali]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>-The Sales Representative is a leading driver of our customer interactions and sales performance They are the face of our customer experience approach and build deep relationships that deliver value for customers and patients in order to drive sales growth in a compliant and ethical manner.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>Responsabilidades<br />~ Impulse el crecimiento competitivo de las ventas<br />~ Identifique y priorice a los clientes de alto potencial a través del análisis de datos (profesionales de la salud y partes interesadas) que influyen en las decisiones de prescripción<br />~ Impulse el rendimiento de las ventas a través de la hábil orquestación de experiencias positivas para los clientes<br />~ Involucrarse y construir relaciones.<br />~ Participe en conversaciones basadas en el valor (en persona y virtualmente) para comprender los desafíos críticos de los clientes, los factores que impulsan la toma de decisiones, los puntos débiles y las oportunidades<br />~ Personalice y organice los recorridos de interacción con el cliente para los profesionales de la salud objetivo reflejando las preferencias de los clientes, aprovechando el contenido disponible y los múltiples canales de interacción<br />~ Fomentar el compromiso trabajando en colaboración con los profesionales sanitarios para desarrollar una colaboración sostenida a lo largo del tiempo para Novartis<br />~ Ofrezca experiencias memorables y centradas en el cliente más allá de la diferenciación clínica escuchando sus necesidades y comprendiendo su entorno sanitario<br />~ Establecer relaciones de trabajo efectivas con líderes de opinión y personas influyentes en el sector médico (a nivel territorial) y desafiar los comportamientos actuales para mejorar el recorrido del paciente (paciente adecuado, momento adecuado)<br />~ Desarrolle conocimientos y conocimientos profundos sobre el cliente<br />~ Recopile información sobre el negocio del cliente para descubrir lo que es importante para él<br />~ Haga un seguimiento de los comentarios de los clientes y traduzca las respuestas en acciones que creen valor adicional y superen las expectativas<br />~ Aproveche las fuentes de datos disponibles para crear, priorizar dinámicamente y ajustar planes relevantes de interacción con el territorio, la cuenta y el cliente<br />~ Compartir la información de los clientes con las partes interesadas internas pertinentes de forma continua para apoyar el desarrollo de contenido, campañas y planes de interacción relacionados con el producto y la indicación.<br />~ Entregue valor a clientes y pacientes<br />~ Colabore de manera compatible con equipos multifuncionales para diseñar e implementar soluciones que aborden las necesidades insatisfechas de los clientes y pacientes.<br />~ Actuar como un socio de confianza para el cliente con el fin de ayudarlo a administrar su negocio; escuchar para aprender; esforzarse por profundizar la relación de una manera obediente y ética; posicionarse para crear soluciones de valor agregado.<br />~ Actuar con integridad y honestidad tratando a los clientes y colegas de manera transparente y respetuosa con una intención clara. Cuando te enfrentes a dilemas éticos, haz lo correcto y habla cuando las cosas no parezcan correctas. Vivir según el Código de Ética y Valores y Comportamientos de Novartis.<br /><br />Key Performance Indicators<br /><br />~ Se completará a nivel local, sobre la base de la orientación que se derivará de los resultados del Consejo de Gestión del Desempeño de la Participación sobre el Terreno del IMI.<br /><br />~Habilidades de venta<br />~Información sobre los clientes<br />~Habilidades de comunicación<br />~Habilidades de influencia<br />~Gestión de conflictos<br />~Habilidades de negociación<br />~Habilidades Técnicas<br />~Gestión de cuentas<br />~Coordinación interfuncional<br />~Sector Sanitario<br />~Excelencia Comercial<br />~Ética<br />~Conformidad<br /><br /> </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Commercial Excellence, Communication Skills, Compliance, Conflict Management, Cross-Functional Coordination, Customer Insights, health care industry, Influencing Skills, Key Account Management, Negotiation Skills, Professional Ethics, Selling Skills, Technical Skills]]></description><link>http://biotechroles.com/sales-representative-dermatology-base-cali-novartis/69d67cbec8e81216cd0caf71</link><guid isPermaLink="true">http://biotechroles.com/sales-representative-dermatology-base-cali-novartis/69d67cbec8e81216cd0caf71</guid><pubDate>Wed, 08 Apr 2026 16:05:18 GMT</pubDate><company>Novartis</company><location>Barranquilla (Pharmaceuticals) / Cali (Oncology)</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Commercial Lead, Vietnam and Thailand]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><ul><li>Lead organization strategic planning and flawless execution to unify company growth either business and people by work with cross functional team and cross-BU</li><li>Supervise Launch Excellence Lead and Sales Operation Team (SO)</li><li>Chief of staff – Act as cluster point of contact either local or regional/global</li><li>Critical leadership position reporting to the CL to manage the books of business, operational effectiveness and growth aspirations for the cluster.</li><li>Manage the end-to-end op plan and op plan process for the cluster inline with region; success of this role will be defined by the seamless execution of the operating plan.</li></ul><p></p><p><b>ROLE RESPONSIBILITIES </b></p><p><b> 1.Organization strategic development</b></p><ul><li>Lead cross BU/category strategy decision and coordinate cross functional team to develop operating plan (OP) and lead teams to set strategic direction, provide guidance and prioritize resource allocation to achieve financial &amp; operating plan ambition.</li><li>Support Cluster Lead for company-wide initiatives includes culture shaping, business review and talent development and any projects assigned.</li><li>Anticipate, influence and negotiate with key stakeholders to gain insights, needs and requirements to develop, build and maintain external partnership and accelerate further growth</li><li>Influence senior leadership within Pfizer and shape external environment to identify new commercial opportunities to accomplish broad business objectives</li></ul><p><b>2.Leadership and team management </b></p><ul><li>Act as cluster point of contact to regional/ EM /global for new commercial initiatives and country/cluster performance monitoring</li><li>The member of leadership team (LT) and key contact point for LT to consolidate and lead organization business/people activities e.g.  POA/Annual plan/talent development plan/internal communication</li><li>Supervise launch excellence process to integrate cross-functional efforts leading to successful breakthrough <span>launches as well as builds market expertise in launch planning and execution. </span></li><li>Lead early stages of new assets strategic planning, as early as 3 years prior to launch. Is responsible for initial assessment and recommendation for Pfizer assets/BD in the pipeline and prioritize launches across categories at the country/cluster level and coordinates resource allocation to support launch planning.</li><li>Lead &amp; Supervise MEET/MAPP (Event) related operation team under Pfizer code of conduct and develop better solution to reduce the waiting time</li></ul><p><b>3.Transformation lead</b></p><ul><li>Point of contact for EM transformation initiative and lead country/cluster to transform culture/ process/ people mindset/ and innovative solution</li></ul><p></p><p><b>QUALIFICATIONS </b></p><ul><li>10-12 years of experience in commercial roles. Healthcare pharmaceutical domain is preferred. Proven successful track record is a must. Strong passion and experience for business management and Innovation.</li><li>Strong ability to unite people under new ideas and ways of working – Strong agent of change to bring others to think and act differently. Ability to evaluate and correct by teaching and coaching the progression of colleagues towards a plan and its goals.</li><li>Demonstrated strong cross-functional working skills to lead, inspire, inform and develop colleagues’ knowledge in relation with business management and the redefinition of the Pfizer Value to customers. Ability to deliver stretching results through others in matrix complex working situations. Excellent communication and presentation skills.</li><li>Knowledge of pharmaceutical industry, evolving Global healthcare environment and emerging digital health movement would be an advantage.</li><li>Willingness and ability to travel nationally and internationally as required</li><li>Strong operational rigor, ability to focus the organization on high end optimization and transformation strategies and programs with exceptional project management and leadership.</li><li>Strong business acumen and commercial expertise to be the go-to person/ second in charge to the CL for all commercial decision making.</li><li>High end communication skills to align, navigate, manage and present to high-level/ high impact stakeholders within the organization.</li></ul><p></p><ul></ul><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Mkt &amp; Sales/Commercial Bus<p></p><p></p>]]></description><link>http://biotechroles.com/commercial-lead-vietnam-and-thailand-pfizer/69d67badc8e81216cd0caf49</link><guid isPermaLink="true">http://biotechroles.com/commercial-lead-vietnam-and-thailand-pfizer/69d67badc8e81216cd0caf49</guid><pubDate>Wed, 08 Apr 2026 16:00:45 GMT</pubDate><company>Pfizer</company><location>Viet Nam - Ho Chi Minh</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Process Engineer (PCP) 15 months training programme]]></title><description><![CDATA[<p><b>Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals</b></p><p></p><p>We are pleased to announce the Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals, a distinguished talent development initiative aimed at cultivating the next generation of skilled professionals for Singapore&#39;s biopharmaceutical manufacturing industry.</p><p></p><p><b>Program Overview:</b></p><ul><li><p><b>Program Type: </b>Mid-Career Change</p></li><li><p><b>Duration: </b>15 months</p></li><li><p><b>Attachment:</b> Local attachment to Pfizer Inc.</p></li><li><p><b>Eligibility:</b></p><ul><li><p>Singapore Citizens or Singapore Permanent Residents</p></li><li><p>Have no prior working experience in the biopharmaceutical sector</p></li><li><p>Mid-Career Candidate: Graduated for at least 2 years prior to point of application</p></li></ul></li><li><p><b>Training Allowances: </b>CPF exempted</p></li></ul><p></p><p>This comprehensive program is meticulously designed to provide participants with the requisite skills and experience to meet the anticipated hiring demand within the biopharmaceutical manufacturing sector.</p><p></p><p>We invite eligible candidates to apply for this exceptional opportunity to advance their careers with one of the industry&#39;s leading organizations.</p><p></p><p><b>Use Your Power for Purpose</b></p><p></p><h3>The Tuas, Singapore active pharmaceutical ingredient (API) manufacturing site is a key strategic manufacturing part of the PGS Network. Many of the Pfizer’s important new innovative medicines are being transferred to the Site to support the overall growth and breakthrough strategy.</h3><p></p><h3>Whether you are managing projects, or liaising with others, your contribution in this team will help in making our work easier and faster so that we can deliver breakthroughs that change patients&#39; lives.</h3><p></p><h1><b>Why Patients Need You</b></h1><p>Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you&#39;ll help bring medicines to the world even faster by imagining what’s possible and taking action.</p><p></p><h1><b>What You Will Achieve</b></h1><p>Working with Pfizer’s dynamic engineering team, you will play a critical role in developing and modifying process formulations, methods and controls to meet desired quality standards. Your production engineering skills will help in recommending and implementing improvements, modifications or additions that will help in solving problems. You will review product requirements in terms of product development compatibility and help Pfizer determine optimum costs and schedules of production.</p><p>As an associate, your focus on the job will contribute in achieving project tasks and goals. It is your domain knowledge, commitment, collaboration and dedication that will help us achieve new milestones and patients across the globe.</p><p></p><h1><b>How You Will Achieve It</b></h1><ul><li><p>Develop Manufacturing / Operating Instructions and necessary Standard Operating Procedures.</p></li><li><p>Develop, maintain and troubleshoot the process control system recipe / models.</p></li><li><p>Carry out technical assessment for evaluation of processes.</p></li><li><p>Investigate, report and troubleshoot findings on both quality and EHS related issues observed during manufacturing or during batch record review.</p></li><li><p>Develop, implement and monitor robust preventive measures for processing issues.</p></li><li><p>Play a proactive role in ensuring the site safety and quality standards are adhered to.</p></li><li><p>Proactively monitor, identify, develop and implement improvements in processes and equipment.</p></li><li><p>Communicate on a regular basis to the plant personnel on process updates.</p></li><li><p>Train the process technicians and fellow process engineers on the process and procedures as required.</p></li></ul><p></p><h1><b><u>Qualifications</u></b></h1><p></p><h2><b>Here Is What You Need (Minimum Requirements)</b></h2><ul><li><p>Degree in Engineering, preferably in Chemical Engineering or Degree in Science with Major in Chemistry</p></li><li><p>Proactive, with strong interpersonal skills</p></li><li><p>Strong written and verbal communication skills</p></li><li><p>Proficiency in Microsoft Applications</p></li><li><p>Ability to work effectively in a team environment and collaborate with cross-functional teams</p></li></ul><p></p><p><b>Bonus Points If You Have (Preferred Requirements)</b></p><ul><li><p>Demonstrated experience in a manufacturing environment</p></li><li><p>Process Engineering and Technical Knowledge</p></li><li><p>Familiarity with Lean Manufacturing principles and Six Sigma methodologies</p></li><li><p>Excellent organizational skills and attention to detail</p></li><li><p>Ability to adapt to changing priorities and work effectively under pressure</p></li><li><p>Strong sense of commitment and dedication, with sense of urgency to get things done and results-driven attitude</p></li></ul><p>  <br />Work Location Assignment: On Premise</p>&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Support Services<p></p><p></p>]]></description><link>http://biotechroles.com/process-engineer-pcp-15-months-training-programme-pfizer/69d67bacc8e81216cd0caf48</link><guid isPermaLink="true">http://biotechroles.com/process-engineer-pcp-15-months-training-programme-pfizer/69d67bacc8e81216cd0caf48</guid><pubDate>Wed, 08 Apr 2026 16:00:44 GMT</pubDate><company>Pfizer</company><location>Singapore - Tuas</location><salary>$25000-35000</salary><type>Full time</type></item><item><title><![CDATA[Operational Excellence Lead]]></title><description><![CDATA[<p><span><b> </b></span></p><p></p><p><span><b>ROLE SUMMARY</b></span></p><p><span>The incumbent reports to the Senior Director, External Supply, Strategy &amp; Operational Excellence (ES S&amp;OE)</span></p><p><span><b>The Director of External Supply (ES), Operational Excellence (OE) is to:</b></span></p><ul><li><p><span>Provide Business facing OE Support to ES Clusters and/or Pfizer Center One (PC1)</span></p></li><li><p><span>Lead/Support/Coach OE solutions in the ES Clusters and/or Pfizer Center One (PC1) e.g. Continuous Improvement Loop, IMEx Deployment, Innovation, Agile Transformation, Complex Investigations in alignment with the ES/OE Strategies</span></p></li><li><p><span>Lead and/or coach Lean/Six Sigma projects for ES Clusters/PC1/CMO and support functions to diagnose and improve processes. This may also be on a regional basis</span></p></li><li><p><span>Build OE &amp; Innovation capabilities at the ES Clusters, PC1 and selected CMOs</span></p></li><li><p><span>Coach the ES Clusters/PC1 on embedding a CI Culture</span></p></li><li><p><span>Lead a Global OE program across External Supply in alignment with the ES/OE Strategies</span></p></li><li><p><span>Lead/support ES Strategies and T5 Initiatives</span></p></li><li><p><span>Lead/support ES IMEx</span></p></li><li><p><span>Be an active member of the ES S&amp;OE team in devising the OE and ES Strategies</span></p></li><li><p><span>Passionate and competent in using AI for Continuous Improvement</span></p></li></ul><p></p><p><span><b> </b></span></p><p><span><b> </b></span></p><p></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><p><span><b> </b></span></p><p><span>Provide Business facing OE Support to ES Clusters and/or PC1</span></p><p><span>-         Drive the ES Clusters/PC1 Governance in alignment with IMEx</span></p><p><span>-         Be a central part of the ES Clusters/PC1 and a facilitator as needed of the weekly, monthly and quarterly cadence of team meetings e.g. facilitate VSLT, BRM. Ensure process confirmations are actively used for all governance.</span></p><p><span>-         Drive a CI Culture and Act as OE SME within the ES Clusters</span></p><p><span>-         Facilitate/Co-lead the ES Cluster/PC1 Strategy and Goal setting</span></p><p><span> </span></p><p><span>Lead/Support/Coach OE solutions in the ES Clusters/PC1 e.g. Continuous Improvement Loop, IMEx Deployment, Innovation, Agile Transformation, Complex Investigations in alignment with the ES/OE Strategies</span></p><p><span>-         Lead/Coach the CI Process within the ES Clusters / PC1 at T4 VSLT and T3/T2 VSOT/VPT levels</span></p><p><span>-         Lead/Support/Coach the deployment of ES OS solutions e.g. Continuous Improvement Loop, IMEx Deployment, Agile Transformation, EIRM, facilitate Innovations Workshops at the BU level</span></p><p><span>-         Coach Complex Investigations using the established process</span></p><p><span> </span></p><p><span>Lead and/or coach Lean/Six Sigma projects for ES Clusters/PC1/CMOs and support functions to diagnose and improve processes. This may also be on a regional basis</span></p><p><span>-         Use CI to identify and lead/coach Lean/Six Sigma projects using M1, M2, M3 methodology</span></p><p><span>-         Work with functions (e.g. GTEL &amp; ESOQ) to identify and execute Lean/Six Sigma opportunities at CMOs</span></p><p><span>-         Work with the ES OE team to ensure appropriate skills are deployed by BU and region</span></p><p><span> </span></p><p><span>Build OE &amp; Innovation capabilities at the ES Clusters/PC1  and selected CMOs</span></p><p><span>-         Build M1, M2, M3, M4, PHP and Innovation capabilities within the ES Cluster/PC1 in conjunction with the PGS OE Teams</span></p><p><span>-         Build M1 and PHP capability at selected CMOs</span></p><p><span> </span></p><p><span>Coach the ES Clusters/PC1 on embedding a CI Culture</span></p><p><span>-         Respectfully challenge the Status Quo and seek to identify Value Add/Non-Value Add</span></p><p><span>-         Embed CI mindsets &amp; behaviors in the BU team and supporting functions</span></p><p><span> </span></p><p><span>Lead a Global OE program across External Supply in alignment with the ES/OE Strategies</span></p><p><span>-         Co Design and lead a Global Program that spans all of ES e.g. Cycle Time, Capability Building, EIRM, Agile Transformations, Cost Savings (eg. EMAP Operating Efficiencies)</span></p><p><span> </span></p><p><span>Lead/Support ES Strategies and T5 Initiatives (Eg. IMEx, etc)</span></p><p><span> </span></p><p><span>Be an active member of the ES S&amp;OE team in devising the OE and ES Strategies</span></p><p><span>-         Contribute to the OE &amp; ES Strategies</span></p><p><span>-         Assist with co-design of OE programs</span></p><p><span>-         Facilitate ES S&amp;OE team meetings</span></p><p><span> </span></p><p></p><p><span> </span></p><p><span>  </span></p><p></p><p><span><b>BASIC QUALIFICATIONS</b></span></p><ul><li><p><span>Bachelor’s Degree in associated discipline is required (i.e., Engineering, Industrial Engineering, Operations Management or Science)</span></p></li><li><p><span>8&#43; years of manufacturing and/or supply experience</span></p></li><li><p><span>5&#43; years hands-on analytics/six sigma/continuous improvement experience</span></p></li><li><p><span>Lean Six Sigma Black Belt trained and certified minimum</span></p></li><li><p><span>AI certified</span></p></li><li><p><span>Incumbent must be fluent both written and verbally in English.</span></p></li></ul><p><span><b> </b></span></p><p><span><b>PREFERRED QUALIFICATIONS</b></span></p><ul><li><p><span>Certified/Trained AI Expert</span></p></li><li><p><span>Certified Innovation Coach</span></p></li><li><p><span>M1 Train the trainer</span></p></li><li><p><span>Languages such as Mandarin, Spanish, Italian and French are preferred but not required</span></p></li><li><p><span>5&#43; years coaching and certifying successful six sigma green belts and black belts  </span></p></li><li><p><span>Proven skills in managing large scale initiatives</span></p></li><li><p><span>Demonstrated coaching skills</span></p></li><li><p><span>Comprehensive knowledge of a broad range of operational excellence methodologies / programs</span></p></li><li><p><span>Ability to define, evaluate and recommend improvement opportunities across the E2E to achieve and sustain improvements</span></p></li><li><p><span>Strong business acumen with manufacturing and supply chain experiences preferred</span></p></li><li><p><span>Demonstrated ability to influence stakeholders at all levels of the organization and a proven track record in change management</span></p></li><li><p><span>Strong communication and interpersonal skills to guide and / or lead diverse teams,</span></p></li><li><p><span>Strong analytical and problem solving</span></p></li><li><p><span>Adaptable to work priorities in response to complex and rapidly changing environment</span></p></li><li><p><span>Ability to navigate ES organization and operate in a multicultural environment</span></p></li><li><p><span>Develop and execute strategies with minimal guidance</span></p></li><li><p><span>undefined</span></p></li></ul>&nbsp;<br>Work Location Assignment:&nbsp;Hybrid<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Manufacturing<p></p><p></p>]]></description><link>http://biotechroles.com/operational-excellence-lead-pfizer/69d67bacc8e81216cd0caf47</link><guid isPermaLink="true">http://biotechroles.com/operational-excellence-lead-pfizer/69d67bacc8e81216cd0caf47</guid><pubDate>Wed, 08 Apr 2026 16:00:44 GMT</pubDate><company>Pfizer</company><location>Singapore - Mapletree Business City</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Mechanic]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p></p><p>Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you&#39;ll play a key role in accelerating the delivery of medicines to the world.</p><p></p><p><b>What You Will Achieve</b></p><p></p><p>In this role, you will:</p><ul><li><p>Serve as a key resource and possibly lead lower levels within your area of expertise, recognized as a &#34;LEAD&#34; or &#34;Subject Matter Expert&#34;.</p></li><li><p>Perform monitoring to the reliability of mechanical system in PGS Jakarta operations</p></li><li><p>Execute maintenance activities to the mechanical system in PGS Jakarta</p></li><li><p>Manage personal time and professional development, taking accountability for your own results, and may lead and allocate the work of others.</p></li><li><p>Contribute to project and departmental tasks, providing direction, training, and potentially acting as a lead worker.</p></li><li><p>Proactively identify and resolve potential problems, considering wider implications beyond the immediate issue.</p></li><li><p>Complete assignments independently, selecting appropriate methods, and ensuring team assignments are completed.</p></li><li><p>Review non-standard work for technical soundness and may review the work of others, adhering to Pfizer standards and guidelines.</p></li><li><p>Perform maintenance, adjustments, and repairs on production, process, facility, and utility equipment, participating in multicraft work activities as needed.</p></li><li><p>Assess priorities and make decisions related to troubleshooting, diagnostics, and proactive maintenance of systems and mechanical equipment cost-effectively.</p></li><li><p>Participate in safety training programs, use tools and equipment safely, and follow equipment schematics, logic diagrams, and engineering drawings.</p></li><li><p>Provide customer training on system implementation in compliance with company standards, government regulations, and make recommendations for improved machine performance.</p></li></ul><p></p><p><b>Here Is What You Need</b> (Minimum Requirements)</p><ul><li><p>Bachelor&#39;s Degree in Mechanical Engineering (D3/D4/S1).</p></li><li><p>Minimum 2-3 years&#43; of Pharmaceutical Manufacturing Experience.</p></li><li><p>Demonstrated aptitude in basic mechanical, pneumatic, and hydraulic skills along with problem-solving techniques.</p></li><li><p>A solid understanding of industry practices and standards, as well as basic mathematics.</p></li><li><p>Familiarity with general trades such as machine construction, electrical, and machine shop work.</p></li><li><p>Well-developed time management and problem-solving skills.</p></li><li><p>Excellent communication skills.</p></li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements):</p><ul><li><p>Bachelor&#39;s Degree (S1)</p></li><li><p>Understanding of Pharma Utility systems and Machine operations.</p></li><li><p>Advanced certifications in relevant technical fields.</p></li><li><p>Experience with advanced diagnostic tools and techniques.</p></li><li><p>Experience using software CMMS, EAMS, SAP PM etc.</p></li><li><p>Knowledge of regulatory requirements and compliance standards.</p></li><li><p>Strong in root cause analysis skills.</p></li></ul>&nbsp;&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p></p><p></p>]]></description><link>http://biotechroles.com/mechanic-pfizer/69d67baac8e81216cd0caf46</link><guid isPermaLink="true">http://biotechroles.com/mechanic-pfizer/69d67baac8e81216cd0caf46</guid><pubDate>Wed, 08 Apr 2026 16:00:42 GMT</pubDate><company>Pfizer</company><location>Indonesia - Cabang Jakarta</location><salary>$12000-25000</salary><type>Full time</type></item><item><title><![CDATA[Regional Healthcare Manager - Strategic Account Manager]]></title><description><![CDATA[<p>The Regional Healthcare Managers in GSAM team is responsible for budget achievements of the region by maximizing business opportunities in the Govt/Reimbursement accounts for biopharma products.</p><p></p><p>The role holder is responsible for managing the team of Government Strategic Account Managers in <b>Govt/Reimbursement accounts </b>and is involved in management of overall commercial performance of the <b>Institutional business and developing key relationships</b>. He / She is responsible for working with sales team and cross-functional Pfizer stakeholders to ensure appropriate level of support for an account, including identification and development of additional revenue opportunities.</p><p></p><p><b>Position Responsibilities:</b></p><p><b>1. Strategic/ Policy</b></p><ul><li><p>Develop the strategic plan for institutional sales in the Govt/Reimbursement accounts for the region by taking a short, mid and long term view of the business</p></li><li><p>Analyze and understand the impact of macroeconomic factors and industry trends on the institutional sales business and create account plans accordingly to optimize sales opportunities</p></li><li><p>Study the sales analytics for each GSAM territory and region for Govt institutional sales to help draw out trends that impact the future business plans and provide inputs to the key accounts manager for driving growth</p></li><li><p>Achieve agreed overall business objectives for each of the assigned accounts</p></li><li><p>Scoping for opportunities in the assigned govt accounts, Shaping therapy, recommendations, formulary inclusion, tender announcement.</p></li><li><p>Maximizing business opportunities by introducing innovative assets / SKUs in existing accounts or winning back lost accounts/SKUs, also work on established portfolios</p></li><li><p>He should be able to understand the state polices towards priority disease areas, funding ecosystem, state health schemes,  NHM projects, centers of excellence created by central govt like rare disease policy.</p></li><li><p>He should also have long terms view of Ayushman bharat and  aligns Pfizer’s global/India focus in therapies along with Govt interest areas.</p></li><li><p>This position also requires to understand and align procurement policies, GFR rules, make india clause and upcoming policies by MOHFW( Ministry)</p></li><li><p>This role requires coordination with DG ESI, DG DGAFS, Railway board, DG GMSD/CGHS.</p></li></ul><p></p><p><b>2. Operational / Process</b><br /><b>Account Management:</b></p><ul><li><p>Stay updated about changes in terms and conditions, criteria for selection of products, information on prices, etc. by liaising with formulary heads, KOLs, hospital Administrators and helping account-wise purchase</p></li><li><p> Work with the GSAM team and other stakeholders towards getting Pfizer products included into the preferred list of products for the accounts managed</p></li><li><p>Monitor progress of accounts managed and evolve action plans as appropriate (monitor account contacts, plan execution, profit, value, volume growth, and market share)</p></li><li><p>Ensuring that business is conducted in line with Company’s policies, ethical practices, Vision, Mission and Core</p></li></ul><ul><li><p>Coordinate with tender manager to ensure his regional assigned tenders are submitted as per schedule.</p></li><li><p>Attend Technical/Financial Bid Meetings along with GSAM if required</p></li><li><p>Attend Price Negotiation Committee Meetings</p></li><li><p>Executing Rate Contract with the help of HO.</p></li><li><p>PO tracking every month for entire team</p></li><li><p>Representations to Govt authorities on various topics</p></li><li><p>Management of BSPs including appointment process including DDQ internal, external and their claims.</p></li></ul><p><b>Customer Engagement:</b></p><ul><li><p>Know the decision making and influencing network (within and those impacting the accounts) for the accounts identified within the territory</p></li><li><p> Develop / maintain effective relationships with national, regional or local bodies / government officials<br />and any other key stakeholders and decision making authorities within prioritized accounts</p></li><li><p> Leverage opportunities for synergy and collaboration (with relevant internal and external stakeholders) to<br />adequately meet the customer needs and achieve the business goals for Pfizer</p></li><li><p> Develop relationships with Key Opinion Leaders who would have a strong influence in institutions in the region</p></li></ul><p><b>Cross Functional Interactions:</b></p><ul><li><p>Coordinate with cross functional teams to deploy support and value propositions created for the Govt/Reimbursement accounts.</p></li><li><p>Provide key account / customer insights to the marketing and strategy teams to help them co-create the marketing / strategic plan for the Govt/Reimbursement accounts</p></li><li><p>Ensure communication of account information, competitor information, and value proposition (insights) to commercial team</p></li><li><p>Work with business team and distribution team to ensure availability/liqidation of products as per the account plans</p></li><li><p>Handle account receivables and payment realization in direct accounts.</p></li><li><p>Managing and developing relationships with Key Stakes holders (Procurement, Administration of CARE&amp; States and NHM,</p></li><li><p>Participate in Audits</p></li><li><p>Coordination with Sales team for demand creation, with medical, market access, public affair. Regulatory for engagement.</p></li><li><p>Registering Pfizer entities with various Govt accounts.</p></li><li><p>Communication with assigned accounts on behalf of pfizer in coordination with RBM, Legal &amp; business.</p></li></ul><p><b>3. People</b></p><ul><li><p>Demonstrate and promote Pfizer global values in all interactions.</p></li><li><p> Demonstrate leadership behaviors</p></li></ul><p><b>4. Financial</b></p><ul><li><p>Ensure achievement of sales budgets from the Govt/Reimbursement accounts of the region.</p></li><li><p>Align budgets and resources based of the region on the account opportunities &amp; business potential to optimize return on investment</p></li><li><p>Tracking of all penalties, inventories of the region.</p></li></ul><p><b>5. Technology</b></p><ul><li><p>Use technology solutions for enabling better information availability.</p></li></ul><p></p><p><b>Qualification / Experience:</b></p><ul><li><p><b>10&#43; years of pharmaceutical experience (sales, operation, account management etc.) preferred</b></p></li><li><p><b>Understanding of Tenders, Regulatory, Financial documents is must,  </b></p></li><li><p><b> Key Account Management in Govt/Reimbursement accounts will be preferred.</b></p></li><li><p> BSc degree required. MBA preferred.</p></li></ul><p></p><p><b>Skills / Knowledge:</b></p><ul><li><p> Commercial Acumen &amp; Customer Management: Demonstrate knowledge of the healthcare market, ability to develop and manage relationships with institutional customers, demonstrate account management &amp; negotiation skills and understand how to prioritize resources and develop business plans.</p></li><li><p>  Account Management: Understand, influence and adapt to changing local healthcare, key customer and stakeholder needs. Assess the portfolio of accounts and prioritize limited resources in order to create ‘wins’ for the account and for Pfizer.</p></li><li><p>Strategic Thinking: Align account needs with Pfizer goals, understand the healthcare and local market trends and accordingly develop appropriate account plans.</p></li><li><p> Collaboration &amp; Cross-Functional Team Work: Build and maintain strong trusting relationships.</p></li><li><p> Learning agility: Demonstrate ability to manage ambiguity and perform at a high level in unfamiliar situations</p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/regional-healthcare-manager-strategic-account-manager-pfizer/69d67ba9c8e81216cd0caf45</link><guid isPermaLink="true">http://biotechroles.com/regional-healthcare-manager-strategic-account-manager-pfizer/69d67ba9c8e81216cd0caf45</guid><pubDate>Wed, 08 Apr 2026 16:00:41 GMT</pubDate><company>Pfizer</company><location>India - Mumbai</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Data Science & AI (Technical Product Owner)]]></title><description><![CDATA[<p>The International Data Science &amp; AI organization is committed to transforming data into actionable intelligence and scalable AI capabilities that enable markets to drive better decisions, improved customer engagement, and measurable business outcomes.</p><p></p><p>We are seeking a Sr Manager – Data Science and AI, to own the critical end‑to‑end AI for Targeting &amp; Segmentation program for international markets, including program strategy, model design, solution, product roadmap, delivery coordination across stakeholders, and value realization. This is a senior team lead role with significant influence, requiring strong cross‑functional leadership across Data Science, Analytics, BT, ICO,  Digital, and country teams to design, deploy, and scale segmentation solutions.</p><p></p><p>The successful candidate will thrive in a fast‑paced, highly collaborative environment, translate business needs into clear product/program requirements, and drive industrialization of segmentation capabilities from pilots through scalable deployments—while operating within governance, privacy, and responsible AI practices.</p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><p><b>AI for Segmentation Program Ownership (International)</b></p><ul><li><p>Own the <b>vision, strategy, and roadmap</b> for the AI for Targeting &amp; Segmentation program across international markets, ensuring alignment to commercial priorities and market needs.</p></li><li><p>Define the <b>program operating model</b>, key deliverables, success measures, and cadence for planning, prioritization, and decision‑making across regions and markets.</p></li><li><p>Serve as the primary point of accountability for program outcomes, coordinating across functions and markets to deliver high‑quality solutions on time and with measurable impact.</p></li></ul><p><b>Roadmap Translation, Requirements, and Delivery Coordination</b></p><ul><li><p>Translate business needs into clear <b>problem statements</b>, <b>requirements, and user stories</b> for Data Science, Analytics Engineering, and Technology teams, including data needs, model requirements, workflows, and integration expectations.</p></li><li><p>Partner closely with Data Science and engineering teams to shape solution design, ensure feasibility, and drive progress from <b>pilot → deployment → scaling</b> while maintaining quality, usability, and robustness.</p></li><li><p>Establish and maintain program plans (milestones, dependencies, risks, and mitigations), and provide transparent updates to stakeholders across geographies and time zones.</p></li></ul><p><b>Cross</b><b>‑</b><b>Functional &amp; Market Partnership (Influence Without Authority)</b></p><ul><li><p>Build strong relationships with international and local stakeholders (Commercial, Marketing, Digital, Field/Operations, Tech/IT) to align on priorities, secure input, and drive adoption.</p></li><li><p>Facilitate workshops and working sessions to align on segmentation objectives, market readiness, change impacts, and enablement needs, ensuring consistent engagement and shared ownership.</p></li><li><p>Coordinate with centralized and regional teams to identify reusable patterns and accelerate cross‑market scaling while respecting local context, constraints, and regulatory requirements.</p></li></ul><p><b>Adoption, Change Management, and Enablement</b></p><ul><li><p>Define and execute an international <b>adoption and change management approach</b>, including market onboarding, training, communications, and “how to use” guidance for segmentation outputs and workflows.</p></li><li><p>Create and maintain program documentation and business‑facing assets (e.g., value proposition, playbooks, FAQs, release notes, training materials, and adoption metrics).</p></li><li><p>Incorporate feedback loops (user feedback, performance monitoring, market learnings) to continuously improve segmentation models, outputs, and end‑to‑end user experience.</p></li></ul><p><b>Governance, Data Privacy, and Responsible AI</b></p><ul><li><p>Ensure program alignment with data governance, privacy, security, and responsible AI practices, coordinating required reviews and documentation with the appropriate governance bodies.</p></li><li><p>Partner with Technology/IT and data teams to ensure appropriate controls for data access, model monitoring, auditability, and lifecycle management.</p></li></ul><p><b>Value Realization, KPIs, and Performance Management</b></p><ul><li><p>Define, monitor, and communicate <b>program success metrics</b> (e.g., adoption, business value, segmentation performance, operational efficiency), and drive actions to close performance gaps.</p></li><li><p>Quantify and communicate value delivered through AI for Segmentation to senior stakeholders, connecting program outcomes to measurable market impact.</p></li></ul><p><b>Ways of Working / Agile Delivery</b></p><ul><li><p>Act as “voice of the user” for international markets in agile delivery teams, helping prioritize work to maximize value and ensure usability and scalability of deliverables.</p></li><li><p>Promote consistent ways of working across markets (templates, standards, release cadence, and minimal viable onboarding kits) to accelerate delivery and reduce rework.</p></li></ul><p></p><p><b>BASIC QUALIFICATIONS </b></p><ul><li><p><b>Bachelor’s degree in analytics related area (Data Science, Computer Engineering, Computer Science, Statistics, Economics, Mathematics, Operations Research, Information Systems, Engineering, or a related discipline)</b></p></li><li><p><b>9&#43; years of relevant work experience delivering Analytics, Data Science, AI/ML, or Digital/Data products in a business environment, with demonstrated end-to-end ownership from problem framing to outcomes</b></p></li><li><p><b>4&#43; years of hands-on Product Management experience</b></p></li><li><p>Demonstrated experience translating business priorities into clear requirements and roadmaps and leading delivery across cross-functional stakeholders (including influence without direct authority)</p></li><li><p>Strong stakeholder management and communication skills: ability to distill complex analytical concepts into clear, decision-oriented insights for technical and non-technical audiences</p></li><li><p>Strong program/project management skills: ability to define scope/deliverables, manage dependencies, monitor progress, and drive implementation and adoption.</p></li><li><p>Experience working with data and analytics ecosystems (e.g., data platforms, BI, analytics engineering) and collaborating with engineering teams to operationalize solutions.</p></li><li><p>Ability to operate effectively in a multi‑country, international environment, partnering across regions and time zones.</p></li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li><p>Advanced degree in Data Science, Computer Engineering, Computer Science, Information Systems or related discipline</p></li><li><p>Experience in segmentation (customer/HCP, account, or analogous segmentation), targeting, portfolio planning, or decision support, including measurement of impact and adoption.</p></li><li><p>Experience in product ownership and/or agile delivery practices for analytics/AI solutions, including backlog management and value-based prioritization.</p></li><li><p>Experience in developing Machine Learning based products, preferably with Large Language Models and GenAI solutions</p></li><li><p>Experience in developing and operating analytic workflows and model pipelines that are parametrized, automated and reusable</p></li><li><p>Experience developing and deploying data and analytic products for use by technical and non-technical audiences</p></li><li><p>Pharma &amp; Life Science commercial functional knowledge</p></li><li><p>Pharma &amp; Life Science commercial data literacy</p></li><li><p>Experience with Dataiku Data Science Studio</p></li></ul><p></p><p><b>PROFESSIONAL CHARACTERISTICS</b></p><ul><li><p><b>Growth Mindset:</b> Actively seeks improvement, evaluates the impact of insights, and helps partners anticipate strategic changes.</p></li><li><p><b>Analytical Thinker:</b> Synthesizes information across data sources into clear insights and recommendations; connects analytics to business drivers and value.</p></li><li><p><b>Strong Communicator:</b> Translates technical outputs into actionable commentary that enables effective decisions; adapts style to audience.</p></li><li><p><b>Relationship Manager / Influencer:</b> Builds durable partnerships across levels and functions; positively influences without formal authority.</p></li><li><p><b>Highly Collaborative:</b> Shares responsibility and credit; works effectively across teams; supports others through knowledge sharing and teamwork.</p></li><li><p><b>Strong Program Manager:</b> Defines scope, success criteria, and action plans; sequences work appropriately; monitors outcomes and drives adoption.</p></li><li><p><b>Proactive Self</b><b>‑</b><b>Starter:</b> Comfortable with ambiguity; prioritizes competing demands; stays current on analytics/AI trends and applies them pragmatically.</p></li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p>Ability to work non-traditional work hours interacting with global teams spanning across the different regions (eg: North America, Europe, Asia)</p><p></p><p><b>ORGANIZATIONAL RELATIONSHIPS</b></p><ul><li><p>Other AI and Data Science COE Teams</p></li><li><p>Other AIDA teams (Domain Delivery, Platforms, and Support)</p></li><li><p>Global Commercial Analytics</p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p></p><p></p>]]></description><link>http://biotechroles.com/senior-manager-data-science-and-ai-technical-product-owner-pfizer/69d67ba7c8e81216cd0caf44</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-data-science-and-ai-technical-product-owner-pfizer/69d67ba7c8e81216cd0caf44</guid><pubDate>Wed, 08 Apr 2026 16:00:39 GMT</pubDate><company>Pfizer</company><location>India - Mumbai</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Laboratory Technician]]></title><description><![CDATA[<p><span><span><b>JOB INFORMATION</b></span></span></p><p></p><p><b>JOB SUMMARY</b></p><p>· The Clinical Research Laboratory Senior Technician’s main responsibility includes proper sample management, storage and shipment on a day-to-day level.</p><p>· Involved in all pre analytical activities in the laboratory and  also in data collection.</p><p>· Perform the schedule of the laboratory for day-to-day activities.</p><p>· Training of new colleagues and updating the training materials.</p><p>· Inventory management and controls for the laboratory.</p><p>· Optimize Operational Control and Effectiveness.</p><p>· Assures close partnership with Lab Project coordinators and Principal Investigator to assure successful study delivery and high quality data.</p><p>· Fosters positive community attitudes and volunteer trust through professional behavior and ongoing communication.</p><p>· Ensures the role of Laboratory Shift Leader like a member of the laboratory staff having a good overview of the Lab &amp; unit operational activity, and solely responsible for coverage during shift.</p><p><br /> </p><p><span><b>JOB RESPONSIBILITIES</b></span></p><p>The Clinical Research Laboratory Senior Technician is responsible for the day-to-day Laboratory work.<br /> </p><p><u>Laboratory</u></p><p>· Ensure the control of the laboratory environment, safety specification, the maintenance and calibration of laboratory material required to conduct clinical trials.</p><p>· Execute lab activities as required by the CMCD both analytical as pre analytical activities</p><p>· Must be able to follow written and oral instructions and comply with safety and laboratory procedures.</p><p>· Creation/review and update SOP’s of the laboratory when it is necessary.</p><p></p><p><u>Laboratory Shift Leader</u></p><p>· To attend to the Shift Report on the clinical floor in the morning and/or evening.</p><p>· To be sure that all samples are ready before the beginning of the activities. The overall responsibility will be maintained until hand over to next shift.</p><p>· Keeps daily Laboratory organization flowing smoothly following the organization (staff allocation and  study schedules) planned by the scheduling team. In case of issues, Laboratory Shift Leader makes arrangements to reorganize the workload in order to ensure correct study/Laboratory conduct with respect to GLP and personnel qualifications: Re-distribute personnel, tasks and reorganizes activities on an efficient manner.</p><p>· Responsible of coordinating Lab colleagues activities during the same shift &amp; anticipate the activity for subsequent shift delegating appropriately the remaining tasks.</p><p>· To be the gateways between the start-up and the operational teams. To have a global vision of studies and be aware of the different specificities and to anticipate the work preparation and delegates appropriately between Lab colleagues.</p><p></p><p><u>Sample Management</u></p><p>· Responsible to ensure quality throughout sample processes and beyond.</p><p>· Manage all necessary preparations in regard to the laboratory for adequate execution of a protocol in a timely manner.</p><p>· Ensure proper lab samples handling (documents for staff use: trolley sheet, centrifugation sheet, urine collection sheet, order Lab supplies, etc…).</p><p>· Identify new lab equipment if necessary.</p><p>· Support new lab technique and software improvements (biomarkers, material, etc…).</p><p>· Assisting in the validation of methods when it is necessary.</p><p></p><p><u>Shipment</u></p><p>· Responsible for PCRU samples shipments (packing, documentation, organization with sender).</p><p></p><p><u>Other</u></p><p>· Others duties/tasks will include but are not limited to:</p><ul><li>Record and communicate or  resolve any discrepancy to study protocols in regards to laboratory.</li><li>Ensure development of new procedures required by the protocol as “superuser” and train staff accordingly.</li><li>May Participate in protocol reviews and provid specialized oversight and technical assistance in regards to the laboratory and liaise with the  Lab Project Coordinator.</li><li>May be assigned to be mentor/sponsor for a new colleague.</li></ul><p></p><p><u>Training</u></p><p>· Participate in training courses as appropriate.</p><p>· Organize and assist in the training of PCRU staff and contractors with less experience and expertise.</p><p>· May Ensure Lab training requirements are fully achieved  for protocol execution and for all protocol related procedures.</p><p>· Responsible for complying with Pfizer Standards, ethical standards, ICH, regulatory and legal requirements, national and European laws on health and safety at work, fire prevention and other appropriate legislation.</p><p></p><p></p><p><span><b>QUALIFICATIONS / SKILLS</b></span></p><p>· Minimum of a Diploma/Bachelor degree Medical Biology or equivalent.</p><p>· Superior written and verbal skills are essential; including the ability to communicate complicated research principles in easily understandable language.</p><p>· Must be available for various shifts (weekends/evenings/nights/public holiday).</p><p>· English language skills is highly recommended, your second language would be French or Dutch.</p><p>· Excellent communication skills.</p><p>· Minimum of 3 years of Laboratory experience.</p><p></p><p><u>Clinical skills</u></p><p>· Successful study conduct of all Clinical Research Unit studies in accordance with ethical, legal, and moral standards, Good Clinical Practices (GCPs) and ISO 17025 requirements and drug development goals.</p><p></p><p><u>Computer skills</u></p><p>· Working knowledge of computers and ability to adapt rapidly and easily to clinical research data systems and associated issues/risks.</p><p></p><p><u>Teamwork:</u></p><p>· Must have the ability to function as an effective team member in diverse workgroups to accomplish business objectives.</p><p>· Demonstrates effective communication with management group and internal/external customers.</p><p>· Group members are able to perform and collaborate in teams to problem solve for increased team productivity.</p><p>· Must be proactive, showing initiative and positive team spirit.</p><p>· Accountability.</p><p></p><p><u>Flexibility</u></p><p>· Demonstrates ability and flexibility to work alternative or additional hours internally and externally (weekends/evenings/nights/public holiday) to provide study activity coverage.</p><p></p><p><u>Language skills</u></p><p>· Written and reading English skills is a must</p><p>· Verbal French and Dutch skills is an asset</p><p></p><p> <br />Work Location Assignment: On Premise<br /> </p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><p style="text-align:left"><i><span>Pfizer discovers, develops, manufactures and distributes medicines and vaccines. Pfizer wants to contribute to better health and wellness for everyone, at every stage of life. Pfizer works with the government and other health partners to provide quality and accessible healthcare. The patient is central to this story.</span></i><span> </span></p><p style="text-align:left"><i><span>Pfizer has four offices in Belgium with which it supports its Belgian and international activities: 1) Anderlecht, where the Pfizer Clinical Research Unit is located. This is a fully equipped phase 1 research center. With that of New Haven (US), it is one of two Phase 1 Pfizer research centers in the world, 2)<span> </span></span></i><i><span>Elsene</span></i><i><span>, the Belgian headquarters, 3)<span> </span></span></i><i><span>Puurs</span></i><i><span>, Pfizer&#39;s production and packaging site, and 4) Zaventem, the international Pfizer&#39;s Logistics Center.</span></i><span> </span></p></div><div><p style="text-align:left"><i><span>More information can be found at<span> </span></span></i><a href="http://www.pfizer.com/" target="_blank"><u><span>www.pfizer.com</span></u></a><i><span>,<span> </span></span></i><a href="http://www.pfizer.be/" target="_blank"><u><span>www.pfizer.be</span></u></a><i><span><span> </span>and on Facebook and Twitter.</span></i><span> </span></p></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer&#39;s aim is to provide equality of opportunity in the recruitment process by avoiding any bias or potential discrimination on any grounds including (but not limited to): sex, age, race, religion or belief, sexual orientation or disability. At Pfizer we are creating an organization and promoting a culture that respects each individual&#39;s unique character and life experiences and reflects the diversity of our society, customers and markets. We will achieve this through fostering and sustaining an environment in which every colleague feels valued and supported.</p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p><p style="text-align:inherit"></p><p style="text-align:left"><u>Handicap &amp; Inclusion</u></p><p style="text-align:left">Notre mission est de libérer le potentiel de nos collaborateurs et nous sommes fiers d&#39;être un employeur inclusif pour les personnes handicapées, garantissant ainsi l&#39;égalité des chances en matière d&#39;emploi pour tous les candidats. Nous vous encourageons à donner le meilleur de vous-même en sachant que nous apporterons tous les ajustements raisonnables pour soutenir votre candidature et votre carrière future. Votre expérience avec Pfizer commence ici !</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Research and Development<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/senior-laboratory-technician-pfizer/69d67ba7c8e81216cd0caf43</link><guid isPermaLink="true">http://biotechroles.com/senior-laboratory-technician-pfizer/69d67ba7c8e81216cd0caf43</guid><pubDate>Wed, 08 Apr 2026 16:00:39 GMT</pubDate><company>Pfizer</company><location>Belgium - Anderlecht</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Professional Health Representative - Vaccine]]></title><description><![CDATA[<p><b>Professional Health Representative - Vaccine</b></p><p></p><p><b>Position Summary</b></p><p>The Professional Health Representative – Vaccine is responsible for driving sustainable business growth</p><p>by effectively promoting assigned products within a defined geographic territory. The role leverages a</p><p>hybrid engagement model, combining face‑to‑face and digital channels, to deliver value‑based,</p><p>science‑driven interactions with healthcare professionals (HCPs) and key stakeholders, in alignment with</p><p>company strategy and compliance standards.</p><p>Operating under the general guidance of the Health Representative Manager, the incumbent maintains full</p><p>accountability for business performance, customer engagement, and financial results within the assigned</p><p>territory.</p><p></p><p><b>Key Responsibilities</b></p><ul><li><p>Customer Engagement &amp; Promotion Deliver high‑quality, science‑based brand messages that support HCPs in addressing patient needs.</p></li><li><p>Execute omnichannel engagement plans aligned with customer preferences, content relevance, and channel effectiveness.</p></li><li><p>Onboard customers to new operating models and digital platforms (e.g., Digital Engagement Portal).</p></li><li><p>Build, maintain, and expand strong professional relationships with HCPs, KOLs, pharmacists, and other healthcare stakeholders.</p></li></ul><p></p><p><b>Product &amp; Disease Knowledge</b></p><ul><li><p>Onboard customers to new operating models and digital platforms (e.g., Digital</p></li><li><p>Provide accurate, approved information on product usage, dosing, safety, and clinical data.</p></li><li><p>Support physicians in disease management through the appropriate use of Pfizer products.</p></li><li><p>Distribute relevant scientific materials, clinical data, guidelines, and product samples where applicable.</p></li></ul><p></p><p><b>Territory &amp; Account Management</b></p><ul><li><p>Manage and develop accounts to ensure optimal product access, formulary inclusion, and sustainable growth.</p></li><li><p>Monitor ordering processes.</p></li><li><p>Identify, develop, and execute territory‑specific plans of action (POA) aligned with business objectives.</p></li><li><p>Explore new business opportunities and expand the reach and impact of the assigned territory.</p></li></ul><p></p><p><b>Collaboration &amp; Cross‑Functional Support</b></p><ul><li><p>Provide actionable market insights, customer feedback, and competitive intelligence to sales and marketing teams.</p></li><li><p>Contribute to marketing campaign planning by sharing real‑world customers and market insights.</p></li><li><p>Support and execute marketing and medical initiatives, including local, regional, and international congresses, workshops, and awareness programs.</p></li><li><p>Participate in speaker nomination and selection processes within the assigned territory.</p></li></ul><p></p><p><b>Reporting &amp; Compliance</b></p><ul><li><p>Accurately document customer interactions, activities, and insights.</p></li><li><p>Prepare and submit regular reports covering sales performance, activities, market feedback, opportunities, and risks.</p></li><li><p>Attend sales meetings, cycle meetings, and general business meetings as required.</p></li><li><p>Maintain full accountability for customer communications (emails, calls, and follow‑ups).</p></li></ul><p></p><p><b>Education &amp; Experience</b></p><ul><li><p>Bachelor’s degree in pharmacy or related pharmaceutical/medical field.</p></li><li><p>Minimum 2 years&#39; experience as a Health/Medical Representative.</p></li><li><p>Vaccine experience is an advantage.</p></li><li><p>Fluency in Arabic and English is required.</p></li></ul><p></p><p><b>Competencies &amp; Capabilities</b></p><ul><li><p>Strong alignment with Pfizer Colleague Competencies and “One Pfizer” culture.</p></li><li><p>Excellent written and verbal communication skills.</p></li><li><p>Strong interpersonal, influencing, negotiation, and change‑agility capabilities.</p></li><li><p>Demonstrated selling excellence, presentation skills, and analytical thinking.</p></li><li><p>Customer‑centric mindset with a strong focus on unmet needs.</p></li><li><p>Ability to manage complexity across territories and accounts.</p></li><li><p>Influence through insights and value‑based conversations.</p></li><li><p>Establish credibility and trust with healthcare stakeholders.</p></li><li><p>Effective orchestration of omnichannel engagement.</p></li><li><p>Embrace data, digital tools, and technology adoption.</p></li><li><p>Navigate complex accounts and collaborate cross‑functionally.</p></li><li><p>Integrate the patient perspective into customer interactions.</p></li></ul><p>  <br /> </p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer Gulf is an equal-opportunity employer, and we are proud of our commitment to creating a diverse and inclusive candidate pool to support and empower our workforce.</p><p style="text-align:inherit"></p><p style="text-align:left">We strive to ensure that our people are heard, seen and cared for by creating an environment that fosters inclusion and inspires colleagues to speak up to promote an engaging and inclusive culture where they can thrive.</p><p style="text-align:inherit"></p><p style="text-align:left">Our diverse workforce represents the patients we serve and the communities in which we operate.</p><p style="text-align:inherit"></p><p style="text-align:left">We look forward to reviewing your application and thank you for your interest.</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/professional-health-representative-vaccine-pfizer/69d67ba6c8e81216cd0caf42</link><guid isPermaLink="true">http://biotechroles.com/professional-health-representative-vaccine-pfizer/69d67ba6c8e81216cd0caf42</guid><pubDate>Wed, 08 Apr 2026 16:00:38 GMT</pubDate><company>Pfizer</company><location>United Arab Emirates - Dubai</location><salary>$55000-85000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Director, Identity Security and Access Management]]></title><description><![CDATA[<p><span><b> ROLE SUMMARY</b></span></p><p></p><p><span>Our Identity Security and Access Management (ISAM) team is responsible for enabling secure and seamless access to Pfizer’s digital resources while protecting against unauthorized access and identity-based threats. This team leads enterprise-wide efforts in privileged access management (PAM), directory services, certificate management, identity and access entitlements, and authentication (MFA, SSO, and federation services), ensuring that access is granted appropriately, monitored continuously, and aligned with regulatory and business requirements.</span></p><p></p><p><span>We are seeking an experienced and strategic individual of Identity Security and Access Management to lead Pfizer’s enterprise ISAM program. The ideal candidate will bring deep expertise in identity governance, access control, and ISAM architecture, with a strong history of designing and managing large-scale programs that enhance security, improve operational efficiency, and support regulatory compliance. This leader will oversee enterprise-wide initiatives across identity governance, identity entitlements, directory services, certificate management, federated identity services, and privileged access management.</span></p><p><span> <b> </b></span></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><ul><li><p><span> <span>Own and drive the strategic vision for Identity Security and Access Management across the organization, aligning ISAM initiatives with broader cybersecurity and business objectives.</span></span></p></li><li><p><span>Develop and manage the ISAM budget, ensuring alignment with organizational goals and effective allocation of resources. Monitor expenditures, forecast future budget needs and identify opportunities for cost optimization.</span></p></li><li><p><span>Lead the transformation of legacy identity management systems and deliver on a multi-year modernization roadmap, including the enterprise-wide implementation of SailPoint.</span></p></li><li><p><span>Champion the adoption of modern ISAM practices and technologies, including Ping Identity, ensuring scalable, secure, and future-ready solutions.</span></p></li><li><p><span>Take ownership of Privileged Access Management, ensuring seamless integration with existing ISAM systems while maintaining operational excellence and legacy support.</span></p></li><li><p><span>Oversee directory services and certificate management processes, ensuring they are secure, available, efficient, and aligned with enterprise standards across a global environment.</span></p></li><li><p><span>Define and execute strategies to enhance identity governance controls, including access request, provisioning, and de-provisioning, with a focus on automation and user experience.</span></p></li><li><p><span>Drive enterprise-wide strategy and execution for MFA, SSO, and Federation services, ensuring secure and seamless authentication across internal and external platforms.</span></p></li><li><p><span>Define and implement identity and access entitlement frameworks, ensuring granular access control aligned with business roles and regulatory requirements.</span></p></li><li><p><span>Ensure integration and interoperability across ISAM capabilities, including PAM, directory services, certificate management, and federated identity, to support a unified and scalable ISAM architecture.</span></p></li><li><p><span>Ensure compliance with internal and external audit requirements, maintaining a high level of security and operational resilience in ISAM systems.</span></p></li><li><p><span>Collaborate with cross-functional teams to ensure ISAM requirements are embedded into the organization’s security architecture and technology strategy.</span></p></li><li><p><span>Lead and mentor a multi-national team through complex ISAM projects, providing clear direction, accountability, and support to deliver high-impact outcomes. </span></p></li><li><p><span>Act as a trusted advisor to senior leadership, translating technical ISAM concepts into strategic business value and influencing decision-making at the executive level.</span></p></li></ul><p><span> </span></p><p><span><b>BASIC QUALIFICATIONS</b></span></p><ul><li><p><span><span>Bachelor’s degree with 12 - 15&#43; years of experience in cybersecurity, identity and access management, or related fields.</span></span></p></li><li><p><span>At least 8 years of direct leadership experience managing enterprise-wide ISAM functions.</span></p></li><li><p><span>Professional certifications such as CISSP or CISM strongly preferred.</span></p></li><li><p><span>Strong background in identity governance, access management, and regulatory compliance, with experience in frameworks such as NIST and ISO.</span></p></li><li><p><span>Deep knowledge of ISAM technologies and best practices, including identity governance tools, SSO, MFA, and PAM solutions.</span></p></li><li><p><span>Experience designing and implementing identity entitlement models and federated identity architectures across hybrid environments.</span></p></li><li><p><span>Strong leadership, communication, and presentation skills, with the ability to translate complex ISAM concepts into business-focused insights for senior executives.</span></p></li></ul><p></p><p><span><b>Preferred Qualifications</b></span></p><ul><li><p><span><span>Experience with ISAM tools and technologies, specifically SailPoint, Ping and CyberArk.</span></span></p></li><li><p><span>Proven track record of leading cross-functional teams and driving strategic ISAM initiatives within a large, complex organization.</span></p></li></ul><p><span><b> </b></span></p><p><span><b>OTHER INFO</b></span></p><ul><li><p><span><span>Periodic international and domestic travel may be required (less than 5%).</span></span></p></li><li><p><span>Work Location Assignment: Must be able to work in the assigned office 2-3 days per week, or as needed by the business.</span></p></li><li><p><span>This role is NOT remote. </span>Work Location Assignment: Hybrid.</p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Information &amp; Business Tech<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/sr-director-identity-security-and-access-management-pfizer/69d67ba6c8e81216cd0caf41</link><guid isPermaLink="true">http://biotechroles.com/sr-director-identity-security-and-access-management-pfizer/69d67ba6c8e81216cd0caf41</guid><pubDate>Wed, 08 Apr 2026 16:00:38 GMT</pubDate><company>Pfizer</company><location>Greece-Thessaloniki Chortiatis</location><salary>$140000-190000</salary><type>Full time</type></item><item><title><![CDATA[Recruiting Onboarding Delivery Associate]]></title><description><![CDATA[<p>Use Your Power for Purpose </p><p></p><p>At Pfizer, the Associate - Regional TA &amp; Onboarding Delivery role centers around delivering an outstanding candidate experience. As part of the Candidate Experience team, you will join a dynamic team committed to attracting top talent and ensuring every candidate feels valued from the first interaction through onboarding and integration. We prioritize a welcoming and supportive environment, actively seeking ways to improve processes and resolve challenges so that candidates and new hires have a seamless, positive journey. By focusing on each individual&#39;s experience, we create a workplace that is inclusive and exceptional, ultimately advancing our mission to enhance patient care and organizational success.</p><p></p><p>What You Will Achieve </p><p></p><ul><li><p>Facilitate talent acquisition by attracting high-quality candidates and streamlining their onboarding process, ensuring a positive experience for all new hires from initial contact through integration.</p></li><li><p>Serve as the primary point of contact for new hires and hiring managers to resolve onboarding questions and issues, including access to relevant tools, technologies, information and events.</p></li><li><p>Execute key operational components of recruitment and onboarding, such as job postings, generating and managing offer documentation, and handling pre-boarding activities.</p></li><li><p>Take ownership of all recruitment and onboarding administration assigned tasks and tickets and make sure that they are resolved efficiently and with a superior level of quality</p></li><li><p>Manage and track pre-hire contingencies and onboarding tasks to ensure compliance, timely completion, and a positive candidate experience.</p></li><li><p>Prepare, update, and verify the accuracy of employee records and onboarding data through reliable data entry practices, supporting audit readiness and regulatory requirements.</p></li><li><p>Execute key operational components of the end to end recruitment and onboarding processes including job posting, offer documentation generation and management, and pre-boarding documentation management</p></li><li><p>Ensure process alignment with country legal and privacy-related requirements, and deliver against agreed Service Level Agreements (SLAs) and Key Performance Indicators (KPIs) for recruitment and onboarding.</p></li><li><p>Identify areas for improvement in recruitment and onboarding processes, supporting the implementation of process enhancements by collaborating with the Regional Talent Acquisition Delivery Lead.</p></li><li><p>Develop and promote effective team collaboration and communication, operate within established procedures, and seek guidance as needed to uphold best practices and support organizational goals.</p></li></ul><p></p><p>Here Is What You Need (Minimum Requirements) </p><p></p><ul><li><p>A BA/BS with at least 1 year of experience, or an associate&#39;s degree with at least 4 years of experience, or a high school diploma (or equivalent) with at least 6 years of relevant experience is required for this role. </p></li><li><p>Proficiency in MS Office to handle tasks efficiently and seamlessly. </p></li><li><p>Strong written and verbal communication skills for effective collaboration and idea articulation. </p></li><li><p>A positive and continuous improvement mindset to adapt in ever-evolving situations. </p></li><li><p>Demonstrated capability to work as a compelling team member within a matrix environment. </p></li><li><p>Ability to manage multiple tasks and prioritize effectively in a fast-paced setting. </p></li><li><p>Strong organizational skills to coordinate workflow and handle documentation logistics. </p></li><li><p>Verbal and written fluency in English to facilitate clear communication and effective collaboration across teams.</p></li><li><p>Demonstrates customer orientation and delivers excellent customer service skills to ensure satisfaction and positive experiences.</p></li><li><p>At least 1 year of experience supporting recruitment and onboarding delivery processes for North America regions, ensuring smooth transitions and compliance with regional requirements.</p></li><li><p>Proficiency in MS Office to handle tasks efficiently and seamlessly.</p></li><li><p>Experience with Workday to manage recruitment processes and support recruitment and onboarding activities.</p></li><li><p>Strong written and verbal communication skills for effective collaboration and idea articulation.</p></li></ul><p></p><p>Bonus Points If You Have (Preferred Requirements): </p><ul><li><p>Ability to utilize various analytical tools effectively for informed decision-making. </p></li><li><p>Excellent interpersonal skills to foster collaborative relationships. </p></li><li><p>Problem-solving skills with a proactive attitude towards challenges. </p></li><li><p>Adaptability to changing environments and processes, demonstrating resilience and flexibility. </p></li><li><p>Experience in project management or coordination to support Talent acquisition initiatives. </p></li><li><p>Enthusiasm for continuous learning and professional development opportunities. </p></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>People Experience<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/recruiting-onboarding-delivery-associate-pfizer/69d67ba5c8e81216cd0caf40</link><guid isPermaLink="true">http://biotechroles.com/recruiting-onboarding-delivery-associate-pfizer/69d67ba5c8e81216cd0caf40</guid><pubDate>Wed, 08 Apr 2026 16:00:37 GMT</pubDate><company>Pfizer</company><location>Costa Rica - Escazu</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Data & AI Engineer]]></title><description><![CDATA[<p><b>Role Summary</b></p><p>The Senior <b>Manager, Data &amp; AI Engineer</b> is a hands-on engineering leadership role responsible for <b>building and scaling data &amp; AI engineering capabilities</b> that enable <b>AIT (AI Transformation)</b> programs across <b>international and local projects</b>. </p><p></p><p>As the AICL Platform Lead, you will play a pivotal role driving end‑to‑end platform capability design (L4&#43;), coordinating with Data Science, Digital, analytics/reporting, and global teams to translate use case needs into reusable platform assets. You will also act as the China coordination point for data governance forums to ensure decisions support trusted, compliant data consumption &amp; AI adoption.</p><p> </p><p>You will design and deliver <b>production-grade data pipelines, semantic/consumption layers, model/LLM serving services, and operational tooling</b> with strong engineering discipline (testing, CI/CD, observability, security/compliance) with principles aligned with International data strategy as applicable</p><p> </p><p>This is a player‑coach role: the individual is expected to lead delivery while remaining technically hands‑on, especially in areas where deep technical judgement and collaboration with Digital are required.</p><p></p><p><b>Key Responsibilities</b></p><p></p><ul><li><p><b>AICL Platform Leadership &amp; Architecture (Core)</b></p><ul><li><p>Lead the design and hands‑on delivery of China AICL capabilities, including AI‑ready data products, semantic/consumption layers, and orchestration patterns.</p></li><li><p>Translate AI and analytics use‑case needs (e.g. DDD) into concrete technical designs and deliverables, moving from PoC or concept into MVP and production‑ready solutions.</p></li><li><p>Ensure AICL components are usable, stable, and reusable, not just architecturally sound.</p></li></ul></li></ul><p></p><ul><li><p><b>Cross‑Functional Alignment (China &#43; Global)</b></p><ul><li><p>Work <b>day‑to‑day with Digital / engineering teams</b> to co‑design and implement AICL solutions, including integration, deployment, testing, and operational handover.</p></li><li><p>Partner closely with Data Science/Digital teams and analytics stakeholders to ensure platform capability aligns with real use cases and adoption pathways.</p></li><li><p>Keep continuous, bidirectional alignment with global counterparts on AI and data platform product evolution, ensuring that global updates, upgrades, and lessons learned are shared proactively, and that China requirements and constraints are fed back into global discussions.</p></li></ul></li></ul><p></p><ul><li><p><b>AI Consumption Enablement: Semantic/Context &amp; Orchestration</b></p><ul><li><p>Drive the enablement of semantic and context layers (e.g., mapping business terms to technical objects, SSOT KPI integration, organization/context enrichment) as foundational AICL capabilities.</p></li><li><p>Guide the design of AI consumption and orchestration patterns (e.g., structured &#43; unstructured retrieval coordination, agent orchestration considerations) as part of AICL L4&#43; capability planning.<b> </b></p></li></ul></li></ul><ul><li><p><b>Data Quality &amp; Observability</b>:</p><ul><li><p>Responsible for data quality and observability across AICL and related platforms, ensuring enterprise standards and AI/analytics criteria are clearly defined and consistently followed by designated teams.</p></li></ul></li></ul><ul><li><p><b>AI/ML Engineering, MLOps &amp; LLMOps</b></p><ul><li><p>Productionize ML/AI solutions: build training/inference pipelines, packaging, deployment, monitoring, and lifecycle management for models and AI services</p></li><li><p>LLM Development: Proven experience in designing and developing LLM-based applications, including RAG systems and AI Agents.</p></li><li><p>Framework Proficiency: Hands-on experience with popular LLM orchestration frameworks such as LangChain, LlamaIndex, or similar tools for building scalable AI solutions.</p></li><li><p>Implement LLMOps practices (prompt testing, runtime monitoring, evaluation/guardrails, hallucination control patterns) for agentic and LLM-enabled solutions where applicable.</p></li><li><p>Collaborate with Data Scientists to integrate models into scalable services and workflows, enabling repeatable delivery and BAU operations.</p></li></ul></li></ul><ul><li><p><b>Backend Services &amp; Platform Engineering</b></p><ul><li><p>Build and maintain Python services and REST/gRPC APIs (e.g., FastAPI) that support inference workflows, metadata/services, internal platforms, and automation.</p></li><li><p>Establish clear API contracts, data models, validation, and secure authN/authZ patterns for enterprise integration.</p></li></ul></li></ul><p></p><p><b>Required Qualifications</b></p><ul><li><p>Bachelor’s, Master’s, or PhD in Computer Science, Statistics, Data Science, Engineering, or a related quantitative field.</p></li><li><p>8&#43; years in data/analytics platforms, dataproduct, or AI enablement roles, with experience leading cross-functional delivery and platform adoption</p></li><li><p>Strong understanding of end-to-end data &amp; AI platform architecture, especially consumption/semantic enablement and platform lifecycle thinking.</p></li><li><p>Strong programming skills in <b>Python</b>; experience building backend services with <b>FastAPI/Flask</b> and designing <b>REST APIs</b>.</p></li><li><p>Hands-on experience developing <b>ETL pipelines</b> using <b>Python &#43; SQL</b>, working with databases and data modeling concepts.</p></li><li><p>Familiar with modern engineering practices (version control, CI/CD concepts, testing, observability), sufficient to lead industrialized delivery with Digital teams.</p></li><li><p>Able to evaluate technical options and make pragmatic decisions under China constraints</p></li><li><p>Data Quality &amp; Observability: Experience implementing and managing frameworks for data quality testing, observability, and alerting.</p></li></ul><ul><li><p>Strong stakeholder management and communication skills (China &#43; global), able to maintain long-term alignment on platform evolution</p></li><li><p>Experience with cloud platforms and operating services in cloud environments (AWS/Azure/GCP); familiarity with containers (Docker) and CI/CD.</p></li><li><p>Strong engineering discipline: testing (unit/integration), code quality, documentation, and operational readiness.</p></li></ul><p><b>Preferred:</b></p><ul><li><p>Strong execution capability in data / analytics / AI platform delivery.</p></li><li><p>Proven experience working hands‑on with engineering or Digital teams to deliver production‑ready data or AI capabilities.</p></li><li><p>Solid understanding of data engineering, consumption layers, and AI‑ready data enablement.</p></li><li><p>Ability to translate business or AI needs into implementable technical solutions.</p></li><li><p>Experience with AI consumption layer, semantic layer/metadata enablement, or orchestration/agent patterns</p></li><li><p>Understanding of RAG / unstructured data enablement considerations and the implications for semantic/context layers</p></li><li><p>Experience in regulated/data-sensitive environments and governance forums (decision framing, standards setting).</p></li><li><p>Familiarity with enterprise governance models and data lifecycle decision processes.</p></li></ul>&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Marketing and Market Research<p></p><p></p>]]></description><link>http://biotechroles.com/data-and-ai-engineer-pfizer/69d67ba5c8e81216cd0caf3f</link><guid isPermaLink="true">http://biotechroles.com/data-and-ai-engineer-pfizer/69d67ba5c8e81216cd0caf3f</guid><pubDate>Wed, 08 Apr 2026 16:00:37 GMT</pubDate><company>Pfizer</company><location>China - Beijing - Beijing</location><salary></salary><type>Full time</type></item><item><title><![CDATA[Director, Science Media Relations]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p><b> </b></p><p>The Director of Global Media Relations leads media relations strategy and day-to-day execution for key research and development functions and divisions of Pfizer. The Director will be a strategic partner in helping shape the public or stakeholder perception of Pfizer through proactive media engagement and risk mitigation strategies that will increase public understanding of Pfizer’s work.</p><p></p><p>The role owns the strategy, preparation, execution and performance of media plans aligned to advance pipeline priorities, strengthen Pfizer’s reputation and credibility, particularly during moments of heightened visibility including but not limited to data readouts, regulatory filings/approvals, collaborations, publications, early discovery efforts and policy.</p><p></p><p>As a leader within Corporate Communications, this role operates as a trusted advisor to business and R&amp;D leadership</p><p>and is fully integrated into Pfizer’s enterprise narrative. It reports to the Senior Director of Pipeline and Portfolio Media Relations and is based in New York City.</p><p></p><p>The role works closely with Executive Communications Center of Excellence (COE), Social and Digital Communications, Research and Development, and business partners to shape how the world understands Pfizer’s science, business, and purpose.</p><p></p><p>This position requires strong executional rigor, editorial judgment, stakeholder management, and the ability to manage complex, high-visibility workflows in a dynamic environment.</p><p></p><p><b>CORE RESPONSIBILITIES</b></p><p><b> </b></p><ul><li><p>Uncover/identify compelling content for scientific earned media storytelling opportunities and the placement of them in high-impact media outlets, including those that may be new and/or emerging in today’s dynamic news environment</p></li><li><p>Continually discover and develop relationships with science-focused earned media outlets and journalists</p></li><li><p>Use combined media, science and competitive landscape knowledge to provide insights for successful engagement strategies</p></li><li><p>Serve as point person for major news outlets interested in Pfizer’s science and research, aligning with the broader team around Pfizer’s pipeline and clinical innovation</p></li><li><p>Arrange and staff with Pfizer’s scientists and science spokespeople, preparing them for successful media engagements related to Pfizer’s core priorities including chronic weight management and vaccine development</p></li><li><p>Function as a translator of Pfizer’s science for media audiences and partner closely with R&amp;D, medical and business partners on story content, proof points and strategy</p></li><li><p>Support development of press materials (Q&amp;As, press releases, leader talking points, preparation documents)</p></li><li><p>Lead development and deployment of high-impact storytelling across traditional and emerging media platforms</p></li><li><p>Define KPIs and success earned media metrics for pipeline efforts and regularly report insights to senior communications leadership</p></li><li><p>Partner with the Senior Director of Pipeline and Portfolio media relations on key catalyst and milestone calendar</p></li><li><p>Advise leaders and manage strategy or reactive responses to safety and medical topics related to Pfizer’s vaccines and/or medicines</p></li><li><p>Lead the development and deployment of high-impact executive digital content across platforms, including written, visual, and video formats</p></li><li><p>Orchestrate scientific congress earned media efforts (e.g., American Diabetes Association, ObesityWeek, IDWeek, ECCMID, World Vaccine Congress), and coordinate with IR regarding press releases, earnings releases, and other disclosures</p></li><li><p>Balance proactive thought leadership and storytelling with disciplined restraint during sensitive or high-risk periods</p></li><li><p>Serve as a partner across groups like Corporate Communications, Policy, Investor Relations, and regional teams to align executive digital activity with enterprise campaigns and critical moments.</p></li><li><p>Share frameworks, insights, and best practices to elevate media relations capability across the organization</p></li></ul><p></p><p><b>QUALIFICATIONS</b></p><p></p><ul><li><p>Minimum required: Bachelor’s degree, preferably in communications, English, social sciences, business/economics, healthcare/pre-med, or related fields.</p></li><li><p>8&#43; years of experience in media relations and communications, including experience with a pharmaceutical, biotech, medical, or other related research environment.</p></li><li><p>Must possess a track record of scientific story placements among top-tier, trade and relevant media.</p></li><li><p>Solid experience in dealing with significant healthcare issues management.</p></li><li><p>Strong understanding of media, digital, social, internal, and executive communications and how they work together; current on best practices and trends.</p></li><li><p>Mastery of AI basics and hands-on knowledge of the use of LLMs in communications work is necessary.</p></li><li><p>Day-to-day direction, by the nature of the business, must be self-initiated.</p></li><li><p>Excellent presentation skills, and persuasiveness are mandatory.</p></li><li><p>Agency background preferred.</p></li><li><p>Ability to manage pressure, meet deadlines and monitor and evaluate results is essential.</p></li><li><p>High attention to detail, strong organizational skills, and sound judgment under pressure.</p></li><li><p>A strong, demonstrated record of collaboration is critical.</p></li><li><p>Excellent strategic thinking, writing, editing, storytelling skills, and editorial judgement with a proven ability to convey complex ideas across formats and channels.</p></li><li><p>Demonstrated resilience, adaptability, and sound judgment in dynamic and ambiguous environments, with the interpersonal presence and credibility to build trust quickly and influence effectively at senior levels.</p></li></ul><p> <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p></p><p>Work Location Assignment: Hybrid</p><p>Last date to apply: April 22, 2026</p>&amp;#xa;The annual base salary for this position ranges from $162,900.00 to $271,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Public Affairs &amp; Communication&amp;#xa;]]></description><link>http://biotechroles.com/director-science-media-relations-pfizer/69d67ba4c8e81216cd0caf3e</link><guid isPermaLink="true">http://biotechroles.com/director-science-media-relations-pfizer/69d67ba4c8e81216cd0caf3e</guid><pubDate>Wed, 08 Apr 2026 16:00:36 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Research Analyst]]></title><description><![CDATA[<p><b>Job Summary</b></p><ul><li><p>​Development and implementation of analytics for new API processes and technology in manufacturing sites. </p></li></ul><ul><li><p>Provide technical support and leadership for supply assurance projects </p></li></ul><p></p><p><b>Job Responsibilities</b></p><ul><li><p>Apply highly specialised analytical skills to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the Development team. </p></li></ul><ul><li><p>Develop, evaluate &amp; verify analytical methods across a range of techniques as required to support projects. </p></li></ul><ul><li><p>Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team. </p></li></ul><ul><li><p>Contribute a range of highly innovative analytical ideas to support global process development projects. </p></li></ul><ul><li><p>Demonstrate problem solving delivering process and analytical understanding. </p></li></ul><ul><li><p>Provide analytical support in technical transfer of analytical methods to manufacturing sites </p></li></ul><ul><li><p>Co-ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands. </p></li></ul><ul><li><p>Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups.  </p></li></ul><ul><li><p>Investigate new technologies and analytical approaches </p></li></ul><ul><li><p>Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines. </p></li></ul><ul><li><p>Contribute to the analytical team program of continuous improvement. </p></li></ul><ul><li><p>Ensure the ongoing safe and efficient operation of facilities. </p></li></ul><p></p><p><b>Qualifications/Skills</b></p><ul><li><p>Extensive knowledge and experience of analytical principles and procedures. </p></li></ul><ul><li><p>Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC-MS/MS, GC-MS, KF. </p></li></ul><ul><li><p>A strong background in impurity isolation and identification using LC-MS to support the development and troubleshooting of chemical processes is desirable. </p></li></ul><ul><li><p>Experience in HPLC/UPLC method development. GC method development experience is desirable. </p></li></ul><ul><li><p>Experience in pGTI method development and quantification is desirable. </p></li></ul><ul><li><p>Experience of method validation and method transfers, including the generation and review of MT and validation protocols and reports is desirable. </p></li></ul><ul><li><p>A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project.  Project management experience a plus here.  </p></li></ul><ul><li><p>The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results.  Develops advanced ideas and guides their development into a final product.  </p></li></ul><ul><li><p>Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes. </p></li></ul><ul><li><p>Excellent interpersonal skills and the ability to work in a collaborative, team driven environment. </p></li></ul><ul><li><p>Excellent written and verbal communication skills. </p></li></ul><ul><li><p><b>For Research Analyst,</b> a PhD in analytical chemistry ideally combined with 0&#43; years’ experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and ideally up to 2&#43; years’ experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role.</p></li></ul><p> <br />Work Location Assignment: On Premise</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p style="text-align:left"><b><span>Additional Information</span></b><span> </span></p></div><div><ul><li><p style="text-align:left"><span><span>In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.</span></span><span> </span></p></li><li><p style="text-align:left"><span><span>Please note there is no relocation support available for this position </span></span></p></li></ul><p style="text-align:inherit"><span><span>​</span></span><span> </span></p></div><div><p style="text-align:left"><b><span>How to apply</span></b><span> </span></p></div><div><ul><li><p style="text-align:left"><span><span>Make a difference today, all suitable candidates should apply with CV below.  We are looking forward to hearing from you!</span></span><span> </span></p></li></ul><p style="text-align:inherit"><span>​</span></p></div></div><div><p style="text-align:left"><u><span>Purpose</span></u><span>  </span></p></div><div><p style="text-align:left"><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</span></span><span> </span></p><p style="text-align:inherit"></p></div><div><p style="text-align:left"><u><span><span>Digital Transformation Strategy </span></span></u></p><p style="text-align:left"><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span><span> </span></p><p style="text-align:inherit"></p></div><div><p style="text-align:left"><u><span><span>Equal Employment Opportunity </span></span></u></p><p style="text-align:left"><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span><span> </span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Research and Development<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/research-analyst-pfizer/69d67ba0c8e81216cd0caf3d</link><guid isPermaLink="true">http://biotechroles.com/research-analyst-pfizer/69d67ba0c8e81216cd0caf3d</guid><pubDate>Wed, 08 Apr 2026 16:00:32 GMT</pubDate><company>Pfizer</company><location>Ireland - Cork - Ringaskiddy</location><salary>$55000-85000</salary><type>Full time</type></item><item><title><![CDATA[Therapy Area Specialist: Neurology & Covid-19 – North West England]]></title><description><![CDATA[<p><b>Therapy Area Specialist: Neurology &amp; Covid-19 – North West England</b></p><p></p><p><b>ROLE SUMMARY</b></p><p>The Therapy Area Specialist (TAS) role within Primary Care Business Unit is a promotional, customer‑facing position responsible for driving excellence in customer engagement, disease education and brand execution across Neurology (Migraine) and COVID treatment pathways. The TAS partners with a broad range of NHS stakeholders—including GPs, pharmacists, PCN leaders, community services and secondary care clinicians—to improve pathway understanding, support appropriate treatment adoption and optimise patient outcomes. Through strong clinical knowledge, insight‑led conversations and compliant promotion, the TAS aims to maximise uptake of medicines in-line with local priorities while delivering agreed business unit KPIs</p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><ul><li><p>Demonstrate sustained in-depth disease, brand and environmental knowledge (patient pathway, stakeholder mapping) to deliver impactful In Call Effectiveness to maximise the value and uptake of our medicines, outcomes and ROI</p></li><li><p>Targeted Customer Engagement of key individual stakeholders and organisations across the patient pathway, in order to secure optimal patient access within the local NHS system, based upon the value of our medicines</p></li><li><p>Develop Key Clinical Experts to advocate the value of and, maximise the appropriate use of our medicines and benefits for patients</p></li><li><p>Account planning &amp; prioritisation; Work with Healthcare Partnership Manager to demonstrate excellence in prioritisation, development &amp; execution of best in class account plans in collaboration with cross functional team  to deliver impactful strategies that accelerate value for Pfizer, Health and Care Systems and Patients</p></li><li><p>Budget Management - Manage Territory and Project budget and ensure that any over or under spend is highlighted in a timely manner to Commercial Manager (CM) to allow resource reallocation.</p></li><li><p>Operate with a Digital First multichannel mindset, demonstrating high capability and deployment of digital technology and channels, to further enhance customer experience, maximise colleague efficiency and ensure optimal patient access to our medicines</p></li><li><p>Role model living our Purpose, Values &amp; Behaviours to ensure that our Culture is diverse &amp; inclusive where everyone can thrive.  A growth orientated mindset demonstrating Courageous thinking, thoughtful risk taking &amp; aspirational goal setting</p></li><li><p>Cross Functional Working – Demonstrate effective working relationship with Commercial Manager CM, Healthcare partnership Manager HPM, Clinical Effectiveness Consultant and Marketing colleagues on specific engagements and projects.</p></li><li><p>Deliver Performance with Integrity; Operate with a strong commitment and adherence to the ABPI Code of Practice and Pfizer policies and procedures.</p></li></ul><p></p><p><b>BASIC QUALIFICATIONS &amp; EXPERIENCE</b></p><ul><li><p>Graduate or Equivalent (ideally Life Sciences).</p></li><li><p>Must have gained the ABPI Medical Representative’s Exam (or equivalent) within first two years of employment as a representative.  Representatives new to the pharmaceutical industry, must take an appropriate exam within their first year of employment as a representative.</p></li><li><p>Fully conversant with requirements of ABPI Code of Practice.</p></li><li><p>Where access  to customer groups have certain entry requirements e.g. credentialling, colleague would be required to comply with these as necessary to fulfil their role.</p></li><li><p>UK pharmaceutical industry experience.</p></li><li><p>Effective working knowledge of NHS structures and the inter-dependencies between Health and Care systems and service providers, across primary care and secondary care.</p></li><li><p>Advanced selling skills and ability to critically appraise &amp; present clinical and real world data with impact.</p></li><li><p>Experience in building long term customer relationships and advocacy development.</p></li><li><p>Promote ongoing learning agility and Continuous Professional Development for self and others, demonstrating a growth mindset.</p></li><li><p>Role model Pfizer values and behaviours to ensure our culture is diverse and inclusive.</p></li><li><p>Driving license.</p></li></ul><p></p><p><b>PREFERRED EXPERIENCE AND QUALIFICATIONS</b></p><p>·     Digital Affinity with multichannel offerings and virtual engagement excellence</p><p>·     Business planning skills – understanding of operational planning process</p><p>·     Previous experience in a secondary care specialty environment.</p><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</b></p><p> ·       Remote worker</p><p>·       The role and customer facing activity will be a mix of face to face &amp; remote working based on customer preference &amp; business need</p><p>·       Occasional night away from home will be required</p><p></p><p><b>OTHER INFORMATION</b></p><p>This role includes the opportunity for promotion to a Senior Grade if promotion eligibility criteria is met (see field promotion criteria guidance). The additional expectations of a Senior are summarised as;</p><p>1.       Is sought out by colleagues as a subject matter/role expert for support and guidance as a result of their sustained high level of performance and expertise</p><p>2.       Supports colleague and peer development as a coach/mentor</p><p>3.       Demonstrates additional proactive Leadership at a Regional/National level (projects/initiatives/meetings) to impact National performance</p><p>4.       With a solution focused growth mindset, consistently seeks new opportunities to drive continuous improvement of internal processes and external customer engagement</p><p>Works cross functionally within BU and across One Pfizer to align and share best practice to deliver on our purpose</p><p></p><p><b>ORGANISATIONAL RELATIONSHIPS</b></p><p>Reports to Commercial Manager</p><p>Internal:  Healthcare Partnership Manager, Clinical Effective Consultant, Therapy Area Specialists , Brand Marketing &amp; Medical colleagues</p><p>External:  A range of health care professions specific to therapy area and brands</p><p></p><p><b>RESOURCES MANAGED</b></p><p>Territory or Region Customer Investment Spend Budget</p><p>Supervision: This role does not have any direct reports</p><p>Work Location Assignment: Remote - Field Based</p><p></p><p><span>The closing deadline for applications is April 19th. </span></p><p><span>All applicants must have the relevant authorisation to live and work in the UK.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>DisAbility Confident</u></p><p style="text-align:left">We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/therapy-area-specialist-neurology-and-covid-19-north-west-england-pfizer/69d67ba0c8e81216cd0caf3c</link><guid isPermaLink="true">http://biotechroles.com/therapy-area-specialist-neurology-and-covid-19-north-west-england-pfizer/69d67ba0c8e81216cd0caf3c</guid><pubDate>Wed, 08 Apr 2026 16:00:32 GMT</pubDate><company>Pfizer</company><location>United Kingdom - Pharm Field Force</location><salary>$65000-90000</salary><type>Full time</type></item><item><title><![CDATA[Snr Quality Engineer, Combo Product External Quality]]></title><description><![CDATA[<p>The Senior Quality Engineer is responsible for carrying out Manufacturing Quality Assurance functions within the plant including resolution of deviations, performance of product impact analysis and corrective and preventive action for events, leading and participating in investigations, approval of standard operating procedures, oversight of the plant calibration program, quality improvement programs, and assurance of cGMP and Abbott policy compliance for the manufacturing plant.<br>
Supports the Quality Engineering group by auditing of commissioning and validation documentation completed by others, authoring and execution of newly identified qualification/validation protocols, review and approval of critical planned maintenance routines, and other quality assurance tasks assigned by the MQA Section Manager and/or the Plant QA Manager.</p><p>Responsibilities</p><ul><li>Responsible for implementing and maintaining the effectiveness of the Quality System.</li><li>Support the ensure that all quality goals are met, and all practices and procedures comply with company policies and applicable regulations for the Quality areas under his/her responsibility.</li><li>Ensures investigations of plant events are completed thoroughly and documented accurately and are included in the plant CAPA system. Performs product impact analyses for plant events and places product on QA hold where appropriate.</li><li>Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.</li><li>Participates on the Validation Review Board as the Manufacturing Quality Assurance function.</li><li>Approves standard operating procedures; ensures procedures comply with policy and make sense.</li><li>Approves calibration requests and ensures that these requests have appropriate product/process limits assigned.</li><li>Auditing of commissioning and validation documentation.</li><li>Develops product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses and FMEA’s. Develops and implements statistical quality programs and process monitoring systems.</li><li>For specific U.S. manufacturing sites, performs batch release.</li></ul>]]></description><link>http://biotechroles.com/snr-quality-engineer-combo-product-external-quality-abbvie/69d627c1c8e81216cd0c7d65</link><guid isPermaLink="true">http://biotechroles.com/snr-quality-engineer-combo-product-external-quality-abbvie/69d627c1c8e81216cd0c7d65</guid><pubDate>Wed, 08 Apr 2026 10:02:41 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Quality Engineer, Combo Product External Quality]]></title><description><![CDATA[<p>The Senior Quality Engineer is responsible for carrying out Manufacturing Quality Assurance functions within the plant including resolution of deviations, performance of product impact analysis and corrective and preventive action for events, leading and participating in investigations, approval of standard operating procedures, oversight of the plant calibration program, quality improvement programs, and assurance of cGMP and Abbott policy compliance for the manufacturing plant.<br>
Supports the Quality Engineering group by auditing of commissioning and validation documentation completed by others, authoring and execution of newly identified qualification/validation protocols, review and approval of critical planned maintenance routines, and other quality assurance tasks assigned by the MQA Section Manager and/or the Plant QA Manager.</p><p>Responsibilities</p><ul><li>Responsible for implementing and maintaining the effectiveness of the Quality System.</li><li>Support the ensure that all quality goals are met, and all practices and procedures comply with company policies and applicable regulations for the Quality areas under his/her responsibility.</li><li>Ensures investigations of plant events are completed thoroughly and documented accurately and are included in the plant CAPA system. Performs product impact analyses for plant events and places product on QA hold where appropriate.</li><li>Maintains an effective liaison and cooperative relationship with other Quality areas and Plant departments.</li><li>Participates on the Validation Review Board as the Manufacturing Quality Assurance function.</li><li>Approves standard operating procedures; ensures procedures comply with policy and make sense.</li><li>Approves calibration requests and ensures that these requests have appropriate product/process limits assigned.</li><li>Auditing of commissioning and validation documentation.</li><li>Develops product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses and FMEA’s. Develops and implements statistical quality programs and process monitoring systems.</li><li>For specific U.S. manufacturing sites, performs batch release.</li></ul>]]></description><link>http://biotechroles.com/sr.-quality-engineer-combo-product-external-quality-abbvie/69d627bdc8e81216cd0c7d64</link><guid isPermaLink="true">http://biotechroles.com/sr.-quality-engineer-combo-product-external-quality-abbvie/69d627bdc8e81216cd0c7d64</guid><pubDate>Wed, 08 Apr 2026 10:02:37 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Safety Operations Portfolio]]></title><description><![CDATA[<p><strong>Purpose:</strong></p><p>This position manages a team of Portfolio Leads and Product Leads who are responsible for Safety Operations-related scientific activities, input and expertise across assets in all therapeutic areas. This position leads the SOPROL (Safety Operations Product Leadership) team. This role works with Therapeutic Area Heads and senior/executive scientific leaders across Global Patient Safety(GPS), Global Medical Affairs, Clinical Development and Regulatory Affairs. The role is responsible for ensuring that accurate, high-quality and timely Safety Operations scientific input and support are provided to PSTs across assets (development and on-market) from discovery to end of life. Safety Operations oversees the intake, processing, and reporting of patient safety information.</p><p><strong>Responsibilities:</strong></p><p>• Develops, communicates and implements the strategy for providing scientific expertise and support across all Safety Operations activities for assets, in support of PST responsibilities and deliverables. This includes but not limited to regulatory responses, submissions and launches, audits/inspections, clinical trial protocol reviews, etc.</p><p>• Responsible for oversight of the accuracy, quality and timeliness of all scientific input for the end-to-end spectrum of Safety Operations activities for pharmaceutical and device assets (in development and on-market). Reviews scientific content through an enterprise and international lens. Provides direction to SOPROL team members to enhance quality of scientific input.</p><p>• Interprets and implements global regulations related to clinical trial and pharmacovigilance supporting all patient safety activities. Collaborates with the QPPV Office in the application of international regulatory requirements in Safety Operations activities.</p><p>• Builds strong collaborative relationships with PST Therapeutic Area leadership and Group Medical Directors, as well as senior leaders in Epidemiology and Medical Aesthetics &amp; Device Safety, Clinical Trial Safety &amp; Insights. Provides Safety Operations scientific recommendations to help optimize safety strategies for high-profile assets.</p><p>• Maintains a comprehensive understanding of the strategic direction of AbbVie’s pipeline and commercial priorities. Applies understanding in making recommendations on ICSR forecasting and broader Safety Operations business planning.</p><p>• Proactively prepares GPS leadership communications to share crucial insights from ICSR data across key assets, that further strengthen safety understanding, narratives and actions.</p><p>• Manges talent development and utilization of SOPROL Portfolio Leads and Product Managers. Engages, inspires, coaches and mentors team.</p><p>• Partners with senior scientific leadership cross-functionally (Global Medical Affairs, Regulatory Affairs, Clinical Development, etc.) to advance the priorities of SOPROL and the broader Safety Operations team, with the goal of supporting high quality scientific decision-making and agility in cross-functional partnerships.</p><ul><li>Manages audit and inspection preparedness, in support of PSTs. Prepares Portfolio Leads and Product Managers for product SME direct participation in front and back rooms.</li></ul><p>• Represents VP Safety Operations in senior leadership scientific discussions on assets. Serves on GPS scientific governance bodies as needed</p><p>• Performs SOPROL responsibilities for sensitive or confidential assets (e.g. related to acquisition deals and company partnerships)</p>]]></description><link>http://biotechroles.com/associate-director-safety-operations-portfolio-abbvie/69d627bac8e81216cd0c7d61</link><guid isPermaLink="true">http://biotechroles.com/associate-director-safety-operations-portfolio-abbvie/69d627bac8e81216cd0c7d61</guid><pubDate>Wed, 08 Apr 2026 10:02:34 GMT</pubDate><company>AbbVie</company><location>South San Francisco, North Chicago</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[CAPA Specialist II]]></title><description><![CDATA[<p>Oversees the plant CAPA Quality System by performing root cause investigations for exceptions/nonconformities/deviations to required procedures and/or specifications for drug product manufacturing and packaging.</p><p><strong>Responsibilities:</strong></p><ul><li>Provides consistent and thorough exception documents and timely resolution of investigations based on CAPA requirements</li><li>Coordinates the exception document process and creates exception documents</li><li>Independently leads complex, high impact investigations</li><li>Ensures all investigations are written according to corporate and site requirements</li><li>Ensures all applicable regulatory requirements are met for the implementation and maintenance of the Quality System</li><li>Ensures all Quality CAPA goals and metrics are met</li><li>Promotes culture of continuous improvement by identifying problems, conducting root cause analysis and confirming appropriate implementation of corrections, corrective and preventive actions</li><li>Maintains an effective liaison and cooperative relationship with other Quality areas and departments within the plant</li></ul>]]></description><link>http://biotechroles.com/capa-specialist-ii-abbvie/69d627b6c8e81216cd0c7d60</link><guid isPermaLink="true">http://biotechroles.com/capa-specialist-ii-abbvie/69d627b6c8e81216cd0c7d60</guid><pubDate>Wed, 08 Apr 2026 10:02:30 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$85000-115000</salary><type>Full-time</type></item><item><title><![CDATA[Systems/Verification Engineer]]></title><description><![CDATA[<p>Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.</p><p>Responsibilities</p><ul><li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li><li>Publish research in peer-reviewed journals and present work at scientific conferences.</li><li>Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program.</li><li>Seize opportunities to pursue project relevant leads that are in line with the group’s strategy.</li><li>Maintain a high level of productivity in the lab.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li><li>May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.</li></ul>]]></description><link>http://biotechroles.com/systemsverification-engineer-abbvie/69d627b2c8e81216cd0c7d5f</link><guid isPermaLink="true">http://biotechroles.com/systemsverification-engineer-abbvie/69d627b2c8e81216cd0c7d5f</guid><pubDate>Wed, 08 Apr 2026 10:02:26 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$95000-145000</salary><type>Full-time</type></item><item><title><![CDATA[QA Technician Warehouse]]></title><description><![CDATA[<p>The primary purpose of this position is to ensure the quality of raw materials , commodities and durable &amp; consumable received, are acceptable per the appropriate quality attributes.</p><p>Responsibilities</p><ul><li>Perform sampling and inspect raw materials, commodities, durable &amp; consumable as per specifications.</li><li>Responsible of the release of material according to materials specification and incoming quality procedures.</li><li>Responsible to enter test results in manufacturing systems such SAP and LIMS .</li><li>Segregate and document the rejected and experimental materials.</li><li>Keep current the specifications, procedures, documents in general from the area.</li></ul>]]></description><link>http://biotechroles.com/qa-technician-warehouse-abbvie/69d627aec8e81216cd0c7d5e</link><guid isPermaLink="true">http://biotechroles.com/qa-technician-warehouse-abbvie/69d627aec8e81216cd0c7d5e</guid><pubDate>Wed, 08 Apr 2026 10:02:22 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$45000-65000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Data Analyst]]></title><description><![CDATA[<p>The&#xa0;<strong>Associate Data Analyst&#xa0;</strong>is responsible for executing all of the reporting, in partnership with internal and external stakeholders. The individual will also partner with internal teams such as pharmacovigilance, local in-country teams, and the device quality assurance team to ensure the appropriate and accurate reporting of complaints. They will interface with regulators and serve as the liaison to the respective team when questions and requests arise.</p><p><strong>Responsibilities</strong></p><ul><li>Decision maker for reportability decisions</li><li>Lead for all vigilance reporting, including local and global submissions</li><li>Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for submissions and escalates requests as appropriate</li><li>Ensures that relevant stakeholders have visibility to the reporting and where they are in the process</li><li>Manages regular reporting needs and external requests (i.e. from the FDA)</li><li>Manage the timeline for end to end reporting</li><li>Owns translation services for reporting</li></ul>]]></description><link>http://biotechroles.com/associate-data-analyst-abbvie/69d627aac8e81216cd0c7d5c</link><guid isPermaLink="true">http://biotechroles.com/associate-data-analyst-abbvie/69d627aac8e81216cd0c7d5c</guid><pubDate>Wed, 08 Apr 2026 10:02:18 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$65000-85000</salary><type>Full-time</type></item><item><title><![CDATA[Tech Lead Engineer]]></title><description><![CDATA[<p>Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.</p><p><strong>Responsibilities</strong></p><ul><li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li><li>Publish research in peer-reviewed journals and present work at scientific conferences.</li><li>Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program.</li><li>Seize opportunities to pursue project relevant leads that are in line with the group’s strategy.</li><li>Maintain a high level of productivity in the lab.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li><li>May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.</li></ul>]]></description><link>http://biotechroles.com/tech-lead-engineer-abbvie/69d627a7c8e81216cd0c7d5b</link><guid isPermaLink="true">http://biotechroles.com/tech-lead-engineer-abbvie/69d627a7c8e81216cd0c7d5b</guid><pubDate>Wed, 08 Apr 2026 10:02:15 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Project Manager]]></title><description><![CDATA[<p>An engineering professional who, working with little or no supervision, applies scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete assignments related to a specific technical field or discipline. A Senior Engineer has general knowledge of other related disciplines beyond their own area of expertise.</p><ul><li>Responsibilities of this engineering grade level inherently include and expand upon the responsibilities established for lower engineering grade levels.</li><li>Responsible for compliance with applicable policies and procedures. Ensures quality and effectiveness of key results of major projects within function through sound design, early risk assessments, and implementation of fallback strategies. Has full awareness of the potential consequences (defects and failure modes) of design changes to established processes. Mitigates risk within functions through sound design, early risk assessments and implementation of fallback strategies.</li><li>Independently plans and conducts high business impact projects within engineering specialty in the Drug Product Manufacturing or Packaging areas. Responsible for achieving the project's financial targets in support of business objectives. Maintains project controls and reporting for cost, scope, and schedule.</li><li>Develops execution strategy including procurement; balances multiple demands; understands the business needs and has a thorough knowledge of the customer and cGMP needs when developing a project scope. Incorporates business foresight of emerging technological trends.</li><li>Facility, Equipment, and Utilities SME responsibilities during Regulatory Agencies Audits. Responsible of preparing documentation packages and presenting information in front of regulatory agents.</li><li>Produces unique and cost-effective results. Establishes alternate use possibilities and incorporates flexibility; balances system costs with benefits provided; oversees design work of internal and external consultants, Creates/modified designs for intermediate problems. Integrates financial with technical data. Analyzes complex interdisciplinary problems and identifies their impact; establishes probabilities; draws conclusions reflecting broad business needs.</li><li>Represents engineering on corporate task forces. Identifies full range of customer/client needs and proposes solutions to address them; makes alterations in products or services to better meet (recognized or unrecognized) customer need. Monitors the improvement of other engineer and may participate in the evaluation of assigned staff/project team members and in the identification of development needs. May supervise other engineers or technicians.</li></ul>]]></description><link>http://biotechroles.com/project-manager-abbvie/69d627a3c8e81216cd0c7d5a</link><guid isPermaLink="true">http://biotechroles.com/project-manager-abbvie/69d627a3c8e81216cd0c7d5a</guid><pubDate>Wed, 08 Apr 2026 10:02:11 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$105000-145000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Northern Virginia/Hagerstown MD/Winchester VA]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-northern-virginiahagerstown-mdwinchester-va-abbvie/69d6279fc8e81216cd0c7d59</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-northern-virginiahagerstown-mdwinchester-va-abbvie/69d6279fc8e81216cd0c7d59</guid><pubDate>Wed, 08 Apr 2026 10:02:07 GMT</pubDate><company>AbbVie</company><location>Hagerstown, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Philadelphia, PA]]></title><description><![CDATA[<p>Purpose</p><p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers.</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance.</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-philadelphia-pa-abbvie/69d6279cc8e81216cd0c7d58</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-philadelphia-pa-abbvie/69d6279cc8e81216cd0c7d58</guid><pubDate>Wed, 08 Apr 2026 10:02:04 GMT</pubDate><company>AbbVie</company><location>Philadelphia, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - North San Antonio, TX]]></title><description><![CDATA[<p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-north-san-antonio-tx-abbvie/69d62798c8e81216cd0c7d57</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-north-san-antonio-tx-abbvie/69d62798c8e81216cd0c7d57</guid><pubDate>Wed, 08 Apr 2026 10:02:00 GMT</pubDate><company>AbbVie</company><location>San Antonio, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Florence, AL]]></title><description><![CDATA[<p>Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-florence-al-abbvie/69d62794c8e81216cd0c7d56</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-florence-al-abbvie/69d62794c8e81216cd0c7d56</guid><pubDate>Wed, 08 Apr 2026 10:01:56 GMT</pubDate><company>AbbVie</company><location>Florence, US-Virtual Office</location><salary>$85000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Product Engineer]]></title><description><![CDATA[<p>As a <strong>Senior Engineer in the Product Development, Science &amp; Technology</strong> team, you will conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.</p><p><strong>Responsibilities</strong></p><ul><li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li><li>Publish research in peer-reviewed journals and present work at scientific conferences.</li><li>Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program.</li><li>Seize opportunities to pursue project relevant leads that are in line with the group’s strategy.</li><li>Maintain a high level of productivity in the lab.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li><li>May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.</li></ul>]]></description><link>http://biotechroles.com/product-engineer-abbvie/69d62791c8e81216cd0c7d53</link><guid isPermaLink="true">http://biotechroles.com/product-engineer-abbvie/69d62791c8e81216cd0c7d53</guid><pubDate>Wed, 08 Apr 2026 10:01:53 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Psychiatry - Cherry Hill, NJ]]></title><description><![CDATA[<p><strong>Purpose</strong></p><p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p><strong>Responsibilities</strong></p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-psychiatry-cherry-hill-nj-abbvie/69d6278dc8e81216cd0c7d51</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-psychiatry-cherry-hill-nj-abbvie/69d6278dc8e81216cd0c7d51</guid><pubDate>Wed, 08 Apr 2026 10:01:49 GMT</pubDate><company>AbbVie</company><location>Cherry Hill Township, US-Virtual Office</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Migraine - North Albany, NY]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-migraine-north-albany-ny-abbvie/69d6278ac8e81216cd0c7d50</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-migraine-north-albany-ny-abbvie/69d6278ac8e81216cd0c7d50</guid><pubDate>Wed, 08 Apr 2026 10:01:46 GMT</pubDate><company>AbbVie</company><location>Albany, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Specialty Representative, Migraine - South Albany, NY]]></title><description><![CDATA[<p>This role is field-based, and candidates should live within a reasonable distance from the primary city. Talent will be hired at a level commensurate with experience.<br>
<br>
Execute brand strategy and tactics in field, sales performance, effectively manage assigned territory and targeted accounts, build strong customer relationships and customer needs solving capability to maximize short and long term sales performance placing the patient into the center of any efforts and operating within AbbVie’s business code of conduct, policies and all applicable laws and regulations.</p><p>Responsibilities</p><ul><li>Deliver sales performance, brand KPIs, financial targets, marketing objectives, etc. to meet or exceed on those objectives.</li><li>Create pre-call plan objectives and execute post-call evaluation to continuously improve sales performance. Effectively handle objections, misunderstandings, concerns and consistently gain logical and reasonable calls to action to close on every sales call.</li><li>Proactively and continuously aspire to serve customer needs, customer expectations and challenges to build trusted customer relationships and to achieve win-win agreements between AbbVie and customers</li><li>Develop and execute a call plan that achieves set call metrics and optimizes coverage and frequency to key customers to maximize access and sales opportunities.</li><li>Continuously build understanding on customer needs and expectations, territory market landscape, competitors, market segments/dynamics, accounts, disease, product, clinical and sales expertise and share this market intelligence information with in-field team, brand team and sales manager to achieve alignment, to anticipate environmental changes and challenges and to optimize brand strategy and its execution.</li><li>Differentiate AbbVie’s value proposition with health providers assigned and identify, develop, and maintain disease state experts and speakers/advocates to maximize brand performance</li></ul>]]></description><link>http://biotechroles.com/specialty-representative-migraine-south-albany-ny-abbvie/69d62786c8e81216cd0c7d4e</link><guid isPermaLink="true">http://biotechroles.com/specialty-representative-migraine-south-albany-ny-abbvie/69d62786c8e81216cd0c7d4e</guid><pubDate>Wed, 08 Apr 2026 10:01:42 GMT</pubDate><company>AbbVie</company><location>Albany, US-Virtual Office</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[District District Manager. ACP - Central]]></title><description><![CDATA[<p><strong>This role is field-based and candidates should live within a reasonable distance from one of the following cities:</strong></p><ul><li><strong>Dallas, TX</strong></li><li><strong>Houston, TX</strong></li><li><strong>Chicago, IL</strong></li><li><strong>Indianapolis, IN</strong></li><li><strong>St Louis, MO</strong></li><li><strong>New Orleans, LA</strong></li></ul><p><strong>Talent will be hired at a level commensurate with experience.</strong></p><p><strong>Responsibilities</strong></p><ul><li>Coordinate in-field activity to achieve results and agreed-upon targets. Maximize market, segment, and team dynamics to drive both top- and bottom-line results.</li><li>Ensure smooth, collaborative efforts in both day to day and long term business execution. Set tone and pace for business process and organization.</li><li>Understand and present a market and franchise/business point of view when leading teams and championing in-field meeting by developing a mastery of product and disease state information, as well as pertinent Market dynamics, including Managed Care landscape.</li><li>Coach, mentor, educate and develop direct and indirect team members to enhance individual skills and elevate overall team performance. Hold direct reports accountable to behaviors and expectations.</li><li>Provide direction and insights to key internal partners in business planning process.</li><li>Consistently exemplify the AbbVie Ways of Working.</li><li>Coordinate commercial activity within in-field teams to ensure targets are reached for increasing sales within an assigned geography. Create, implement, and communicate District Sales Plan and monitor progress.</li></ul>]]></description><link>http://biotechroles.com/district-district-manager.-acp-central-abbvie/69d62784c8e81216cd0c7d4d</link><guid isPermaLink="true">http://biotechroles.com/district-district-manager.-acp-central-abbvie/69d62784c8e81216cd0c7d4d</guid><pubDate>Wed, 08 Apr 2026 10:01:40 GMT</pubDate><company>AbbVie</company><location>Chicago, US-Virtual Office</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Global Financial Audit]]></title><description><![CDATA[<p>AbbVie’s Internal Audit (IA) function plays a valuable role in protecting and enhancing the organization’s value by providing risk-based and objective assurance, advice and insights. The function is guided by a disciplined, collaborative approach that is aligned with AbbVie’s strategy and the IIA standards with a focus on constant innovation and talent development.</p><p>Reporting to the Finance Audit Director, the Finance Audit Associate Director will have responsibility for planning, executing and reporting on assigned internal audits as well as developing and implementing key improvements to department processes. Finance Audit assignments may be performed anywhere in the world AbbVie operates. The Finance Audit Associate Director will also work as part of the department’s overall management team to perform and maintain an annual risk assessment which forms the basis of our annual audit plan. Other responsibilities include aiding the Director in developing talent strategies and effectively managing direct reports and audit teams.</p><p>Given the extent of the department’s interactions with the business and other functions, excellent communication and relationship building skills are required together with the ability to deal with ambiguity and exercise critical thinking to effectively influence senior business management and peers while acting as a catalyst for positive change. Strong people management skills are essential.</p><p>Responsibilities</p><ul><li>Audit Planning, Execution &amp; Reporting (~70%)<ul><li>In collaboration with the rest of the IA management team, assist the Directors in the development and execution of a comprehensive risk-based global internal audit program through proactive involvement and research of industry and profession best practices.</li><li>Directly manage and perform multiple Financial and Operational internal audits simultaneously with the objective of assessing the design and operating effectiveness of internal controls, efficiency of operations, compliance with corporate policies and procedures and generally accepted accounting principles.</li><li>Provide management with valuable recommendations and insights to strengthen the control environment.</li><li>Manage internal projects and process improvement initiatives.</li><li>Maintain the highest standards of professionalism and independence in the execution of duties.</li></ul></li><li>Other (~30%)<ul><li>Coach and mentor audit staff.</li><li>Proactively liaise with various business and corporate functions management providing counsel and input on risk and control issues facing their functions.</li><li>Manage and perform key departmental process improvement initiatives including internal quality assurance; assist with audit issue trend analysis and reporting.</li><li>Manage and perform special projects including providing controls consulting expertise to the business.</li><li>Assist with preparation of quarterly Leadership presentations, as needed.</li></ul></li></ul><p>&#xa0;</p><p>Equal Opportunity Employer Minorities/Women/Veterans/Disabled&#xa0;</p>]]></description><link>http://biotechroles.com/associate-director-global-financial-audit-abbvie/69d62780c8e81216cd0c7d4c</link><guid isPermaLink="true">http://biotechroles.com/associate-director-global-financial-audit-abbvie/69d62780c8e81216cd0c7d4c</guid><pubDate>Wed, 08 Apr 2026 10:01:36 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$150000-200000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Captain]]></title><description><![CDATA[<p><strong>Purpose</strong></p><p>The Senior Captain is responsible for the operation of the company aircraft. When assigned to a flight, the captain has the final authority regarding the operation of the aircraft. Ensures that all flight and ground operations are conducted at the highest levels of safety and comply with federal aviation regulations, applicable foreign regulations, department and company policies and procedures.</p><p><strong>Responsibilities</strong></p><ul><li>Responsible for the airworthiness of the aircraft to which assigned, and for the safety of the passengers and crew on board. The captain accomplishes the duties of pilot-in-command, as defined by Federal Aviation Regulations, the aircraft flight manual, and the department policy and operations manual, and is operationally responsible for all phases of the flight.</li><li>Keeps informed and trained on international flight operations.</li><li>Plan and execute all aspects of international flights.</li><li>Obtain the training and skills necessary to obtain a type rating for appropriate aircraft.</li><li>Assists the Head&#xa0;of Aviation and Director of Flight Operations – Chief Pilot in maintaining and developing relevant company policies and procedures.</li><li>Develop and maintain a complete knowledge, understanding and a mastery of the aircraft systems.</li><li>Makes decisions to start, delay, or cancel flights, or deviate from planned routes, or destinations, when operating conditions dictate.</li><li>As a team member, always confers with other crewmembers to obtain as much information as possible to determine the best course of action.</li><li>Maintains open channels of communication with all crewmembers.</li><li>Responsible for maintaining highest standards of safety through acquiring all pertinent knowledge pertaining to any flights, pilot proficiency training and continuing education.</li><li>Develops and maintains thorough understanding about the operation and location of all aircraft emergency, survival and medical equipment.</li><li>Keeps fully informed on FAA and foreign regulations, and department policy pertaining to operations.</li><li>Keeps informed of latest industry, aircraft, or equipment developments that may impact the department.</li><li>Serves in an advisory capacity to the Head&#xa0;of Aviation, Director of Flight Operations and Director of Maintenance regarding aircraft flight operations.</li><li>Monitors crew performance and delegates duties required for the safe and efficient operation of the aircraft.</li><li>Develop and maintain the ability to communicate effectively with passengers, corporate executives and customers and express verbal and written thoughts coherently and logically.</li><li>Assures safety and security of aircraft while away from home base.</li><li>Maintains flight manuals and navigation charts, as required. Completes appropriate flight logs and paperwork for each flight.</li><li>Responsible for post-flight activities, including proper storage and protection of aircraft, cleaning and restocking while away from home base.</li><li>Must always act with a clear customer focus.</li><li>Provides leadership and direction to others by setting a positive example, always demonstrating teamwork and professionalism at all times, treating co-workers with respect, and encouraging others to do their best.</li><li>Mentors, teaches, and shares knowledge with all less-experienced crewmembers.</li><li>Completes assigned collateral duties.</li></ul>]]></description><link>http://biotechroles.com/senior-captain-abbvie/69d6277fc8e81216cd0c7d4b</link><guid isPermaLink="true">http://biotechroles.com/senior-captain-abbvie/69d6277fc8e81216cd0c7d4b</guid><pubDate>Wed, 08 Apr 2026 10:01:35 GMT</pubDate><company>AbbVie</company><location>North Chicago, Waukegan</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Strategic Medical Writing]]></title><description><![CDATA[<p>The Director, Strategic Medical Writer provides strategic leadership and direction for clinical and regulatory writing projects for one large or multiple compounds within a therapeutic area within budget, with quality, and in accordance with timelines.</p><p><u><strong>Responsibilities:</strong></u></p><ul><li>Directly leads people leader(s)&#xa0;and multiple individual contributors located in geographically disbursed locations with oversight of both internal and external staff. Ensures effective management of external business partners such as CROs who are employed to deliver clinical documents according to established standards and processes.</li><li>Participates in continual improvement across Strategic Medical Writing best practices, processes, and performance. Leads execution of cross-functional initiatives.</li><li>Effectively utilizes project management tools/techniques to drive multiple projects; responsible for overall project management for a large number of projects simultaneously.</li><li>Works with cross-functional project teams to develop project objectives, strategies, corresponding timelines, and milestones. Coordinates activities and communications on writing projects/submissions utilizing cross-functional skills/expertise and drug development knowledge. Holds team members to the project tasks/deliverables.</li><li>Collects appropriate metrics for assigned therapeutic area(s).</li><li>Maintains expert knowledge of US and international regulations, requirements, and guidance associated with preparation of regulatory documentation and serves as a company-wide subject matter expert and liaison for other functions to ensure the application of highest industry standards. Learns and applies therapeutic area and product knowledge to scientific projects and business improvement projects. May serve as a consultant/liaison in partnerships with other companies.</li><li>Maintains inspection readiness for assigned remit. Acts as the organizational representative in regulatory inspections and quality audits.</li></ul><p>Significant Work Activities:&#xa0;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required</p>]]></description><link>http://biotechroles.com/director-strategic-medical-writing-abbvie/69d6277bc8e81216cd0c7d48</link><guid isPermaLink="true">http://biotechroles.com/director-strategic-medical-writing-abbvie/69d6277bc8e81216cd0c7d48</guid><pubDate>Wed, 08 Apr 2026 10:01:31 GMT</pubDate><company>AbbVie</company><location>North Chicago, US-Virtual Office</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Global Procurement Systems]]></title><description><![CDATA[<p><strong>Job Description:</strong> The Manager, Global Procurement Systems supports the Global Procurement Systems &#xa0;Sr. Manager within R&amp;D Procurement (RDP). This role will be responsible for driving operational excellence, supporting process governance, and collaborating across global teams to ensure the successful delivery of high-quality system solutions. &#xa0;&#xa0;This role also involves proactively supporting and optimizing production environment, addressing ongoing system issues and needs, and fostering continuous improvement and innovation for the business and user community.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Function as a global point of contact within R&amp;D Procurement (RDP) for Procurement program initiatives, collaborating closely with the Sr. Manager, Global Procurement Systems.</li><li>Lead and support process transformation and continuous improvement initiatives including standardization, simplification, and technology innovation related to yearly system releases.</li><li>Provide support for end-to-end business processes. Maintain accountability for defect tracking and issue resolution. Collaborate with BTS on LMIC monthly maintenances releases.&#xa0; Lead and execute UAT activities and ensure release notes are effectively communicated to end users.&#xa0;</li><li>Drive the formulation and implementation of group goals and objectives to ensure the Systems Team excels in managing training materials and system documentation. Proactively lead initiatives that optimize the team's effectiveness and accountability in all related responsibilities.</li><li>Facilitate requirements gathering by partnering collaboratively with stakeholders to understand their needs &#xa0;and&#xa0; provide strategies to effectively achieve process improvement goals that can be enabled via technology.</li><li>Contribute to identifying future optimization opportunities to meet business needs and provide insights for operational improvements and alternate strategies, methodologies and best practices.</li><li>Collaborate with and support BTS teams, &#xa0;to ensure successful implementation and deployment of maintenance and full releases.</li><li>Provide operational process expertise during migrations, business expansions (M&amp;A/divestitures), and other change initiatives.&#xa0; Requires the ability to review and understand life sciences contracts and amendments, determine proper document alignment, and support accurate database corrections during migrations.</li><li>Identify and bridge knowledge gaps with BTS during requirements gathering sessions to ensure all business needs are accurately captured and met.&#xa0; Assess and define integration requirements to enable seamless interoperability with other systems.</li><li>Create and implement dashboards to provide analytics and KPI reporting . Track and report on key global metrics to &#xa0;evaluate the &#xa0;effectiveness of improvement initiatives and support the adoption and sustainability of new processes.</li><li>Assist in developing solid business cases for new initiatives, helping prepare executive presentations in alignment with overall AbbVie strategy.</li></ul>]]></description><link>http://biotechroles.com/manager-global-procurement-systems-abbvie/69d62778c8e81216cd0c7d45</link><guid isPermaLink="true">http://biotechroles.com/manager-global-procurement-systems-abbvie/69d62778c8e81216cd0c7d45</guid><pubDate>Wed, 08 Apr 2026 10:01:28 GMT</pubDate><company>AbbVie</company><location>North Chicago, North Chicago</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Regional Access Manager Immunology (all genders) (Vollzeit / unbefristet)]]></title><description><![CDATA[<p>Als Regional Access Manager Immunology (all genders) bist du das strategische Bindeglied zwischen den&#xa0;Healthcare&#xa0;Ecosystem&#xa0;Managern (HEMs) und der&#xa0;restlichen&#xa0;Market Access-Organisation. Du sorgst für einen strukturierten und beidseitigen Austausch praxisrelevanter&#xa0;Erkenntnisse, wodurch diese systematisch in die Entwicklung und Umsetzung von Marktzugangsstrategien einfließen.&#xa0;Du&#xa0;verstehst regionale Steuerungsmechanismen&#xa0;in dem Dir zugeordneten Therapiegebiet und bringst Dich strategisch in die Entwicklung von Vertragsstrategien mit Krankenkassen oder Krankenhäusern ein.&#xa0;Darüber hinaus übernimmst du&#xa0;nach Bedarf&#xa0;die Leitung oder Mitwirkung an nationalen Versorgungsprojekten, mit dem Ziel, die Patientenversorgung zu verbessern und den Zugang zu&#xa0;AbbVie’s&#xa0;Produkten nachhaltig zu optimieren.&#xa0;</p><p>&#xa0;</p><p>Wichtigste Aufgaben:&#xa0;</p><ul><li>Zentrale&#xa0;Schnittstelle&#xa0;für den strukturierten, bidirektionalen Austausch von&#xa0;relevanten&#xa0;Erkenntnissen&#xa0;und Informationen&#xa0;für die Strategieentwicklung und deren Umsetzung&#xa0;zwischen HEMs und&#xa0;anderen Market Access Bereichen&#xa0;</li><li>Sammlung, Analyse und&#xa0;zeitnahe&#xa0;Kommunikation von regionalen&#xa0;Insights&#xa0;zu&#xa0;Marktentwicklungen,&#xa0;Veränderungen in der Kostenträgerlandschaft, Wettbewerbsdynamiken&#xa0;und&#xa0;gesundheitspolitischen Entwicklungen&#xa0;sowie&#xa0;Ableitung&#xa0;strategischer Handlungsempfehlungen&#xa0;&#xa0;</li><li>Bei Bedarf&#xa0;Leitung&#xa0;von&#xa0;oder Mitwirkung an&#xa0;nationalen&#xa0;Versorgungsprojekten, die auf die Verbesserung des Patientenzugangs&#xa0;oder&#xa0;der Versorgungsqualität ausgerichtet sind&#xa0;</li><li>Enge&#xa0;Zusammenarbeit mit Market Access Managern und&#xa0;Contracting&#xa0;Managern&#xa0;bei der Entwicklung von&#xa0;maßgeschneiderten&#xa0;Vertragsstrategien für verschiedene Kostenträgersegmente&#xa0;und proaktives kontinuierliches Monitoring&#xa0;der Performance von&#xa0;Vertragsmodellen&#xa0;</li><li>Entwicklung von Kundenmaterialien für das HEM-Team&#xa0;gemeinsam mit den Market Access Managern,&#xa0;sowie die Anpassung dieser&#xa0;an die Anforderungen lokaler Kostenträger und aktueller&#xa0;Marktentwicklungen&#xa0;</li><li>Entwicklung&#xa0;von&#xa0;Schulungsinhalten&#xa0;für die&#xa0;Sales Teams zu Market Access Themen in Zusammenarbeit mit den Sales&#xa0;Enablement&#xa0;Specialists&#xa0;</li></ul>]]></description><link>http://biotechroles.com/regional-access-manager-immunology-(all-genders)-(vollzeit-unbefristet)-abbvie/69d62774c8e81216cd0c7d44</link><guid isPermaLink="true">http://biotechroles.com/regional-access-manager-immunology-(all-genders)-(vollzeit-unbefristet)-abbvie/69d62774c8e81216cd0c7d44</guid><pubDate>Wed, 08 Apr 2026 10:01:24 GMT</pubDate><company>AbbVie</company><location>Wiesbaden, Wiesbaden</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Sales Enablement Specialist (all genders) (Vollzeit oder Teilzeit 80%)]]></title><description><![CDATA[<p>Als&#xa0;Sales&#xa0;Enablement&#xa0;Specialist (all genders) bist du der&#xa0;primäre&#xa0;Ansprechpartner der Sales Teams&#xa0;zu&#xa0;Market Access-Themen.&#xa0;Du&#xa0;unterstützt&#xa0;diese&#xa0;mit Wissen, Tools und Ressourcen&#xa0;für&#xa0;Fragestellungen&#xa0;rund um den Marktzugang und Erstattungsfähigkeit&#xa0;von&#xa0;AbbVie’s&#xa0;Produktportfolio.&#xa0;Zudem beantwortest Du bei Bedarf&#xa0;Fragen von Fachkräften im Gesundheitssystem&#xa0;zu unserer Produktpalette.&#xa0;</p><p>&#xa0;</p><p>Wichtigste Aufgaben:&#xa0;</p><ul><li>Hauptansprechpartner der Sales Teams für Market Access-bezogene Fragestellungen und&#xa0;verantwortlich für&#xa0;deren&#xa0;zeitnahe&#xa0;Beantwortung&#xa0;oder ggf.&#xa0;Unterstützung bei der Lösungsfindung&#xa0;</li><li>Beantwortung&#xa0;von Fragen seitens medizinischem Fachpersonal (HCPs) zu Market Access Themen&#xa0;auf verschiedenen Kommunikationswegen, bei Bedarf auch&#xa0;Durchführung von virtuellen Meetings mit&#xa0;HCPs ggf. unter Einbeziehung&#xa0;des Sales-Teams&#xa0;sowie enge Zusammenarbeit mit den&#xa0;HEM&#xa0;in Fällen&#xa0;besonderer, regionaler&#xa0;Herausforderungen&#xa0;</li><li>Regelhafte Dokumentation und&#xa0;Auswertung der&#xa0;internen und externen&#xa0;Fragestellungen&#xa0;und&#xa0;Weiterleitung relevanter Erkenntnisse&#xa0;an die&#xa0;Market Access Organisation&#xa0;&#xa0;</li><li>Schulung und Unterstützung der&#xa0;Sales-Teams&#xa0;bei Market Access Themen, Richtlinien und Prozessen. Teilnahme&#xa0;an&#xa0;ausgewählten&#xa0;Sales-Tagungen&#xa0;bei Bedarf&#xa0;</li><li>Durchführung von&#xa0;Onboarding-Schulungen&#xa0;für neue Sales-Mitarbeiter&#xa0;&#xa0;</li><li>Entwicklung von&#xa0;Schulungsunterlagen&#xa0;für Sales-Teams&#xa0;(z.B.Q&amp;As,&#xa0;Leitfäden)&#xa0;</li></ul>]]></description><link>http://biotechroles.com/sales-enablement-specialist-(all-genders)-(vollzeit-oder-teilzeit-80percent)-abbvie/69d62771c8e81216cd0c7d43</link><guid isPermaLink="true">http://biotechroles.com/sales-enablement-specialist-(all-genders)-(vollzeit-oder-teilzeit-80percent)-abbvie/69d62771c8e81216cd0c7d43</guid><pubDate>Wed, 08 Apr 2026 10:01:21 GMT</pubDate><company>AbbVie</company><location>Wiesbaden, Wiesbaden</location><salary>$65000-90000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Engineering Manager]]></title><description><![CDATA[<p>As<strong>&#xa0;Senior Engineering Manager</strong>, you will be the&#xa0;technical leader for the site. You will have responsibility for all Engineering and Maintenance activities related to the facility and production equipment. This includes managing the following areas: production support, all facets of engineering (mechanical, process, controls, electrical), validation, maintenance, capital planning and spending and technical support for new product launches.</p><p><strong>Responsibilities</strong></p><ul><li>Financial responsibility for the Maintenance and Engineering Budgets</li><li>financial responsibility for Capital Spending</li><li>Partner with cross-functional peers to ensure the success of the plant goals and objectives</li><li>Develop appropriate Engineering and Maintenance strategies aligned with the business</li><li>Assure his/her personnel and the personnel they serve work in a safe environment and with the proper safety tools and procedures</li><li>Maintain the proper compliance level in the job they perform</li><li>Assure the proper human resources, tools and equipment are in place to assure the expected service</li><li>Assure his/her personnel have the proper training and education to perform the required job and service.</li><li>Negotiate, secure, oversee &amp; ensure that resources are available to meet the demands of the projects and goals of the site</li><li>Continually look for opportunities for process optimization, cost avoidance and cost reduction</li><li>All aspects of people leadership: setting expectations, coaching, counseling, developing, evaluating, feedback, hiring, discipline, and separations related to Engineering and Maintenance staff.<br>
&#xa0;</li></ul>]]></description><link>http://biotechroles.com/senior-engineering-manager-abbvie/69d6276ec8e81216cd0c7d41</link><guid isPermaLink="true">http://biotechroles.com/senior-engineering-manager-abbvie/69d6276ec8e81216cd0c7d41</guid><pubDate>Wed, 08 Apr 2026 10:01:18 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Packing Operator]]></title><description><![CDATA[<p>· Maintain a clean and organized work area throughout and at the end of each shift.</p><p>· Work safely and follow all plant and department health, safety, and environmental policies.</p><p>· Report safety concerns and observations using the Eachieve system.</p><p>· Follow all current departmental SOPs and cGMP practices.</p><p>· Stay up to date with all required cGMP and safety training using ELMS.</p><p>· Execute packaging tasks to ensure timely product delivery and complete all required documentation.</p><p>· Set up and clear packaging lines efficiently, preparing equipment and machines for operation in compliance with SOPs and cGMPs.</p><p>· Troubleshoot equipment issues and work with Maintenance Technicians for mechanical adjustments, reducing downtime and product defects.</p><p>· Operate and monitor computerized production machinery, maintaining high quality standards.</p>]]></description><link>http://biotechroles.com/packing-operator-abbvie/69d6276bc8e81216cd0c7d3f</link><guid isPermaLink="true">http://biotechroles.com/packing-operator-abbvie/69d6276bc8e81216cd0c7d3f</guid><pubDate>Wed, 08 Apr 2026 10:01:15 GMT</pubDate><company>AbbVie</company><location>Westport, Westport</location><salary>$38000-52000</salary><type>Full-time</type></item><item><title><![CDATA[Software / Control Engineer]]></title><description><![CDATA[<p>As <strong>Software / Control Engineer, </strong>you are responsible for basic configuration and programming per AbbVie’s change management procedures for the manufacturing process, utilities and facilities control systems. This position performs system troubleshooting during and outside business hours as necessary. Responsible for the maintenance of assigned site operations technologies (OT) systems per applicable departmental procedures.</p><p><strong>Responsibilities</strong></p><ul><li>Develop basic control configuration or programming in accordance with the design documents to meet the functional requirements.</li><li>Provide first line technical support to Project Engineers, Maintenance, Production and Technical Operation personnel in automation related problems as need arises. Provides training for OT Systems users in automation technologies and process control applications.</li><li>Diagnose and troubleshooting Control System hardware, software, and networking issues, replace defective components as needed.</li><li>Perform site OT systems (DCS, PLC’s, SCADA, and Data Historian) upgrades and data migrations activities.</li><li>Develop and execute qualification protocols plus associated technical documentation like System’s Functional and\or Design Specifications following OT Systems lifecycle validation activities.</li><li>Perform scheduled OT Systems administration and maintenance tasks such as operating systems (OS) and anti-virus updates, users accounts managements, critical data back-up and others.</li><li>Evaluate and provide input and recommendations regarding control system improvements. Establish monitoring and reporting project techniques to support equipment performance reliability.</li><li>Provide production support during off-peak hours. This might require working overtime, overnight or on weekends.</li><li>Conform to EHS management system requirements and compliance obligations, promote continuous improvement, and consider EHS aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal, and any other program applicable according to the position duties.</li></ul>]]></description><link>http://biotechroles.com/software-control-engineer-abbvie/69d62767c8e81216cd0c7d3e</link><guid isPermaLink="true">http://biotechroles.com/software-control-engineer-abbvie/69d62767c8e81216cd0c7d3e</guid><pubDate>Wed, 08 Apr 2026 10:01:11 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$85000-115000</salary><type>Full-time</type></item><item><title><![CDATA[Spécialiste Senior Paie – France]]></title><description><![CDATA[<p>Purpose</p><p>This Senior Payroll Analyst will be responsible for processing and correcting payroll transactions for specific countries as assigned (generally larger, more complex countries), supporting pre-payroll activities, year-end payroll activities, reviewing and verifying files generated internally or by global payroll vendors (GPV), enforcing key payroll deadlines, as well as answering employee/manager queries.</p><p>Responsibilities</p><p>List up to 10 main responsibilities for the job. Include information about the accountability and scope.</p><ul><li>Partnering with internal stakeholders and with Global Payroll Vendor (GPV) to process payroll and resolve payroll transactions that are in error</li><li>Review and validate payroll files (eg. Payroll Reconciliation File, Bank File) and reports generated internally or by the GPV and approve for processing.</li><li>Support pre-payroll activities (eg. finalize data entry, review master data file quality, and confirm time/payroll data completeness).</li><li>Assist in resolving input errors (and other errors) from the third party vendors or internal AbbVie stakeholders.</li><li>Assist in resolving Bank Errors (with AbbVie Treasury’s support).</li><li>Support Year-End Payroll processing activities (eg. develop and provide payroll calendar, review year-end tax reports and notify AbbVie employees of availability of tax information).</li><li>Respond to internal AbbVie stakeholders (Tax, Treasury, Finance and BHR) with regard to questions or issues they have raised around payroll data and/or payroll reports.</li><li>Answer employee/manager queries or assist GPV with other queries it cannot resolve.</li><li>Lead smaller global, regional and country specific projects and participate on global project teams.</li><li>Some travel may be required.</li></ul><p><strong>Objectif</strong><br>
Le/la Senior Payroll Analyst sera responsable du traitement et de la correction des transactions de paie pour certains pays assignés (généralement les plus grands et les plus complexes), du support des activités pré-paie et de fin d’année, de la vérification et validation des fichiers générés en interne ou par les prestataires globaux de paie (GPV), du respect des échéances clés de paie, ainsi que de la réponse aux questions des employés et managers.</p><p><strong>Responsabilités</strong></p><ul><li>Collaborer avec les parties prenantes internes et les prestataires globaux de paie (GPV) pour traiter la paie et corriger les erreurs.</li><li>Examiner et valider les fichiers de paie (ex. : fichier de rapprochement de paie, fichier bancaire) ainsi que les rapports générés en interne ou par le GPV, et approuver leur traitement.</li><li>Soutenir les activités pré-paie (ex. : finalisation de la saisie des données, contrôle de la qualité des données de base, vérification de l’exhaustivité des données de temps et de paie).</li><li>Aider à résoudre les erreurs de saisie (et autres erreurs) provenant de prestataires tiers ou des équipes internes.</li><li>Contribuer à la résolution des erreurs bancaires (avec le support de la trésorerie AbbVie).</li><li>Participer aux activités de clôture annuelle de la paie (ex. : élaboration du calendrier de paie, vérification des rapports fiscaux de fin d’année, communication aux employés).</li><li>Répondre aux parties prenantes internes (Fiscalité, Trésorerie, Finance, BHR) concernant les questions liées aux données ou rapports de paie.</li><li>Répondre aux questions des employés/managers ou assister le GPV pour les demandes non résolues.</li><li>Piloter des projets globaux, régionaux ou locaux de petite envergure et participer à des équipes projets globales.</li><li>Des déplacements occasionnels peuvent être requis.</li></ul>]]></description><link>http://biotechroles.com/specialiste-senior-paie-france-abbvie/69d62765c8e81216cd0c7d3d</link><guid isPermaLink="true">http://biotechroles.com/specialiste-senior-paie-france-abbvie/69d62765c8e81216cd0c7d3d</guid><pubDate>Wed, 08 Apr 2026 10:01:09 GMT</pubDate><company>AbbVie</company><location>Martillac, Krakow</location><salary>$65000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Supply Chain Manager]]></title><description><![CDATA[<p>As<strong> Supply Chain Manager</strong>, you are responsible for supervising warehouses supporting distribution, manufacturing or site&#xa0;services such as MRO or delivery services in the Tempe site. You ensure the Manager’s expectations<br>
for routine activities are met and may manage medium projects within the area while being responsible<br>
for ensuring facilities meet AbbVie external or internal customer expectations and support.</p><p>You are expected to maintain all Quality, Regulatory, Financial and Global Trade compliance<br>
expectations for the area and must ensure full compliance with FDA, DEA, OSHA, GTC, TSA and<br>
other regulatory expectations. Maintain efficient and compliant operations to ensure readiness to meet any internal, customer or regulatory audit. Required to maintain a safe and secure<br>
facility ensuring employee safety and product integrity. The Supervisor is expected to meet<br>
assigned goals and KPI’s and assure capacity, systems and technology is capable of supporting<br>
the assigned area.</p><p><strong>Responsibilities</strong></p><ul><li>Ensure area compliance with applicable Corporate and Divisional Policies and procedures</li><li>Be able to troubleshoot and execute problem solving with minimal supervision</li><li>Ensure daily, weekly and monthly assignments are completed per schedule</li><li>Ensure direct reports are appropriately trained to complete assigned tasks and complete<br>
formal written and verbal performance reviews as scheduled</li><li>Monitor daily work operations and provides direction to supervisors, group leaders, or other staff to achieve unit or departmental goals</li><li>Interact with internal and external customers, by meeting regularly, responding to requests<br>
and explaining procedures</li><li>Develop work schedules for department by assessing priorities, workload and available<br>
resources.</li><li>Maintain personnel records (e.g., work schedules, vacation schedules, leaves) and makes or<br>
directs modifications in the database to reflect actual change</li><li>Develops and/or identifies new work processes and the improved utilization of human and<br>
material resources within the assigned area or related departments, facilitates others<br>
participation in the continuous improvement program, and investigates and solves basic<br>
problems that impact work processes and personnel within a unit or department</li></ul>]]></description><link>http://biotechroles.com/supply-chain-manager-abbvie/69d62762c8e81216cd0c7d3c</link><guid isPermaLink="true">http://biotechroles.com/supply-chain-manager-abbvie/69d62762c8e81216cd0c7d3c</guid><pubDate>Wed, 08 Apr 2026 10:01:06 GMT</pubDate><company>AbbVie</company><location>Tempe, US-Virtual Office</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Supplier Quality Manager]]></title><description><![CDATA[<p>The Supplier Quality Manager performs a key function in the Quality relationship building, QA oversight and issue resolution with suppliers/TPMs in support of AbbVie’s commercial and pipeline supply chains. The individual will work collaboratively across Technical, Manufacturing, Quality, Product Support and Research and Development teams in direct support of supplier management. In this role, the supplier quality manager is the primary quality contact to specific strategic supplier partners. This individual will be responsible for assuring investigations, CAPAs, change management, and audit readiness meet agency and Abbvie expectations. The individual will provide on site supplier support and upskilling to ensure the key suppliers are improving quality performance and ready for agency inspections.</p><ul><li>Build and maintain strong relationships with regional suppliers to support AbbVie’s pipeline and on market product portfolio.</li><li>Assure authenticity of commercial and pipeline product supply chains by performing on-site visits with suppliers to verify business operations and potential areas of improvement.</li><li>Conduct quality business reviews with identified suppliers to assure customer interface of necessary communication to support new product launches.</li><li>Drive remediation efforts with suppliers including PAI readiness and issue resolution.</li><li>Leverage technical expertise to assist in issue resolution at suppliers including investigation review and CAPA planning.</li><li>Ensure all quality expectations related to suppliers in New Product Introductions (NPI) are met.</li><li>Participate in process validation campaigns at Suppliers and provide validation overviews to Quality Business unit.</li><li>Execute audit readiness and upskilling at suppliers in preparation to external and internal quality audits</li><li>Coordinate remediation efforts when poor audit performance is identified at EU suppliers.</li></ul>]]></description><link>http://biotechroles.com/senior-supplier-quality-manager-abbvie/69d6275ec8e81216cd0c7d3a</link><guid isPermaLink="true">http://biotechroles.com/senior-supplier-quality-manager-abbvie/69d6275ec8e81216cd0c7d3a</guid><pubDate>Wed, 08 Apr 2026 10:01:02 GMT</pubDate><company>AbbVie</company><location>Shanghai, Shanghai</location><salary>$120000-180000</salary><type>Full-time</type></item><item><title><![CDATA[AMI Digital & COE Manager, Allergan Aesthetics]]></title><description><![CDATA[<p><strong>About AMI :</strong> Allergan Medical Institute (AMI) is a department within Allergan Aesthetics (AA) with a unique offering of first-class medical education to the healthcare professionals (HCPs) in order to increase their knowledge in medical aesthetics and help them develop state of the art clinical practice.</p><p>The AMI Digital &amp; COE Manager is a high-impact individual contributor responsible for spearheading the Korea Digital Super gap Strategy through an integrated omnichannel approach. This role focuses on maximizing Healthcare Professional (HCP) engagement by managing the 24/7 AMI Digital World ecosystem and establishing a state-of-the-art physical Center of Excellence (COE).<br>
The successful candidate will manage digital acquisition and advertisement strategies across various social media channels to expand the AMI HCP pool and effectively leverage digital assets against physical training programs.<br>
This position requires a professional with deep expertise in VEEVA, virtual training architecture, and a proven track record in navigating complex regulatory landscapes (MA, Legal, RA, and Compliance) to deliver industry-leading medical education.</p><p><strong>1. Digital Ecosystem, Virtual Curriculum &amp; Omnichannel Strategy</strong><br>
•Omnichannel Learning Leadership: Strategically manage and develop AMI Digital World (DW 3.0), providing a seamless 24/7 self-paced learning journey for Healthcare Professionals (HCPs).<br>
•Digital Strategy &amp; Holistic Promotion: Establish and execute robust advertisement and promotion strategies across various social media channels (including Kakao Channel, Instagram, etc.) and SMS management to expand the AMI HCP pool.<br>
•Synergy with Offline Programs: Actively promote and highlight offline programs (Hands-on, Nationwide) through digital channels. This includes pre- and post-event digital engagement, managing "Replay" services on DW3, and leveraging digital assets to maximize the impact of physical training.<br>
•System &amp; VEEVA Mastery: Serve as the technical Subject Matter Expert (SME) for Absorb LMS, PRISM, and VEEVA systems, managing the strict end-to-end approval process for all digital and clinical materials.<br>
•Virtual Training Specialization: Design and execute high-impact webinar series and virtual training formats, ensuring all localized content aligns with the AMI IMCO &amp; Korea strategy.</p><p><br>
<strong>2. COE Establishment &amp; Facility Strategic Execution</strong><br>
•Greenfield Facility Establishment: Lead the initial setup, demonstration center establishment plan, and operational execution of the AMI COE, ensuring the facility supports 50–100 pax small-group trainings and clinical demonstrations.<br>
•Regulatory &amp; Compliance Orchestration: Navigate complex internal approval gates by collaborating extensively with Medical affairs(MA), Legal, Regulatory Affairs (RA), and Office of Ethics/Compliance (OEC) to ensure 100% adherence to protocols.<br>
•Conflict &amp; Stakeholder Management: Utilize highly skilled communication and negotiation techniques to manage internal conflicts and align diverse interests during the COE’s setup and operational phases.<br>
•Operational Excellence: Oversee the daily operations and maintenance of the COE, ensuring a professional, high-standard environment that reflects the brand's global prestige.</p><p><br>
<strong>3. Strategic Agility, Collaboration &amp; Dynamic Scope</strong><br>
•Cross-Functional Synergy: Work closely with Hands-on and Nationwide Managers to create a unified educational ecosystem, ensuring digital and offline initiatives are perfectly leveraged against each other.<br>
•Strategic Functional Partnership: Support the AMI Lead as a key functional partner, providing critical expertise in the execution of the annual AMI operating plan.<br>
•Adaptability &amp; Dynamic Scope: Please note that the responsibilities listed above are not exhaustive. This role requires a high degree of adaptability; project details and focus areas may change or expand based on Regional/International guidelines, team strategies, and evolving project requirements.<br>
•Performance Accountability: Manage program budgets, vendor relationships, and AMI dashboards to ensure accurate measurement of ROI and effectiveness.</p>]]></description><link>http://biotechroles.com/ami-digital-and-coe-manager-allergan-aesthetics-abbvie/69d6275bc8e81216cd0c7d31</link><guid isPermaLink="true">http://biotechroles.com/ami-digital-and-coe-manager-allergan-aesthetics-abbvie/69d6275bc8e81216cd0c7d31</guid><pubDate>Wed, 08 Apr 2026 10:00:59 GMT</pubDate><company>AbbVie</company><location>Seoul, Seoul</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Product Specialist Haemathology]]></title><description><![CDATA[<p><strong>Job Description</strong></p><p>AbbVie is seeking a Senior Product Specialist to lead the launch and market growth of our Haemathology portfolio. In this vital role, you will partner with healthcare professionals across hospitals, applying your expertise in Haemathology to drive patient access, optimize product utilization, and execute strategic territory plans. If you thrive in a collaborative, data-driven environment and are passionate about advancing patient care through innovative therapies, we invite you to join us and help shape the future of Haemathology.</p><p>&#xa0;</p><p><strong>Purpose Statement</strong></p><p>Drive the launch and growth of AbbVie’s Haemathology product by engaging hospital teams and executing territory plans. Build strong relationships with healthcare professionals to support patient access treatment and ensure appropriate product use, while working with Brand and Field Teams to implement strategies and achieve sales targets.</p><p>&#xa0;</p><p><strong>Main Responsibilities</strong></p><ul><li>Build and maintain trusted, long-term relationships with oncologists, specialist nurses, pharmacists, and other key stakeholders to support patient access and optimal product use.</li><li>Tailor scientific and product discussions to HCP needs, patient pathways, and local context.</li><li>Develop and execute territory and strategic account plans aligned with launch objectives and brand strategy.</li><li>Achieve sales targets and performance KPIs across the assigned geography.</li><li>Identify growth opportunities by understanding treatment pathways, stakeholder influence, and market dynamics.</li><li>Leverage AI-driven tools and analytics to enhance customer engagement, optimize territory planning, and support data-informed decision-making.</li><li>Collaborate with Brand and In-Field teams to share insights, inform strategy, and ensure effective brand execution.</li><li>Maintain up-to-date knowledge of Haemathology, clinical data, and the evolving treatment landscape.</li><li>Manage territory budget and promotional spend responsibly to support launch objectives and optimize resources.</li></ul>]]></description><link>http://biotechroles.com/senior-product-specialist-haemathology-abbvie/69d62757c8e81216cd0c7d20</link><guid isPermaLink="true">http://biotechroles.com/senior-product-specialist-haemathology-abbvie/69d62757c8e81216cd0c7d20</guid><pubDate>Wed, 08 Apr 2026 10:00:55 GMT</pubDate><company>AbbVie</company><location>Dublin, Dublin</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Brand Manager, Allergan Aesthetics  (New created position)]]></title><description><![CDATA[<p><strong>This is a new added headcount for our Botox line, and this role will be reporting into the senior brand manager and involves many exciting new product launches activities.&#xa0;</strong></p><p><strong>CORE JOB RESPONSIBILITIES&#xa0;</strong></p><ul><li>Assist the Botox brand lead to design Botox marketing strategy and execution plans and carry out&#xa0;</li><li>Assist the Botox brand lead to manage the short-term &amp; mid-term business planning process based on solid market insights and assumptions.&#xa0;</li><li>Build and maintain relationships with KOLs in order to ensure the value proposition of brands&#xa0;</li><li>Assist the Botox brand lead to develop the customer engagement plan to enhance customer awareness&#xa0;and preference of product differentiation&#xa0;</li><li>Ensure the integrity of marketing activities in accordance with local, regional and corporate compliance&#xa0;policies&#xa0;</li><li>Assist the Botox brand lead to lead collaboration efforts with sales force, other functions and marketing&#xa0;managers&#xa0;</li><li>Analyze market trends and sales potential to make monthly proposed forecast with suggested action plans&#xa0;to achieve the proposed forecast.</li><li>Contribute to the development of the strategy through the Brand Planning process in line with strategy&#xa0;defined by Global Brand Team and assist the adequate involvement of multiple functions as relevant for&#xa0;the Brand.&#xa0;</li></ul>]]></description><link>http://biotechroles.com/associate-brand-manager-allergan-aesthetics-(new-created-position)-abbvie/69d62753c8e81216cd0c7d1f</link><guid isPermaLink="true">http://biotechroles.com/associate-brand-manager-allergan-aesthetics-(new-created-position)-abbvie/69d62753c8e81216cd0c7d1f</guid><pubDate>Wed, 08 Apr 2026 10:00:51 GMT</pubDate><company>AbbVie</company><location>Seoul, Seoul</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Technical Support Specialist]]></title><description><![CDATA[<ul><li>Plays a central role in higlighting and implementing continuous improvement ideas and operational excellence opportunities identified through tracking and monitoring of production performance</li><li>Assists with the development of lean and continuous improvement skills throughout the manufacturing organisation.</li><li>Assists in the pre-campaign planning of Drug Products and APIs, in reviewing lessons learned from previous campaigns with operations personel and supports post-campaign activities.</li><li>May act as a delegate for the DP and Synthroid Operations Leads for certain activities and tasks based on level of experience and competence.</li><li>Assists and may lead Root Cause Analyses and indentification of Corrective/Preventative Actions as part of deviation investigation processes.</li><li>Assists in following up and closing operations related CAPAs and compliance suggestions.</li><li>Personally responsible for adhering to all SOPs related to Quality, Safety and Environmental Compliance. Should act as role model for the identification and implementation of Positive Compliance interventions.</li><li>Implements changes to Operating SOPs as required.</li><li>May represent operations on introductions and execution of NPI projects.</li><li>Assists in the identifiaction, implementation and execution of key Manufacturing and Site Strategies</li></ul>]]></description><link>http://biotechroles.com/technical-support-specialist-abbvie/69d62750c8e81216cd0c7d11</link><guid isPermaLink="true">http://biotechroles.com/technical-support-specialist-abbvie/69d62750c8e81216cd0c7d11</guid><pubDate>Wed, 08 Apr 2026 10:00:48 GMT</pubDate><company>AbbVie</company><location>Sligo, Sligo</location><salary>$45000-65000</salary><type>Full-time</type></item><item><title><![CDATA[Project Coordinator (Neuroscience Marketing)]]></title><description><![CDATA[<p>The Project Coordinator&#xa0;(PC) is primarily responsible for providing operational and administrative support to the marketing and sales team.&#xa0; 70% of the PC's time will be dedicated to important administrative tasks, working closely with internal team members to drive efficiency and compliance.&#xa0; The remaining 30% will be focused on ensuring strategically important marketing projects remain on track to deliver against objectives.&#xa0; The PC role is internally focused and does not directly manage external stakeholder relationships.</p><p>The Project Coordinator&#xa0;reports to the team Brand Lead.</p><p>Administrative &amp; Internal Project Support (70%)</p><ul><li>Provide day-to-day project coordination and administrative support, collaborating with marketing and sales functions</li><li>Schedule and organise internal team meetings, document actions/decisions, and ensure timely follow-up on deliverables</li><li>Maintain project documentation, governance records, and highest compliance standards specific to the brand team initiatives</li><li>Track operational project milestones, actions, risks, and escalation points, reporting to project owners</li><li>Assist with internal approvals, compliance checks, and process adherence (e.g., relevant industry codes)</li><li>Identify and implement process improvements to enhance efficiency and scalability</li><li>Raise purchase orders and liaise with finance to ensure prompt payment to agencies and clinicians</li></ul><p>Marketing Activity Tracking &amp; Enablement (30%)</p><ul><li>Coordinate and monitor the delivery of marketing activities, ensuring timelines and objectives are met</li><li>Facilitate internal workflows for content review and approval, ensuring compliance with relevant codes and policies</li><li>Organise cross-functional input and manage timelines for key promotional initiatives</li><li>Monitor, report, and escalate progress and risks associated with brand marketing projects</li></ul>]]></description><link>http://biotechroles.com/project-coordinator-(neuroscience-marketing)-abbvie/69d6274dc8e81216cd0c7d10</link><guid isPermaLink="true">http://biotechroles.com/project-coordinator-(neuroscience-marketing)-abbvie/69d6274dc8e81216cd0c7d10</guid><pubDate>Wed, 08 Apr 2026 10:00:45 GMT</pubDate><company>AbbVie</company><location>Maidenhead, Maidenhead</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Product Specialist Oncology - Lombardia, Trentino Alto Adige]]></title><description><![CDATA[<p><strong>Key Responsibilities:</strong></p><ul><li>Performs scientific information activities for physicians in accordance with Legislative Decree 24/04/2006 No. 219, the Farmindustria Code of Ethics, regional guidelines on drug scientific information regulations, and, where applicable, Legislative Decree 5 August 2022 No. 137.</li><li>Develops a deep knowledge of the therapeutic areas covered and the relative market.</li><li>Reports all information about adverse drug effects to the Scientific Service and the company's Pharmacovigilance team, in line with current regulations and company procedures.</li><li>Prepares and plans interviews and meetings with healthcare professionals and tracks relevant information obtained in order to improve the scientific efficacy in subsequent meetings.</li><li>Performs support activities aligned with scientific drug information, manages the reporting and information flows according to company directives with the aim to develop territorial interactions. Updates reports using the company tools.</li><li>Conducts non-promotional educational and information activities for healthcare operators (both prescribing and non-prescribing professionals) involved in patient care, according to company directives.</li><li>Knows and applies company procedures for scientific information activities and manages related materials, scientific and technological supports</li><li>Supports company functions in activities aimed at ensuring the correct supply/provision of products.</li><li>Shares relevant information with the Area Manager, In Field Team members and colleagues at headquarters to anticipate changes and implement company strategies.</li></ul>]]></description><link>http://biotechroles.com/product-specialist-oncology-lombardia-trentino-alto-adige-abbvie/69d62749c8e81216cd0c7d0f</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-oncology-lombardia-trentino-alto-adige-abbvie/69d62749c8e81216cd0c7d0f</guid><pubDate>Wed, 08 Apr 2026 10:00:41 GMT</pubDate><company>AbbVie</company><location>Milan, Roma</location><salary>$65000-95000</salary><type>Full-time</type></item><item><title><![CDATA[Director of Sales, SENSORA]]></title><description><![CDATA[<p><span style="font-size: 16px;">Eko builds AI and digital tools to enable every healthcare provider to more accurately detect heart and lung disease – the leading causes of death globally. Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on millions of patients around the world. With Eko, clinicians can detect cardiac and pulmonary disease with higher accuracy, diagnose with more confidence, manage treatment effectively, and ultimately give their patients the best care possible.</span></p>
<p><span style="font-size: 16px;">We have strong venture capital backing from investors like Artis Ventures, Questa Capital, Highland Capital, and Mayo Clinic Ventures.</span></p>
<p><span style="font-size: 16px;">Recognized by TIME magazine in 2025 as one of the world’s top healthcare technology companies, Eko is one of the fastest growing digital health companies with products used around the world at some of the most prestigious health systems.</span></p>
<p><span style="font-size: 16px;">We have more than 8 FDA clearances including novel AI algorithms, and we invest heavily in quality clinical research and R&amp;D to build and validate exceptional products for patients we care deeply about.</span></p>
<p><span style="font-size: 16px;">We’ve built a mission driven, high performing, talented, and diverse team of engineers, physicians, PhD’s, creatives, and technologists. We are committed to investing in each other and our mission to ensure all patients have access to high quality care.</span></p>
<p><span style="font-size: 16px;">We are headquartered in Emeryville, California and privately-held with world class investors and partners.</span></p><div><br></div><h3>About the Role&nbsp;</h3>
<div>The Head of SENSORA Sales owns enterprise revenue growth for Eko’s SENSORA platform. This is a senior, hands-on role combining direct enterprise selling with sales leadership. The role operates as a player-coach, personally leading complex health system sales while building and scaling a small enterprise sales team as the SENSORA business grows. The Head of SENSORA Sales is responsible for the end-to-end enterprise sales motion, from pipeline development through close, and works closely with cross-functional partners to drive successful adoption across hospitals and integrated delivery networks.</div></br><b>As Head of Sales - SENSORA at Eko, You Will: </b></br>
<li>Own new business generation and enterprise revenue for SENSORA across large hospitals and integrated delivery networks, from prospecting through contract execution.</li>
<li>Personally lead and close complex, multi-stakeholder enterprise sales cycles, including 6- and 7-figure opportunities.</li>
<li>Develop and execute territory and account strategies across key enterprise segments, including health systems, physician groups, and value-based care networks.</li>
<li>Build, mentor, and manage a small initial team of enterprise sellers, expanding the team over time as the business scales.</li>
<li>Establish trusted, multi-threaded relationships with senior clinical, IT, finance, and executive stakeholders within health systems.</li>
<li>Develop and present ROI-driven business cases that align SENSORA’s clinical and operational value with health system priorities.</li>
<li>Navigate enterprise procurement processes, including legal, privacy, security, value analysis, and clinical governance reviews.</li>
<li>Partner cross-functionally with Product, Clinical, Marketing, Implementation, and Customer Success teams to support pilots, evaluations, and enterprise rollouts.</li>
<li>Maintain accurate forecasting, pipeline management, and account data within CRM systems.</li>
<li>Act as a voice of the customer, providing input into go-to-market strategy, product roadmap, pricing, and enterprise messaging.</li>
<li>Ensure compliance with company policies and applicable laws and regulations.</li>
<li>Other duties as assigned.</li>
<li>Note: Job duties may change at any time with or without notice.es may change at any time with or without notice.</li>
</br><b>As Head of Sales - SENSORA at Eko, You Have:</b></br>
<li>Bachelor’s degree or equivalent practical experience.</li>
<li>10+ years of enterprise sales experience in digital health, MedTech, or healthcare SaaS.</li>
<li>Proven track record of closing complex enterprise deals with large hospitals and health systems.</li>
<li>Experience selling new or category-creating technologies into healthcare environments.</li>
<li>Demonstrated ability to operate as both a senior individual contributor and sales leader.</li>
<li>Strong knowledge of health system procurement, value analysis, contracting, and privacy/security processes.</li>
<li>Experience building ROI-based value propositions for clinical and executive audiences.</li>
<li>Proficiency with CRM systems and enterprise sales forecasting tools.</li>
<li>Strong communication, organizational, and problem-solving skills.</li>
<li>Ability to perform the essential functions of the role with or without reasonable accommodation.ccommodation.</li>
</br><p><span style="font-size: 16px;">Compensation is market-based and reflects the cost of labor across different U.S. geographic locations. The specific salary is based on several factors, including market location, and may vary depending on job-related knowledge, skills, and experience.</span></p>
<p><span style="font-size: 16px;">Eko is proud to be an equal opportunity employer and welcome people of different backgrounds, experiences, abilities and perspectives. We are committed to building a diverse and inclusive team.</span></p>]]></description><link>http://biotechroles.com/director-of-sales-sensora-eko/69d5d398c8e81216cd0c684a</link><guid isPermaLink="true">http://biotechroles.com/director-of-sales-sensora-eko/69d5d398c8e81216cd0c684a</guid><pubDate>Wed, 08 Apr 2026 04:03:36 GMT</pubDate><company>Eko</company><location>Remote, US</location><salary>$180000-280000</salary><type>Full Time</type></item><item><title><![CDATA[Customer Success Manager - CRO Clinical Operations]]></title><description><![CDATA[<div>Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.</div>
<div>&nbsp;</div>
<div>At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a&nbsp;<a href="https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6">public benefit corporation</a>&nbsp;(PBC), legally bound to balancing the interests of customers, employees, society, and investors.</div>
<div>&nbsp;</div>
<div>As a&nbsp;<a href="https://careers.veeva.com/work-anywhere/">Work Anywhere</a>&nbsp;company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.</div>
<div>&nbsp;</div>
<div>Join us in&nbsp;<a href="https://www.youtube.com/watch?v=TaPSP8cCSKY&amp;ab_channel=Forbes">transforming the life sciences industry</a>, committed to making a positive impact on its customers, employees, and communities.</div><div><br></div><h3><strong>The Role</strong></h3>
<div>&nbsp;</div>
<div>As a Customer Success Manager, you will be responsible for ensuring our CROs customers’ success with Veeva’s Clinical Operations’ products and services. You will serve as a liaison between Veeva and key customer stakeholders to foster collaboration, triage escalations, and highlight value through proactive engagement.
<div>
<p>We're seeking a driven Clinical Operations expert who thrives in a customer-facing environment. The role demands a strong communicator with a passion for building enduring, trusted relationships with key decision-makers, and a collaborative spirit for working in a cross-functional environment to improve the overall customer experience.</p>
</div>
</div></br><b>What You'll Do</b></br><div>

<li>Support 4-6 global CRO customers post-implementation with Veeva Clinical Operations applications (e.g. eTMF, CTMS, Study Startup, etc.)</li>
<li>Act as a trusted advisor and own the relationship with your customers’ application owners to understand their objectives and challenges</li>
<li>Liaise with Veeva strategy, sales, product and/or services’ stakeholders to address customer needs</li>
<li>Lead meetings with customers to demonstrate success and identify additional opportunities to add value</li>
<li>Provide strategic guidance to optimize use of Veeva applications and help create a&nbsp; customer roadmap based on their business goals and needs</li>
<li>Facilitate customer to customer or customer to Veeva connections for collaboration opportunities and industry learning</li>

</div></br><b>Requirements</b></br><div>

<li>7+ years of experience in Clinical Operations within life sciences industry</li>
<li>Experience working in large global Clinical Research Organizations (CROs)</li>
<li>Customer-facing consulting experience</li>
<li>Experience managing relationships with key decision makers and application owners</li>
<li>Ability to travel up to 25%</li>
<li>Qualified candidates must be legally authorized to be employed in United States. Veeva Systems does not anticipate providing sponsorship for employment visa status for this employment position</li>

</div></br><div>
<div><span style="font-size: 10px;">#LI-Remote</span></div>
<div><span style="font-size: 10px;">#LI-MidSenior</span></div>
</div><div><br></div><div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>]]></description><link>http://biotechroles.com/customer-success-manager-cro-clinical-operations-veeva/69d5d388c8e81216cd0c6842</link><guid isPermaLink="true">http://biotechroles.com/customer-success-manager-cro-clinical-operations-veeva/69d5d388c8e81216cd0c6842</guid><pubDate>Wed, 08 Apr 2026 04:03:18 GMT</pubDate><company>Veeva</company><location>North Carolina - Raleigh</location><salary>$110000-150000</salary><type>Full-Time</type></item><item><title><![CDATA[Director, Marketing (Brand Lead)]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a class="postings-link" href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<b>&nbsp;</b><span style="font-size: inherit">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div><div><br></div><div><span style="color: #000000;"><strong><u>Summary</u>: </strong></span><span style="color: #000000;">The <strong>Director, Marketing</strong> is responsible for leading the US promotional launch of Orca-T, Orca Bio’s first commercial product. This individual will be a critical member of the Marketing team and broader Commercial team, leading workstreams to collect and interpret HCP insights, develop engagement strategies, shape and test Brand messaging, and build promotional tactics. The Director, Marketing will have a wide remit including HCP, payer, and patient audiences, personal and non-personal tactical development, and omnichannel media strategy. Planning for multiple launch scenarios, completing promotional readiness, and contributing to Commercial and organizational Launch Readiness will be core responsibilities for this role. Reporting into the VP/Head of Marketing, this individual will collaborate closely with the cross-functional Orca team including Medical Affairs, Sales, Operations, Regulatory, IT, and Legal.</span></div></br><b>Responsibilities</b></br><div>
<ul type="disc" style="margin-top: 0in; margin-bottom: 0in;">
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Leads the promotional launch of Orca-T, driving robust pre-launch, launch, and post-launch strategies and omnichannel tactics that maximize market penetration and product adoption</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Drives development of unique and effective HCP engagement strategies aligned to Orca-T Brand strategy</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Collaborate with the Market Development team and other Commercial personnel to shape a comprehensive HCP Marketing tactical plan, budget, and performance plan aligned to Brand KPIs to enable a robust promotional launch</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Lead Orca-T message development across HCP and patient audiences, including insights generation and analysis</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Lead the execution of a full HCP-facing tactical suite for personal and non-personal channels, including PRC review and approval, for Day 0, Now Approved, and Campaign assets</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Contribute to omnichannel strategy, deployment, and management</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Manage agency partners effectively to deliver consistent results</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Contribute to advisory board content, execution, and analysis</span></li>
<li style="color: #000000; margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif;"><span style="color: #000000;">KOL Engagement at major congresses, advisory boards, and site visits as necessary to support Commercial onboarding workstreams</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Lead consistent engagement with Sales team to ensure optimization of messaging and assets</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Effectively manage the promotions tactical budget to Launch Readiness and Orca-T launch</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Manage one Product Marketing FTE</span></li>

</ul></div></br><b>Qualifications</b></br><div>
<ul type="disc" style="margin-top: 0in; margin-bottom: 0in;">
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Bachelor’s degree in Life Sciences, Marketing, Finance, or related required; an MBA or other advanced degree is preferred</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">10 years of biopharmaceutical experience, including at least 7 years of experience in Marketing, Commercial Strategy, and/or Sales</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Experience in hematology/oncology and/or bone marrow transplantation and marketing complex, novel products in therapeutic areas of high unmet need</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Proven ability to prioritize and manage multiple projects simultaneously, including market research, message development, promotional tactics, advertising campaigns, and associated PRC and OPDP processes</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Track record of cross-functional collaboration</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Prior people management experience preferred</span></li>
<li style="margin-bottom: 0in; line-height: normal; margin-top: 0in; margin-right: 0in; font-size: 11pt; font-family: Calibri, sans-serif; color: #000000;"><span style="color: #000000;">Willingness to travel up to 20%</span></li>

</ul></div></br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div><div><br></div><div><b style="font-size: 18px">Who we are</b></div><div><br></div><div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div><div><br></div><div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div><div><br></div><div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div><div><br></div><div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div><div><br></div><div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div><div><br></div><div><b style="font-size: 18px">Notice to staffing firms</b></div><div><br></div><div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/director-marketing-(brand-lead)-orca-bio/69d5d374c8e81216cd0c683c</link><guid isPermaLink="true">http://biotechroles.com/director-marketing-(brand-lead)-orca-bio/69d5d374c8e81216cd0c683c</guid><pubDate>Wed, 08 Apr 2026 04:03:00 GMT</pubDate><company>Orca Bio</company><location>Remote</location><salary>$180000-260000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Director, Commercial Manufacturing]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863" class="postings-link">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<strong>&nbsp;</strong><span style="font-size: inherit;">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div>
<div>&nbsp;</div>
<div>We have built a state-of-the-art, 100,000-square-foot manufacturing facility in Sacramento, CA (7910 Metro Air Pkwy) to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies.</div><div><br></div><p>The <strong>Director, Commercial Manufacturing </strong>is responsible for leadership of cell therapy manufacturing operations and production support functions to ensure reliable, compliant, and timely delivery of patient-specific therapies. This role drives consistent batch execution, operational discipline, and cross-functional alignment to meet on-time patient delivery while maintaining the highest standards of quality and safety.</p>
<p>The Director will build and sustain robust production systems, embed lean manufacturing principles, and lead continuous improvement initiatives to scale operations in a dynamic, GMP-regulated environment.</p></br><b>Physical Demands</b></br>
<li><em>Production Associate Roles</em>: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment.</li>
<li><em>Most roles</em> must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.</li>
</br><b>Work Conditions</b></br>
<li><em>Many roles</em> must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs, as well as regularly participate in video-based meetings. Also, may be required to work scheduled overtime, weekends, or holidays based on business needs.</li>
</br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Who we are</strong></div>
<div>&nbsp;</div>
<div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div>
<div>&nbsp;</div>
<div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div>
<div>&nbsp;</div>
<div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div>
<div>&nbsp;</div>
<div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div>
<div>&nbsp;</div>
<div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Notice to staffing firms</strong></div>
<div>&nbsp;</div>
<div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/director-commercial-manufacturing-orca-bio/69d5d374c8e81216cd0c683d</link><guid isPermaLink="true">http://biotechroles.com/director-commercial-manufacturing-orca-bio/69d5d374c8e81216cd0c683d</guid><pubDate>Wed, 08 Apr 2026 04:03:00 GMT</pubDate><company>Orca Bio</company><location>Sacramento, CA</location><salary>$180000-260000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Associate, Packaging Operations and Cold Chain Handling - Night Shift]]></title><description><![CDATA[<div>More than one million people in the United States today are fighting blood cancer. While a traditional <a class="postings-link" href="https://www.mayoclinic.org/tests-procedures/allogeneic-stem-cell-transplant/pyc-20384863">allogeneic stem cell transplant</a> has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks.<b>&nbsp;</b><span style="font-size: inherit">With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.</span></div><div><br></div><div><span style="font-size: 16px;">The <strong>Associate, Packaging Operations and Cold Chain Handling</strong></span><strong style="font-size: 16px;">&nbsp;- Night Shift </strong><span style="font-size: 16px;">supports critical operations related to the receipt of patient materials (leukapheresis/blood), cryopreservation of cellular products, and preparation and coordination of final drug product shipments.&nbsp; This role will operate with a deep understanding of GMP manufacturing, cell therapy processes, and the ability to execute multiple tasks in a fast-paced environment.</span></div>
<div>&nbsp;</div>
<div><strong style="font-size: 16px;">Night Shift Hours Worked:</strong></div>
<div><span style="font-size: 16px;">• 6:00pm to 6:30am </span><em><strong style="font-size: 16px;">or</strong></em></div>
<div><span style="font-size: 16px;">• 6:30pm to 7:00am</span></div>
<div>&nbsp;</div>
<div><strong style="font-size: 16px;">Work Week Schedule:</strong></div>
<div><span style="font-size: 16px;">• &nbsp;Sunday, Monday, Tuesday + every other Wednesday </span><em><strong style="font-size: 16px;">or</strong></em></div>
<div><span style="font-size: 16px;">• &nbsp;Thursday, Friday, Saturday + every other Wednesday&nbsp;</span></div></br><b>Physical Demands</b></br>
<li><em>Production Associate Roles</em>: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment.</li>
<li>Must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed. Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.</li>
</br><b>Work Conditions</b></br>
<li>Must be able to work at either Orca Bio Sacramento location (3400 Business Dr. or 7910 Metro Air Pkwy) based on operational needs.</li>
<li>Must be comfortable regularly participating in video-based meetings.</li>
<li>May be required to work scheduled overtime, weekends, or holidays based on business needs.</li>
</br><div>The anticipated annual salary range for this job is based on prior experience in the role/industry, education, location, internal equity, and other job-related factors as permitted by law. For remote-based positions, this range may vary based on your local market. You will also be eligible to receive pre-IPO equity, in addition to competitive medical, dental, and vision benefits, PTO, 401(k) plan, life and accidental death and disability coverage, and parental leave benefits. Other perks include subsidized daily lunches and snacks at our on-site locations.</div><div><br></div><div><b style="font-size: 18px">Who we are</b></div><div><br></div><div>We are driven by a passion for science and compassion for patients. We act with urgency to ensure our treatments are one day accessible to all who need them.</div><div><br></div><div>We live by our core values of passion, courage, and integrity. Excellence in our work means the chance to unlock a better quality of life for our patients, and with that comes tremendous responsibility.</div><div><br></div><div>We innovate on a path that hasn’t been paved. We embrace an entrepreneurial spirit and take calculated risks to achieve our mission. We aren’t afraid to ask “why not” and challenge the status quo.</div><div><br></div><div>We maintain a start-up culture of camaraderie and leadership by example, regardless of title.</div><div><br></div><div>We’re proud to be an equal opportunity employer, and recognize that celebrating our differences creates stronger, lasting solutions that better serve our team, our patients and their healthcare providers.</div><div><br></div><div><b style="font-size: 18px">Notice to staffing firms</b></div><div><br></div><div>Orca Bio does not accept resumes from staffing agencies with which we do not have a written agreement and specific engagement for a particular opening. Our employment activities, inquiries and offers are managed through our HR/Talent team, and all candidates are presented through this channel only. We do not accept unsolicited resumes, and we rarely outsource recruitment.</div>]]></description><link>http://biotechroles.com/associate-packaging-operations-and-cold-chain-handling-night-shift-orca-bio/69d5d374c8e81216cd0c683b</link><guid isPermaLink="true">http://biotechroles.com/associate-packaging-operations-and-cold-chain-handling-night-shift-orca-bio/69d5d374c8e81216cd0c683b</guid><pubDate>Wed, 08 Apr 2026 04:03:00 GMT</pubDate><company>Orca Bio</company><location>Sacramento, CA</location><salary>$55000-75000</salary><type>Regular, Full-Time Employee</type></item><item><title><![CDATA[Senior Director, Financial Planning and Analysis]]></title><description><![CDATA[<div><u style="font-size: 11pt;"><strong>Who is BlueRock?</strong></u></div>
<div><span style="font-size: 11pt;">BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique </span><strong style="font-size: 11pt;"><em>cell+gene</em></strong><span style="font-size: 11pt;">&nbsp;platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.</span></div>
<div><span style="font-size: 11pt;">The convergence of cell biology and genetic engineering is creating fundamental new ways to impact disease. Founded in 2016 to capitalize on these technological breakthroughs, we are advancing our novel&nbsp;</span><strong style="font-size: 11pt;"><em>cell+gene</em></strong><span style="font-size: 11pt;">&nbsp;platform to develop, manufacture, and deliver an entirely new generation of authentic and engineered cell therapies across three therapeutic areas: neurology, cardiology, and immunology.</span></div>
<div>&nbsp;</div>
<div><u style="font-size: 11pt;"><strong>What Are We Doing?</strong></u></div>
<div><span style="font-size: 11pt;">Our&nbsp;foundational science&nbsp;harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit. </span></div>
<div><span style="font-size: 11pt;">We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options. </span></div>
<div><span style="font-size: 11pt;">We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives.</span></div>
<div><strong style="font-size: 11pt;">&nbsp;</strong></div>
<div><strong style="font-size: 11pt;">Senior Director, Financial Planning &amp; Analysis (FP&amp;A)</strong></div>
<div><u style="font-size: 11pt;"><strong>Position Overview</strong></u></div>
<div><span style="font-size: 11pt;">The&nbsp;Senior Director, Financial Planning &amp; Analysis (FP&amp;A)&nbsp;will serve as the company’s&nbsp;strategic finance architect, reporting to the SVP, Head of Finance. Operating with a high degree of autonomy, this leader will&nbsp;shape BlueRock’s enterprise financial strategy into a coherent financial narrative, translating corporate vision into actionable financial frameworks that drive long-term value creation. This role will inform capital allocation and investment decisions, and enable executive and Board decision-making through rigorous analysis and insight.</span></div>
<div><span style="font-size: 11pt;">As the head of FP&amp;A, the incumbent will lead and orchestrate the enterprise-wide planning, forecasting, and performance management, while acting as a thought partner to Executive Management and Chief of Staff on key financial, strategic, and operational decisions. This highly visible role will shape how the company prioritizes investments, evaluates trade-offs, allocates capital across the portfolio, and communicates its strategy internally and externally. While this role will have some direct business partnering responsibilities for key functions, this role will primarily be focused on ensuring the financial storyline and key investments are tied to BlueRock’s Corporate Strategy.</span></div>
<div><span style="font-size: 11pt;">The Senior Director will also lead and scale the FP&amp;A function, evolving processes, tools, and governance to support the company’s growth, pipeline progression, and long-range objectives.</span></div>
<div>&nbsp;</div>
<div><u style="font-size: 11pt;"><strong>Key Responsibilities</strong></u></div>
<div>&nbsp;</div>
<div><strong style="font-size: 11pt;">Strategic Leadership &amp; Decision Support</strong></div>
<div><span style="font-size: 11pt;">Serve as a finance advisor to Executive Leadership, shaping BlueRock’s capital allocation and portfolio strategy through data-driven insights.</span></div>
<div><span style="font-size: 11pt;">Define and articulate the enterprise financial narrative, connecting corporate strategy, operational milestones, long-range plans, and external messaging</span></div>
<div><span style="font-size: 11pt;">Act as a key thought partner to the Chief of Staff and senior program and functional leadership to ensure financial plans clearly reflect strategic priorities and trade-offs</span></div>
<div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 11pt;">Lead comprehensive scenario modeling and strategic initiative evaluations that guide investment decisions and risk-return assessments.</span></div>
<div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 11pt;">Establish frameworks for financial decision-making that embed strategic discipline across the company.</span></div>
<div><span style="font-size: 11pt;">&nbsp;</span></div>
<div><strong style="font-size: 11pt;">Planning, Forecasting &amp; Performance Management</strong></div>
<div><span style="font-size: 11pt;">Lead the end-to-end annual SBP and long-range planning cycles, from strategic design through execution and communication</span></div>
<div>·<span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 11pt;">Oversee an agile forecasting model that identifies and manages value drivers, risks, and opportunities in real time.</span></div>
<div><span style="font-size: 11pt;">Ensure financial rigor and accountability by building strong partnerships with R&amp;D, Program Management, and operational functions.</span></div>
<div><span style="font-size: 11pt;">Develop and deliver executive-level management reporting that supports timely and informed decision-making</span></div>
<div><span style="font-size: 11pt;">Support the Bemdaneprocel Product Team (Bemda PT) as the key Finance lead to support decision making and go/no go decisions.</span></div>
<div><strong style="font-size: 11pt;">&nbsp;</strong></div>
<div><strong style="font-size: 11pt;">Executive &amp; Board Engagement</strong></div>
<div><span style="font-size: 11pt;">Prepare and present high-quality financial materials for Executive Committee, including strategic deep dives</span></div>
<div><span style="font-size: 11pt;">Provide clear, concise financial perspectives to support Board discussions on strategy, capital deployment, and long-term value creation</span></div>
<div><strong style="font-size: 11pt;">&nbsp;</strong></div>
<div><strong style="font-size: 11pt;">FP&amp;A Function &amp; Process Excellence</strong></div>
<div><span style="font-size: 11pt;">Build and mentor a high-performing FP&amp;A organization, establishing a multi-year vision aligned with the company’s strategic trajectory</span></div>
<div><span style="font-size: 11pt;">Evaluate emerging analytics technologies (including AI-driven insights) to enhance decision-making quality and efficiency.</span></div>
<div><span style="font-size: 11pt;">Partner with Accounting to ensure alignment between financial planning, reporting, and actual results</span></div>
<div><span style="font-size: 11pt;">Collaborate with the People &amp; Culture team to enhance internal cost planning and maintain BlueRock’s operations within clearly defined financial guardrails.</span></div>
<div><span style="font-size: 11pt;">&nbsp;</span></div>
<div><strong style="font-size: 11pt;">Cross-Functional Partnership</strong></div>
<div><span style="font-size: 11pt;">Collaborate with R&amp;D, Program Management, People &amp; Culture, and other functions to integrate operational plans into a cohesive financial view</span></div>
<div><span style="font-size: 11pt;">Support financial oversight of sponsored research agreements, partnerships, and other collaborations</span></div>
<div><span style="font-size: 11pt;">Provide ad hoc analytical support on strategic and operational topics as needed</span></div>
<div><strong style="font-size: 11pt;">&nbsp;</strong></div>
<div><strong style="font-size: 11pt;">Minimum Qualifications</strong></div>
<div><span style="font-size: 11pt;">Bachelor’s degree required; Master’s degree (MBA, MS, or equivalent) preferred</span></div>
<div><span style="font-size: 11pt;">14+ years of experience across FP&amp;A, public accounting, banking, consulting, or related fields</span></div>
<div><span style="font-size: 11pt;">7+ years supporting pre-clinical and clinical-stage drug development; commercial experience a plus</span></div>
<div><span style="font-size: 11pt;">Demonstrated experience influencing enterprise-level strategic and capital allocation decisions</span></div>
<div><span style="font-size: 11pt;">Strong track record of building and leading high-performing FP&amp;A teams</span></div>
<div><span style="font-size: 11pt;">Experience implementing and scaling financial planning and reporting tools</span></div>
<div><span style="font-size: 11pt;">Advanced proficiency in Excel, PowerPoint, and financial modeling; strong systems aptitude</span></div>
<div><span style="font-size: 11pt;">Deep understanding of accounting principles and financial statements</span></div>
<div><span style="font-size: 11pt;">Exceptional ability to synthesize complex data into clear strategic insights and recommendations</span></div>
<div><span style="font-size: 11pt;">Executive-level communication skills with a consultative, business-partner mindset</span></div>
<div><span style="font-size: 11pt;">&nbsp;</span></div>
<div><u style="font-size: 11pt;"><strong>Equal Opportunity Workplace: </strong></u><em><span style="font-size: 11pt;">At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace.&nbsp; Please let us know if you require disability-related accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs.</span></em></div>
<div><span style="font-size: 11pt;">&nbsp;</span></div></br><b>undefined</b></br>undefined</br><b>undefined</b></br>undefined</br>]]></description><link>http://biotechroles.com/senior-director-financial-planning-and-analysis-bluerock/69d5d363c8e81216cd0c6837</link><guid isPermaLink="true">http://biotechroles.com/senior-director-financial-planning-and-analysis-bluerock/69d5d363c8e81216cd0c6837</guid><pubDate>Wed, 08 Apr 2026 04:02:43 GMT</pubDate><company>BlueRock</company><location>Cambridge, Massachusetts</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Director, Process Development]]></title><description><![CDATA[<div>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values,&nbsp;<strong>Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome</strong>, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.</span></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><strong><span style="font-size: 11.0pt; line-height: 115%;">Position Overview</span></strong></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;">Kyverna is seeking a </span><span style="font-size: 11.0pt; line-height: 115%;"><strong>Sr. Director, Process Development</strong> to lead a team of scientists and engineers responsible for the development of robust processes used to isolate, modify, expand, and purify autologous engineered T-cell products. This individual develops the overall process optimization and innovation strategy, leads the technical transfer of process improvements to external partners, authors/reviews regulatory documents, aligns plans with health authorities, and supports the manufacture of clinical and commercia supplies. This individual designs experiments and creates objectives, timelines, resource plans, and budgets to support the company’s goals. The role requires strong partnership with functions within technical operations including Analytical Development, Quality, and Manufacturing, and with other internal and external stakeholders. The ideal candidate has a strong technical background in late-stage/commercial cell therapy development, approval and commercialization, and has strong leadership, strategic planning, communication, and project management skills.</span></p>
<p style="margin: 0in 0in 8pt; line-height: 115%; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11.0pt; line-height: 115%;"><br><strong>Department:</strong> Technical Development<br><strong>Location:</strong> Emeryville, CA (Hybrid: 2 days a week) or West Coast Remote<br><strong>Reports To:</strong> Executive Director, Head of Technical Development<br></span></p>
</div></br><b>Responsibilities</b></br><ul style="margin-bottom: 0in; margin-top: 0px;">
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Identify life-cycle management process improvement options that improve robustness, increase capacity, and reduce cost of goods to support the company’s aspirations to be the leader in the autoimmune CAR T space.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Partner with the life-cycle team leaders, clinical development, commercial, and business development teams to create the optimization and innovation roadmap.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Identify opportunities for team synergies and/or product improvements across different products and platforms.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Lead the process development function including the in-house laboratories.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Manage the design and execution of process development plans, including studies that support pre-clinical and clinical development stages.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Design process characterization plans and process control strategies.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Support the optimization of plasmids, vectors, and product delivery methods.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Lead the execution of laboratory studies, technical assessments for engineering and process changes, and documentation generation pertaining to process development, qualification, and validation.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Oversee the execution of studies that support process development, process characterization, and life-cycle change management to ensure on time delivery of projects.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Author and review process related documents, including risk assessments, technical protocols and reports, batch records, change controls, investigation reports, and corrective and preventative actions. </span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Author and review CMC sections of regulatory documents in support of both clinical trial (IND/IMPD) and commercial therapeutic applications (BLA/MAA).&nbsp;&nbsp;&nbsp; </span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Product Supply Strategy</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Support the characterization of critical raw materials (cell banks, plasmids, reference standards, etc.).</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Support the creation of the product supply strategy, including assessments for in-house versus outsourced activities.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Design processes that ensure compliance with Good Manufacturing Practices (cGMP) and other regulatory requirements.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Manage the tech transfer for clinical and commercial manufacturing.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Team Leadership and Development</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Build a high functioning and performing team that’s delivers meaningful results.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Foster a culture of innovation, collaboration, and continuous improvement.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Provide mentorship, guidance, and career development opportunities for team members.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Regulatory and Quality Compliance</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Ensure all development activities comply with regulatory standards, including expectations from FDA, EMA, and other global health authorities.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Collaborate with the Quality team to implement and maintain SOPs, quality systems, and documentation.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Develop and manage the overall process development budget operational and capital expenses and resource plan.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Allocate resources effectively to meet project timelines and objectives.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Collaboration and Communication&nbsp; </span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Establish and ensure strong relationships with key partners in Analytical Development, Manufacturing, Quality, Clinical and Regulatory.&nbsp; </span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Function as a key liaison with internal and external stakeholders on process development topics.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Develop and maintain relationships with contract development and manufacturing organizations (CDMOs) and other external partners.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Serve as the accountable technical interface between Kyverna Process Development and the process development department of CDMO partners.</span></li>
<li style="margin: 0in 0in 0in 0px; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 11pt;">Represent the company in interactions with regulatory agencies, industry conferences, and scientific meetings.</span></li>
</ul></br><b>Qualifications</b></br><ul type="disc" style="margin-bottom: 0in; margin-top: 0px;">
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Advanced degree (PhD) in cell biology, Immunology, Molecular Biology, Chemical Engineering, Biotechnology or equivalent is preferred.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">15+ years of experience in the biotechnology or pharmaceutical industry with a focus on late-stage/commercial cell therapy, biologics, or related field</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Proven expertise in CAR-T (or other ex-vivo gene modified) cell therapy process development, process characterization, tech transfer and comparability assessment.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Knowledge of regulatory requirements and quality standards for cell therapies.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Experience advancing product development on closed automated platforms or practical know-how of application of process automation in support of cell therapy processes is preferred.&nbsp;</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Established track record of success supporting early and late-stage CMC and clinical product development teams.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Expertise with cGMP manufacturing as well as associated regulations and requirements for pharmaceuticals and devices.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Excellent interpersonal, verbal and written communication skills.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to function efficiently and independently in a changing environment.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to foster a strong team-first environment to enable delivery of company goals.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Demonstrated success in leading high performing development teams and growing talent.</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Demonstrated capacity to think creatively when addressing complex situations.&nbsp;</li>
<li style="line-height: normal; margin-top: 0in; margin-right: 0in; margin-bottom: 8pt; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to collaborate and communicate effectively with Kyverna Leadership, Analytical Development, Manufacturing, Quality, Clinical and Regulatory teams and with external business partners and Regulatory Authorities.</li>
</ul></br><div><span style="font-size: 9pt; line-height: 115%;">The national salary range for this position is from $250,000 to $275,000 USD annually. This salary range is an estimate of what we reasonably expect to pay for this posted position, and the actual salary may vary based on various factors, including without limitation individual education, experience, tenure, skills and abilities, as well as internal equity and alignment with market data.&nbsp; This position is also eligible for bonus, benefits, and participation in Company’s stock plan.</span></div>]]></description><link>http://biotechroles.com/sr.-director-process-development-kyverna/69d5d35dc8e81216cd0c6835</link><guid isPermaLink="true">http://biotechroles.com/sr.-director-process-development-kyverna/69d5d35dc8e81216cd0c6835</guid><pubDate>Wed, 08 Apr 2026 04:02:37 GMT</pubDate><company>Kyverna</company><location>Emeryville, CA</location><salary>$180000-260000</salary><type>Full Time</type></item><item><title><![CDATA[Senior Director, Business Development and Alliance Management]]></title><description><![CDATA[<p>The Senior Director of Business Development and Alliance Management will lead strategic initiatives to identify, evaluate, and secure partnerships that accelerate Janux’s pipeline and platform capabilities. This role combines business development expertise and alliance management to shape corporate strategy and maintain a competitive edge in the evolving biotech landscape.</p></br><b>ESSENTIAL FUNCTIONS AND RESPONSIBILITIES</b></br>
<li>Proactively identify and evaluate strategic growth opportunities through potential collaboration partnerships that align with Janux’s pipeline, platform, and corporate objectives.</li>
<li>Participate in and, as appropriate, lead deal structuring, negotiation, and execution, ensuring alignment with Janux’s long‑term strategic and financial goals.</li>
<li>Coordinate the execution of strategic initiatives, by developing and tracking implementation plans, ensuring focus and discipline to achieve organizational goals.</li>
<li>Oversee alliance management activities, ensuring effective communication, issue resolution, and achievement of partnership objectives. Play a critical part in managing and strengthening external collaborations.</li>
<li>Serve as a key point of escalation and problem‑solving for partnership challenges, working cross‑functionally to drive successful outcomes.</li>
<li>Partner with internal teams (R&amp;D, Clinical Development, Legal, Finance, and Program Management) to ensure aligned execution and value realization across collaborations.</li>
<li>Partner closely with internal stakeholders and external organizations to ensure effective governance, seamless execution, and strategic alignment across a dynamic portfolio of partnerships.</li>
<li>Represent Janux at industry conferences, investor meetings, and strategic forums, and provide concise summaries of key insights to the organization.</li>
</br><b>EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES</b></br><div>

<li>Advanced degree in Life Sciences, Business, or related field; MBA or PhD preferred.</li>
<li>10+ years of experience in biotech/pharma business development and alliance management with a strong preference for oncology and autoimmune modalities.</li>
<li>Proven track record of executing strategic partnerships, alliance management, and licensing deals.</li>
<li>Strong understanding of biopharma R&amp;D, clinical development, and regulatory pathways.</li>
<li>Exceptional negotiation, communication, and leadership skills.</li>
<li>Ability to thrive in a fast-paced, lean biotech environment.</li>

<p>&nbsp;</p>
<p><strong>Travel Requirements</strong></p>
<ul type="disc">
<li>Domestic and/or international travel may be required.</li>

</ul></div></br><div><b style="font-size: 12pt">Job Type:&nbsp;</b><span style="font-size: 12pt">Full-time</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">Benefits:</b></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Annual bonus program</span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Incentive stock option plan</span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">401k plan with flat non-elective employer contribution </span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Comprehensive medical insurance with 90-100% employer-paid premiums </span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Dental and vision insurance</span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity) </span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Unlimited PTO  </span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Generous holiday schedule; includes summer and winter company shutdown </span></div><div><span style="font-size: 10pt;">·</span><span style="font-size: 7pt;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt;">Relocation assistance</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">Schedule:</b></div><div><span style="font-size: 10pt">·</span><span style="font-size: 7pt">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt">Monday to Friday</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">Work authorization:</b></div><div><span style="font-size: 10pt">·</span><span style="font-size: 7pt">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt">United States (Required)</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">Additional Compensation:</b></div><div><span style="font-size: 10pt">·</span><span style="font-size: 7pt">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt">Annual targeted bonus %</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">Work Location:</b></div><div><span style="font-size: 10pt">·</span><span style="font-size: 7pt">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="font-size: 12pt">On site (San Diego, CA)</span></div><div><span style="font-size: 12pt">&nbsp;</span></div><div><b style="font-size: 12pt">EQUAL OPPORTUNITY EMPLOYER:</b></div><div><span style="font-size: 12pt">Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.</span></div><div><br></div><div><br></div><div><b><span style="font-size: 16px">Notice to Recruiters and Third-Party Agencies</span></b></div><div><span style="font-size: 16px">The Talent Acquisition team manages the recruitment and employment process for Janux. To protect the interests of all parties involved, Janux will only accept resumes from a recruiter once a fully-executed search agreement is in place. Agencies are hereby specifically directed not to contact Janux employees directly in an attempt to present candidates. Janux will consider any candidate for whom an Agency and/or Recruiter has submitted an unsolicited resume to have been referred, free of any charges or fees.</span></div>]]></description><link>http://biotechroles.com/senior-director-business-development-and-alliance-management-janux/69d5d359c8e81216cd0c6834</link><guid isPermaLink="true">http://biotechroles.com/senior-director-business-development-and-alliance-management-janux/69d5d359c8e81216cd0c6834</guid><pubDate>Wed, 08 Apr 2026 04:02:33 GMT</pubDate><company>Janux</company><location>San Diego, CA</location><salary>$180000-280000</salary><type></type></item><item><title><![CDATA[Backend Engineer Tech Lead - Bloom]]></title><description><![CDATA[<div>At Sword, we’re building AI to heal billions and unlock humanity’s full potential. In doing so, we’re pioneering AI Care, a fundamentally new approach to healthcare built for medical reasoning, safety, and real-time treatment, not generic technology applied after the fact. As both a clinical-centric frontier AI lab and an applied AI platform, Sword is reimagining how care is delivered at scale, removing traditional barriers like appointments, waiting rooms, and stigma so more people can access the care they need—and ultimately get back to lives lived in full.<br><br>Since 2020, Sword has expanded across physical therapy, women’s health, cardiometabolic, and mental health, and is now moving beyond the session to a fully AI-native, 24/7 care program that brings physical activity, therapeutic exercise, psychotherapy, nutrition, and behavior change into one connected experience. More than 700,000 members across three continents have completed over 10 million AI sessions, helping 1,000+ enterprise clients avoid more than $1 billion in unnecessary healthcare costs. Backed by 42 clinical studies, 44+ patents, and more than $500 million raised from leading investors including Khosla Ventures, General Catalyst, and Founders Fund, Sword is defining a new standard for healthcare.</div><div><br></div><div>
<p>As a Backend Tech Lead, you will establish the technical vision and scale the AI-driven infrastructure powering Bloom’s real-time clinical care. You will lead and mentor a high-performance engineering team, ensuring excellence through automated pipelines, robust architecture, and continuous skill development. By partnering with Product and Infrastructure teams, you will drive the software lifecycles necessary to expand our care categories across every life stage. Your role balances hands-on technical leadership with a focus on team motivation, performance monitoring, and the recruitment of top-tier talent. Ultimately, you will bridge technical innovation with operational success to keep Bloom at the forefront of accessible health technology.</p>
<p>&nbsp;</p>
<p>Today, 1 in every 3 women suffer from a pelvic-health disorder and Bloom is here to change that.</p>
<p>Sword Health developed Bloom to connect millions of women with accessible pelvic-health care, using the most innovative technology available today. Bloom includes customized guidance from Pelvic Health Specialists, an intra-vaginal biofeedback device, and a mobile app to track real-time results and progress. Women meet with Pelvic Health Specialists remotely and progress through the program from the comfort of home, on their own time.</p>
<p>Starting with pelvic health and now expanding into menopause, fertility, pregnancy, and postpartum care, Bloom is powered by the same AI Care model driving Sword's platform: a continuous interaction between the member, an AI health specialist (Phoenix), and a human clinician.</p>
<p><br>To get to know more about our Tech Stack, check <a href="https://stackshare.io/sword-health/sword-health">here</a>.</p>
</div></br><b></b></br><div><strong>AI</strong>&nbsp;<strong>Proficiency at Sword Health</strong>
<p>AI fluency is a core expectation at Sword Health. Every candidate is assessed against our three-level framework — be ready to share real examples of how AI is already part of how you work.</p>

<li>
<p>Explorer (Level 1) — Uses AI daily to boost personal productivity</p>
</li>
<li>
<p>Builder (Level 2) — Creates workflows and tools that elevate the whole team</p>
</li>
<li>
<p>Integrator (Level 3) — Embeds AI into products and processes at scale</p>
</li>

<p>Every hire must demonstrate at least Level 1. The expected level will vary depending on the seniority of the role.</p>
</div></br><b>What you’ll be doing:</b></br>
<li>Lead a team, establishing a technical vision, resolving technical disagreements and ensuring the success of delivered solutions.</li>
<li>Oversee day-to-day operations, delegating tasks and set deadlines/goals.</li>
<li>Stay up to speed with all web technologies, software architecture principles and design patterns, investing in continual improvements.</li>
<li>Use appropriate engineering practices, such fully automated development pipelines and testing.</li>
<li>Understanding the current lifecycle and development of new lifecycles with emphasis on software quality processes.</li>
<li>Work closely with our infrastructure team and other tech leads to define and improve our software and infrastructure architecture.</li>
<li>Maintaining a productive and inspiring working environment for development teams, actively participating in the training/building skills, provide coach, monitoring performance, motivating the team, recognize high performance and reward accomplishments.</li>
<li>Together with the HR team and assisting Hiring Manager, help on R&amp;D process, motivation and retention of new members.</li>
</br><div><span data-sheets-root="1">*This range includes base, variable and equity<br><br>These compensation bands are just the starting point. Once someone joins and proves they’re outlier talent, we adjust quickly to ensure their compensation aligns with their impact.<br><br>Our job titles may span more than one career level. Actual pay is determined by skills, qualifications, experience, location, market demand, and other factors. Compensation details listed in this posting reflect the base salary and any potential variable, bonus or sales incentives, and the Company’s estimation of the value of private company stock options, if applicable. The pay range is subject to change, future value of company stock options is not guaranteed, and compensation may be modified in the future. In addition to our total compensation, Sword offers a number of benefits as listed below.</span></div>
<div>&nbsp;</div>
<div><strong>Portugal - Sword Benefits &amp; Perks:</strong></div>
<div>&nbsp;</div>
<div>• Health, dental and vision insurance</div>
<div>• Meal allowance</div>
<div>• Equity shares</div>
<div>• Remote work allowance</div>
<div>• Flexible working hours</div>
<div>• Work from home</div>
<div>• Discretionary vacation</div>
<div>• Snacks and beverages</div>
<div>&nbsp;</div>
<div><strong>Note:</strong>&nbsp;Please note that this position does not offer relocation assistance. Candidates must possess a valid EU visa and be based in Portugal.</div>
<div>&nbsp;</div>
<div>Sword Health complies with applicable Federal and State civil rights laws and does not discriminate on the basis of Age, Ancestry, Color, Citizenship, Gender, Gender expression, Gender identity, Gender information, Marital status, Medical condition, National origin, Physical or mental disability, Pregnancy, Race, Religion, Caste, Sexual orientation, and Veteran status.</div>]]></description><link>http://biotechroles.com/backend-engineer-tech-lead-bloom-sword-health/69d5d344c8e81216cd0c6832</link><guid isPermaLink="true">http://biotechroles.com/backend-engineer-tech-lead-bloom-sword-health/69d5d344c8e81216cd0c6832</guid><pubDate>Wed, 08 Apr 2026 04:02:12 GMT</pubDate><company>Sword Health</company><location></location><salary>$160000-220000</salary><type></type></item><item><title><![CDATA[Director/Senior Director, GCP & GLP QA (Hybrid)]]></title><description><![CDATA[<div><b>Who we are</b></div><div><br></div><div>REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities.</div><div><br></div><div><strong style="font-size: 12pt;">The opportunity&nbsp;</strong></div>
<div>&nbsp;</div>
<div>The (Sr.) Director, GCP &amp; GLP QA will ensure robust quality assurance systems and procedures are in place to cover REGENXBIO’s pre-clinical activities through clinical trial operations.&nbsp; You will also ensure non-clinical and clinical study execution are compliant with applicable GLP, GCLP, and GCP regulatory requirement as well as regulatory compliance of both internal functions and outsourced activities through oversight of audit activities, utilizing internal and external resources.&nbsp; You will have the opportunity to interface and collaborate with representatives from Clinical Operations, Biometrics, Clinical Development, Regulatory Affairs, Bioanalytical and Preclinical functions.&nbsp;</div></br><b>What you’ll be doing</b></br>
<li>Develops/improves quality programs and procedures to promote, facilitate, and ensure compliance with domestic and international regulatory and industry standards and implement risk-based methodologies to improve efficiencies</li>
<li>Authors and/or reviews and approves Standard Operating Procedures (SOPs)</li>
<li>Reviews/approves or audits clinical and regulatory documentation and other clinical data to ensure accuracy and data integrity for GCP, GLP and GCLP activities as required</li>
<li>Evaluates internal systems and external clinical sites and vendors to determine acceptable compliance to applicable regulations and guidelines.&nbsp; Includes but is not limited to: Clinical Investigator Sites, External CROs/Vendors, Laboratories (clinical and non-clinical), and Trial Master Files</li>
<li>Provides QA support for risk assessment and remediation, and identification and investigation/CAPA of Critical Quality Issues as needed</li>
<li>Oversees/approves non-clinical and clinical supplier and site audit/assessment schedules and facilitates the selection of contract auditors to support the clinical auditor program, as required and per defined budget</li>
<li>Participates in or leads internal and vendor audits to ensure patient safety and data integrity</li>
<li>Oversees clinical quality event and CAPA process</li>
<li>Develops and delivers training on good clinical practice concepts and specific GCP procedures</li>
<li>Represents QA at internal clinical and GCLP team meetings</li>
<li>Supports key quality processes, metrics and indicators to measure trends and improve key quality determinants of GCP and supporting GxP operations</li>
<li>Effectively communicates progress and issue resolution to appropriate internal/external stakeholders</li>
<li>Stays up-to-date with current regulatory changes and industry trends and translates new requirements back to the company’s policies and procedures</li>
<li>Facilitate/lead QA activities for GLP/GCP regulatory inspection management</li>
<li>Promotes a culture of quality and operational excellence through leadership of clinical quality function and partnering with other departments throughout the organization</li>
<li>Plans, resources, and manages staff to ensure efficient operations and encourage development of capabilities</li>
<li>Must be able to travel up to 10-20% of time</li>
</br><b>We set our employees up for success.  To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:</b></br>
<li>BS, preferably in a biological science</li>
<li>Must have direct job experience in a Clinical QA or GLP QA role</li>
<li>Extensive experience conducting and overseeing audits</li>
<li>Extensive knowledge of FDA and EU regulations as well as ICH guidelines</li>
<li>Minimum of 10 years of experience in a Quality Assurance/Quality Systems/Clinical QA position in biopharma / biologics / cellular therapy / gene therapy in a regulated environment</li>
<li>Excellent interpersonal skills and ability to effectively interact with and influence different functional groups at multiple levels of the company</li>
<li>Ability to interpret regulations and practically apply them to procedures</li>
<li>Excellent oral and written communication skills for effectively interfacing with internal and external organizations</li>
<li>Strong project management skills</li>
<li>Ability to manage multiple priorities with aggressive timelines and changing priorities</li>
<li>Must have excellent attention to detail</li>
<li>Possesses strong critical and logical thinking</li>
<li>Basic proficiency in MS PowerPoint, Excel and Word</li>
</br><div><strong style="font-size: 12pt;">Why You Should Apply</strong></div>
<div><span style="font-size: 12pt;">&nbsp;</span></div>
<div><span style="font-size: 12pt;">By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us.&nbsp; By joining our team, you’ll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally.</span></div>
<div><span style="font-size: 12pt;">&nbsp;</span></div>
<div><span style="font-size: 12pt;">We&nbsp;are proud to&nbsp;offer a comprehensive&nbsp;rewards&nbsp;package which includes&nbsp;a&nbsp;market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more!&nbsp;The estimated compensation range for this role is $190,000 to $330,000 annually. The actual salary offered to the final candidate depends on a number of factors&nbsp;such as&nbsp;relevant work experience, skills, education, and years of experience.</span></div>]]></description><link>http://biotechroles.com/directorsenior-director-gcp-and-glp-qa-(hybrid)-regenxbio/69d5d339c8e81216cd0c682f</link><guid isPermaLink="true">http://biotechroles.com/directorsenior-director-gcp-and-glp-qa-(hybrid)-regenxbio/69d5d339c8e81216cd0c682f</guid><pubDate>Wed, 08 Apr 2026 04:02:01 GMT</pubDate><company>Regenxbio</company><location>Remote</location><salary>$160000-220000</salary><type></type></item><item><title><![CDATA[Director, Integrated Insights and Strategy (IIS) Strategy, Abrysvo Adult]]></title><description><![CDATA[<p><span><b>ROLE SUMMARY</b></span></p><p></p><p><span>Pfizer is seeking an experienced <b>Director of Integrated Insights &amp; Strategy (IIS)</b> to serve as a senior strategic thought partner to U.S. brand leadership for a high‑value vaccine. Reporting to the IIS Therapeutic Area Team Lead, this role will act as the senior member of a brand‑aligned team of strategists, responsible for identifying and activating performance opportunities that unlock brand value and advising the business on drivers of transformational change.</span></p><p><span> </span></p><p><span>As part of IIS within Pfizer’s <b>Global Commercial Analytics (GCA)</b> organization, you will help frame complex business challenges in a way that enables clear decision‑making and effective execution to drive impact and unlock value. IIS integrates insights from multiple analytic disciplines across GCA, leading day‑to‑day problem solving, stakeholder engagement, and team leadership. IIS applies deep functional expertise, strong intellectual curiosity, and proprietary GCA analytic capabilities to deliver high‑quality, actionable insights while building trusted partnerships and developing new IIS colleagues.</span></p><p><span> </span></p><p><span>The ideal candidate comes with a proven track record of high-value brand consultancy, with experience framing, designing, and executing solutions to complex business challenges. They will bring in-depth knowledge of multiple analytic disciplines, with a keen understanding of output and quality/timely insight derivation. Their team orientation and collaborative approach, along with their outstanding listening skills and ability to manage through influence, will enable their exceptional intellectual and analytical curiosity to shine. Comfort operating with senior brand leaders, a polished executive presence, and excellent written and verbal communication skills are essential. Success in this role also requires the ability to work proactively and independently when needed, while collaborating effectively to drive change across a matrixed organization.</span></p><p><span> </span></p><p><span><span><b>Commercial Brand Strategy</b></span></span></p><ul><li><p><span><span>Serve as a senior strategic thought partner to U.S. commercial teams, framing and answering high‑impact business questions related to brand strategy, tactics, and investment decisions</span></span></p></li><li><p><span><span>Lead patient‑journey–based business reviews aligned to operating and budgetary goals, surfacing performance opportunities and optimization levers for cross‑functional teams</span></span></p></li><li><p><span><span>Synthesize insights across market research and analytics into clear, compelling narratives with actionable recommendations for senior leadership</span></span></p></li><li><p><span><span>Define key learning objectives and lead the development of integrated market research and analytic plans to address priority business needs</span></span></p></li><li><p><span><span>Build and maintain strong, trusted relationships with Commercial and cross‑functional stakeholders to drive effective strategy development and decision‑making</span></span></p></li></ul><p><span><span><b> </b></span></span></p><p><span><span><b>Promotional Strategy &amp; Execution Insights</b></span></span></p><ul><li><p><span><span>Establish and monitor performance metrics in partnership with cross‑functional teams to assess and enhance the effectiveness of marketing campaigns</span></span></p></li><li><p><span><span>Diagnose performance gaps and recommend data‑driven optimization actions and corrective strategies</span></span></p></li><li><p><span><span>Integrate campaign‑level insights into broader analytic perspectives to inform resource allocation and customer strategy decisions</span></span></p></li><li><p><span><span>Contribute to shaping the forward‑looking vision for brand strategy and execution</span></span></p></li></ul><p><span><span><b> </b></span></span></p><p><span><span><b>Operating Plan Support</b></span></span></p><ul><li><p><span><span>Lead development of Operating Plans in close partnership with key Pfizer stakeholders</span></span></p></li><li><p><span><span>Collaborate with the IIS Lifecycle Strategist (forecasting) and US marketing leads to ensure strategic and financial alignment</span></span></p></li></ul><p><span><span><b> </b></span></span></p><p><span><span><b>Collaboration with Other Analytics Teams</b></span></span></p><ul><li><p><span><span>Orchestrate integration of insights across market research, data science, performance analytics, and media to deliver a unified point of view</span></span></p></li><li><p><span><span>Partner with analytics teams to advance the use of novel data sources</span></span></p></li><li><p><span><span>Contribute to capability advancement through thought leadership and knowledge sharing across the analytics community</span></span></p></li><li><p><span><span>Build AI fluency by applying AI tools in daily work to support better decisions, problem‑solving, and efficiency</span></span></p></li></ul><p></p><h1><b><span><span>Basic Qualifications</span></span></b></h1><ul><li><p><span>BA/BS in Marketing, Psychology, Mathematics, Statistics, or Engineering or similar related field required</span></p></li><li><p><span>8&#43; years in consulting, finance or market analytics</span></p></li><li><p><span>5&#43; years at a high-value level (e.g., US &amp; Global) developing data-driven brand strategy for major assets (&gt;$1B)</span></p></li><li><p><span>Ability to develop analytic plans and lead research projects with a budget of &gt;$1M annually</span></p></li><li><p><span>Demonstrated experience framing, designing, and executing solutions to complex, high‑impact business challenges</span></p></li><li><p><span>Deep expertise across multiple analytic disciplines, including primary market research and secondary data, with strong standards for rigor, quality, and timely insight delivery</span></p></li><li><p><span>Proven track record as a trusted strategic thought partner to senior brand leaders, with the ability to influence decision‑making without formal authority</span></p></li><li><p><span>Highly collaborative and team‑oriented, with strong listening skills and the ability to lead and manage through influence in a matrixed environment</span></p></li><li><p><span>Strong intellectual and analytical curiosity, with the ability to apply creative, innovative thinking to business problem‑solving</span></p></li><li><p><span>Polished executive presence with comfort engaging senior leaders; exceptional presentation and storytelling skills, both verbal and written</span></p></li><li><p><span>Ability to proactively drive work forward independently while collaborating effectively to influence and lead change across all levels of the organization</span></p></li><li><p><span>Excellent communication skills, with the ability to distill complex ideas into clear, actionable messages</span></p></li><li><p><span>Advanced proficiency in PowerPoint and Excel</span></p></li></ul><h1><br /><b><span><span>Preferred Qualifications</span></span></b></h1><ul><li><p><span>MS or MBA preferred</span></p></li><li><p><span>3&#43; years of vaccines experience</span></p></li><li><p><span>Understanding of IQVIA (DDD, LAAD) and other secondary data sources</span></p></li></ul><p><br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.<br /> </p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><p>Limited business travel required</p><p><br /><span><b>OTHER JOB DETAILS</b></span></p><ul><li><span><b>Last Day to Apply</b>: April 13, 2026</span></li><li><span><b>Work Location Assignment</b>: Hybrid, 2-3 days onsite/week, US, UK or EU Commercial Pfizer site required (per Pfizer’s Log in for Your Day Policy)</span></li></ul>&amp;#xa;The annual base salary for this position ranges from $162,900.00 to $271,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/director-integrated-insights-and-strategy-iis-strategy-abrysvo-adult-pfizer/69d576b7c8e81216cd0c4c8f</link><guid isPermaLink="true">http://biotechroles.com/director-integrated-insights-and-strategy-iis-strategy-abrysvo-adult-pfizer/69d576b7c8e81216cd0c4c8f</guid><pubDate>Tue, 07 Apr 2026 21:27:19 GMT</pubDate><company>Pfizer</company><location>United States - Pennsylvania - Collegeville</location><salary>$180000-240000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist]]></title><description><![CDATA[<p><b>COMPANY OVERVIEW</b></p><p><b> </b></p><p>At Pfizer, our purpose is to deliver breakthroughs that transform patients&#39; lives. Central to this mission is our Research and Development team, dedicated to translating advanced science and innovative technologies into impactful therapies and vaccines.  In this role, you will be at the forefront of this effort, ensuring that our daily activities align with our unwavering commitment to quality. Your work will accelerate the delivery of best-in-class medicines to patients globally, fulfilling Pfizer&#39;s commitment to making a meaningful difference in healthcare.</p><p></p><p><b>ROLE SUMMARY</b></p><p></p><p>The Internal Medicine Research Unit (IMRU) at Pfizer seeks a Principal Scientist to lead discovery efforts focused on anti-inflammatory mechanisms in cardiovascular diseases. The successful candidate will drive target identification and early drug development, leveraging both in vitro and in vivo systems to explore immune and cardiovascular biology.  In addition to drug discovery responsibilities, publication in high-impact journals and presentation of research are encouraged. The ideal candidate will bring strong scientific acumen, deep knowledge of immunology and cardiovascular disease, leadership potential, and a collaborative mindset to advance Pfizer’s mission in cardiovascular innovation.</p><p><b> </b></p><p><b>ROLE RESPONSIBILITIES</b></p><p><b> </b></p><ul><li><p>Lead and execute in vitro and in vivo studies to identify novel therapeutic targets and support drug discovery related to immune dysfunction in cardiovascular diseases</p></li><li><p>Apply state-of-the-art cellular, molecular, and animal model techniques to investigate immune mechanisms in cardiovascular pathology</p></li><li><p>Collaborate with cross-functional teams and contribute to project strategy, experimental design, data interpretation, and decision-making in a matrixed research environment</p></li><li><p>Mentor junior scientists and contribute to a culture of scientific rigor, innovation, and collaboration</p></li><li><p>Communicate findings through internal presentations, external conferences, and peer-reviewed publications</p></li></ul><p></p><p><b>QUALIFICATIONS</b></p><p><b> </b></p><p>Basic Qualifications:</p><ul><li><p>Ph.D. in Immunology, Cardiovascular Biology, or a related field, with postdoctoral research experience</p></li><li><p>A minimum of 3 years of relevant industry experience in drug discovery or translational research</p></li><li><p>Demonstrated expertise in inflammation and immunology and/or cardiovascular disease biology</p></li><li><p>Proficiency in both in vitro (e.g., primary immune or vascular cell assays) and in vivo (e.g., rodent models of atherosclerosis) experimental systems</p></li><li><p>Strong analytical and problem-solving capabilities, supported by a track record of impactful scientific contributions</p></li><li><p>Excellent written and verbal communication skills, with the ability to effectively present complex scientific concepts</p></li><li><p>Proven ability to work collaboratively in multidisciplinary teams</p></li></ul><p></p><p>Preferred Qualifications:</p><ul><li><p>Experience in leveraging human data sources (e.g., genetics, multi-omics, clinical datasets) to inform and guide therapeutic discovery and development</p></li><li><p>Proven leadership and mentoring experience, with a commitment to fostering scientific excellence and team development</p></li><li><p>Experience in leading drug discovery projects, with a demonstrated ability to drive scientific strategy and execution</p></li></ul><p></p><p>  <br /> </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p>Ability to work in a laboratory environment; capacity to lift and move laboratory materials and equipment (up to 25 lbs) as needed.</p><p></p><p><u>Additional Information: </u></p><ul><li>Relocation support available</li><li>Work Location Assignment: On Premise</li><li>Last Day to Apply: April 17, 2026</li></ul>&amp;#xa;The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div><p style="text-align:inherit"></p></div></div></div></div></div></div></div>&amp;#xa;Research and Development&amp;#xa;]]></description><link>http://biotechroles.com/principal-scientist-pfizer/69d576b6c8e81216cd0c4c8e</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-pfizer/69d576b6c8e81216cd0c4c8e</guid><pubDate>Tue, 07 Apr 2026 21:27:18 GMT</pubDate><company>Pfizer</company><location>United States - Massachusetts - Cambridge</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Workfront Business Product Lead, Director]]></title><description><![CDATA[<p>We are transforming how content is created, reviewed, and delivered – fast, compliant and at scale. Our End-to-End Content Strategy connects AI, automation, data and smart workflows to deliver high-quality content globally.</p><p></p><p>At the center of this transformation is a connected product ecosystem, powered by AI-enabled solutions, and data-driven insights, combined with streamlined processes that enhance productivity and maximize marketing ROI. Our commitment is clear: to deliver a streamlined, compliant, user-centric AI-enabled content experience that supports our business globally.</p><p></p><p>If you are passionate about innovation, collaboration and building products that sit at the intersection of strategy, user experience and technology, join us. Be part of a team that’s setting the North Star for content excellence, leveraging AI and automation to unlock new possibilities and deliver meaningful impact globally.</p><p></p><p><span class="emphasis-3"><b>ROLE PURPOSE</b></span></p><p><b> </b></p><p>The <b>Workfront Business Product Lead</b> drives the success of marketing teams by leveraging marketing automation through <b>Adobe Workfront</b>, developing and delivering product offerings that support end-to-end workflows for colleagues and agency partners.<br /><br />This role serves as the voice of the customer, shaping product strategy and prioritization to improve operational execution, user experience, and measurable outcomes.</p><p></p><p>This role is responsible for translating business priorities into scalable product capabilities, guiding the evolution from foundational enablement to intelligent automation.</p><p></p><p>This role is accountable for execution excellence—from early concept and prototyping through enterprise-wide adoption—driving measurable outcomes in user productivity, quality, compliance confidence, and speed to market.</p><p></p><p>This is an exciting position that has an opportunity to partner with AI teams for further integration.</p><p></p><p></p><p><span class="emphasis-3"><b>ROLE RESPONSIBILITIES </b></span></p><p><b>Product Strategy​ and Value Delivery</b></p><ul><li><p>Shape and refine Workfront product strategy and vision that delivers value to customers, aligned to marketing organization priorities.</p></li><li><p>Develop and deliver innovative product offerings supporting end-to-end workflows for internal teams and agency partners</p></li><li><p>Lead work management improvements that strengthen Workfront as a central hub for operational execution—connecting teams and streamlining workflows</p></li><li><p>Build and curate a prioritized backlog to address fundamental gaps impacting Workfront user experience and operational efficiency</p></li><li><p>Establish and maintain product governance, including prioritization frameworks, decision rights, and cross‑functional alignment mechanisms</p></li><li><p>Ensure transparency into backlogs and product performance through data -driven metrics (e.g., adoption, efficiency, reuse, impact) to inform ongoing optimization</p></li><li><p>Manage Stakeholder buy-in, business requirement alignment and coordination of digital delivery to market release plans</p></li></ul><p></p><p><b>Cross-functional Collaboration and Stakeholder management</b>​</p><ul><li><p>Collaborate with business, engagement, and operations leaders to incorporate user feedback, adoption signals, and market readiness into product decisions</p></li><li><p>Collaborate with internal digital teams, UX experts, and stakeholders to implement a roadmap that streamlines processes while capturing critical metadata for optimization</p></li><li><p>Partner with peer platform owners to ensure seamless integration across the broader marketing and technology ecosystem</p><p></p></li></ul><p><b>Change Management, Enablement and Continuous improvement​</b></p><ul><li><p>Enable product rollout and scaling efforts, ensuring organizational readiness across processes, systems, and support teams</p></li><li><p>Partner with Content at Scale and change management teams to deliver cohesive onboarding, communications, and adoption experiences</p></li><li><p>Lead continuous improvement cycles that incorporate user feedback, performance data, and evolving business needs into future releases and roadmap planning</p></li><li><p>Clearly articulate value propositions that map back to business needs</p><p></p></li></ul><p><span class="emphasis-3"><b>BASIC QUALIFICATIONS</b></span></p><ul><li><p>8&#43; years in product management/platform delivery</p></li><li><p>Bachelor&#39;s degree required</p></li><li><p>Experience with regulated workflows in pharma/life sciences strongly preferred​​</p></li><li><p>Experience stabilizing/optimizing Workfront environments user experience improvement efforts</p></li><li><p>Familiarity with integrated ecosystems spanning Workfront and adjacent platforms (e.g., DAM-related dependencies)</p></li><li><p>Experience influencing and managing cross‑functional stakeholders with conflicting viewpoints to drive consensus and progress</p></li><li><p>Proficient in mapping user journeys to uncover challenges and opportunities for experience optimization</p></li><li><p>Skilled at translating insights into innovative solutions and well‑defined user stories for development teams</p></li><li><p>Knowledge of marketing operations is considered a strong asset​</p></li><li><p>Exceptional analytical skills to interpret usage data and derive actionable insights​</p></li><li><p>Strong communication skills, able to engage senior stakeholders and align diverse technical and business teams​ BA/BS in business, engineering, computer science, or other related fields</p></li><li><p>Passion for user-centric design and AI innovation, with a collaborative mindset and resilience in fast-paced, matrixed environments​</p></li><li><p>Excellent communication and influence skills, comfortable engaging executive stakeholders and global teams</p></li></ul><p><br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.<br /><br /><span class="emphasis-3"><b>PREFERRED QUALIFICATIONS</b></span></p><ul><li>Experience with regulated workflows in pharma/life sciences strongly preferred​​</li><li>Master’s degree in business, Computer Science, Marketing, or a related field; MBA or advanced certification in Product Management/AI preferred​<br /> </li></ul><p><span class="emphasis-3"><b>OTHER JOB DETAILS</b></span></p><ul><li><span><b>Last Day to Apply:</b> April 20, 2026</span></li><li><span><b>Work Location Assignment: </b>Hybrid, 2-3 days onsite/week, US Commercial Pfizer site required (per Pfizer’s Log in for Your Day Policy)</span><br /> </li></ul><p>#AdobeWorkFront #ProductManager #JIRA</p>&amp;#xa;The annual base salary for this position ranges from $162,900.00 to $271,500.00.* In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;* The annual base salary for this position in Tampa, FL ranges from $146,600.00 to $244,400.00.&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/workfront-business-product-lead-director-pfizer/69d576b5c8e81216cd0c4c8d</link><guid isPermaLink="true">http://biotechroles.com/workfront-business-product-lead-director-pfizer/69d576b5c8e81216cd0c4c8d</guid><pubDate>Tue, 07 Apr 2026 21:27:17 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Associate Scientist, Diagnostic Assays]]></title><description><![CDATA[<p><b>Role Summary</b></p><p></p><p>The position requires an analyst to perform ligand-binding and diagnostic assay activities, including but not limited to assay development and clinical testing. The position also requires documentation of new methods and writing summary reports to related work activities. As an integral member of our dynamic team, the incumbent must have a strong work ethic, be highly collaborative with the other group members, have an understanding of robotic methods used in assay development, experience in bioanalytical method validation, and work in cross-functional teams. All of the above includes practicing laboratory safety at all times and adherence to GLP compliance.</p><p></p><p><b>Role Responsibilities</b></p><ul><li><p>Perform all functions to support assay development and analysis of non-clinical and clinical samples.</p></li><li><p>Perform assays to support critical assay reagent testing, assay development/ troubleshooting.</p></li><li><p>Present progress on assay development projects to colleagues and senior management.</p></li><li><p>Collect, collate and analyze data on a per project basis to support troubleshooting, qualification and other lab projects.</p></li><li><p>Assist in ordering supplies from internal inventory and order/prepare reagents/supplies necessary for assay work.</p></li><li><p>Assist in updating and writing documents associated with assays, including information/data archiving, SOPs and status reports.</p></li><li><p>Stay current on all departmental and corporate training.</p></li><li><p>Build team skills and collaborate effectively within the work group.</p></li></ul><p></p><p><b><u>Qualifications</u></b></p><p><b>Must-Have</b></p><ul><li><p>BA/BS with 0 to 2 years of experience</p></li><li><p>Laboratory experience in a biology, immunology and/or microbiology</p></li><li><p>Good verbal and written communication skills are required</p></li><li><p>Proficiency in the use of Word, Excel, PowerPoint and relevant scientific software.</p></li></ul><p></p><p><b>Nice-to-Have</b></p><ul><li><p>Pharmaceutical and biotech drug discovery experience</p></li><li><p>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving.</p></li></ul><p></p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><ul><li><p>Sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis.</p></li></ul><p></p><p><br /><b>Work Location Assignment: On Premise</b></p>&amp;#xa;The annual base salary for this position ranges from $60,200.00 to $100,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Research and Development&amp;#xa;]]></description><link>http://biotechroles.com/associate-scientist-diagnostic-assays-pfizer/69d576b4c8e81216cd0c4c8c</link><guid isPermaLink="true">http://biotechroles.com/associate-scientist-diagnostic-assays-pfizer/69d576b4c8e81216cd0c4c8c</guid><pubDate>Tue, 07 Apr 2026 21:27:16 GMT</pubDate><company>Pfizer</company><location>United States - New York - Pearl River</location><salary>$85000-110000</salary><type>Full time</type></item><item><title><![CDATA[AI-ZJ2-高级医学信息沟通专员-杭州]]></title><description><![CDATA[<h2 style="color:!important"><span style="color:#000000"><b><span style="font-size:inherit">Prior Job Description&#xff08;既往职位描述&#xff09;</span></b></span></h2><ul><li style="font-size:inherit !important"><p style="font-size:inherit !important"><b><span style="font-size:inherit">工作职责&#xff1a;</span></b></p><p style="font-size:inherit !important"><span style="font-size:inherit">在公司政策和程序指引下传达医学信息,以合法合规方式达成公司指标&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">及时提供市场信息并做出适当建议&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">申请和报销 PIM、院内会和MICS区域内的院间会&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">与客户建立良好关系&#xff0c;保持公司形象&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">能够就合规要求严于律己&#xff0c;严格管理自己的行为&#xff0c;确保日常工作全部遵循公司政策、行业准则以及相关法律法规政策&#xff0c;包括但不限于&#xff1a;积极完成合规培训&#xff1b;严守诚信&#xff0c;保持真实透明&#xff0c;如实准确报销真实发生且符合公司政策的费用&#xff1b;如对工作中遇有合规疑问主动向经理、卫星团队/法务/内控/合规团队咨询。</span></p><p style="font-size:inherit !important"></p><p style="font-size:inherit !important"><b><span style="font-size:inherit">任职条件&#xff1a;</span></b></p><p style="font-size:inherit !important"><span style="font-size:inherit">认可公司价值观&#xff0c;为人诚实正直&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">具有良好的沟通能力和强烈的学习愿望&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">工作积极&#xff0c;乐观向上&#xff0c;善于自我激励和承受压力&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">大专或以上学历&#xff0c;医学&#xff0c;药学&#xff0c;生命科学等相关专业优先&#xff1b;</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">熟练使用MS Office&#xff0c;英语良好。</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">内部候选人申请岗位空缺还须确保本人在前12个月内在辉瑞工作期间无合规警告以上处分记录并需对过往接受的任何等级的合规处分记录进行如实披露&#xff0c;以及没有正在被调查中 。</span></p><p style="font-size:inherit !important"><span style="font-size:inherit">  </span></p><p style="font-size:inherit !important"><span style="font-size:inherit">  </span></p></li></ul><ul><li style="font-size:inherit !important"><p></p></li></ul>&nbsp;&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/ai-zj2-pfizer/69d576b3c8e81216cd0c4c8b</link><guid isPermaLink="true">http://biotechroles.com/ai-zj2-pfizer/69d576b3c8e81216cd0c4c8b</guid><pubDate>Tue, 07 Apr 2026 21:27:15 GMT</pubDate><company>Pfizer</company><location>China - Zhejiang - Hangzhou</location><salary>$28000-45000</salary><type>Full time</type></item><item><title><![CDATA[Pharmaceutical Attendant B1 M19]]></title><description><![CDATA[<p><span class="emphasis-3"><b>Use Your Power for Purpose</b></span></p><p>Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them.</p><p></p><p></p><p><span class="emphasis-3"><b>What You Will Achieve</b></span></p><p>In this role, you will:</p><ul><li><p>Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.</p></li><li><p>Manage personal time and professional development, being accountable for results.</p></li><li><p>Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.</p></li><li><p>Identify and solve moderately routine problems.</p></li><li><p>Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.</p></li><li><p>Ensure work is reviewed for accuracy, quality, and adherence to standards.</p></li><li><p>Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run.</p></li><li><p>Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations.</p></li><li><p>Perform in-process quality inspections, and seek to implement process and safety improvements.</p></li></ul><p></p><p></p><p><span class="emphasis-3"><b>Here Is What You Need </b></span>(Minimum Requirements)</p><ul><li><p>High School Diploma or GED with 2&#43; years of relevant experience</p></li><li><p>Strong analytical and problem-solving skills</p></li><li><p>Excellent problem-solving and decision-making skills</p></li><li><p>Excellent communication and interpersonal skills</p></li><li><p>Ability to work independently and as part of a team</p></li><li><p>Detail-oriented with strong organizational skills</p></li></ul><p></p><p></p><p><b><span class="emphasis-3">Bonus Points If You Have</span> </b>(Preferred Requirements)</p><ul><li><p>Previous experience in cGMPs (current Good Manufacturing Practices) environment</p></li><li><p>Proficiency in using manufacturing software and tools</p></li><li><p>Ability to adapt to changing priorities and work in a fast-paced environment</p></li><li><p>Demonstrated leadership skills and ability to mentor team members</p></li><li><p>Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity</p></li></ul><p></p><p>  </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><ul><li><p><span>Must be able to lift 10-20 lbs. frequently and up to 45 lbs. sporadically, including lifting above shoulders.</span></p></li><li><p><span>Must be able to withstand exposure to inks, solvents, heat, steam and liquids.</span></p></li><li><p><span>Walk and stand for up to 8 to 12 hours depending on assigned area.</span></p></li><li><p><span>Must be able to aseptically gown.</span></p></li><li><p><span>Vision must be correctable to 20/20.</span></p></li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><ul><li><p><span>Able to work rotating shifts, holidays, nights and weekends as required</span></p></li><li><p><span>Must be able to gown aseptically and retain certification.</span></p></li></ul><p></p><p></p><p><span class="emphasis-3">Other Job Details:</span></p><ul><li><p>Last day to apply: April 14th</p></li><li><p>Work Location Assignment: On site</p></li></ul>&amp;#xa;The salary for this position ranges from $18,99 to $31,65 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Kansas - Mcpherson location.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Manufacturing&amp;#xa;]]></description><link>http://biotechroles.com/pharmaceutical-attendant-b1-m19-pfizer/69d576b0c8e81216cd0c4c8a</link><guid isPermaLink="true">http://biotechroles.com/pharmaceutical-attendant-b1-m19-pfizer/69d576b0c8e81216cd0c4c8a</guid><pubDate>Tue, 07 Apr 2026 21:27:12 GMT</pubDate><company>Pfizer</company><location>United States - Kansas - McPherson</location><salary>$42000-55000</salary><type>Full time</type></item><item><title><![CDATA[Junior Associate]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. </p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li>Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.</li><li>Manage personal time and professional development, being accountable for results.</li><li>Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.</li><li>Identify and solve moderately routine problems.</li><li>Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.</li><li>Ensure work is reviewed for accuracy, quality, and adherence to standards.</li><li>Operate assembly and packaging equipment according to Standard Operating Procedures and Batch Records, ensuring equipment is operational post-maintenance with accurate and complete maintenance logs.</li><li>Monitor, evaluate, and adjust processes or packaging equipment to enhance quality and efficiency, performing calculations for percent accountabilities, reconciling numerical values, and executing all manual packaging and inspection duties as required by the operating unit.</li></ul><p></p><p><b>Here Is What You Need </b>(Minimum Requirements)</p><ul><li>High School Diploma or GED with 2&#43; years of relevant experience</li><li>Proficiency in math and reading skills for understanding Standard Operating Procedures, Good Manufacturing Practices (also cGMP), and Batch Record comprehension</li><li>Ability to follow instructions provided in written, oral, or diagram form</li><li>Capability to perform tasks under demanding conditions</li><li>Basic computer skills for data entry and equipment operation</li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements)</p><ul><li>Experience in a pharmaceutical or manufacturing environment</li><li>Knowledge of Good Manufacturing Practices (GMP)</li><li>Familiarity with automated packaging equipment</li><li>Strong problem-solving skills</li><li>Ability to work independently with minimal supervision</li><li>Excellent communication skills</li><li>Strong attention to detail</li><li>Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity</li></ul>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Manufacturing<p></p><p></p>]]></description><link>http://biotechroles.com/junior-associate-pfizer/69d576b0c8e81216cd0c4c89</link><guid isPermaLink="true">http://biotechroles.com/junior-associate-pfizer/69d576b0c8e81216cd0c4c89</guid><pubDate>Tue, 07 Apr 2026 21:27:12 GMT</pubDate><company>Pfizer</company><location>India - Vizag</location><salary>$8000-15000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate, Analytics]]></title><description><![CDATA[<p>The Global Commercial Analytics (GCA) team within the Chief Marketing Office (CMO) organization is dedicated to transforming data into actionable intelligence, enabling the business to remain competitive and innovative in a data-driven world.  We play a pivotal role in extracting insights from large and complex datasets to drive strategic decision-making. Collaborating closely with various subject matter experts across various fields, our team leverages advanced statistical analysis, machine learning techniques, and data visualization tools to uncover patterns, trends, and correlations within the data. Additionally, we are dedicated to delivering new, innovative capabilities by deploying cutting-edge Machine learning algorithms and artificial intelligence techniques to solve complex problems and create value.</p><p></p><p>As a hands-on <b>Senior Associate Analytics</b> within Commercial Decision Analytics, you will design, build, analytics solutions that optimize field force sizing, territory alignment, and commercial ROI across brands and markets. You will collaborate closely with Commercial, Sales Leadership, and Insights teams to transform data into actionable recommendations, deliver clear visualizations and business-ready presentations, and support MMM (Marketing Mix Modeling) in pharma contexts. This is an individual contributor role—not a people manager—ideal for someone who thrives on building, analyzing, and storytelling with data.</p><p></p><p><b>Role Responsibilities:</b></p><p><b>Field Force Sizing &amp; Optimization</b></p><ul><li><p>Build analytical frameworks to determine optimal rep counts, structures, and deployment by market/brand/therapeutic area.</p></li><li><p>Develop models for coverage, reach, frequency, and workload-driven territory design.</p></li><li><p>Support scenario planning/simulation to evaluate alignment strategies and their impact on KPIs.</p></li></ul><p><b>Territory Alignment</b></p><ul><li><p>Execute end-to-end territory alignment workflows using potential, workload, and segmentation data.</p></li><li><p>Maintain assignment rules, constraints, and performance baselines for territory changes<b>.</b></p></li></ul><p><b>Commercial ROI &amp; MMM</b></p><ul><li><p>Contribute to pharma MMM (e.g., regression/Bayesian models with adstock/carryover) to quantify the impact of field, digital, email, media.</p></li><li><p>Build ROI calculators and budget allocation recommendations for launch and established brands<b>.</b></p></li></ul><p><b>Analytics &amp; Visualization</b></p><ul><li><p>Develop Tableau/ PowerBI dashboards and ad hoc reports that translate complex analysis into actionable insights for senior stakeholders.</p></li><li><p>Build data pipelines and self-service assets in Dataiku; author queries in SQL; implement analyses in Python<b>.</b></p></li></ul><p><b>Data Management &amp; Quality</b></p><ul><li><p>Ensure data integrity, freshness, and documentation across CRM, sales, claim/prescription, and market datasets.</p></li><li><p>Contribute to data governance and standardization of metrics/definitions.</p></li></ul><p><b>Stakeholder Collaboration &amp; Storytelling</b></p><ul><li><p>Partner with Commercial, Sales, and Insights teams to understand requirements and present findings clearly, including recommendations and trade-offs.</p></li><li><p>Develop business-ready presentations in PowerPoint synthesizing insights and next-best actions<b>.</b></p></li></ul><p><b>Cross-Functional Collaboration </b></p><ul><li><p>Work closely with Analytics Engineering to ensure the data ecosystem is conducive for data science modeling purposes.</p></li><li><p>Partner with Digital teams to enhance data science capabilities, aligning efforts to leverage digital data sources effectively.</p></li><li><p>Foster collaboration with other teams to ensure seamless integration of data science initiatives across the organization&#39;s infrastructure, promoting efficiency and effectiveness in leveraging data for informed decision-making.</p></li></ul><p></p><p><b>Education and Experience:</b></p><ul><li><p><b>Bachelor’s/Master’s in Statistics, Data Science, Engineering, Economics, or related quantitative field.</b></p></li><li><p><b>Experience: 2–4 years in Commercial Pharma analytics or Sales/Marketing analytics, with hands-on exposure to field force/territory analytics and MMM.</b></p></li></ul><p><b>Skills: </b></p><ul><li><p><b>Tableau / Power BI, SQL, Python, Excel (advanced), PowerPoint (executive storytelling)</b></p></li><li><p><b>Experience with both traditional SQL and modern NoSQL data stores including SQL, and large-scale distributed systems such as Hadoop and or working in Snowflake/Databricks</b></p></li><li><p>Communication: Excellent verbal/written skills to elicit requirements, explain methodology, and present insights to senior business leaders.</p></li><li><p>Experience with supporting commercial strategies and tactics, experience in pharmaceutical or healthcare industry is preferred.</p></li></ul><p><b>Preferred/Good-to-Have</b></p><ul><li><p>Knowledge of Statistical modeling and ML Techniques</p></li></ul><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Marketing and Market Research<p></p><p></p>]]></description><link>http://biotechroles.com/senior-associate-analytics-pfizer/69d576b0c8e81216cd0c4c88</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-analytics-pfizer/69d576b0c8e81216cd0c4c88</guid><pubDate>Tue, 07 Apr 2026 21:27:12 GMT</pubDate><company>Pfizer</company><location>India - Mumbai</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Electrical Maintenance & project Engineer]]></title><description><![CDATA[<h2>Required Qualifications</h2><h3><b>Education</b></h3><ul><li><p>Bachelor’s Degree / Diploma in <b>Electrical Engineering or Electrical &amp; Electronics Engineering</b></p></li></ul><h3><b>Experience</b></h3><ul><li><p>4–6 years of experience (adjustable) in: Electrical engineering for filling or packaging lines Manufacturing plants or industrial project environments</p></li><li><p>Hands‑on experience in <b>installation and commissioning</b> preferred</p></li></ul><p><b>Key Responsibilities</b></p><h3><b>Project Engineering &amp; Execution</b></h3><ul><li><p>Execute electrical scope for <b>new filling line installations, line expansions, and modifications</b></p></li><li><p>Review and finalize: Electrical single-line diagrams (SLD) Power distribution layouts Cable schedules and routing Equipment and panel specifications</p></li><li><p>Coordinate with project stakeholders to meet <b>scope, schedule, cost, and quality targets</b></p></li></ul><h3><b>Electrical Systems &amp; Equipment</b></h3><ul><li><p>Design and supervise electrical systems including: MCCs, PCCs, VFD panels, machine control panels Power distribution for fillers, cappers, labelers, conveyors, case packers Motors, drives, sensors, and actuators (electrical interface)</p></li><li><p>Ensure correct power requirements, grounding, and protection devices</p></li><li><p>Interface with OEM machines and system integrators for electrical integration</p></li></ul><h3><b>Installation, Testing &amp; Commissioning</b></h3><ul><li><p>Supervise electrical installation, cable laying, termination, and panel installation</p></li><li><p>Conduct: Insulation resistance (IR) tests Continuity and earthing checks Power‑up inspections and electrical safety checks</p></li><li><p>Support and execute: FAT, SAT, and site commissioning activities Electrical troubleshooting during startup and trial runs</p></li></ul><h3><b>Safety, Compliance &amp; Standards</b></h3><ul><li><p>Ensure compliance with: Electrical safety standards and statutory regulations Machine safety requirements (interlocks, emergency stops, guarding)</p></li><li><p>Participate in: Risk assessments, HAZOP, and electrical safety audits</p></li><li><p>Ensure documentation and installations comply with <b>ISO, GMP, IS/IEC/NEC standards</b> as applicable</p></li></ul><h2><b>Technical Skills</b></h2><ul><li><p>Strong knowledge of: Industrial electrical systems and power distribution Motors, VFDs, MCCs, relays, breakers, and panels Machine electrical safety and interlocks</p></li><li><p>Ability to read and interpret: Electrical SLDs, wiring diagrams, layout drawings</p></li><li><p>Working knowledge of: PLC panel interfaces and automation coordination Electrical testing tools and commissioning procedures</p></li></ul><p></p>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p></p><p></p>]]></description><link>http://biotechroles.com/electrical-maintenance-and-project-engineer-pfizer/69d576afc8e81216cd0c4c87</link><guid isPermaLink="true">http://biotechroles.com/electrical-maintenance-and-project-engineer-pfizer/69d576afc8e81216cd0c4c87</guid><pubDate>Tue, 07 Apr 2026 21:27:11 GMT</pubDate><company>Pfizer</company><location>India - Vizag</location><salary>$12000-22000</salary><type>Full time</type></item><item><title><![CDATA[Associate Manager-Instrumentation]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>At Pfizer, we believe that every role contributes to our mission of improving patients&#39; lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you&#39;ll play a pivotal role in accelerating the delivery of medicines to the world.</p><p></p><h2>Job Summary</h2><p>The Instrumentation Engineer – Filling Line Project is responsible for <b>design, specification, installation, configuration, testing, and commissioning of instrumentation and control systems</b> for filling and packaging lines. The role ensures accurate measurement, reliable control, compliance with safety and quality standards, and seamless integration with automation systems to achieve desired line performance.</p><h2>Required Qualifications</h2><h3><b>Education</b></h3><ul><li><p>Bachelor’s Degree / Diploma in <b>Instrumentation Engineering, Electronics, or Related Discipline</b></p></li></ul><h3><b>Experience</b></h3><ul><li><p>6–10 years of experience (adjustable) in: Instrumentation &amp; automation for filling or packaging lines Manufacturing plants or greenfield/brownfield projects</p></li><li><p>Hands-on experience in <b>project commissioning</b> preferred</p></li></ul><h2>Key Responsibilities</h2><h3><b>Project Engineering &amp; Execution</b></h3><ul><li><p>Execute instrumentation scope for <b>filling line projects</b> (new lines, upgrades, and expansions)</p></li><li><p>Review and finalize: Instrument index and specifications I/O lists and control philosophy Wiring diagrams, loop diagrams, and hook-up drawings</p></li><li><p>Coordinate with mechanical, electrical, and automation teams during project execution</p></li></ul><h3><b>Instrumentation &amp; Control Systems</b></h3><ul><li><p>Specification, selection, and installation of instruments such as: Flow, pressure, level, temperature transmitters Load cells, weighing systems, check weighers Vision systems, barcode scanners, sensors, and actuators Control valves, variable frequency drives (VFDs), analyzers</p></li><li><p>Ensure proper integration of instruments with <b>PLC / DCS / SCADA systems</b></p></li><li><p>Support OEM machines such as fillers, cappers, labelers, and conveyors</p></li></ul><h3><b>Installation &amp; Commissioning</b></h3><ul><li><p>Supervise field installation and termination of instruments</p></li><li><p>Perform loop checking, calibration, and functional testing</p></li><li><p>Support <b>FAT, SAT, and site commissioning activities</b></p></li><li><p>Troubleshoot instrumentation, signal, and communication issues during startup</p></li></ul><h3><b>Calibration &amp; Validation</b></h3><ul><li><p>Ensure instruments are calibrated as per standards and maintain calibration records</p></li><li><p>Support <b>IQ, OQ, PQ activities</b> (especially for GMP environments)</p></li><li><p>Prepare test protocols, commissioning reports, and as-built documentation</p></li></ul><h3><b>Safety, Quality &amp; Compliance</b></h3><ul><li><p>Ensure compliance with <b>EHS standards, machine safety norms, and electrical/instrumentation codes</b></p></li><li><p>Participate in HAZOP, risk assessments, and interlock testing</p></li><li><p>Ensure compliance with <b>GMP, ISO, HACCP, and regulatory requirements</b> (as applicable)</p></li></ul><h3><b>Operational Support</b></h3><ul><li><p>Support performance optimization, troubleshooting, and line stabilization</p></li><li><p>Develop preventive maintenance plans and spare instrument lists</p></li><li><p>Train operations and maintenance personnel on instrumentation systems</p></li></ul><h2>Technical Skills</h2><ul><li><p>Strong knowledge of: Industrial instrumentation and measurement principles PLC systems (Siemens, Rockwell, Schneider, etc.) Field instruments, sensors, and actuators Industrial communication protocols (Profibus, Profinet, Ethernet/IP)</p></li><li><p>Ability to read and interpret: P&amp;IDs, loop diagrams, wiring drawings</p></li><li><p>Familiarity with: FAT / SAT procedures Calibration standards and documentation systems</p></li></ul><h2>Soft Skills &amp; Competencies</h2><ul><li><p>Strong coordination and communication skills</p></li><li><p>Analytical and troubleshooting capability</p></li><li><p>Ability to work under tight project schedules</p></li><li><p>Site execution and vendor management skills</p></li><li><p>Team-oriented approach with strong ownership</p></li></ul>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p></p><p></p>]]></description><link>http://biotechroles.com/associate-manager-instrumentation-pfizer/69d576aec8e81216cd0c4c85</link><guid isPermaLink="true">http://biotechroles.com/associate-manager-instrumentation-pfizer/69d576aec8e81216cd0c4c85</guid><pubDate>Tue, 07 Apr 2026 21:27:10 GMT</pubDate><company>Pfizer</company><location>India - Vizag</location><salary>$18000-30000</salary><type>Full time</type></item><item><title><![CDATA[Medical Affairs Scientist (Izmir Based)]]></title><description><![CDATA[<p>MAIN RESPONSIBILITIES / DUTIES</p><p>To provide deep medical &amp; scientific expertise to support healthcare professionals, professional associations, patient groups and other relevant decision makers. This includes the following:</p><p>•Develop and deliver the local medical strategy and life-cycle clinical plans for Pfizer’s inline and pipeline medicines in nominated therapy area</p><p>•Communicate the safe and appropriate use and the value of Pfizer medicines in order to improve patient outcomes, enhance clinical practice and support business needs at the national, regional and corporate level</p><p>•Demonstrate the value of our innovative medicines, e.g. through real world evidence</p><p>• Create industry leading digital educational and scientific content that is timely, relevant, balanced, interactive, innovative and easily digestible</p><p>•Champion the patient voice when developing and implementing medical strategies</p><p>•Provide subject matter expertise and high-quality scientific exchange, bringing in insights (both formally with CRM tools and informally) into the organization to shape strategy</p><p>•Provide focused, relevant information in response to clinician needs and the needs of their patients</p><p>•Establish Pfizer as a key research partner within National Life Sciences</p><p>•Establish deep and lasting relationships with healthcare professionals and other relevant decision makers</p><p>•Create constructive and effective cross-functional partnerships with internal departments and external stakeholders</p><p>•Review and approve (where applicable) medical materials and activities within scope of the MoH, AIFD and company codes</p><p>Partnerships</p><p>•Provide medical &amp; scientific expertise to healthcare professionals, professional associations, patient groups and other relevant decision makers through scientific communications</p><p>•Establish Pfizer as a key research partner within National Life Sciences by building academic and research collaborations within the nominated therapy area</p><p>•Establish deep and enduring peer-to-peer relationships with leading healthcare professionals and specialists, including on-traditional partners and key decision makers</p><p>•Understand clinicians’ insights around current standard of care and strengthen their knowledge of the value of our medicines to the patients and decision makers</p><p>•Liaise with healthcare professionals to effectively communicate and manage drug safety issues</p><p>•Provide specialist medical and scientific input to the nominated internal teams in order to support the appropriate use of Pfizer medicines and successful implementation of Pfizer’s initiatives and programs</p><p>Data Generation and Publications</p><p>•Identifies data gaps for pipelines assets and develops local RWD/RWE for the demonstration of the value of our products and market access.</p><p>•Acquire and maintain in-depth scientific expertise of Pfizer medicines within nominated therapy area as well as of key competitors (including those in development)</p><p></p><p>• Deliver key medical and scientific activities within the medical plan, e.g. high-quality educational materials, generation of real-world evidence, non-interventional studies, database studies and registries (in collaboration with the Health &amp; Value team) and ensure timely publication of data</p><p>• Provide medical expertise to evaluate requests to support medical education, quality improvement, health services research, investigator sponsored research (ISR) and clinical research collaborations</p><p>Clinical Development</p><p>• Provide medical/scientific input into protocol feasibility assessments for clinical trial proposals</p><p>• Identify appropriate investigators / sites for Pfizer-sponsored clinical trials</p><p>• Work together with clinical research colleagues and in collaboration with global teams to drive the timely completion of Pfizer-sponsored clinical trials</p><p>• Provide input into clinical development teams to ensure design and selection of trials relevant to Turkey needs, leveraging clinician, payer and patient insights</p><p>• Effectively implement approved compassionate use and named patient supply programs to ensure appropriate access to Pfizer medicines in response to clinician requests</p><p>Data Communication and Medical Insights</p><p>• Present high-quality, accurate, balanced and specific information to healthcare professionals and other relevant decision makers in response to unsolicited requests for information</p><p>• Create industry leading and impactful scientific and medical content through a range of digital channels and formats that is timely, relevant, balanced, interactive, innovative and easily digestible. This may include videos, webinars, interactive pdfs, peer reviewed publications, congress materials, clinical trials and real-world data</p><p>• Ensure medical insights are brought into the organization to shape future strategies</p><p>• Lead local advisory boards to gain clinical and patient insights</p><p>• Work with patients and patient organizations to understand unmet medical need and to ensure the patient voice is at the center of medical strategies and projects</p><p>• Present the medical perspective on selected topics during media briefings</p><p>• Provide scientific insights and support to field and head office based commercial colleagues</p><p>• Review and approve (where applicable) medical materials and activities within scope of the MoH, AIFD and company codes</p><p>Cross Functional Medical Activity</p><p>• Provide medical expertise into regulatory and market access strategies for pipeline assets, including early licensing &amp; access schemes, regulatory and HTA submissions and adaptive pathways</p><p>• Provide medical expertise for regulatory labelling updates, risk management plans and license maintenance</p><p>• Provide clinical input to Medical Information to facilitate the maintenance of an accurate, relevant and high-quality database of standard response documents/creation of new responses</p><p>• Develop and maintain strong cross-functional working between global and local country teams</p><p>• Identifies opportunities for customer focused digital solutions and contributes to their creation in partnership with MAS/Digital Medical.</p><p>• Performs the medical customer facing activities for the assigned products, according to the priorities defined with the Manager, and liaises with the other medical colleagues, if applicable</p><p>• Review and sign-off to ensure compliance of promotional materials and company sponsored activities such as local promotional meetings and events with local SPCs and requirements.</p><p>• Works closely with the MAEL, MAS/Digital Medical, the MAS/Real World Data Expert, the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional team, including customer-facing roles</p><p>REQUIRED SKILL SET</p><p>Technical</p><p>• Understanding in the following areas:</p><p>o Medical plans and budget management</p><p>o Medical governance and cross-functional teams’ collaboration</p><p>o Medical writing and comprehensive medical review of documents</p><p>o Communication skills to different stakeholders and across different channels</p><p>o External engagement competencies, including networking and stakeholders mapping &amp; management</p><p>• Performance driven with professional demeanor and strong collaboration skills</p><p>• Ability to focus on priorities, resilience, organization, and project management competencies</p><p>• Sense of responsibility and accountability, quality orientation</p><p>• Strategic, agile, innovative and growth mindset</p><p>• Language Requirements: Fluent in Turkish and English</p><p>Personal skills:</p><p>• Performance driven with professional demeanor</p><p>• Ability to lead complex projects with multiple external and internal stakeholders</p><p>• Business acumen and high level of industry understanding</p><p>• Customer oriented mindset</p><p>• Ability to act in midst of uncertainty</p><p>• Self-management &amp; ability to manage heavy workload</p><p>• Experience in setting up networks and develop them</p><p>• Excellent communication skills</p><p>• ’Can do’ &amp; pioneering attitude, solution driven</p><p>• Sense of responsibility and accountability, quality orientation</p><p>Managerial: N/A</p><p>Certifications: N/A</p><p>Education:</p><p>Medical Doctor or Pharmacist with Ph.D.</p><p>Experience:</p><p>Preferred qualifications</p><p>• Pharmaceutical industry experience within medical affairs</p><p>• Good knowledge of the national healthcare and medicine funding/reimbursement systems</p><p>• Knowledge of health economics, pharmacovigilance and regulatory affairs</p><p>• Experience in RWD/RWE generation in healthcare</p><p>• Experience in clinical research</p><p> <br />Work Location Assignment: Remote - Field Based</p><p></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><p style="text-align:left"><u><span><span>Purpose</span></span></u><span><span> </span> </span></p></div><div><p style="text-align:left"><span><span><b>Breakthroughs that change patients&#39; lives...</b> At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>School of Leaders</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>Flexibility</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!</span></span><span> </span></p></div><div><p style="text-align:inherit"><span><span> </span></span><span> </span></p></div><div><p style="text-align:left"><u><span><span>Equal Employment Opportunity</span></span></u><span><span> </span></span></p><p style="text-align:left"><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span><span> </span></p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>]]></description><link>http://biotechroles.com/medical-affairs-scientist-izmir-based-pfizer/69d576aec8e81216cd0c4c84</link><guid isPermaLink="true">http://biotechroles.com/medical-affairs-scientist-izmir-based-pfizer/69d576aec8e81216cd0c4c84</guid><pubDate>Tue, 07 Apr 2026 21:27:10 GMT</pubDate><company>Pfizer</company><location>Turkey - Izmir</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Senior Health Representative - (Vaccines Hospital - Dong Nai/An Giang/Kien Giang/Can Tho/Dong Thap)]]></title><description><![CDATA[<p>We are looking for 3 positions:</p><ul><li>1 position in Dong Nai</li><li>1 position in An Giang/Kien Giang</li><li>1 position in Can Tho/Dong Thap</li></ul><p></p><p>The Pfizer Health Representative will be the central contact in connecting customers within their accounts to therapies that advance wellness, prevention, treatments, and cures to the most feared diseases of our time. Central to the Health Representative’s role will be the introduction of a new &amp; promoted medicines and innovative digital service that will help elevate Health Care Professionals’ patient care. The role is consultative; spanning Pfizer’s entire resource and product portfolio for their customer base and one that will result in long standing and truly valued relationships with customers. The Heath Representative will draw on healthcare knowledge and understanding of the health and pharmaceutical industry, as well as Pfizer and the product portfolio, so that customers achieve the solutions they need.</p><p>The Health Representative should be proficient at planning and executing an effective relationship strategy and building/ maintaining effective, long-term business relationships at the senior executive level with key decision makers and influencers.  The Health Representative identifies and prioritises Pfizer opportunities through understanding customers’ business and strategic imperatives.  The Health Representative is responsible for developing and executing an effective account plan for each account and is part of the Integrated Account Team (IAT).</p><p> <b><span>The Health Representative is responsible for supporting their customers with their designated portfolio within a defined geographical territory that includes both metro and regional areas.</span></b></p><p></p><p><b><span>ROLE RESPONSIBILITIES</span></b></p><ul><li><p>Driving identified customers to the digital service offerings, opening a world of trusted materials and support that can be tailored to their needs and those of their patients. Ensuring customers gain best value from the services, in conjunction with the <span>Pfizer Virtual Health Representative team who are on hand providing virtual support.</span></p></li><li><p>Leading relationships with Health Care Professionals <span>within a defined geographical territory</span> as well as providing support virtually.  </p></li><li><p>Gaining deep understanding of Health Care Professional needs, sharing expert product advice, tailoring data, delivering promotional activities, aligning the customer lifecycle with that of the Pfizer portfolio and connecting them to relevant internal Pfizer people whenever they need it.   </p></li><li><p>Provide objective and scientifically sound medical information regarding Pfizer&#39;s product portfolio and the diseases states treated. Incorporating the use of educational programs, outcome and other tools which identify the greatest opportunities for improving patient care.  </p></li><li><p> Seeking and developing awareness of external market conditions to drive exceptional customer support and insights, connecting customer discussions with external trends and internal developments within Pfizer.</p></li><li><p>Establishing a strong working relationship with the <span>Pfizer VHSS, KAM and SME Teams</span> and sharing insights from customers to make our digital service offering even better.</p></li><li><p>Managing and achieving annual targets and ensuring adherence to Compliance, Legal, Medical and Regulatory requirements.  </p></li><li><p>Ensure relevant inline medicines prescribed by HCP’s have CFC commercial support.</p></li><li><p>Share relevant brand and therapy area updates with HCP’s.</p></li><li><p>Ability to convey relevant messages across multiple medicines and therapy areas.</p></li><li><p>Strong customer relationship focus, <span>establishing trusting</span> relationships, quick to navigate <span>complex hospital</span> stakeholder environment, experts in secondary care environment and or Primary Care.</p></li><li><p>Has a thorough understanding of the environment and challenges of their key HCPs and acts to come back to the business so we can find solutions to their needs in managing <span>our patients and</span> identify opportunities.</p></li><li><p>Strong capabilities in leveraging <span>virtual/digital channels</span> with at least 50% of interactions to be virtual.</p></li><li><p>Single point of contact for relevant Pfizer medicines for their accounts.</p></li><li><p>Able to understand how products across the <span>business interplay</span> with each other.</p></li><li><p>Ability to have <span>a product POA change</span> based on needs of customer and <span>their patients.</span></p></li><li><p>Ensures a customer centric – comprehensive approach to the way HCP’s treat their patients with all Pfizer brands that are relevant to the customer.</p></li></ul><p><b><span>Customer Engagement:</span></b></p><ul><li><p>Leads, coordinates, and manages the long term, consultative, customer relationship to become the customer’s trusted business advisor.  Extends the relationship beyond transactional to needs analysis based. </p></li><li><p>Demonstrates expertise in relationship skills, creatively delivers innovation and thought leadership, and represents the full spectrum of Pfizer value. </p></li><li><p>Responsible for overall service excellence within the account and is the customer advocate internally at Pfizer.</p></li></ul><p><b><span>Account Management:</span></b></p><ul><li><p>Maximises opportunity across the Pfizer portfolio, monitors progress with key accounts and evolves Account Plans as appropriate.</p></li><li><p>Analyses and understands the local environment, account business, and aligned Pfizer priorities to create Account Plans, and utilises insights to create and execute value propositions of mutual benefit.</p></li></ul><p><b><span>Leadership:</span></b></p><ul><li><p>Applies a proficiency in business acumen, including understanding of the account business, industry, economic trends, issues, and competition. Shares insights gained with cross functional colleagues and IAT.</p></li><li><p>Develops and leads the Account Plan and coordinates the cross functional team, demonstrating highest level of teamwork and professionalism.</p></li><li><p>As part of the IAT supports the development, negotiation, and implementation within accounts.</p></li></ul><p><b><span>QUALIFICATIONS</span></b></p><ul><li><p><span>Graduated from Pharmacy/Medicine University/</span>College.  </p></li><li><p><span>2- 3 years of experience on Field force</span></p></li><li><p>Curiosity and an entrepreneurial mindset.</p></li><li><p>Analytical skills to identify the connections between data, products and the needs of both Health Care Professionals and patients.</p></li><li><p>Written and verbal communication skills to help build trusted, sustainable relationships with your internal and external stakeholders.  </p></li><li><p>Solid understanding of the digital space and a willingness to keep learning and upskilling.</p></li><li><p>Strategic thinking and planning to help customers see beyond the day-to-day.  </p></li><li><p>Agility, adaptability to change and seasoned negotiation skills.</p></li><li><p>Commercial and business acumen, managing financial budgets, driving sales and achieving performance measures.</p></li><li><p>Able to connect with customers virtually and in person.</p></li><li><p>Can-do attitude and a work ethic underpinned by determination and commitment</p></li><li><p>Strong compliance mindset.</p></li><li><p>Not being subject to any of the following circumstances:  facing a criminal prosecution, serving a court’s sentence or ruling; being suspended from practice or doing works related to pharmacy under the court’s sentence or ruling; orhaving limited legal capacity.</p></li><li><p><span>Good command in English is preferred.</span></p></li></ul><p> <br />Work Location Assignment: Hybrid</p><p></p><p> -----</p><p><b>Important Notice for Applicants</b><br />At Pfizer, we value your privacy and security. Please note:</p><ul><li><p>All job applications must be submitted <b>only through our official channels</b>:</p></li><li><p>Pfizer Careers Website: <a href="https://www.pfizer.com/about/careers" target="_blank">Careers | Pfizer</a></p></li><li><p>Verified LinkedIn page: <a href="https://www.linkedin.com/" target="_blank">https://www.linkedin.com/</a></p></li><li><p>Verified local job board - Pharma360: <a href="https://pharma360.vn/viec-lam/" target="_blank">Công ty dược tuyển dụng dược sĩ đại học - Việc làm dược sĩ Pharma360</a></p></li></ul><p></p><p>We <b>never request payment, bank details, or confidential personal information</b> during the recruitment process.</p><p></p><p>If you receive suspicious messages or job offers outside these channels, please report them immediately to <b>[ProtectPfizer&#64;pfizer.com] </b></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/senior-health-representative-vaccines-hospital-dong-naian-giangkien-giangcan-thodong-thap-pfizer/69d576aec8e81216cd0c4c83</link><guid isPermaLink="true">http://biotechroles.com/senior-health-representative-vaccines-hospital-dong-naian-giangkien-giangcan-thodong-thap-pfizer/69d576aec8e81216cd0c4c83</guid><pubDate>Tue, 07 Apr 2026 21:27:10 GMT</pubDate><company>Pfizer</company><location>Viet Nam - Ho Chi Minh</location><salary>$25000-40000</salary><type>Full time</type></item><item><title><![CDATA[Senior Health Representative (Vaccines - South/Central)]]></title><description><![CDATA[<p><span><span><b>ROLE SUMMARY</b></span></span></p><p><span><span>The Senior HR Vaccine will be the central contact in connecting customers within their accounts to therapies that advance wellness, prevention, treatments, and cures to the most feared diseases of our time. Central to the Health Representative’s role will be the introduction of a new &amp; promoted medicines and innovative digital service that will help elevate Health Care Professionals’ patient care. The role is consultative; spanning Pfizer’s entire resource and product portfolio for their customer base and one that will result in long standing and truly valued relationships with customers. The Senior Heath Representative will draw on healthcare knowledge and understanding of the health and pharmaceutical industry, as well as Pfizer and the product portfolio, so that customers achieve the solutions they need.</span></span></p><p><span><span>The Senior HR Vaccine should be proficient at planning and executing an effective relationship strategy and building/ maintaining effective, long-term business relationships at the senior executive level with key decision makers and influencers.  The Senior Health Representative/ Brand Communication Manager identifies and prioritizes Pfizer opportunities through understanding customers’ business and strategic imperatives.  The Account Management Executive/ Brand Communication Manager is responsible for developing and executing an effective account plan for each account</span></span></p><p><span><span>The Senior HR Vaccine is responsible for supporting their customers with their designated portfolio within a defined geographical territory that includes both metro and regional areas.</span></span></p><p><span><span> </span></span><span><span> </span></span></p><p><span><span><b>ROLE RESPONSIBILITIES</b></span></span></p><p><span><span>1. <b>Territory Management</b></span></span></p><ul><li><span><span>Develop a customer database with detailed records of hospitals/ health centers/ target organizations/ health care professionals, etc.</span></span></li><li><span><span>Evaluate, classify, and identify precise target customers. Prioritize potential territories.</span></span></li><li><span><span>Establish &amp; maintain a close relationship with key accounts by ensuring company services meet their requirements.</span></span></li><li><span><span>Monitor market trends and competitor activity in assigned territory.</span></span></li><li><span><span>Collect and report Market intelligence to Supervisor &amp; Marketing team.</span></span></li></ul><p><br /><span><span>2. <b>Planning and organizing:</b></span></span></p><ul><li><span><span>Utilize customer database for preparing weekly &amp; monthly working plans, daily detailing calls, resource allocation plans, <i>including virtual or onsite symposium for HCPs in accounts </i>or direct-to-consumer marketing activities.</span></span></li><li><span><span>Analyses and understands the local environment, account business, and aligned Pfizer priorities to create Account Plans, and utilizes insights to create and execute value propositions of mutual benefit.</span></span></li><li><span><span>Develops and leads the Account Plan and coordinates the cross functional team, demonstrating highest level of teamwork and professionalism.</span></span></li></ul><p><br /><span><span>3. <b>Business development</b></span></span></p><ul><li><span><span>Develop new business opportunities with existing and potential clients.<br />Ensure good execution of all Sales &amp; Marketing programs in assigned territory. Strictly track and provide feedback on the programs to upper levels.</span></span></li><li><span><span>Implement effective daily sales calls, monthly key activities and maintain records. Address product complaints promptly.</span></span></li></ul><p><br /><span><span>4. <b>Others</b></span></span></p><ul><li><span><span>Well update product knowledge, as well as health care scientific backgrounds.</span></span></li><li><span><span>Manage Company and department reports in a timely and correct manner.<br />Ensure activities comply with the Company Business Code of Conduct and all local applicable laws within the scope of function responsibility.</span></span></li><li><span><span>Carry special work as assigned by Management.</span></span></li></ul><p><span><span> </span></span></p><p><span><span><b>QUALIFICATIONS</b></span></span></p><ul><li><span><span>Graduated from Pharmacy/Medicine University/College.</span></span></li><li><span><span>2- 3 years of experience on Field force</span></span></li><li><span><span>Curiosity and an entrepreneurial mindset.</span></span></li><li><span><span>Analytical skills to identify the connections between data, products and the needs of both Health Care Professionals and patients.</span></span></li><li><span><span>Written and verbal communication skills to help build trusted, sustainable relationships with your internal and external stakeholders.  </span></span></li><li><span><span>Solid understanding of the digital space and a willingness to keep learning and upskilling.</span></span></li><li><span><span>Strategic thinking and planning to help customers see beyond the day-to-day.  </span></span></li><li><span><span>Agility, adaptability to change and seasoned negotiation skills.</span></span></li><li><span><span>Commercial and business acumen, managing financial budgets, driving sales and achieving performance measures.</span></span></li><li><span><span>Able to connect with customers virtually and in person.</span></span></li><li><span><span>Can-do attitude and a work ethic underpinned by determination and commitment</span></span></li><li><span><span>Strong compliance mindset.</span></span></li><li><span><span>Not being subject to any of the following circumstances:  </span></span><ul><li><span><span>facing a criminal prosecution, serving a court’s sentence or ruling; being suspended from practice or doing works related to pharmacy under the court’s sentence or ruling; or</span></span></li><li><span><span>having limited legal capacity.</span></span></li></ul></li><li><span><span>Good command in English is preferred.</span></span></li></ul><p></p><p> <br />Work Location Assignment: Hybrid</p><p></p><p>-----</p><p><b>Important Notice for Applicants</b><br />At Pfizer, we value your privacy and security. Please note:</p><ul><li><p>All job applications must be submitted <b>only through our official channels</b>:</p></li><li><p>Pfizer Careers Website: <a href="https://www.pfizer.com/about/careers" target="_blank">Careers | Pfizer</a></p></li><li><p>Verified LinkedIn page: <a href="https://www.linkedin.com/" target="_blank">https://www.linkedin.com/</a></p></li><li><p>Verified local job board - Pharma360: <a href="https://pharma360.vn/viec-lam/" target="_blank">Công ty dược tuyển dụng dược sĩ đại học - Việc làm dược sĩ Pharma360</a></p></li></ul><p></p><p>We <b>never request payment, bank details, or confidential personal information</b> during the recruitment process.</p><p></p><p>If you receive suspicious messages or job offers outside these channels, please report them immediately to <b>[ProtectPfizer&#64;pfizer.com]</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/senior-health-representative-vaccines-southcentral-pfizer/69d576adc8e81216cd0c4c82</link><guid isPermaLink="true">http://biotechroles.com/senior-health-representative-vaccines-southcentral-pfizer/69d576adc8e81216cd0c4c82</guid><pubDate>Tue, 07 Apr 2026 21:27:09 GMT</pubDate><company>Pfizer</company><location>Viet Nam - Ho Chi Minh</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[France Country Compliance Lead]]></title><description><![CDATA[<p><span style="color:#000000">France Country Compliance Lead (CCL) role is responsible for: (1) overseeing the implementation of Pfizer’s compliance program in the country of France and cluster; (2) leading and supporting key proactive and strategic initiatives to assess and mitigate global risks across the country and cluster; (3) supporting, as needed and requested, risk management initiatives focused on global or regional risks relevant to Pfizer.</span></p><p></p><p></p><p><span style="color:#000000">The CCL is responsible for partnering with local leaders to ensure a culture of integrity and simplicity and efficient and effective risk management in France and cluster.  The CCL supports the identification and effective management of key risk areas in collaboration with business leadership and local risk management functions, and provides oversight, strategic direction, and operational support for the implementation of all elements of an effective compliance program.</span></p><p></p><p><span style="color:#000000">The position will serve as the primary compliance and risk advisor to France’s country leadership team, supporting a culture of quality and integrity, and assessing and mitigating risks across all business units.  The CCL will collaborate with regional compliance leader’s forum(s) to ensure consistent deployment of Pfizer’s compliance program.</span></p><p></p><p><span style="color:#000000">The role will provide subject matter expertise to support mitigation of Anti Bribery Anti-Corruption (ABAC) related risk management, including diligence and approvals.</span></p><p></p><p><span style="color:#000000">The position will partner closely with above market compliance leads and other global and regional functions within Pfizer’s Compliance Division (e.g., Risk Assessment, Monitoring, Pfizer’s Anti-Corruption Program Office (ACPO), and International Commercial Office (ICO)) and outside (e.g., Legal, HR, Promotional Compliance, Corporate Affairs).  The position reports to the Pfizer’s ICO, VMG, and France, France, and Japan Compliance Lead.</span></p><p></p><p><span style="color:#000000">France country responsibility includes all business units, divisions, and functions located in France.  France compliance lead responsibility includes global projects and cluster management.</span></p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><p><b> </b></p><p><span style="color:#000000"><b>Be the Compliance Leader: </b>Develops and drives France compliance and risk program including through development of plan addressing the risk profile of the market.  Overall, responsible for effective compliance program designed to prevent and detect systematic non-compliance and drive ownership of compliance.</span></p><p> </p><p><span style="color:#000000"><b>Culture of Compliance: </b>Develop a comprehensive strategy and operational approach to establish a culture of accountability, integrity, and compliance to prevent systemic non-compliance across France.  Develop and implement or coordinate integrity culture-related resources and communication, including updating business leadership on on-going environment and emerging risks, cultural challenges, significant compliance developments involving the business, and global compliance-related initiatives.</span></p><p></p><p><span style="color:#000000"><b>Governance</b>: Oversee local risk management governance to ensure effective risk-management oversight, assessment and prioritization of quality and compliance risks, and design of effective mitigation in line with all elements of effective risk management; Chair and coordinate the cross-functional market Risk Management Forums including local risk management functions to ensure strategic, comprehensive and optimized execution against integrated risk assessments, mitigation and monitoring plans; and represent Pfizer and Pfizer’s ethical priorities before external stakeholders (e.g. industry associations);</span></p><p> </p><p><span style="color:#000000"><b>Risk Assessment: </b>Guide the execution of annual risk assessments to support local risk prioritization; contribute to the development of a strategic direction for above-market Compliance mitigation activities based on the risk assessment results.</span></p><p><span style="color:#000000">Coordinate, lead, and/or support risk mitigation activities through strategic advice, policy/procedure support, training, communication campaigns, and monitoring in partnership with cross-functional risk management partners for priority risk areas.</span></p><p><span></span> </p><p><span style="color:#000000"><b>Policies and Training</b>: Support implementation of corporate and divisional policies and procedures within business units and the development of regional/local specific guidance or policies as needed; Partner with relevant SMEs to identify policy and training needs and implement an effective policy and training framework for the country in consultation with key business and risk management partners; identify training needs across the country and develop a training curriculum and program in key areas.</span></p><p> </p><p><span style="color:#000000"><b>Monitoring:</b> Identify monitoring needs in line with local risk assessment and coordinate or execute monitoring plans; Partner or coordinate with monitoring functions.</span></p><p> </p><p><span style="color:#000000"><b>Corrective Action</b>: Collaborate with Investigations, Monitoring, Audit, and other risk management functions to develop and implement interim corrective actions, implement agreed upon programmatic remediation and drive execution of remediation steps related to the Compliance Program.</span></p><p><b> </b></p><p><span style="color:#000000"><b>Third Party Support</b>: Collaborate with necessary stakeholders to ensure the proper policies and oversight structures are in place to identify and mitigate risks related to third parties, including but not limited to business development transactions.</span></p><p> </p><p><b>Artificial Intelligence and Scalable Risk Management Practices: </b>Lead driving evolution of the market compliance program toward scalable AI, data‑ and technology‑enabled risk identification, monitoring, and advisory models, aligned with global compliance transformation initiatives.  Provide strategic oversight for emerging technology, digital, data, and AI‑related compliance risks, ensuring alignment with evolving regulatory and ethical expectations.</p><p> </p><p><span style="color:#000000"><b>Global Compliance Division or France Markets Priority Implementation</b>: Coordinate with appropriate stakeholders to implement key divisional or cluster priorities and support development and localization of global or cluster risk area solutions.</span></p><p><b> </b></p><p><b>Lead or support for Global/Regional Risk Management and Cluster</b>: When assigned, lead cluster compliance program and support initiatives and programs designed to identify, mitigate, and/or monitor areas of emerging or established risk on a global or cluster level.</p><p></p><p></p><p><b>QUALIFICATIONS</b></p><p><b> </b></p><ul><li><p>University degree in Law, Finance, Business, Medicine, or Science with strong academic background;</p></li><li><p>10&#43; years professional experience in Compliance, Legal, Finance, Commercial, or Business Operations;</p></li><li><p>Understanding of the US FCPA, local regulatory environments (as relating to Compliance &amp; Risk Management), relevant international and local Codes of Practice, guidelines, and regulations;</p></li><li><p>Track record in developing meaningful solutions and appropriate controls for innovative business initiatives;</p></li><li><p>Fluent French language skill is a MUST.</p></li></ul><p></p><p></p><p><b>COMPETENCIES</b></p><p></p><ul><li><p>Strong analytical, organizational, problem solving and strategic thinking skills; with ability to see the big picture as well as the detailed and specific relationships between business topics;</p></li><li><p>Ability to partner with key in-market business leaders as an advisor;</p></li><li><p>Ability to encourage innovation and take appropriate risks to challenge the status quo;</p></li><li><p>Identifies multiple solutions or innovative options in solving highly complex problems with direct impact on the business projects in France;</p></li><li><p>Ability to lead, manage and motivate team of direct reports;</p></li><li><p>Exercises foresight and judgment in making complex decisions;</p></li><li><p>Acts independently on self-initiated projects with impact beyond France;</p></li><li><p>Ability to encourage innovation and take appropriate risks to challenge the status quo;</p></li><li><p>Excellent written and oral communication skills in local language and English; ability to summarize and articulate complex concepts clearly and efficiently;</p></li><li><p>Ability to assess, understand and communicate risk profile and key healthcare compliance risk areas;</p></li><li><p>Strong communication skills to drive and message compliance culture as leader;</p></li><li><p>Ability to understand local culture and sensibilities and to communicate effectively in a global environment;</p></li><li><p>Ability to prioritize time and resources;</p></li><li><p>Self-directed; ability to work both autonomously and as part of a team to resolve complex matters; and</p></li></ul><ul><li><p>Understanding of principles of escalation and independence.</p></li></ul><p></p><p>The role is a Hybrid role.  The colleague is expected to work onsite and may log in for your day as per company policy.  Business travel is expected 10% or less within France and Europe or any other location of the business meeting.</p>&nbsp;<br>Work Location Assignment:&nbsp;Hybrid<br><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Égalité des chances &amp; Emploi<span> </span></u></p><p style="text-align:left">Nous croyons que des équipes diversifiées et inclusives sont essentielles à la réussite d&#39;une entreprise. En tant qu&#39;employeur, Pfizer s&#39;engage à valoriser la diversité et l’inclusion sous toutes ses formes. Cette diversité se reflète également à travers les patients et les communautés que nous servons. Ensemble, continuons à bâtir une culture qui encourage, soutient et responsabilise nos employés.</p><p style="text-align:inherit"></p><p style="text-align:left"><u>Handicap &amp; Inclusion</u></p><p style="text-align:left">Notre mission est de libérer le potentiel de nos collaborateurs et nous sommes fiers d&#39;être un employeur inclusif pour les personnes handicapées, garantissant ainsi l&#39;égalité des chances en matière d&#39;emploi pour tous les candidats. Nous vous encourageons à donner le meilleur de vous-même en sachant que nous apporterons tous les ajustements raisonnables pour soutenir votre candidature et votre carrière future. Votre expérience avec Pfizer commence ici !</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Legal Affairs<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/france-country-compliance-lead-pfizer/69d576acc8e81216cd0c4c81</link><guid isPermaLink="true">http://biotechroles.com/france-country-compliance-lead-pfizer/69d576acc8e81216cd0c4c81</guid><pubDate>Tue, 07 Apr 2026 21:27:08 GMT</pubDate><company>Pfizer</company><location>France - Rives de Paris</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Quality Control Analyst]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p></p><p>Everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. You will play a crucial role in improving patients&#39; lives by ensuring the highest standards of Good Manufacturing Practices (GMP) are met. Your work will directly contribute to the safety and efficacy of our products, making a tangible difference in the lives of patients worldwide.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><p></p><ul><li><p>Perform analytical testing accurately and efficiently following Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.</p></li><li><p>Perform Analytical Method Transfer, Analytical Method Validation and Analytical Method verification as well as Cleaning Method Development and Validation in accordance with Standard Operating Procedures (SOPs), adhering to ALCOA principles and Data Integrity requirements.</p></li></ul><ul><li><p>Interpret and evaluate data in terms of accuracy, precision and potential Good manufacturing Practices impact and recommend appropriate corrective actions.</p></li><li><p>Support to QC Method trouble shooting.</p></li><li><p>Support the troubleshooting and resolution of equipment and testing issues, ensuring operational readiness.</p></li><li><p>Manage and maintain reagents and laboratory consumables inventories, ensuring they are valid and stored correctly.</p></li><li><p>Support routine data review following written procedures.</p></li><li><p>Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.</p></li><li><p>Maintain training to current standards and procedures on all assigned curriculums</p></li><li><p>Participate in Laboratory investigations and propose CAPA for the identified root cause.</p></li><li><p>Contribute to the completion of improvement projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.</p></li></ul><ul><li><p>Manage personal time and professional development, being accountable for results.</p></li></ul><ul><li><p>Maintain data integrity and ensure compliance with company SOPs, GLP and cGMP regulations.</p></li><li><p>Use IMEX &#34;way of working&#34; for day-to-day operations, problem solving, escalation and continuous improvements.</p></li><li><p>Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures for site and QC laboratories are followed.</p></li></ul><p></p><p><b>Here Is What You Need</b> (Minimum Requirements):</p><p></p><ul><li><p>Bachelor&#39;s degree (Chemistry, Biology, Biotechnology or similar)</p></li><li><p>At least five years of working experience with HPLC techniques in analytical laboratory (knowledge of working in Empower environment is a plus)</p></li><li><p>Demonstrated technical skills in method transfer, method validation and cleaning validation.</p></li><li><p>Knowledge of laboratory equipment, testing, and techniques</p></li><li><p>Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.</p></li><li><p>Excellent organizational skills and strong ability to multi-task across various projects and activities</p></li><li><p>Strong written and verbal communication skills (French and English)</p></li><li><p>High level of attention to detail</p></li><li><p>Self-motivated and able to work in minimal direction</p></li><li><p>Broad experience with Microsoft Office products</p></li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements):</p><p></p><ul><li><p>Proven track record in leading continuous improvement projects</p></li><li><p>Strong problem-solving skills and attention to detail</p></li><li><p>Ability to manage multiple priorities and meet deadlines.</p></li><li><p>Ability to work independently and as part of a team</p></li><li><p>Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels</p></li><li><p>Adaptability and willingness to learn new techniques and procedures</p></li><li><p>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.</p></li></ul><p> <br />Work Location Assignment: On Site</p><p><b>Worker Type: </b>Regular</p><p></p>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Quality Assurance and Control<p></p><p></p>]]></description><link>http://biotechroles.com/quality-control-analyst-pfizer/69d576aac8e81216cd0c4c80</link><guid isPermaLink="true">http://biotechroles.com/quality-control-analyst-pfizer/69d576aac8e81216cd0c4c80</guid><pubDate>Tue, 07 Apr 2026 21:27:06 GMT</pubDate><company>Pfizer</company><location>Morocco - El Jadida</location><salary>$12000-22000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist, In Vitro Pharmacology]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p></p><p>At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will directly impact the development of therapies and vaccines that improve patients&#39; lives globally. By leveraging advanced science and cutting-edge technologies, you will play a crucial role in transforming innovative ideas into life-changing medical solutions. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your contributions will be vital in accelerating the delivery of top-tier medicines to patients worldwide.</p><p></p><p><b>What You Will Achieve</b></p><p></p><p>The key strategic focus within the Internal Medicine Research Unit (IMRU) is identifying novel therapies for the treatment of obesity and cardiovascular diseases. As a member of the In Vitro Pharmacology team, you will be playing a significant role in the early drug discovery process by developing <i>in vitro</i> screening assays using pharmacology expertise in GPCRs, enzymes, and other target protein classes. In addition, you will contribute to the mechanistic understanding of emerging therapeutic hits, support lead optimization efforts, and work collaboratively with project teams and across partner lines to advance programs into the clinic. Strong technical and problem-solving skills, self-motivation, communication skills, and the ability to both lead as well as thrive as part of a team are essential.</p><p></p><p>In this role, you will:</p><p></p><ul><li><p>Develop assays for <i>in vitro</i> screening using binding, signaling and functional endpoints and support low to medium throughput screening.</p></li><li><p>Validate <i>in vitro</i> cell models using immortalized, primary cells, and co-culture systems and adapt to cell-based screening assays at the required throughput.</p></li><li><p>Independently conceptualize, design and conduct <i>in vitro</i> studies aimed at dissecting the complex molecular pharmacology of emerging therapeutic modulators targeting GPCRs, enzymes, and other protein classes within the IMRU portfolio.</p></li><li><p>Apply rigorous data analytical methods to ensure robust scientific interpretation of results.</p></li><li><p>Translate experimental results to advance understanding of target biology and help define how physiological endpoints are impacted by pharmacological agents.</p></li><li><p>Facilitate and co-author manuscript submissions and publication to high impact peer-reviewed journals.</p></li><li><p>Maintain an awareness of ‘cutting edge’ scientific and technical developments in preclinical to clinical translation and apply these to advance portfolio programs.</p></li><li><p>Ensure that all research/discovery work is conducted with highest quality and ethical guidelines and in accordance with relevant regulatory, QC, and compliance guidelines.</p></li></ul><p></p><p></p><p><b>Here Is What You Need</b> (Minimum Requirements)</p><p></p><ul><li><p>BA/BS and 12 years or MS and 9 years or PhD and 4 years of relevant experience in biochemistry, cell biology and/or pharmacology. Industry and cardiometabolic experience are a plus.</p></li><li><p><b>Experience supporting <i>in vitro</i> screening in a drug discovery environment involving a diverse mix of GPCR, enzyme, and other protein classes as pharmacological targets,</b> with<b> strong plate-based pharmacology background.</b> Lab automation experience is a plus.</p></li><li><p>Experience with <b>Mechanism of Action (MoA)</b> or <b>molecular pharmacology </b>work, including hands-on experience with traditional and novel screening methodologies and concepts related to<b> GPCR and enzyme drug discovery, signaling and trafficking.</b></p></li><li><p>Background on cell-based assay development and extensive mammalian cell culture experience.</p></li><li><p>Scientific rigor with demonstrated ability to review critically available data and think independently and creatively in formulating and testing novel scientific hypotheses.</p></li><li><p>Excellent communication and interpersonal skills and ability to work independently and as part of an interdisciplinary team in a collaborative environment.</p></li><li><p><b>Strong scientific writing skills supported by a successful record of publications in high-impact pharmacology journals and presentations at international conferences (Google Scholar links etc.)</b></p></li><li><p>Ability to mentor junior colleagues both technically and scientifically.</p></li></ul><p></p><p>  </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p></p><p>Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis. Ability to perform laboratory bench and tissue culture work.</p><p><br />Relocation support available<br /><br />Work Location Assignment: On Premise</p>&amp;#xa;The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div><p style="text-align:inherit"></p></div></div></div></div></div></div></div>&amp;#xa;Research and Development&amp;#xa;]]></description><link>http://biotechroles.com/principal-scientist-in-vitro-pharmacology-pfizer/69d576aac8e81216cd0c4c7f</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-in-vitro-pharmacology-pfizer/69d576aac8e81216cd0c4c7f</guid><pubDate>Tue, 07 Apr 2026 21:27:06 GMT</pubDate><company>Pfizer</company><location>United States - Massachusetts - Cambridge</location><salary>$160000-240000</salary><type>Full time</type></item><item><title><![CDATA[Cardiovascular Health and Science Professional (HSP) - Manhattan S, NY]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p></p><p>All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues can grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and can impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.</p><p>Pfizer has a deep heritage and leadership in cardiovascular disease, and we are committed to providing breakthroughs that change patients’ lives.  An integral part of Internal Medicine, the Cardiology (CARD) Team’s mission is to promote a breakthrough therapy for patients suffering from NVAF or VTE. </p><p></p><p>The CARD Health &amp; Science Professional (HSP) is responsible for increasing territory sales and relationship development with assigned customers and accounts by engaging in product promotion and determining the best strategies to manage their business. </p><p>A CARD HSP should possess customer, market, and business acumen, analytical skills, and strong product and disease state knowledge; demonstrate ability to drive sales, promotional and strategic business development and management skills, and in-depth customer engagement expertise both in-person and virtually; demonstrate outstanding communication and teamwork skills; be adept in the operation of digital and virtual tools; and be effective at working remotely in collaboration with cross-functional internal teams to address customer needs and compliantly deliver on Pfizer business objectives.</p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><ul><li><p>Drives sales in assigned territory</p></li><li><p>Engages with customers both face to face and virtually</p></li><li><p>Develops and implements effective business and territory call plans; effectively identifies and implements live/virtual engagement strategies with customer to maximize overall effectiveness and impact</p></li><li><p>Effectively builds rapport and relationships with customers in both live and virtual environments; uses judgment to maintain customer engagement by successfully utilizing existing and ever-changing digital tools effectively for successful customer engagement</p></li><li><p>Understands and leverages internal reports and analytics to assist with identifying, developing, and implementing strategic business opportunities</p></li><li><p>Compliantly leverages product and disease state knowledge to appropriately educate providers on unbranded and branded product value proposition for relevant patient populations and effectively and strategically utilizes approved clinically oriented disease state information and patient resources, as applicable</p></li><li><p>Demonstrates strong teamwork capabilities to collaborate effectively and compliantly across the organization to address customer inquiries and advance Pfizer objectives.</p></li><li><p>Completes all administrative expectations on time and compliantly.</p></li></ul><p></p><p><b>BASIC QUALIFICATIONS</b></p><ul><li><p>Applicant must have a bachelor’s degree and 0-3 years of experience; OR an associate’s degree with 4&#43; years of experience; OR a high school diploma (or equivalent) and 6&#43; years of <u>relevant</u> experience. </p></li><li><p>Professional Sales or Promotional Activity</p></li><li><p>Small Business Owner or other Entrepreneurial experience, Marketing, Customer Service and/or Account Management</p></li><li><p>Relevant Healthcare/Scientific roles (e.g., RN, Pharmacist, PT, OT, etc.)</p></li><li><p>Educator (e.g., Teacher, Principal)</p></li><li><p>Full Time Military experience</p></li><li><p>Must live within 25 miles of the border of the territory.</p></li><li><p>Valid US driver’s license and driving record in compliance with company standards. Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired</p></li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li><p>1 year of pharmaceutical, biotech, medical sales and/or medical related marketing.</p></li><li><p>Strong track record of sales or marketing success, strong territory management skills, outstanding communications skills, as well as demonstrated teamwork, leadership ability and accountability.</p></li><li><p>Experience with applicable disease states, therapeutic area, and products. </p></li><li><p>Knowledge of posted territory customers and markets (prescribers/HCPs/institutions/organizations).</p></li><li><p>Reside within the territory boundaries.</p></li></ul><p></p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><ul><li><p>Ability to travel to all accounts/office locations within territory</p></li><li><p>Depending on size of territory and business need, candidates may be required to stay overnight as necessary</p></li></ul><p></p><p><b>ADDITIONAL JOB DETAILS:</b></p><ul><li><p>Last day to apply: <b>April 21, 2026</b></p></li><li><p>Geography includes: Downtown Manhattan &amp; West Brooklyn (Carroll Gardens, Sunset Park, Red Hook, Park Slope, Dumbo, Downtown Brooklyn)</p></li></ul><p></p><p>The annual base salary for this position ranges from $76,000 - $199,600. <b>During initial new hire sales training, you will be classified as a salary non-exempt employee which entitles you to overtime pay. Upon your training certification, you will become an overtime exempt employee. </b>In addition, this position offers an additional quarterly Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States. </p>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/cardiovascular-health-and-science-professional-hsp-manhattan-s-ny-pfizer/69d576aac8e81216cd0c4c7e</link><guid isPermaLink="true">http://biotechroles.com/cardiovascular-health-and-science-professional-hsp-manhattan-s-ny-pfizer/69d576aac8e81216cd0c4c7e</guid><pubDate>Tue, 07 Apr 2026 21:27:06 GMT</pubDate><company>Pfizer</company><location>United States - New York - Remote</location><salary>$95000-140000</salary><type>Full time</type></item><item><title><![CDATA[Director, HTA, Value & Evidence (HV&E), PCOA]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p></p><p>As a leading biopharmaceutical company, Pfizer is dedicated to the discovery and delivery of high value therapies across a variety of disease areas. It is our mission to bring innovative medicines to patients that significantly improve their lives, and our priority is to ensure patients have access to these medicines.</p><p></p><p>The Health Technology Assessment (HTA), Value &amp; Evidence (HV&amp;E) team is responsible for ensuring patients have affordable, timely access to medicines and vaccines by advancing innovative value and evidence solutions — to inform healthcare decision-making.</p><p></p><p>The Patient-Centered Outcomes Assessment (PCOA) team is part of HV&amp;E and is responsible for ensuring that patient experience data are adequately captured in Pfizer clinical development programs to be deemed as valid scientific evidence supporting registration, access, and healthcare decision-making.</p><p></p><p>The PCOA Director is responsible for development and execution of fit-for-purpose PCOA strategies in clinical trials and observational studies to support registration, access, and reimbursement for Pfizer’s portfolio of innovative therapies.</p><p></p><p>The PCOA Director is an integral member of the HV&amp;E organization and serves as a critical partner to cross-functional stakeholders in R&amp;D, CMO, RWE, and Commercial organizations. As PCOA subject matter expert, the Director fosters a team culture of collaborative knowledge sharing and co-creation.</p><p></p><p><b>ROLE RESPONSIBILITIES </b></p><ul><li>Develops and executes PCOA strategies to support therapeutic area/asset specific clinical development plans, global HV&amp;E strategies, integrated evidence plans, and commercial strategies.</li><li>Effectively collaborates with cross-functional stakeholders to ensure that the PCOA strategies and related deliverables are fit-for-purpose and aligned with the overall program goals.</li><li>Ensures that PCOA strategies are aligned with the most current regulatory and HTA guidance documents (e.g., FDA, EMA, JCA).</li><li>Leads qualitative and quantitative evidence generation research to inform and support PCOA strategies.</li><li>Provides technical expertise in the implementation, analysis, interpretation, and communication of clinical outcome assessment (COA) data.</li><li>Manages a global network of consultants and contract organizations to execute the COA evidence generation deliverables (e.g., qualitative COA development evidence, psychometric analyses, COA qualification dossiers).</li><li>Maintains awareness of new research methods, tools, and data sources to ensure study methods represent current state of the science.</li><li>Promotes the value of patient-centered outcome assessments across Pfizer through education and training.</li></ul><p></p><p></p><p><b>BASIC QUALIFICATIONS </b></p><p></p><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><ul><li>Advanced academic degree (e.g., MSc, MPH, PhD, DrPH, ScD, PharmD) in relevant field such as, public health, psychology, health economics, epidemiology, pharmacy administration, or other research-focused health outcomes field.</li><li>Minimum 5 years of experience with PhD/DrPH/ScD/PharmD or minimum of 7 years of experience with MSc/MPH in consulting, pharmaceutical industry, or academia in COA research or related health outcomes research.</li><li>Advanced understanding of COA research methodology (qualitative and quantitative methodology) </li><li>Knowledge of regulatory guidance documents (FDA, EMA) </li><li>Strong analytical and synthesis skills of qualitative and quantitative data demonstrated in scientific publications </li><li>Experience with developing new or validating existing COA measures in multiple therapeutic areas or assets  </li><li>Experience preparing regulatory briefing documents and COA dossiers to support COA-based labeling. </li><li>Scientific rigor, autonomy, and sense of initiative. </li><li>Demonstrated ability to work effectively in a fast-paced environment, in a cross-functional, matrix team setting as well as independently. </li><li>Technical competency in systematic literature reviews and qualitative research. </li><li>Technical competency in use of ePRO/eCOA and linguistic validation of COAs. </li><li>Demonstrated strong project management skills (ability to manage multiple projects budget planning, vendor management, managing competing deadlines and rapidly shifting priorities) </li><li>Excellent interpersonal skills required; ability to understand and respond to multiple internal and external customers and influence in a matrix environment </li><li>Excellent oral and written English communication skills required </li></ul><p></p><p><b>PREFERRED QUALIFICATIONS </b></p><ul><li>Knowledge of basic elements of psychometric analysis</li><li>Leading PCOA strategy discussions during formal meetings with global regulatory agencies </li></ul><p></p><p><b>Other Job Details:</b></p><ul><li>Last Date to Apply for Job: <b>April 21st, 2026.</b></li><li>Ability to travel domestically and internationally </li><li>NOT eligible for Relocation Package</li><li>This position is hybrid and requires working onsite 2 to 3 days per week</li></ul><p></p><p>#LI-PFE</p>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Market Access&amp;#xa;]]></description><link>http://biotechroles.com/director-hta-value-and-evidence-hvande-pcoa-pfizer/69d576a8c8e81216cd0c4c7d</link><guid isPermaLink="true">http://biotechroles.com/director-hta-value-and-evidence-hvande-pcoa-pfizer/69d576a8c8e81216cd0c4c7d</guid><pubDate>Tue, 07 Apr 2026 21:27:04 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-260000</salary><type>Full time</type></item><item><title><![CDATA[Engineering Maintenance Technician]]></title><description><![CDATA[<p>Job Description</p><p><b><span>Why Patients Need You</span></b></p><p>Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you&#39;ll help bring medicines to the world even faster by imagining what’s possible and taking action.</p><p></p><p><b><span>What You Will Achieve</span></b></p><p>Working with Pfizer’s dynamic engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment.</p><p>As an Engineering Maintenance Technician, your knowledge and skills will contribute towards the goals and objectives of the team.  Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams.</p><p>It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.</p><p></p><p><b><span>How You Will Achieve It</span></b></p><ul><li>Contribute to completion of projects, manage own time to meet agreed targets, develop plans for short-term work activities on own projects.</li><li>Provide engineering support to develop scope of work, project execution plans, and associated engineering studies for equipment and component installation, modification etc.</li><li>Provide necessary operational support as needed.</li><li>Review preventive and corrective work order activities and provide equipment maintenance history review.</li><li>Manage technical writing and document review.</li><li>Ensure calibration compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices.</li><li>Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans.</li><li>Partner with Production and Quality Team Leads on troubleshooting and scheduling.</li><li>Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture.</li><li>Facilitate and participate in the investigation teams created to determine root cause of exemption reports, QARs and laboratory investigation reports. Serve as a liaison between quality, Operations and regulatory/Compliance to facilitate timely closure of investigations.</li><li>Assist in the development the Preventative Maintenance program. Engage with site sustaining Engineering Operations for input and best practice.</li><li>Work with Engineering teams in building the Maintenance Management database system (EAMS) </li></ul><p></p><p><b><u><span>Qualifications</span></u></b></p><p></p><p><b><span>Must-Have</span></b></p><ul><li>Diploma/Degree in an Engineering/Technical Discipline or Electrical/Mechanical Trade Qualification</li><li>3&#43; years of experience</li><li>Experience with Root Cause Failure Analysis PM/PdM optimization, and/or Failure Modes and Effects Analysis</li><li>Strong knowledge and understanding of Current Good Manufacturing Practices {part of GxP}</li><li>Excellent oral and written communication skills</li><li>Experience with commissioning, qualification, start-up, and production support activities is desirable</li><li>Experience executing Engineering tasks using Engineering Maintenance Management systems such as EAMS.</li><li>Strong hands-on troubleshooting capability across mechanical and electrical systems.</li><li>Ability to interpret electrical, mechanical, pneumatic, and logic diagrams.</li><li>Experience with process automation systems, PLC diagnostics, and instrumentation is desirable.</li><li>Good computer literacy and documentation skills. Working knowledge of MS Excel</li></ul><p></p><p><b><span>Nice-to-Have</span></b></p><ul><li>Bachelor’s  degree</li><li>Relevant pharmaceutical experience</li></ul><p></p><p><b><span>What We Offer .. Why Choose Pfizer</span></b></p><p></p><ul><li>Competitive Salary and Shift Allowance<b>*</b></li><li>Multiple Permanent Positions Available</li><li>Annual Bonus and Share Schemes</li><li>Pension Scheme</li><li>Long Term Income Protection</li><li>Healthcare for You and Your Family</li><li>Career Development Opportunities</li><li>Subsidised Canteen</li><li>Health and Wellbeing Initiatives</li><li>On-site Gym and Saloon</li><li>Sports and Social Club (Swim Society, Women&#39;s Mentoring Programme, Pfizer Pride &amp; many more)</li><li>Diverse and inclusive workplace</li></ul><p></p><p>It is a 4 cycle shift role for 24/7 Operation<b>*</b><br />Work Location Assignment: On Premise</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><div><div><p style="text-align:left"><b><span>Additional Information</span></b><span> </span></p></div><div><ul><li><p style="text-align:left"><span><span>In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.</span></span><span> </span></p></li><li><p style="text-align:left"><span><span>Please note there is no relocation support available for this position </span></span></p></li></ul><p style="text-align:inherit"><span><span>​</span></span><span> </span></p></div><div><p style="text-align:left"><b><span>How to apply</span></b><span> </span></p></div><div><ul><li><p style="text-align:left"><span><span>Make a difference today, all suitable candidates should apply with CV below.  We are looking forward to hearing from you!</span></span><span> </span></p></li></ul><p style="text-align:inherit"><span>​</span></p></div></div><div><p style="text-align:left"><u><span>Purpose</span></u><span>  </span></p></div><div><p style="text-align:left"><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.</span></span><span> </span></p><p style="text-align:inherit"></p></div><div><p style="text-align:left"><u><span><span>Digital Transformation Strategy </span></span></u></p><p style="text-align:left"><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span><span> </span></p><p style="text-align:inherit"></p></div><div><p style="text-align:left"><u><span><span>Equal Employment Opportunity </span></span></u></p><p style="text-align:left"><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span><span> </span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>Disability Inclusion</u></p><p style="text-align:left">Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</p></div><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Engineering<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/engineering-maintenance-technician-pfizer/69d576a7c8e81216cd0c4c7a</link><guid isPermaLink="true">http://biotechroles.com/engineering-maintenance-technician-pfizer/69d576a7c8e81216cd0c4c7a</guid><pubDate>Tue, 07 Apr 2026 21:27:04 GMT</pubDate><company>Pfizer</company><location>Ireland - Dublin - Grange Castle</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Marketing Manager/Brand Manager-Dermatology-Shanghai]]></title><description><![CDATA[<p></p><p></p><p><b>POSITION SUMMARY</b></p><p></p><p>Own portfolio strategy to maximize the franchises business to achieve earnings and revenues objectives and lifecycle management; Assist the Brand Owner to build marketing capabilities of the product management team to achieve effectiveness and efficiency of the business. Define and Drive Country Specific TA and Brand Strategy. Interface with WWT and  global/local functional team as TA portfolio (or big strategic brand) lead.</p><p></p><p><b>Responsibilities</b></p><p>Brand Management</p><ul><li><p>Lead the development of brand strategies to optimize the business, including brand/business plan and LRF, and lifecycle management</p></li><li><p>Lead the AD growth initiatives</p></li><li><p>Cross-functional AD leadership – across Field Force, medical, legal, regulatory, etc  to get alignment</p></li><li><p>Interface with WWT to gain support</p></li><li><p>Forecast brand performance and track progress towards target</p></li><li><p>Prepare report for internal communication</p></li></ul><p></p><p>Organization Effectiveness and self Development</p><ul><li><p>Assist brand owner to develop effective campaign/activity to support the growth of business</p></li><li><p>Assist brand owner to establish competency requirement for every marketing position and performance standard for the major market programs</p></li><li><p>Develop subordinates through coaching and training programs to deliver results</p></li></ul><p></p><p>Resource Management</p><ul><li><p>Lead team in strategic brand budget planning and control</p></li><li><p>Allocate and manage in country portfolio budget and evaluate P&amp;L</p></li></ul><p></p><p></p><p><b>POSITION RESPONSIBILITIES </b></p><p><b>Accountable</b></p><p>Lead portfolio strategies and plan Review and actively contribute to brands  plan and A&amp;P allocation Lead the review of  product life cycle management strategy with cross function team. Review the key Campaigns Development and execution Lead the OP plan and  work with SFE on target, FTE allocation Interface with WWT to gain support on relevant TA or brand</p><p></p><p><b>Shared Accountability</b></p><p>s Develop TA life cycle management strategy with CTAL and WWT</p><p>s Develop effective structure with CTAL and BU Head.</p><p>s Develop MKT team competency with CTAL</p><p></p><p></p><p><b>ORGANIZATIONAL RELATIONSHIPS</b></p><p>Marketing Director /Business Unit Leads Global Cross Function Legal Lead Market Access Lead Medical Affairs Lead Regulatory  Lead GCO Marketing services, Business Analytics &amp; Insights (BAI) SBD lead</p><p></p><p></p><p><b>EDUCATION AND EXPERIENCE </b></p><p><b>Qualifications: </b></p><p>Bachelor degree in Medical or Medicine, Master degree and MBA preferred Proficient  oral and written English 7 or above years marketing experience with above 18 months Marketing Manager and people manager experience</p><p></p><p></p><p><b>TECHNICAL SKILLS REQUIREMENTS</b></p><p>Indicate the technical skills required and/or preferred, as applicable.</p><p>Expect candidates to demonstrate these competencies (people manager roles):</p><ul><li><p>Demonstrates business acumen</p></li><li><p>Acts decisively</p></li><li><p>Seizes accountability</p></li><li><p>Holds people accountable</p></li><li><p>Grows-others</p></li><li><p>Leads change</p></li><li><p>Self-awareness</p></li><li><p>Commits to “One Pfizer”</p></li><li><p>Builds effective teams</p></li></ul><p></p><p>Expect candidates to demonstrate these commercial /management competencies</p><ul><li><p>Marketing , Customer and Competitor Insight</p></li><li><p>Marketing Execution</p></li><li><p>Strategic and Operational Business/Marketing Planning</p></li><li><p>Data analysis, interpretation and communications</p></li><li><p>Performance and Program Metrics</p></li><li><p>Exceptional interpersonal skills</p></li><li><p>Exceptional collaboration/negotiation (w/Customer Marketing roles in country, FF, CTALs, BU Leads/CM)</p></li><li><p>Exceptional prioritization –among/across brands, resource-constrained context;</p></li><li><p>Vendor management</p></li><li><p>Proficiency in the local language as well as English proficiency</p></li></ul><p>                                                               </p><p>  <br /> </p>&nbsp;&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Marketing and Market Research<p></p><p></p>]]></description><link>http://biotechroles.com/marketing-managerbrand-manager-dermatology-shanghai-pfizer/69d576a7c8e81216cd0c4c79</link><guid isPermaLink="true">http://biotechroles.com/marketing-managerbrand-manager-dermatology-shanghai-pfizer/69d576a7c8e81216cd0c4c79</guid><pubDate>Tue, 07 Apr 2026 21:27:03 GMT</pubDate><company>Pfizer</company><location>China - Shanghai - Shanghai</location><salary>$60000-120000</salary><type>Full time</type></item><item><title><![CDATA[Vaccines Area Business Manager - Newark, NJ]]></title><description><![CDATA[<div><div><p><b><span>ROLE SUMMARY</span></b><span><span> </span></span><span> </span></p></div><p></p><div><p><span><span>The Vaccines Area Business Manager (ABM) will report into the Regional Business Director (RBD) and will work with customer-facing (Accounts and Pharmacy) and Headquarters (HQ) teams across the organization.  The ABM will<span> </span></span><span>be responsible for</span><span><span> </span>the supervision and leadership of 12-14 representatives within the Northeast area, sales performance of the business portfolio of products, and business knowledge of the area landscape to assess key stakeholders plus future trends within the business marketplace. This position will require regular in field and virtual coaching and observation of Field Representatives and frequent customer contact as well as the development of a strong, effective partnership with accounts, retail, and marketing colleagues.  The ABM will ensure compliant execution by team members, driving understanding of relevant policies and<span> </span></span><span>guidance</span><span><span> </span>and advancing a culture of integrity. </span></span><span> </span></p></div><div><p></p><p><b><span>ROLE RESPONSIBILITIES </span></b><span><span> </span></span><span> </span></p></div><div><ul><li><p><span><span>Responsible for supervising operations of the Area to include hiring, live coaching, virtual coaching, representative development, performance management, and the assignment of key &#34;priority&#34; accounts within the medical community, managing12-14 representatives. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Develops and implements strategic plans for the Area, business plan, and overall responsibility for budgets at District level in alignment with RBD expectations.  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Plans, organizes, and<span> </span></span><span>monitors</span><span><span> </span>performance to achieve the business potential of the Area and Region. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensuring effective territory<span> </span></span><span>representatives</span><span><span> </span></span><span>utilization</span><span><span> </span>of promotional material, making valuable contribution to the formulation of marketing plans for the year, measuring efficient implementation of the plans in the<span> </span></span><span>field</span><span><span> </span>and undertaking regular assessment of marketing activities as an integral part of the total marketing operations  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Proactive data analysis to<span> </span></span><span>identify</span><span><span> </span>market trends  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Collaborates,<span> </span></span><span>identifies</span><span>, &amp; motivates key account development and opportunities that<span> </span></span><span>impact</span><span><span> </span>regional/national business  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Build relationships with customers (including KOLs) and key stakeholders (including members of the Area and Region Management Teams, Channel Partners, and other cross-functional partners) and<span> </span></span><span>utilizes</span><span><span> </span>content appropriately for engagement  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Develops external advocates and contributes to advocacy and community engagement (as necessary)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Understands and champions the value of cross-functional collaboration to deliver on customer needs, while ensuring that compliance guardrails are respected by representatives </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Coaches’ representatives on seamlessly connecting cross-functional colleagues reactively to address customer needs and how to use digital tools  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Effectively plan and conduct plan of action and other meetings with Area Management Teams, Channel Partners, and other cross-functional partners  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Collaborate effectively in an integrated account team  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensures cross-functional partnerships within all of Pfizer’s Markets / customers to build up effective relationships and face-to-face selling  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Leads cross functional partnerships ensuring patient services are being met (as necessary)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Maintains enhanced product and/or portfolio, disease state, and market knowledge to respond accurately to all questions<span> </span></span><span>regarding</span><span><span> </span>products, policies, and business-related issues from customers &amp; reps  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Able to expertly<span> </span></span><span>operate</span><span><span> </span>digital and virtual tools/platforms  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Leverages insights from new analytics tools (e.g., 360-degree customer insights)  </span></span><span> </span></p></li></ul></div></div><div><div><ul><li><p><span><span>Demonstrates advanced virtual communication skills (e.g., empathy, listening, asking probing questions)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Retains flexible time management (e.g., time allocation of F2F v. virtual engagements to meet business<span> </span></span><span>objectives</span><span><span> </span>to maximize HCP engagement across large(r) geographies)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Works with all members of Area to coach and counsel on improvement of performance and skill execution of selling skills, product knowledge, and capabilities needed for successful representative development, including the development of business plans  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ensures actions of self and team are fully compliant; has complete understanding of all relevant compliance policies and processes; escalate issues, as necessary, and ensures<span> </span></span><span>appropriate commitment</span><span><span> </span>to integrity within their team  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Implements and upholds Area Standards with sales colleagues </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Applies situational leadership skills (e.g., knowing when to intervene aligning coaching to colleague’s developmental level)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Employs multiple and interactive methods of coaching across all engagement types (e.g., F2F coaching in front of customers, when appropriate a virtual ‘ride along’,)  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Builds<span> </span></span><span>strong team</span><span><span> </span>culture, colleague engagement, and morale  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Promotes a feedback culture and continuous improvement mindset in team to assess quality of customer experience  </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Set team goals and hold team members accountable for consistent adherence i (e.g., time management, technical knowledge, communication, compliance, and use of technology) </span></span><span> </span></p></li></ul></div><div><p><b><span> </span></b><span> </span></p></div><div><p><b><span>Basic Qualifications </span></b><span><span> </span></span><span> </span></p></div><div><ul><li><p><span><span>Bachelor’s Degree Required </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Must live within 50 miles of the Area boundary </span></span><span> </span></p></li></ul></div><div><ul><li><p><span>6 years of previous pharmaceutical, biotech, or medical marketing/sales experience with at least 3-5 years spent in a position with demonstrated leadership across Peer and Customer Groups.</span> <span><span> </span> </span></p></li></ul></div><div><ul><li><p><span><span>Experience working with key thought leaders or high influence customers in large group practices, hospitals, or managed care organizations preferred. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>This position will require travel as needed to develop internal and external relationships. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Valid US driver’s license and driving record in compliance with company standards</span><span>. <span> </span></span><span>Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Candidate<span> </span></span><span>demonstrates</span><span><span> </span>a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. </span></span><span> </span></p></li></ul></div><div><p></p><p><b><span>Preferred Qualifications</span></b><span><span> </span></span><span> </span></p></div></div><div><div><ul><li><p><span><span>MBA or relevant graduate degree preferred </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>5 or more<span> </span></span><span>years</span><span><span> </span>people management experience preferred and ability to develop and motivate others, lead through change, and deliver on Pfizer business imperatives is necessary to be successful in this role. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Vaccines experience and<span> </span></span><span>expertise</span><span><span> </span>strongly preferred </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Ability to develop and reinforce team<span> </span></span><span>expertise</span><span><span> </span>on broader portfolio of content to show ‘Science First’ mindset </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Cross-functional collaboration mindset to<span> </span></span><span>facilitate</span><span><span> </span>‘One Pfizer’ commitment to customer </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Feedback culture mindset, </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Additional</span><span><span> </span>digital training to ensure personal adherence, as well as leadership by example for team adherence (incl. contracting permissions/guidelines) </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Model/leader for change, agility, and adaptability </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellence in engaging customers and coaching team members in a hybrid environment,<span> </span></span><span>including:</span><span><span> </span>Enhanced competency level on virtual and digital tools/platforms </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Data-driven resource management to ensure proper channel deployment </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong organizational and analytical skills are also<span> </span></span><span>required</span><span><span> </span>and ability to analyze and draw<span> </span></span><span>appropriate conclusions</span><span><span> </span>using sales data/call reporting software/applications and able to adapt to Pfizer&#39;s long-term technology model in bringing Pfizer information to market. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Demonstrated ability both to think strategically and to execute flawlessly to deliver results </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Strong<span> </span></span><span>track record</span><span><span> </span>of collaborative and motivational leadership and internal stakeholder management skills </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Enterprise thinking;<span> </span></span><span>anticipates</span><span><span> </span>consequences </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excellent facilitation skills </span></span><span> </span></p></li></ul><p></p><p><b><span>Other Job Details:</span></b></p><p><span>Last day to apply: April 20, 2026</span></p><p></p><p><span>The annual base salary for this position ranges from $139,000 - $280,400.<span>  </span>In addition, this position offers an additional<span>  </span>Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States. </span></p></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/vaccines-area-business-manager-newark-nj-pfizer/69d576a6c8e81216cd0c4c78</link><guid isPermaLink="true">http://biotechroles.com/vaccines-area-business-manager-newark-nj-pfizer/69d576a6c8e81216cd0c4c78</guid><pubDate>Tue, 07 Apr 2026 21:27:02 GMT</pubDate><company>Pfizer</company><location>United States - New Jersey - Remote</location><salary>$140000-180000</salary><type>Full time</type></item><item><title><![CDATA[Vaccines Area Business Manager - Atlanta S, GA]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b>  </p><div><div><div><div><div><div><div><div><div><p></p><p>The Vaccines Area Business Manager (ABM) will report into the Regional Business Director (RBD) and will work with customer-facing (Accounts and Pharmacy) and Headquarters (HQ) teams across the organization.  The ABM will be responsible for the supervision and leadership of 12-14 representatives within the Northeast area, sales performance of the business portfolio of products, and business knowledge of the area landscape to assess key stakeholders plus future trends within the business marketplace. This position will require regular in field and virtual coaching and observation of Field Representatives and frequent customer contact as well as the development of a strong, effective partnership with accounts, retail, and marketing colleagues.  The ABM will ensure compliant execution by team members, driving understanding of relevant policies and guidance and advancing a culture of integrity.  </p><p></p><p><b>ROLE RESPONSIBILITIES </b>  </p><ul><li><p>Responsible for supervising operations of the Area to include hiring, live coaching, virtual coaching, representative development, performance management, and the assignment of key &#34;priority&#34; accounts within the medical community, managing12-14 representatives.  </p></li></ul><ul><li><p>Develops and implements strategic plans for the Area, business plan, and overall responsibility for budgets at District level in alignment with RBD expectations.   </p></li></ul><ul><li><p>Plans, organizes, and monitors performance to achieve the business potential of the Area and Region.  </p></li></ul><ul><li><p>Ensuring effective territory representatives utilization of promotional material, making valuable contribution to the formulation of marketing plans for the year, measuring efficient implementation of the plans in the field and undertaking regular assessment of marketing activities as an integral part of the total marketing operations   </p></li></ul><ul><li><p>Proactive data analysis to identify market trends   </p></li></ul><ul><li><p>Collaborates, identifies, &amp; motivates key account development and opportunities that impact regional/national business   </p></li></ul><ul><li><p>Build relationships with customers (including KOLs) and key stakeholders (including members of the Area and Region Management Teams, Channel Partners, and other cross-functional partners) and utilizes content appropriately for engagement   </p></li></ul><ul><li><p>Develops external advocates and contributes to advocacy and community engagement (as necessary)   </p></li></ul><ul><li><p>Understands and champions the value of cross-functional collaboration to deliver on customer needs, while ensuring that compliance guardrails are respected by representatives  </p></li></ul><ul><li><p>Coaches’ representatives on seamlessly connecting cross-functional colleagues reactively to address customer needs and how to use digital tools   </p></li></ul><ul><li><p>Effectively plan and conduct plan of action and other meetings with Area Management Teams, Channel Partners, and other cross-functional partners   </p></li></ul><ul><li><p>Collaborate effectively in an integrated account team   </p></li></ul><ul><li><p>Ensures cross-functional partnerships within all of Pfizer’s Markets / customers to build up effective relationships and face-to-face selling   </p></li></ul><ul><li><p>Leads cross functional partnerships ensuring patient services are being met (as necessary)   </p></li></ul><ul><li><p>Maintains enhanced product and/or portfolio, disease state, and market knowledge to respond accurately to all questions regarding products, policies, and business-related issues from customers &amp; reps   </p></li></ul><ul><li><p>Able to expertly operate digital and virtual tools/platforms   </p></li></ul><ul><li><p>Leverages insights from new analytics tools (e.g., 360-degree customer insights)   </p></li></ul><ul><li><p>Demonstrates advanced virtual communication skills (e.g., empathy, listening, asking probing questions)   </p></li></ul><ul><li><p>Retains flexible time management (e.g., time allocation of F2F v. virtual engagements to meet business objectives to maximize HCP engagement across large(r) geographies)   </p></li></ul><ul><li><p>Works with all members of Area to coach and counsel on improvement of performance and skill execution of selling skills, product knowledge, and capabilities needed for successful representative development, including the development of business plans   </p></li></ul><ul><li><p>Ensures actions of self and team are fully compliant; has complete understanding of all relevant compliance policies and processes; escalate issues, as necessary, and ensures appropriate commitment to integrity within their team   </p></li></ul><ul><li><p>Implements and upholds Area Standards with sales colleagues  </p></li></ul><ul><li><p>Applies situational leadership skills (e.g., knowing when to intervene aligning coaching to colleague’s developmental level)   </p></li></ul><ul><li><p>Employs multiple and interactive methods of coaching across all engagement types (e.g., F2F coaching in front of customers, when appropriate a virtual ‘ride along’,)   </p></li></ul><ul><li><p>Builds strong team culture, colleague engagement, and morale   </p></li></ul><ul><li><p>Promotes a feedback culture and continuous improvement mindset in team to assess quality of customer experience   </p></li></ul><ul><li><p>Set team goals and hold team members accountable for consistent adherence i (e.g., time management, technical knowledge, communication, compliance, and use of technology)  </p></li></ul><p><b> </b> </p><p><b>Basic Qualifications </b>  </p><ul><li><p>Bachelor’s Degree Required  </p></li></ul><ul><li><p>Must live within 50 miles of the Area boundary  </p></li></ul><ul><li><p><span>6 years of previous pharmaceutical, biotech, or medical marketing/sales experience with at least 3-5 years spent in a position with demonstrated leadership across Peer and Customer Groups.</span>  </p></li></ul><ul><li><p>Experience working with key thought leaders or high influence customers in large group practices, hospitals, or managed care organizations preferred.  </p></li></ul><ul><li><p>This position will require travel as needed to develop internal and external relationships.  </p></li></ul><ul><li><p>Valid US driver’s license and driving record in compliance with company standards.  Any DUI/DWI or other impaired driving citation within the past 7 years will disqualify you from being hired. </p></li></ul><ul><li><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.  </p></li></ul><p></p><p><b>Preferred Qualifications</b>  </p><ul><li><p>MBA or relevant graduate degree preferred  </p></li></ul><ul><li><p>5 or more years people management experience preferred and ability to develop and motivate others, lead through change, and deliver on Pfizer business imperatives is necessary to be successful in this role.  </p></li></ul><ul><li><p>Vaccines experience and expertise strongly preferred  </p></li></ul><ul><li><p>Ability to develop and reinforce team expertise on broader portfolio of content to show ‘Science First’ mindset  </p></li></ul><ul><li><p>Cross-functional collaboration mindset to facilitate ‘One Pfizer’ commitment to customer  </p></li></ul><ul><li><p>Feedback culture mindset,  </p></li></ul><ul><li><p>Additional digital training to ensure personal adherence, as well as leadership by example for team adherence (incl. contracting permissions/guidelines)  </p></li></ul><ul><li><p>Model/leader for change, agility, and adaptability  </p></li></ul><ul><li><p>Excellence in engaging customers and coaching team members in a hybrid environment, including: Enhanced competency level on virtual and digital tools/platforms  </p></li></ul><ul><li><p>Data-driven resource management to ensure proper channel deployment  </p></li></ul><ul><li><p>Strong organizational and analytical skills are also required and ability to analyze and draw appropriate conclusions using sales data/call reporting software/applications and able to adapt to Pfizer&#39;s long-term technology model in bringing Pfizer information to market.  </p></li></ul><ul><li><p>Demonstrated ability both to think strategically and to execute flawlessly to deliver results  </p></li></ul><ul><li><p>Strong track record of collaborative and motivational leadership and internal stakeholder management skills  </p></li></ul><ul><li><p>Enterprise thinking; anticipates consequences  </p></li></ul><ul><li><p>Excellent facilitation skills  </p></li></ul><p></p><p><b>Other Job Details:</b></p><p>Last day to apply: April 20, 2026</p><p></p><p>The annual base salary for this position ranges from $139,000 - $280,400.  In addition, this position offers an additional  Sales Incentive bonus. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits| (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to any location outside of the United States.<span> </span></p></div></div></div></div></div></div></div></div></div>&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Sales&amp;#xa;]]></description><link>http://biotechroles.com/vaccines-area-business-manager-atlanta-s-ga-pfizer/69d576a6c8e81216cd0c4c77</link><guid isPermaLink="true">http://biotechroles.com/vaccines-area-business-manager-atlanta-s-ga-pfizer/69d576a6c8e81216cd0c4c77</guid><pubDate>Tue, 07 Apr 2026 21:27:02 GMT</pubDate><company>Pfizer</company><location>United States - Georgia - Remote</location><salary>$130000-180000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Automation Network Engineer]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>At Pfizer, we believe that every role contributes to our mission of improving patients&#39; lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you&#39;ll play a pivotal role in accelerating the delivery of medicines to the world.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li><p>Contribute to moderately complex projects, managing time effectively to meet targets.</p></li><li><p>Apply skills and knowledge to contribute to team efforts.</p></li><li><p>Use judgment to modify methods and techniques as needed.</p></li><li><p>Monitor and complete periodic reviews, including the validation master plan for automation engineering.</p></li><li><p>Demonstrate exceptional planning, organizing, time management, and team participation skills.</p></li><li><p>Take responsibility for routine and preventive maintenance, ensuring equipment and facilities operate safely and efficiently.</p></li></ul><p></p><p><b>Here Is What You Need </b>(Minimum Requirements)</p><ul><li><p>High school diploma (or equivalent) with 8&#43; years of experience or Associate’s degree with 6&#43; years of experience or BA/BS with 2&#43; years of experience or MBA/MS with any years of relevant experience</p></li><li><p>Proven experience in Automation Engineering</p></li><li><p>Proficiency in drafting software test plans, user requirements, and system design documents</p></li><li><p>Hands-on experience with Automation Compliance projects</p></li><li><p>Familiarity with process controls equipment</p></li><li><p>Robust understanding of Networks, Computerized Systems, Compliance regulations, and standards</p></li><li><p>Strong teamwork spirit and excellent communication skills</p></li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements)</p><ul><li><p>Relevant pharmaceutical experience</p></li><li><p>Network Certification</p></li><li><p>Understanding of programming and proficiency in at least one language</p></li><li><p>Knowledge of Good Manufacturing Practices (GMP)</p></li><li><p>Ability to train others effectively</p></li><li><p>Strong problem-solving skills</p></li><li><p>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use</p></li></ul><p>  </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><ul><li><p>Requires routine sitting, standing, walking, listening and talking</p></li><li><p>Acute mental and visual attention at all times</p></li><li><p>Handle multiple projects while managing frequent interruptions</p></li><li><p>Requires moderate lifting or moving up to 25 pounds (lbs)</p></li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><ul><li><p>Requires regular onsite attendance </p></li><li><p>Must have the ability to work effectively under strict deadlines</p></li><li><p>Must be able and willing to work beyond office hours which may include weekends and holidays</p></li><li><p>Must be capable of supporting up to 10% travel (domestic and international) </p></li></ul><p></p><p><b>Other Job Details:</b></p><ul><li><p><b>Last Date to Apply for Job: March 21,2026</b></p></li><li><p><span>Work Location Assignment: Must be able to work from assigned Pfizer office </span>2-3 days per week, or as needed by the business</p></li></ul><p></p>&amp;#xa;The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Engineering&amp;#xa;]]></description><link>http://biotechroles.com/sr-automation-network-engineer-pfizer/69d576a5c8e81216cd0c4c76</link><guid isPermaLink="true">http://biotechroles.com/sr-automation-network-engineer-pfizer/69d576a5c8e81216cd0c4c76</guid><pubDate>Tue, 07 Apr 2026 21:27:01 GMT</pubDate><company>Pfizer</company><location>United States - Kansas - McPherson</location><salary>$105000-145000</salary><type>Full time</type></item><item><title><![CDATA[Lider de Utilities]]></title><description><![CDATA[<div><div><div><p><b><span>Objetivo de la Posición</span></b><span> </span></p><p></p></div></div><div><div><p><span><span>Todo lo que hacemos, todos los días, está en línea con un compromiso inquebrantable con la calidad y la entrega de productos seguros y efectivos a los pacientes.  Nuestra cultura de calidad basada en la ciencia y el riesgo es flexible, innovadora y orientada al cliente. Ya sea que esté involucrado en el desarrollo, mantenimiento, cumplimiento o análisis a través de programas de investigación, su contribución tendrá un impacto directo en los pacientes.</span></span><span> </span></p><p></p></div><div><p><span><span>Liderara las actividades relacionadas a<span> </span></span><span>Servicios</span><span><span> </span></span><span>de la Planta Buenos Aires. </span></span><span> </span></p></div><div><p><span> </span></p></div></div></div><div><p><b><span>R</span><span>esponsabilidades</span><span><span> </span>generales del área</span></b><span> </span></p></div><div><p></p><p><span><span>El<span> </span>Líder de Servicios<span> </span>garantiza la disponibilidad<span> </span>de los equipos que proveen servicios de Planta,</span><span><span> </span></span><span>cumpliendo con el presupuesto de gastos correspondiente</span><span>.<span> </span></span><span>Además</span><span><span> </span>es responsable del sistema eléctrico de toda la planta.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>R</span><span>esponsabilidades</span><span><span> </span></span><span>Específicas</span><span><span> </span>de la posición</span></b><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Responsabilidades específicas:</span></b><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>- Participar activamente en la confección de especificaciones técnicas para la compra de</span><span><span> </span>equipos<span> </span></span><span>de servicios<span> </span></span><span>nuevos y sus instalaciones.</span></span><span> </span></p></div><div><p><span><span>- Confeccionar<span> </span></span><span>Ia</span><span><span> </span>programaci</span><span>ó</span><span>n del mantenimiento correctivo/preventivo/ predictiv</span><span>o</span><span><span> </span>de</span><span><span> </span></span><span>los equipos de<span> </span></span><span>servicios y/o eléctricos<span> </span></span><span>con<span> </span></span><span>Ia</span><span><span> </span>correspondiente descripci</span><span>ó</span><span>n de tareas asociadas<span> </span></span></span><span><span>y</span><span><span> </span></span></span><span><span>documentaci</span><span>ó</span><span>n.</span></span><span> </span></p></div><div><p><span><span>-<span> </span></span></span><span><span>Reportar cualquier desviación identificada y participar activamente en su investigación y prevención de recurrencia.</span></span><span> </span></p></div><div><p><span><span>- Participar en la<span> </span></span><span>revisión</span><span><span> </span>de prácticas y Procedimientos mediante el sistema de<span> </span></span></span><span><span>Control<span> </span></span></span><span><span>de Cambios.</span></span><span> </span></p><p></p></div><div><p><span><span>Mantenimiento de<span> </span></span><span>Utilities</span></span><span> </span></p><p></p></div><div><p><span><span>- Organizar el Mantenimiento de equipos de servicios centrales de planta</span><span><span> </span>de Solidos y Capsulas Blandas</span><span>.</span></span><span> </span></p></div><div><p><span><span>- Verificar el correcto funcionamiento de los equipos de servicios<span> </span></span><span>manteniéndolos<span> </span></span><span>en perfecto estado de eficiencia, cumpliendo con los programas de</span><span><span> </span></span><span>mantenimiento preestablecidos.</span></span><span> </span></p></div><div><p><span><span>- Realizar el seguimiento y trato de proveedores en los distintos servicios contratados.</span></span><span> </span></p></div><div><p><span><span>- Asegurar el cumplimiento de los costos, consumes e<span> </span></span><span>índices</span><span><span> </span></span><span>energéticos establecidos, como así también del presupuesto de gastos.</span></span><span> </span></p></div><div><p><span><span>-<span> </span></span></span><span><span>Reportar cualquier desviación identificada y participar activamente en su investigación y prevención de recurrencia.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span><span>Otras Actividades de FFL:</span></span><span> </span></p><p></p></div><div><p><span><span>- Cumplir<span> </span></span><span>y<span> </span></span><span>verificar el cumplimiento de las normas<span> </span></span><span>cGMP</span><span><span> </span></span><span>y<span> </span></span><span>EHS.</span></span><span> </span></p></div><div><p><span><span>- Aprobar el diseño de<span> </span></span><span>Ia</span><span><span> </span>documentación técnica asociada al sector.</span></span><span> </span></p></div><div><p><span><span>- Promover la ejecución de proyectos de mejoras a través de la aplicación de<span> </span></span><span>herramientas de Mejora Continua. </span></span><span> </span></p></div><div><p><span><span>-<span> </span></span><span>Definir e implementar la estrategia para lograr resultados medidos por métricas establecidas y para mejorar continuamente el rendimiento operativo.</span></span><span> </span></p></div><div><p><span><span>- Ad</span></span><span><span>ministrar<span> </span></span><span>el</span><span><span> </span>presupuesto financier</span><span>o del sector</span></span><span><span> </span></span><span> </span></p></div><div><p><span><span>- Participar activamente de las redes de Pfizer<span> </span></span><span>y<span> </span></span><span>otras actividades promovidas por<span> </span></span><span>Ia</span><span><span> </span>corporación.</span></span><span> </span></p></div><div><p><span><span>- Seleccionar, liderar<span> </span></span><span>y<span> </span></span><span>motivar al personal a su cargo a fin de alcanzar los objetivos fijados. Realizar<span> </span></span></span><span><span>la evaluación de rendimiento del personal. </span></span><span> </span></p></div><div><p><span><span>- Asegurar el cumplimiento del entrenamiento requerido para el personal, inicial<span> </span></span><span>y<span> </span></span><span>continuo.</span></span><span> </span></p></div><div><p><span><span>- Crear e implementar planes de desarrollo de sus reportes directos.</span></span><span> </span></p></div><div><p><span><span>-Desarrollar planes de sucesión para su posición<span> </span></span><span>y<span> </span></span><span>Ia</span><span><span> </span>de sus reportes directos. Seguir las<span> </span></span><span>buenas prácticas de Reclutamiento y selección</span><span>.</span></span><span> </span></p></div><div><p><span><span>- Colaborar en las actividades que lleven a lograr un adecuado ambiente Laboral para todos los colegas.</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Recursos que gestionará </span></b><span> </span></p></div><div><p><span><span>Presupuesto M&amp;R</span></span><span> </span></p></div><div><p><span><span>Supervisor de técnicos</span></span><span> </span></p></div><div><p><span><span>Técnicos: eléctrico/<span> </span></span><span>utilities</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Principales clientes internos:</span><span> </span></b><span> </span></p></div><div><p><span><span>Manufactura,<span> </span></span><span>Contratistas,<span> </span></span><span>Procurement</span><span>, Finanzas,<span> </span></span><span>Laboratorios, Ingeniería Industrial</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Rol a quien delegará sus tareas en caso de suplencia:</span><span> </span></b><span> </span></p></div><div><p><span><span>Gerente de EMU</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><b><span>Rol del que puede<span> </span></span><span>ser<span> </span></span><span>suplente/mentor/referente</span></b><span><span>:</span><span> </span></span><span> </span></p></div><div><p><span><span> </span><span>Gerente de EMU</span><span><span> </span>/<span> </span></span></span><span><span>Supervisor de técnicos</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span> </span><b><span>Educación / Capacitación:</span></b><span> </span></p></div><div><div><div><div><p><span><span>Requerido:</span></span><span> </span></p></div><div><p><span><span>Título Universitario en carrera relacionada</span></span><span> </span></p></div><div><p><span><span>M</span><span>anejo fluido de idioma<span> </span></span><span>Ingles</span><span><span> </span>(escrito y oral</span><span>)</span></span><span> </span></p></div><div><p><span> </span><span><span>Deseado:</span></span><span> </span></p></div></div><div><div><p><span><span>Posgrado Universitario en carrera relacionada</span></span><span> </span></p></div><div><p><span> </span></p></div></div></div></div><div><p><span> </span><b><span>Experiencia Laboral:</span></b><span> </span></p></div><div><div><div><div><p><span><span>Requerido:</span></span><span> </span></p></div><div><p><span><span>Mínimo<span> </span></span><span>5</span><span><span> </span>años en<span> </span></span><span>Ia</span><span><span> </span>industria</span></span><span> </span></p></div><div><p><span><span>F</span><span>armacéutica</span><span><span> </span>en trabajos relacionados</span><span>.</span></span><span> </span></p></div></div><div><div><p><span><span>Deseado:</span></span><span> </span></p></div><div><p><span><span>Mínimo<span> </span></span><span>5</span><span><span> </span>años en<span> </span></span><span>posición similar</span><span>.</span></span><span> </span></p></div></div></div></div><div><p><span> </span></p></div><div><div><div><b><span>Comentarios adicionales:</span><span><span> </span>Competencias que requiere el rol</span></b><span> </span></div><div><div><ul><li><p><span><span>Demuestra conocimiento del negocio</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Habilidades técnicas/funcionales</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Actúa decisivamente</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Lidera el cambio</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Asume su responsabilidad y logra el sentido de responsabilidad en otros</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Desarrolla</span></span><span><span><span> </span>a otros y construye equipos efectivos</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Excelente capacidad para relacionarse con el personal de otras áreas. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Capacidad de evaluar y detectar oportunidades de mejoras. </span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Habilidades de comunicación y transmisión de conocimientos.</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Si bien todas las competencias Pfizer para Colegas corresponden a la posición, las siguientes se aplican con mayor frecuencia:</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Habilidades técnicas/funcionales</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Asume su responsabilidad</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Crea relaciones de colaboración</span></span><span> </span></p></li></ul></div><div><ul><li><p><span><span>Actúa decisivamente </span></span><span> </span></p></li></ul></div><div><p><span> </span></p></div><div><p><b><span>Sistemas claves que requiere acceso:</span></b><span> </span></p></div><div><p><span><span>eQMS</span><span>, QTS,<span> </span></span><span>SAP, PDOCs</span><span>,</span><span><span> </span>EAMS,<span> </span></span><span>PEPs</span></span><span> </span></p></div><div><p><span> </span></p></div><div><p><span> </span></p></div></div></div></div><p></p><p></p><ul><li><p></p></li></ul><p> <br /> </p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>Engineering<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/lider-de-utilities-pfizer/69d576a4c8e81216cd0c4c74</link><guid isPermaLink="true">http://biotechroles.com/lider-de-utilities-pfizer/69d576a4c8e81216cd0c4c74</guid><pubDate>Tue, 07 Apr 2026 21:27:00 GMT</pubDate><company>Pfizer</company><location>Argentina - Buenos Aires</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Manager, Operational Strategy Lead]]></title><description><![CDATA[<p><span style="color:#494949"><b>ROLE SUMMARY</b></span></p><p></p><p><span style="color:#494949">Operational Strategy Lead role is a member of the Global Clinical Supply Operations (GCSO) (part of the Clinical Development &amp; Operations Global Clinical Supply Group). </span></p><p></p><p><span style="color:#494949">Our purpose is to provide clinical packaging, labeling, and logistics solutions to deliver quality patient-focused clinical supplies to the patient. </span></p><p></p><p><span style="color:#494949">GCSO provide quality clinical supplies in a compliant, timely, innovative and cost-effective manner. We continuously strive to improve our systems, processes and capabilities in collaboration with our internal Pfizer and external partners in support of developing breakthroughs to change patients’ lives.Operational Strategy Leads are accountable for developing an integrated E2E CSO operational strategy for Pfizer clinical programs and clinical studies</span></p><p></p><p><span style="color:#494949">OSLs partner with Supply Chain Leads (SCL) and Clinical Research Pharmacists (CRP) closely to develop comprehensive and patient-focused operational strategies for their assigned programs</span></p><p></p><p><span style="color:#494949">OSLs are accountable for implementing the operational strategy delivering clinical supplies to support the clinical studies for their assigned programs. OSL achieves excellence by focusing on patients, working with integrity and professionalism. </span></p><p></p><p><span style="color:#494949">OSLs utilize knowledge of Supply Chain process, their expertise in clinical supply packaging, labelling, and distribution, and project management skills to establish comprehensive operational strategies and collaborate with internal and external partners to deliver clinical supplies to support clinical studies. OSLs work closely with other functional roles in GCSO and across GCS and Quality Assurance (QA) to ensure timely and accurate execution of clinical packaging, labelling, and distribution operations. </span></p><p><span style="color:#494949"><br />Substantial training is provided to ensure OSLs can perform all duties and tasks an OSL is accountable and responsible for. </span></p><p><span style="color:#494949"> </span></p><p><span style="color:#494949">OSLs proactively manage risks through risk identification and risk mitigation plans and have detailed execution and monitoring plans to enable the overall design input on a program basis and effective execution of clinical supply packaging, labeling, and distribution.</span></p><p></p><p><span style="color:#494949"><b>KEY RESPONSIBILITIES</b></span></p><p></p><ul><li><p><span style="color:#494949">The Operational Strategy Lead (OSL) is accountable for developing and implementing mid-to long-term supply chain strategies for assigned clinical assigned programs and initiatives. This includes forecast and execution of key packaging, labelling, distribution, and logistics events. The OSL is also accountable for monitor the effectiveness of their operational strategies, and partnering with functional lines in Clinical Supply Operations (CSO) to ensure seamless implementation of operational strategies and delivery of clinical supplies.</span></p></li><li><p><span style="color:#494949">Substantial training will be provided to ensure OSLs can perform all duties and tasks an OSL is responsible for. </span></p></li><li><p><span style="color:#494949">OSLs represent GCSO on Clinical Supply Team (CST) for their assigned programs.</span></p></li><li><p><span style="color:#494949">OSLs are responsible for ensuring that the overarching strategy &amp; scenario planning for the program/protocol is developed with and shared within appropriate stakeholders.</span></p></li><li><p><span style="color:#494949">OSLs monitor and provide input to GCSO level program/protocol dashboards part of program management support.</span></p></li><li><p><span style="color:#494949">OSLs directly oversee delivery of of GCSO activities (clinical packaging and labelling operations and trial distribution) to ensure that all clinical study timelines are support and met. </span></p></li><li><p><span style="color:#494949">Ensures GCSO inspection readiness as part of program management support.</span></p></li><li><p><span style="color:#494949">Participates or Leads GCSO strategic and/or Continuous Improvement (CI) initiatives.</span></p></li><li><p><span style="color:#494949">Provides program-level forecast and special needs to vendors.</span></p></li><li><p><span style="color:#494949">Provides Packaging, Labeling, and Distribution/Storage cost estimation.</span></p></li><li><p><span style="color:#494949">Support integration activities when needed.</span></p></li><li><p><span style="color:#494949">OSL is the GCSO point of contact with Supply Chain Leads (SCL) and Clinical Research Pharmacist (CRP) on GCSO operational strategy, and projects will be assigned at a program level. This position, working independently and influencing others without having a direct reporting relationship, coordinates the fulfilment of customer requests while providing excellent customer service. This role strives to utilize technology and industry trend information to proactively contribute to improving effectiveness of integrated packaging, labelling, and distribution strategies.</span></p></li><li><p><span style="color:#494949">Develops positive and collaborative partnerships with key stakeholders across partner lines.  Proactively ensure quality and compliance through risk identification and mitigation plans, strategic planning and execution, and overall design input. </span></p></li><li><p><span style="color:#494949">Assists GCSO Leadership with strategic development of CSO roles to support evolving needs of stakeholders and patients.</span></p></li><li><p><span style="color:#494949">Evaluates current processes and make recommendations for continuous improvement in the Packaging and Distribution operating models.</span></p></li><li><p><span style="color:#494949">Supports fiscal accountability to projects by refining project specific costs. </span></p></li><li><p><span style="color:#494949">Partners with CSO functional line leaders to further develop/refine human resource capacity analysis for CSO to align resource with project needs according to portfolio priorities</span></p></li><li><p><span style="color:#494949">Ensures compliance with all legal requirements (e.g., EHS, cGMP, GCP, import/export, Quality Standards, 21 CFR Part 11) by creating and maintaining a culture committed to quality; accountable for maintaining training and compliance required for the role; enhance quality and compliance on a site and patient basis utilizing risk and mitigation plans; and assess cross functional impact of procedure/ process changes to CSO processes.</span></p></li><li><p><span style="color:#494949">Interfaces directly with GCS and other groups across Pfizer in order to provide timely and responsive guidance and issue resolution regarding clinical packaging and distribution activities. </span></p></li><li><p><span style="color:#494949">Establishes Program level integrated GCSO operational strategies with Clinical Supply Teams (CST). Contribute to decisions on country feasibility and strategy discussions well in advance of the protocol decisions. Ownership of timing and challenges on country movements in order to meet project requirements.</span></p></li><li><p><span style="color:#494949">Ensures excellent customer service through the development of strong working relationships with key customers and partners leaders to facilitate open lines of communication regarding project priorities, and issue resolution.</span></p></li><li><p><span style="color:#494949">Triage issues and provide appropriately detailed updates to CSO leadership.</span></p></li><li><p><span style="color:#494949">Utilizes project management skills to develop robust packaging and distribution/ logistics planning and management tools; optimize operational strategy to ensure patient continuity; high quality project oversight and activity review.</span></p></li><li><p><span style="color:#494949">When executing packaging, labeling, and distribution operations, the responsibilities include:<br />• Partner with the Supply Chain Leads (SCLs) to review and interpret the clinical protocol to develop practical and efficient packaging designs for Clinical Supplies. Partnering with the SCLs to generate and approve the Clinical Packaging Request (CPR).<br />• Coordinating and communicating multiple study packaging and/or labelling requirements across a network of global contract packaging organizations. </span></p></li></ul>&nbsp;<br>Work Location Assignment:&nbsp;Hybrid<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Purpose</u> </span></span></span></p><p style="text-align:left"><span><span><span><b>Breakthroughs that change patients&#39; lives</b>... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Digital Transformation Strategy </u></span></span></span></p><p style="text-align:left"><span><span><span>One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Flexibility </u> </span></span></span></p><p style="text-align:left"><span><span><span>We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the <span><span><span class="WKM0">conversation!  </span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><u>Equal Employment Opportunity</u> </span></span></span></p><p style="text-align:left"><span><span><span>We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><u>DisAbility Confident</u></p><p style="text-align:left">We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!</p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Logistics &amp; Supply Chain Mgmt<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/sr-manager-operational-strategy-lead-pfizer/69d576a4c8e81216cd0c4c73</link><guid isPermaLink="true">http://biotechroles.com/sr-manager-operational-strategy-lead-pfizer/69d576a4c8e81216cd0c4c73</guid><pubDate>Tue, 07 Apr 2026 21:27:00 GMT</pubDate><company>Pfizer</company><location>United Kingdom - Sandwich</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Pfizer Patient Services (PPS), Affordability Analytics]]></title><description><![CDATA[<p><b>Role Summary</b></p><p></p><p>Patient Solution Insights &amp; Analytics, part of Pfizer Patient Services (PPS), harnesses the power of data to drive robust analytics and insight development that inform Pfizer&#39;s most critical business questions. The Patient Solution Insights and Analytics team&#39;s rigorous analytical expertise is depended on as the compass and decision support for the enterprise. Our dynamic, exciting team of subject-matter experts comes from diverse backgrounds and experiences, including data science, digital analytics, finance, market research, and consulting. As a team, we collaborate to turn data into meaningful insights that will have a direct impact on patient&#39;s lives and the future of Pfizer, as a data-driven organization.</p><p></p><p>This role is dynamic, fast-paced, highly collaborative, and covers a broad range of strategic topics that are critical to our business. The successful candidate will join PPS colleagues who are dedicated to helping drive improvements to Pfizer’s patient service programs through proactive thought leadership, innovative research capabilities, and the ability to communicate complex and dynamic information in new and creative ways</p><p></p><p><b>Role Responsibilities</b></p><p></p><p>This role is accountable for supporting the delivery data driven-insights &amp; solutions for patient services programs, and will partner with functional leads for Pfizer’s Business Analytics community, Pfizer Business Technology, Specialty Pharmacy Providers (SPP) center of excellence and external SPP customer, legal and compliance to develop and implement models, insights, and data products that drive each brands’ strategic priorities.</p><ul><li>Perform sophisticated syntheses across multiple insight sources (i.e., secondary analytics, primary strategy, and stakeholder feedback) to deliver impactful and relevant patient services strategy recommendations</li><li>Identify KPIs to monitor and diagnose program performance and operational execution, across the patient journey</li><li>Maintain data governance standards to ensure consistency and clarity in program metrics / business rule implementation over time</li><li>Work within a high-performing team of insights professionals, responsible for delivering integrated insights, program measurement analytics, reporting, and launch support</li><li>Monitor and manage research and analytics program budgets, identifying opportunities for cost savings, and ensuring financial compliance</li></ul><p></p><p>Technical skills</p><ul><li>Strong Analytical, coding skills (such as: Python, R, SQL, etc.), MS Excel and PowerPoint skills</li><li>Familiar with, and experienced at, different insight development methods across secondary data analytics and primary market research</li><li>Previously demonstrated experience in using innovative techniques to monitor, simulate and analyze complex data sets</li><li>Ability to assess and direct vendor technical capabilities and manage risks in the analytic process</li></ul><p></p><p><b>Basic Qualifications</b></p><p></p><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><ul><li>Bachelor’s degree required. Master of Science strongly preferred in a quantitative or engineering discipline</li><li>6&#43; years’ experience in Biopharma, analytics, strategic consulting, business, or related area</li><li>2&#43; years of hands-on coding experience in SQL or other data analytics tools in life sciences (e.g., Python, R, SAS)</li><li>Experience with the pharma ecosystem and datasets including physician-level prescribing, institutional sales data, payer-prescriber-level data, formulary data, Rebates, Symphony claims, Copay claims</li><li>Prior experience with patient services programs, including specific programmatic components, spanning: Affordability Programs (e.g., Copay, eVoucher), Field Access Support, Hub / Prior Authorization Support, Pharmacy / Distribution Workflows (i.e., retail, specialty pharmacy, and buy-and-bill)</li><li>Demonstrated success in a highly fast-paced setting</li><li>Ability to execute business direction, priorities, and action plans</li><li>Demonstrated analytical capabilities and critical thinking skills</li><li>Exceptional written and verbal communication skills, and prior experience in presenting to functional leaders</li><li>Strong customer service orientation</li><li>Ability to receive and implement direction from senior colleagues to achieve meaningful outcomes and create business impact</li><li>Commitment to receiving development and coaching from leadership </li></ul><div><p></p></div><p><b>Other Job Details:</b></p><ul><li><b>Last Date to Apply for Job: April 20th, 2026.</b></li><li>Ability to travel based on business needs</li><li>Location: NYHQ or PA - Collegeville</li><li>NOT eligible for Relocation Package</li><li>This position is hybrid and requires working onsite 2 to 3 days per week</li></ul><p></p><p>#LI-PFE</p>&amp;#xa;The annual base salary for this position ranges from $124,400.00 to $207,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-pfizer-patient-services-pps-affordability-analytics-pfizer/69d576a3c8e81216cd0c4c72</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-pfizer-patient-services-pps-affordability-analytics-pfizer/69d576a3c8e81216cd0c4c72</guid><pubDate>Tue, 07 Apr 2026 21:26:59 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Institutional Customer Communications & Marketing]]></title><description><![CDATA[<p><b><span>Use Your Power for Purpose</span></b></p><p><span>The US Commercial organization, which is in the Global Hospital &amp; Biosimilars organization, is comprised of over 200 products, spanning more than 10 therapeutic areas, with annual revenue of over $2.5B.</span></p><p><span> </span></p><p><span>The Senior Manager, Institutional Customer Communications &amp; Marketing, is responsible for leading the development and execution of customer communications and marketing materials to maximize revenue, support customer reputation, drive new initiatives for US Hospital and Biosimilar products, and advance internal communications and culture for U.S. Commercial within Global Hospital &amp; Biosimilars organization.</span></p><p><span> </span></p><p><span>The Senior Manager will execute a variety of communications for the business, including supply/availability updates, product opportunities, and market actions via channels including customer letters, field force talking points, Q&amp;As, customer emails, internal communications and more. The colleague will write, develop, and manage customer communications, working with and seeking input from cross-functional team members including Institutional Customer Marketing and Communications, Sterile Injectables Portfolio, Pfizer Global Supply, Corporate Affairs, Customer-Facing Colleagues, Trade, Customer Service, Legal, Regulatory and other teams as needed. In addition, the individual in this role will also assists the Director, Institutional Customer Communications with responses to media and stakeholder inquiries and issues management needs in partnership with Corporate Affairs, as well as assist with leadership and internal communications content including newsletters/internal emails, town halls and internal meetings, and more on an ad hoc basis.</span></p><p><span> </span></p><p><span>The Senior Manager, Institutional Customer Communications &amp; Marketing, reports directly to the Customer Marketing and Communications Lead.</span></p><p><span> </span></p><p><b>What You Will Achieve</b></p><p><span><i>Communications</i></span></p><ul><li><p><span>Lead development of communications plans and written customer communications on supply/availability, product opportunities, market actions, contract opportunities and more for sterile injectable, surgical, and biosimilars portfolios.</span></p></li><li><p><span>Draft customer letters/emails, field force talking points, Q&amp;As, and stakeholder messaging based on input from cross-functional teams including Portfolio, Sales, Account Management, Pfizer Global Supply, Customer Service, Customer Marketing and Communications, Medical/Regulatory/Legal, Corporate Affairs and more.</span></p></li><li><p><span>Develop messaging to support responses to media and stakeholder inquiries and other issues management needs, partnering with Corporate Affairs colleagues.</span></p></li><li><p><span>Draft US Hospital and Sales Force internal communications content including newsletters, internal emails and presentations to support business communication needs.</span></p></li><li><p><span>Track and measure communications and marketing metrics.</span></p></li><li><p><span>Assist in the development of slide content and leadership talking points for internal meetings including Sales forums, all-colleague meetings, and annual Plan of Action meetings.</span></p></li><li><p><span>Assist in messaging support for market sustainability, pricing-related communications, and thought leadership to support the  portfolio.</span></p></li></ul><p></p><p><span><i>Marketing</i></span></p><ul><li><p><span>Assist in messaging support for market sustainability, pricing-related communications, and thought leadership to support the  portfolio.</span></p></li></ul><p></p><p><b>Here Is What You Need (Minimum Requirements)</b></p><ul><li><p>Applicant must have a bachelor&#39;s degree with at least 6 years of experience; OR a master&#39;s degree with at least 5 years of experience; OR a PhD with 1&#43; years of experience</p></li><li><p><span>Experience in B2B, customer/commercial and/or corporate communications. </span></p></li></ul><p></p><p><b>Bonus Points If You Have (Preferred Requirements)</b></p><ul><li><p><span>Excellent written and oral communications skills.</span></p></li><li><p><span>Additional experience in internal communications and/or marketing preferred.</span></p></li><li><p><span>Proven track record of delivering effective, creative communications to advance business goals.</span></p></li><li><p><span>Strong writing, editing, and project management experience; track record of reliable and timely communication planning and execution.</span></p></li><li><p><span>Demonstrated understanding of how communications strategy connects to and advances business strategy.</span></p></li><li><p><span>Track record of providing support to senior corporate executives and working comfortably with senior executives and across cross-functional teams.</span></p></li><li><p><span>Proven ability to work effectively and inclusively in teams with diverse internal and external stakeholders; influence, negotiation and stakeholder management skills.</span></p></li><li><p><span>Overall communications skills including communications strategy; communications plans targeted to audiences; researching/writing/editing messaging documents, talking points, editorial features, scripts and other materials; oversight of multimedia production; communication channels including digital/social; measurement and reporting.</span></p></li><li><p><span>Strong knowledge of healthcare and biopharmaceuticals industries. Preferred knowledge of hospital generics / sterile injectables market and/or experience supporting sales teams (knowledge of sales tools, sales cycle, customer profiles, etc.).</span></p></li><li><p><span>Able to work to tight deadlines, manage multiple projects at once and maintain professionalism under pressure.</span></p></li><li><p><span>Proactive self-starter, and able to work independently. Entrepreneurial mindset.</span></p></li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p>Travel ~15%</p><p><br />Work Location Assignment: Hybrid</p>&amp;#xa;The annual base salary for this position ranges from $124,400.00 to $207,400.00.* In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;* The annual base salary for this position in Tampa, FL ranges from $111,900.00 to $186,500.00.&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-institutional-customer-communications-and-marketing-pfizer/69d576a3c8e81216cd0c4c71</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-institutional-customer-communications-and-marketing-pfizer/69d576a3c8e81216cd0c4c71</guid><pubDate>Tue, 07 Apr 2026 21:26:59 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$155000-210000</salary><type>Full time</type></item><item><title><![CDATA[Director, Research & Development Support]]></title><description><![CDATA[<p><b>ROLE SUMMARY</b></p><p></p><p>A career at Pfizer offers opportunity, ownership, and impact.</p><p>All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop careers that offer both individual and company success; to be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and to make a difference in the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose: to innovate and bring therapies to patients that significantly improve their lives.<br /> </p><p>The Research &amp; Development (R&amp;D) Support and Services Lead for Clinical and Research is a member of the R&amp;D Support &amp; Services organization. In R&amp;D Support and Services, our mission is to create business value for the R&amp;D functions of Pfizer through the delivery of impactful and sustainable technology solutions, as well as by providing the talent for project execution excellence and application support—bringing medicines to patients.<br /> </p><p>The R&amp;D Support and Services Lead play a critical role in achieving our mission. The Lead “owns” the applications portfolio for Clinical and Research, providing oversight for all service management functions, including availability, performance, and business continuity. The Lead is at the center of the action, ensuring SLAs are met by our Application Support &amp; Maintenance providers, interfacing with infrastructure shared service teams, and working with Digital and business lines to ensure a stable application portfolio vital for advancing drug candidates to regulatory submission.</p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><p></p><p>Lead the support for clinical and research portfolios.</p><ul><li>People Management: Build, mentor, and empower a high-performing team, cultivating a culture of innovation, accountability, and continuous learning.</li><li>In partnership with the Business, Digital Creation Center, Shared Service teams, and vendor partners, define and manage the SLAs and OLAs for the R&amp;D applications in a manner compliant with Digital Service Management methodologies. The key outcome is improved effectiveness of service delivery, measured through periodic reporting to stakeholders at the appropriate level of detail and content.</li><li>Apply innovative thinking to identify, design, and implement automation opportunities. Focus on implementing automation, self-service, and GenAI capabilities.</li><li>Change Management: Responsible for understanding the impact and value of proposed and executed application and systems changes, the approval process, and the outcomes. Ensure that maintenance requests are managed within contracted maintenance volume through effective governance.</li><li>Perform Life Cycle Management (upgrade planning, understanding technology roadmaps to create a path forward that is consistent with the application’s use, importance, value, and performance requirements). Output is a Life Cycle Three-Year Plan.</li><li>Performance Analysis: Review application performance and monitor data to understand how the system is performed and proactively direct necessary corrective actions to meet SLAs and customer requirements.</li><li>Manage the software licenses associated with the set of applications in partnership with Procurement. This includes financial planning and optimizing the value of software licenses.</li><li>Responsible for Incident Management and Problem Management activities when necessary.</li><li>Define and evolve the support model/plan for new applications.</li><li>Support audits and inspections as required, addressing questions regarding areas such as computer operations, access controls, and change management.</li><li>Support shared service initiatives while representing the needs of the R&amp;D portfolio.</li><li>Ensure disaster recovery compliance through the facilitation of DR designs, ownership of DR testing, and maintenance of supporting documentation.</li><li>Partner with project teams during the development lifecycle (help develop support/deployment plans and other key deliverables, including acceptance of production releases and go/no-go decisions) and ensure application production readiness (support model, monitoring, SLAs, budget).</li></ul><p></p><p><b>BASIC QUALIFICATIONS </b></p><ul><li>Graduate degree in Information Management, Computer Science, Engineering, Technology Management, Financial Management, or Business Management.</li><li>7&#43; years of experience as an information technology professional in one or more roles, such as Operations Director, systems engineer, support specialist, technology team lead, or technology manager.</li><li>Experience and demonstrated competencies in working with teams in a matrixed organization, building and nurturing relationships, and effective engagement resulting in successful outcomes.</li><li>Demonstrated capabilities and experience collaborating and working effectively in team settings, frequently in virtual teams, with business partner and customer engagement responsibilities.</li></ul><p></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li>Prior experience in managing application support and services in research and/or clinical settings is highly desirable.</li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><ul><li>Should be able to travel up to 20% of the time.</li><li>Some weekend and off-hours work is expected, as the position has business continuity and operational responsibilities that require coordination of activities during off-hours and weekends, especially when application stability and usability are impacted.</li></ul><p></p><p><b>ORGANIZATIONAL RELATIONSHIPS</b></p><p>Provide the primary groups or key role(s) that this role will interact with as a regular part of the role responsibilities. Include any external interactions as appropriate.</p><ul><li>Build trusted relationships with partners (Shared Services, Platform, Network, Global Information Security, Infrastructure, DRM, etc.) who support and manage various components of applications, and work through them to influence decisions that are beneficial to the daily operations of our supported Digital organizations.</li><li>Build and manage trusted relationships with key stakeholder groups, including client partners, creation center leads, and business leads.</li></ul><p><br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p><br />Work Location Assignment: Hybrid</p><p></p><p><span>Last Date to Apply for Job: 4/14/2026</span></p><p>Additional Posting Locations: Cambridge, MA; Collegeville, PA; Groton, CT</p>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Information &amp; Business Tech&amp;#xa;]]></description><link>http://biotechroles.com/director-research-and-development-support-pfizer/69d576a1c8e81216cd0c4c70</link><guid isPermaLink="true">http://biotechroles.com/director-research-and-development-support-pfizer/69d576a1c8e81216cd0c4c70</guid><pubDate>Tue, 07 Apr 2026 21:26:57 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Senior Scientist 1, In Vivo Pharmacology]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;Position&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;This Senior Scientist 1, In Vivo Pharmacology will be working within the pharmacology team and supporting the analysis of animal and human tissues to understand target engagement, potential biomarkers and their relationship to efficacy in disease models. This position requires a person to be highly skilled in numerous molecular biology techniques including the development and execution of immunoassays, PCR techniques for gene expression analysis, flow cytometry and possibly immuno-histochemical techniques. An interest and desire to learn high resolution microscopy and single molecule tracking technology would be a plus. The position interacts with numerous project teams of clinical, chemistry, biology and pharmacology scientists. This is an opportunity to significantly impact Eikon’s drug discovery pipeline and work in a fast-paced and highly energetic environment.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;About You&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;You have a desire to contribute to a face paced, energetic, scientifically driven group. You are a highly skilled molecular biologist with experience working with whole tissues who is versatile and able to pivot between multiple techniques in a fast-paced environment. You have great communication skills and are able to describe your data to colleagues, management and project teams. You’re conscientious and with great attention to detail, documentation and organization are second nature. You are excited about being a foundational member of a rapidly growing team.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;What You’ll Do&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Support the in vivo characterization of novel chemical entities by performing the ex-vivo molecular analysis on tissues from both clinical and pre-clinical disease models to understand target engagement and resulting efficacy.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Engage with clinical or animal scientist colleagues to understand study designs and timelines for studies. Be prepared to analyze tissues from studies as they are available. &amp;nbsp;Work with numerous molecular techniques to analyze the tissues and report data to pharmacology and project teams.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Develop, optimize, and validate biomarker assays using tool compounds to either build on ideas from research biology or perform novel development.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Work flexibly across numerous drug development programs in various therapeutic areas.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Potentially mentor research associates in performing PD assays from tissues to encourage cross-training on techniques. Maintain excellent and timely lab notebook entries.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Be a technical leader that can provide feedback on the project team. Contribute to study reports to be used for regulatory filings.&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;A Postdoc fellowship plus 2 years; or Ph.D. plus minimum 5 years of relevant experience; or Master&#39;s plus 14 years of relevant experience; or Bachelor&#39;s plus 16 years of relevant experience.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Experience working in drug discovery with an emphasis on molecular biology and experience analyzing whole tissues (e.g. serum, tumor, whole organ tissue etc.)&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Experience with cell culture, immuno-assay development and optimization (e.g. ELISA and MSD), real time and conventional PCR techniques and flow-cytometry; immune-histochemistry skills a plus.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Management and/or training of &amp;nbsp;research associates possibly, accurate capturing and presentation of results and authoring of selected study reports.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Ability to organize results and present to larger project teams both in clinical and research settings.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;You thrive in team environments, seek opportunities for collaboration and value team members success as much as your own.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Excellent written and oral communication skills; attention to detail and meticulous lab notebook entries.&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;401k plan with company matching​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Mental health and wellness benefits​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Weeklong summer and winter holiday shutdowns​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Generous paid time off and holiday policies​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Life/AD&amp;amp;D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&amp;amp;D policies ​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Enhanced parental leave benefit​&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;Daily subsidized lunch program when on-site​&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 12pt;&quot;&gt;The expected salary range for this role is $152,000 to $166,250 depending on skills, competency, and the market demand for your expertise.&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; font-family: arial, helvetica, sans-serif;&quot;&gt;We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-1-in-vivo-pharmacology-eikon-therapeutics/69d48242c8e81216cd0c0602</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-1-in-vivo-pharmacology-eikon-therapeutics/69d48242c8e81216cd0c0602</guid><pubDate>Tue, 07 Apr 2026 04:04:18 GMT</pubDate><company>Eikon Therapeutics</company><location>New York, NY</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Head of Member Growth and Engagement]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;About us&lt;/h3&gt;
&lt;p&gt;At Pomelo Care, we are redefining the healthcare journey for women and children. As the leading virtual medical practice in our field, we provide a continuous circle of support—from the first steps of family building and the complexities of pregnancy to the nuances of postpartum, pediatric, and midlife care. We aren&#39;t just a clinic; we are a multidisciplinary engine of clinicians, engineers, and problem-solvers dedicated to closing the gaps in traditional care. By leveraging a high-touch, technology-driven platform, we identify risks early and deliver deeply personalized, 24/7 virtual care. We are here to prove that better data and patient-centered care lead to better outcomes, raising the standard of care for families nationwide.&lt;/p&gt;&lt;/div&gt;&lt;h3&gt;&lt;strong&gt;About The Role:&amp;nbsp;&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;As the Head of Member Growth and Engagement, you will serve as the primary architect and operator of our revenue engine, owning the entire member lifecycle from lead identification through long-term retention. We are looking for a leader who balances the tactical precision needed to hit monthly revenue targets with the strategic vision to re-engineer our enrollment and retention journeys. In this role, you will collaborate across marketing, tech, and operations to unlock step-change improvements in performance and build a world-class member growth and engagement organization.&lt;/p&gt;
&lt;p&gt;This role reports to our VP of Marketing and can be based anywhere in the continental US.&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;What You&#39;ll Do:&amp;nbsp;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Orchestrate the end-to-end member growth and retention strategy, aligning cross-functional roadmaps to drive step-change improvements in business performance.&lt;/li&gt;
&lt;li&gt;Own the P&amp;amp;L-defining metrics of the business, including Enrollment Rate, LTV:CAC, and Monthly Retention.&lt;/li&gt;
&lt;li&gt;Partner with Strategic Finance to model performance inputs and establish long-term enrollment and engagement targets.&lt;/li&gt;
&lt;li&gt;Architect the end-to-end member journey, identifying high-impact engagement touchpoints and implementing automated interventions to mitigate churn.&lt;/li&gt;
&lt;li&gt;Translate annual financial goals into rigorous monthly and weekly operational plans to ensure the business is always paced to exceed revenue targets.&lt;/li&gt;
&lt;li&gt;Maintain a high-fidelity feedback loop with the executive team, providing transparent reporting on KPIs, campaign performance, and revenue pacing.&lt;/li&gt;
&lt;li&gt;Directly oversee a multi-disciplinary team across Outreach, Lifecycle Marketing, and Marketing Operations to foster a high-performance, data-driven culture.&lt;/li&gt;
&lt;li&gt;Identify and diagnose performance gaps in real-time, deploying rapid-response tactics to protect in-month revenue and retention targets.&lt;/li&gt;
&lt;li&gt;Influence the technical roadmap for CRM and marketing automation to ensure the organization has the precision instrumentation required for scale.&lt;/li&gt;
&lt;li&gt;Partner with Product and Engineering to co-author roadmaps and define KRs, ensuring technical resources are prioritized against commercial impact and that teams are held accountable for moving the needle on growth and retention metrics.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;Who You Are:&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of experience with at least 4+ years in senior leadership within subscription models, operating with a P&amp;amp;L owner’s mindset and total bottom-line accountability.&lt;/li&gt;
&lt;li&gt;Can quantify every action, treating a 1% shift in retention as a critical financial lever rather than just a marketing metric.&lt;/li&gt;
&lt;li&gt;Possess the technical depth to partner with Product and Engineering to architect the infrastructure your revenue engine requires.&lt;/li&gt;
&lt;li&gt;Ability to move fluidly between high-level strategy and granular data, diagnosing root causes quickly and doing the math to ensure goals are reachable.&lt;/li&gt;
&lt;li&gt;A proven leader of multi-disciplinary teams who influences cross-functional roadmaps to unlock step-change growth.&lt;/li&gt;
&lt;li&gt;Ability to thrive on owning a number and proactively deploy tactics to close performance gaps before they impact the quarter.&lt;/li&gt;
&lt;li&gt;Comfortable balancing growth-hungry urgency with a deep respect for product integrity and the long-term member experience.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Why you should join our team&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;By joining Pomelo, you will get in on the ground floor of a fast-moving, well-funded, and mission-driven startup that always puts the patient first. You will learn, grow and be challenged, and have fun with your team while doing it.&lt;/p&gt;
&lt;p&gt;We strive to create an environment where employees from all backgrounds are respected. We also offer:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Competitive healthcare benefits&lt;/li&gt;
&lt;li&gt;Generous equity compensation&lt;/li&gt;
&lt;li&gt;Unlimited vacation&lt;/li&gt;
&lt;li&gt;Membership in the First Round Network (a curated and confidential community with events, guides, thousands of Q&amp;amp;A questions, and opportunities for 1-1 mentorship)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Pomelo, we are committed to hiring the best team to improve outcomes for all mothers and babies, regardless of their background. We need diverse perspectives to reflect the diversity of problems we face and the population we serve. We look to hire people from a variety of backgrounds, including but not limited to race, age, sexual orientation, gender identity and expression, national origin, religion, disability, and veteran status.&lt;/p&gt;
&lt;h3&gt;Compensation&lt;/h3&gt;
&lt;p&gt;Our salary ranges are based on paying competitively for our company’s size and industry, and are one part of the total compensation package that also includes equity, benefits, and other opportunities at Pomelo Care. In accordance with New York City, Colorado, California, and other applicable laws, Pomelo Care is required to provide a reasonable estimate of the compensation range for this role. Individual pay decisions are ultimately based on a number of factors, including qualifications for the role, experience level, skillset, geography, and balancing internal equity. Given that this role is open to candidates of different skill levels, determining a salary range is challenging. A reasonable estimate of the current salary range is $220,000 to $250,000. We expect most candidates to fall in the middle of the range. We also believe that your personal needs and preferences should be taken into consideration, so we allow some choice between equity and cash.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h3&gt;&lt;strong&gt;Potential Fraud Warning&lt;br&gt;&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;&lt;em&gt;&lt;br&gt;Please be cautious of potential recruitment fraud. With the increase of remote work and digital hiring, phishing and job scams are on the rise with malicious actors impersonating real employees and sending fake job offers in an effort to collect personal or financial information.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Pomelo Care will never ask you to pay a fee or download software as part of the interview process with our company. Pomelo Care will also never ask for your personal banking or other financial information until after you have signed an offer of employment and completed onboarding paperwork that is provided by our People Operations team. All official communication with Pomelo Care People Operations team will come from domain email addresses ending in @pomelocare.com. &lt;/em&gt;&lt;br&gt;&lt;br&gt;&lt;em&gt;If you receive a message that seems suspicious, we encourage you to pause communication and contact us directly at &lt;a href=&quot;mailto:careers@pomelocare.com&quot;&gt;careers@pomelocare.com&lt;/a&gt;&amp;nbsp; to confirm its legitimacy. For your safety, we also recommend applying only through our official &lt;a href=&quot;https://www.pomelocare.com/careers&quot;&gt;Careers&lt;/a&gt; page. If you believe you have been the victim of a scam or identity theft, please contact your local law enforcement agency or another trusted authority for guidance.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/head-of-member-growth-and-engagement-pomelo-care/69d48242c8e81216cd0c0601</link><guid isPermaLink="true">http://biotechroles.com/head-of-member-growth-and-engagement-pomelo-care/69d48242c8e81216cd0c0601</guid><pubDate>Tue, 07 Apr 2026 04:04:18 GMT</pubDate><company>Pomelo Care</company><location>United States</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Global Drug Substance Commercialization, Conjugation]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;&lt;strong&gt;Join our Mission to Protect Humankind!&lt;/strong&gt;&lt;/h3&gt;
&lt;div&gt;Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;WHAT&lt;/strong&gt;&amp;nbsp;we do is every bit as important as&amp;nbsp;&lt;strong&gt;HOW&lt;/strong&gt;&amp;nbsp;we do it!&amp;nbsp;Our work together is guided by four enduring core values:&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;*MODEL EXCELLENCE:&amp;nbsp; The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.&lt;/div&gt;&lt;/div&gt;&lt;h3&gt;&lt;strong&gt;Summary:&lt;/strong&gt;&lt;/h3&gt;
&lt;p&gt;The Senior Manager for Drug Substance (DS) Commercialization has the responsibility for launch readiness and commercial supply of the conjugate drug substance. The conjugate product strategy will transition from the Process Development organization to Manufacturing Science and Technology (MSAT) during late-stage product development.&amp;nbsp; This role focuses on technical launch planning and execution by bringing best-practices and coordinating cross-functional efforts for regulatory filings, facility readiness, and launch supplies.&lt;/p&gt;
&lt;p&gt;This role also provides leadership to ensure that the organization is equipped to effectively communicate the scientific and commercial rationale for conjugation process to internal stakeholders, relevant CMOs, and to regulatory agencies. The incumbent will be highly skilled in written communication, especially in regard to authoring Health Authority submissions (IND/BLA). The role will also require the ability to interact effectively with people of diverse backgrounds and perspectives. The incumbent will also work with the organization to ensure on-time execution and appropriate planning for commercial lifecycle management.&lt;/p&gt;
&lt;p&gt;This position will be reporting into the Director for Global DS Commercialization, Conjugation. The Sr. Manager will collaborate on overall program strategy, with primary responsibility and accountability for the drug substance strategy.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Manufacturing Science and Technology (MSAT) is responsible for successfully and seamlessly transitioning the vaccine process from Process Development to Commercial, developing and executing technical launch and commercialization strategy, continuously improving process robustness through to end of lifecycle, and ensuring best possible patient outcomes while creating value for the enterprise. As part of the Commercial Manufacturing and Supply Chain organization, MSAT will lead the technical and process support for end-to-end commercial manufacturing, including Polysaccharides, Carrier Proteins, Conjugation across all Drug Substances (DS). The range of activities will include DS technology transfer support, process characterization experiments in support of validation, process improvement, evaluation of novel process technologies, and investigation of process related manufacturing issues, ensuring continuous improvement in process robustness throughout the product life cycle etc.&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;Essential Functions:&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;DS Commercialization – &lt;/strong&gt;Provide strategic and scientific leadership for polysaccharide to protein conjugation with internal and external stakeholders and ensure successful execution of launch plans and post-launch commercial activities.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Organization &lt;/strong&gt;– Build a strong and highly-skilled team for the global network with special focus on manufacturing processes. Support resourcing recommendations on staffing requirements to meet organizational goals.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Process robustness&lt;/strong&gt; – Continuously improve process understanding and process robustness by putting systems in place to monitor, trend, and optimize operations.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Interface&lt;/strong&gt; - Collaboration with cross-functional teams across the network, including Regulatory, CMC, Quality, Supply Chain, Procurement, and Process Engineering, to drive the successful development and commercial launch of the conjugate drug substance. Provides technical representation into initial technology transfer, product launch, product lifecycle, to the end of life/product retirement and for defining/developing the next generation of production technologies.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Tech-transfer new technologies&lt;/strong&gt; - Ensure robust processes exist to support technical transfers and integration of new technologies.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Support&lt;/strong&gt; &lt;strong&gt;technical services&lt;/strong&gt; - Support of our internal and external manufacturing network, including materials management and data analytics.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Process validation and comparability&lt;/strong&gt; - Provide support for the execution of process validation and process comparability activities.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Regulatory&lt;/strong&gt; - Engage In technical reviewing and authoring of regulatory filings and responding to questions received from health authorities. Effectively communicate the scientific and commercial rationale for DS processes to the Boards of Health for regulatory submissions for commercialization.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Communicate&lt;/strong&gt; - Effectively and efficiently communicate process performance to key stakeholders (internal-facing and external-facing). Connect and build strong working relationships with others, demonstrating strong emotional intelligence and an ability to communicate clearly and persuasively.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Executing for Results - &lt;/strong&gt;Set clear and challenging goals and take accountability for driving results. Comfortable with ambiguity and uncertainty; the ability to adapt nimbly and lead others through complex situations.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Leadership&lt;/strong&gt; - Contribute with the DS Commercialization lead and as member of the Global Manufacturing Operations, with an aim to ensure effective and efficient delivery of our life-enhancing therapies to our patients. Delegate effectively, celebrate diversity within the team, and manage team performance with a strong focus on colleague development.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Travel&lt;/strong&gt; - 10-30% travel required.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;Requirements:&amp;nbsp;&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Degree(s) in Chemical or Biochemical Engineering, Chemistry, Biochemistry, or related discipline with a minimum of 5+ years of relevant experience for Ph.D., 8+ years for M.S./M.A., or 12+ years for B.S./B.A.&lt;/li&gt;
&lt;li&gt;Experience in development, tech transfer, scale-up or production of polysaccharide/protein conjugate vaccines&lt;/li&gt;
&lt;li&gt;Experience in MSAT or Process Development in supervisory and/or matrixed team roles.&lt;/li&gt;
&lt;li&gt;Able to leverage deep technical knowledge in a collaborative manner to achieve collective goals.&lt;/li&gt;
&lt;li&gt;Excellent organization, problem solving and strategic planning skills.&lt;/li&gt;
&lt;li&gt;Highly skilled in both verbal and written communication, especially in regards to authoring Health Authority submissions (IND/BLA) with the ability to interact effectively with people of diverse backgrounds and perspectives.&lt;/li&gt;
&lt;li&gt;Proactively recognizes needs and potential challenges, and independently identifies and implements effective steps and solutions.&lt;/li&gt;
&lt;li&gt;The ability to seek and analyze data from a variety of sources to support decisions and to align others with the organization&#39;s overall strategy.&lt;/li&gt;
&lt;li&gt;An entrepreneurial and creative approach to developing new, innovative ideas that will stretch the organization and push the boundaries within the industry.&lt;/li&gt;
&lt;/ul&gt;
&lt;div&gt;&lt;strong&gt;Reports to: &lt;/strong&gt;Director, Global MSAT Commercialization Lead, Conjugation&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Location: &lt;/strong&gt;San Carlos, CA or North Carolina&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Compensation:&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;The compensation package will be competitive and includes comprehensive benefits and an equity component.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Salary Range: &lt;/strong&gt;$165,000 – $193,000 (SF Bay Area). Salary ranges for non-California locations may vary.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;em&gt;We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-global-drug-substance-commercialization-conjugation-vaxcyte/69d4823ec8e81216cd0c05fd</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-global-drug-substance-commercialization-conjugation-vaxcyte/69d4823ec8e81216cd0c05fd</guid><pubDate>Tue, 07 Apr 2026 04:04:14 GMT</pubDate><company>Vaxcyte</company><location>San Carlos, California, United States</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Process Development Chemist]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions. &lt;br&gt;&amp;nbsp;&lt;br&gt;We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;What You’ll Do:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking an experienced Senior Scientist, Process Development Chemist with experience in the area(s) of small molecule and/or peptide manufacturing to participate in development and commercialization activities for a complex drug substance program. This role requires deep process development expertise, strong technical ownership, and a strong background in synthetic and analytical chemistry.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Required location: Waltham, MA&amp;nbsp;(hub-based, onsite 3-4 days per week)&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support drug substance process development activities for complex, multistep manufacturing processes executed at external CMOs&lt;/li&gt;
&lt;li&gt;Partner with senior technical leads to support scale‑up, process characterization, and Process Performance Qualification (PPQ) activities&lt;/li&gt;
&lt;li&gt;Review, analyze, and interpret development, scaleup, and manufacturing data generated by CMOs to support technical decision making&lt;/li&gt;
&lt;li&gt;Contribute to the development and implementation of robust process control strategies aligned with CMC and GMP expectations&lt;/li&gt;
&lt;li&gt;Author and review technical documentation including development reports, manufacturing summaries, and supporting validation documentation&lt;/li&gt;
&lt;li&gt;Support technology transfer and technical oversight of external CMOs during development, GMP manufacturing, and validation activities&lt;/li&gt;
&lt;li&gt;Participate in CMO meetings, troubleshoot technical issues, and support root cause investigations and corrective actions&lt;/li&gt;
&lt;li&gt;Collaborate cross-functionally with Analytical Development, Quality, Regulatory, and Supply Chain to support program milestones&lt;/li&gt;
&lt;li&gt;Ensure clear documentation, data integrity, and compliance with regulatory and quality expectations across external partners&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Required Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in Organic Chemistry, BS/MS in Chemical Engineering with a strong background in organic chemistry with 5-8 years of relevant pharmaceutical or biotechnology industry experience&lt;/li&gt;
&lt;li&gt;Experience supporting small molecule and/or peptide drug substance process development, scaleup, or GMP manufacturing in a CMO or virtual development environment&lt;/li&gt;
&lt;li&gt;Exposure to late-stage development activities such as process characterization, validation, or PPQ support&lt;/li&gt;
&lt;li&gt;Working knowledge of CMC requirements, GMP principles, and regulatory expectations&lt;/li&gt;
&lt;li&gt;Ability to critically evaluate external data, identify risks, and communicate technical conclusions clearly&lt;/li&gt;
&lt;li&gt;Strong collaboration, communication, and organizational skills&lt;/li&gt;
&lt;li&gt;Comfort working in a fast‑paced, highly cross‑functional, externally focused operating model&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience working directly with external CMOs and contract laboratories&lt;/li&gt;
&lt;li&gt;Exposure to regulatory submissions or inspection readiness activities&lt;/li&gt;
&lt;li&gt;Familiarity with Quality-by-Design (QbD), risk assessments, and control strategy development&lt;/li&gt;
&lt;li&gt;Experience supporting development or commercialization programs in a virtual biotech organization&lt;/li&gt;
&lt;li&gt;&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;PhD in Organic Chemistry, or BS/MS in Chemical Engineering with a strong organic chemistry background, &lt;em&gt;(Advanced degree preferred; equivalent experience will be considered)&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$143,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$175,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;For Full Time Roles:&lt;/strong&gt; This range represents the company’s good-faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants—because your well-being and future matter to us.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;EQUAL EMPLOYMENT OPPORTUNITY INFORMATION:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;E-Verify:&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Kailera Therapeutics, Inc. uses E-Verify to confirm the identity and employment eligibility of all new hires.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(255, 255, 255);&quot;&gt;&amp;nbsp;#LI-Hybrid&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-process-development-chemist-kailera/69d48228c8e81216cd0c05fc</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-process-development-chemist-kailera/69d48228c8e81216cd0c05fc</guid><pubDate>Tue, 07 Apr 2026 04:03:52 GMT</pubDate><company>Kailera</company><location>Waltham, Massachusetts</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Ophthalmology Medical Affairs]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Company:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;At Annexon Biosciences we are a biopharmaceutical company advancing a late-stage clinical platform of novel therapies for people living with devastating classical complement-mediated neuroinflammatory diseases of the body, brain, and eye. Our novel scientific approach targets upstream C1q to block the classical complement inflammatory cascade before it starts, and its therapeutic candidates are designed to provide meaningful benefits across multiple autoimmune, neurodegenerative and ophthalmic diseases. With proof-of concept data in Guillain-Barré syndrome, Huntington’s disease and geographic atrophy, we are rigorously advancing our mid-to late-stage clinical trials to bring new potential treatments to patients as quickly as possible. At Annexon, you’ll be part of a team committed to making an impact together.&amp;nbsp;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;For more information on Annexon and our pipeline, check out our site &lt;/span&gt;&lt;a href=&quot;https://annexonbio.com/&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;Annexon Biosciences&lt;/span&gt;&lt;/span&gt;&lt;/a&gt; &lt;span data-contrast=&quot;none&quot;&gt;&amp;amp; &lt;/span&gt;&lt;a href=&quot;https://annexonbio.com/pipeline/&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;Annexon Pipeline&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;span data-contrast=&quot;none&quot;&gt;. We trade on Nasdaq under the ticker symbol ANNX and are headquartered in Brisbane, CA.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We&#39;re seeking&amp;nbsp;&lt;strong&gt;exceptional talent&lt;/strong&gt; from all backgrounds to fuel our growth. At Annexon, we&#39;re building a diverse, equitable, and inclusive workplace. We value unique perspectives and unconventional paths. If you&#39;re the best candidate for the job, even if you don&#39;t perfectly fit the traditional mold, we encourage you to apply.&amp;nbsp;Learn more about our commitment to diversity, equity, inclusion, and our company&amp;nbsp;&lt;a href=&quot;https://annexonbio.com/our-culture/&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;culture&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;span data-contrast=&quot;auto&quot;&gt;!&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Position:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The &lt;strong&gt;Vice President, Ophthalmology Medical Affairs&lt;/strong&gt; will be responsible for representing Annexon Biosciences with a network of external thought leaders and driving Global Medical Affairs activities in complement-mediated diseases in Ophthalmology.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Responsibilities include:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;As a key member of the ophthalmology core team, provide deep medical and scientific expertise on medical affairs, launch, and lifecycle strategies.&lt;/li&gt;
&lt;li&gt;Lead the full spectrum of the Medical Affairs functions that are responsible for the development and implementation of the Global medical strategy across the following areas:
&lt;ul&gt;
&lt;li&gt;Medical Affairs Operations – focused on communication, medical education, advisory management, and patient advocacy.&lt;/li&gt;
&lt;li&gt;Medical Science Liaison – directed at work with practicing physicians, key opinion leaders, academic physicians, and other health care providers who deliver care to the targeted patient populations for which Annexon products are directed.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Partner closely with the organization in the establishment of our market access strategies that enables plans for pricing, reimbursement, and access.&lt;/li&gt;
&lt;li&gt;Establish appropriate strategic partnerships with internal leaders in clinical development, regulatory affairs, safety, operations, research, and commercial.&lt;/li&gt;
&lt;li&gt;Extend and grow the established professional relationships with the external expert community to maintain cutting edge knowledge about the disease areas in which we operate, standards of practice within those areas, and the evolving unmet medical need.&lt;/li&gt;
&lt;li&gt;Enrich the relationship we have with patients and patient advocacy groups for both clinical trials and commercial planning, and understanding of needs that we can better serve.&lt;/li&gt;
&lt;li&gt;Represent Annexon as an organization, and present data at advisory boards, , clinical investigator meetings, congresses, symposia, and other scientific forums.&lt;/li&gt;
&lt;li&gt;Remain at the forefront of the relevant science and competitive landscape.&lt;/li&gt;
&lt;li&gt;Collaborate with legal, compliance, and regulatory authorities to ensure proper and ethical interactions between medical affairs personnel and external stakeholders.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Education, Experience, and Skills:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Required:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Advanced degree (MD, PhD, or PharmD) preferred.&lt;/li&gt;
&lt;li&gt;A minimum of 15 years Medical Affairs experience within the biopharma industry.&lt;/li&gt;
&lt;li&gt;Prior experience in product launch or launches in ophthalmology.&lt;/li&gt;
&lt;li&gt;Skilled at engagement and scientific exchange with the external medical community and has an established network of medical and clinical contacts.&lt;/li&gt;
&lt;li&gt;Proven ability to lead, manage, and motivate others in a multi-functional matrix environment.&lt;/li&gt;
&lt;li&gt;Experience in global/regional/local medical practice and healthcare ecosystems.&lt;/li&gt;
&lt;li&gt;Knowledge of Good Clinical Practices (GCP), region regulations and guidelines, and applicable international regulatory requirements.&lt;/li&gt;
&lt;li&gt;Finance/budgeting and resource management experience.&lt;/li&gt;
&lt;li&gt;Skilled at effectively presenting ideas and documenting complex medical/clinical concepts in both written and oral communication.&lt;/li&gt;
&lt;li&gt;History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues.&lt;/li&gt;
&lt;li&gt;Ensures representation of the patient perspective/ “voice of patient”.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Salary Range: $354,200 - $377,000&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Location:&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Annexon Biosciences is located in Brisbane, California and preference is given to candidates in the San Francisco Bay Area.&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Benefits:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;17&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;A stimulating and rewarding workplace includes flexible work schedules, remote opportunities and the ability to achieve a work-life balance.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;17&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Shuttle service from BART, CalTrain and the Ferry.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;17&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Annexon offers a competitive base salary and equity participation, employee stock purchase plan, as well as a comprehensive health benefit package that includes medical, dental, vision, 401(k), flexible spending plans, and other benefits.&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Annexon Biosciences&lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt; is an Equal Opportunity Employer, and we prohibit discrimination or harassment of any kind.&amp;nbsp; We are committed to fostering an environment where ALL people are welcome and supported. &lt;/span&gt;&lt;/em&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better business results. Creativity and innovation flourish in an environment of openness, inclusion, and mutual respect.&lt;/span&gt;&lt;/em&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;]]></description><link>http://biotechroles.com/vice-president-ophthalmology-medical-affairs-annexon-biosciences/69d48223c8e81216cd0c05fb</link><guid isPermaLink="true">http://biotechroles.com/vice-president-ophthalmology-medical-affairs-annexon-biosciences/69d48223c8e81216cd0c05fb</guid><pubDate>Tue, 07 Apr 2026 04:03:47 GMT</pubDate><company>Annexon Biosciences</company><location>San Francisco Bay Area</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Program Manager, Global Clinical Training and Programming (EMEA) - London]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our mission: to eliminate every barrier to mental health.&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology,&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://www.springhealth.com/our-approach&quot;&gt;&lt;strong&gt;Precision Mental Healthcare&lt;/strong&gt;&lt;/a&gt;, empowers us to deliver the right care at the right time—whether it’s therapy, coaching, medication, or beyond—tailored to each individual’s needs.&lt;/p&gt;
&lt;p&gt;We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we’ve been able to generate a &lt;a href=&quot;https://www.springhealth.com/news/first-net-roi-performance-guarantee-in-mental-health?utm_medium=DSMN8&amp;amp;utm_source=LinkedIn&quot;&gt;&lt;strong&gt;net positive ROI&lt;/strong&gt;&lt;/a&gt; for employers and we are the only company in our category to earn &lt;a href=&quot;https://www.springhealth.com/news/validation-institute-certifies-spring-health-delivers-net-savings-for-customers&quot;&gt;&lt;strong&gt;external validation&lt;/strong&gt;&lt;/a&gt; of net savings for customers.&lt;/p&gt;
&lt;p&gt;We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We’re just getting started—join us on our journey to make mental healthcare accessible to everyone, everywhere.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;Reporting to the Director of Clinical Training, the Senior Program Manager, Clinical Training and Global Programming will develop the strategy for Spring Health’s global training and programming, serve as the SME for global webinars/WellSprings, coordinate the logistics for training and programming, ensure quality member experience for the global population, meet with customers to develop customized training and programming for our larger global accounts. This is a full time remote position seated in Europe, Middle East, or Africa. Travel will be required up to 30% of the time for in person trainings.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you’ll do:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the primary Project Manager for Global (Non US) Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Serve as a SME on Global Clinical Training and Programming, including across time zones, cultures and languages&lt;/li&gt;
&lt;li&gt;Develop and implement a Global Clinical Training and Programming strategy that is sustainable for continued growth&lt;/li&gt;
&lt;li&gt;Coordinate logistics such as creating virtual events platforms, finding clinical providers, ensuring materials are prepared, tracking reporting and evaluation metrics&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Work closely with large Jumbo customers to consult on Training and Programming planning, including partnering with internal stakeholders to consult, manage and advise customers.&lt;/li&gt;
&lt;li&gt;Work closely with the Global team regarding strategy and implementation&lt;/li&gt;
&lt;li&gt;Partner with US Program Managers to plan and coordinate training and programming&lt;/li&gt;
&lt;li&gt;Ensure we are measuring training and program effectiveness&lt;/li&gt;
&lt;li&gt;If possible, involved in some delivery and/or producing of events&lt;/li&gt;
&lt;li&gt;Will take a leadership role in planning for global programming related to events such as World Mental Health Day&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What success looks like in this role:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and roll out a Global Training and Programming calendar, procedures and process to request and deliver clinical events globally&lt;/li&gt;
&lt;li&gt;Optimize efficiency for meeting customer needs related to Clinical Programming and Training&lt;/li&gt;
&lt;li&gt;Maintain customer satisfaction with training/programming as measured by average Kirkpatrick level 1 scores above 4.5 out of 5.0.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What you’ll bring:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Clinical license or equivalent in your country&lt;/li&gt;
&lt;li&gt;3-5 years of experience in facilitation and event planning&lt;/li&gt;
&lt;li&gt;You have complete knowledge and understanding of the unique global challenges, potential solutions, and Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Work on problems of diverse scope where analysis of information requires evaluation of identifiable factors. You build solutions based on limited information and precedent and adapt existing approaches to resolve issues.&lt;/li&gt;
&lt;li&gt;Enhance relationships with senior internal/external partners who are not familiar with the subject matter. You adapt style and messaging to varying audiences and often advise on difficult matters.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Program Management and data evaluation&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Google Suite, Zoom, and additional events platforms as needed&lt;/li&gt;
&lt;li&gt;You have a solid understanding of instructional design and content development, including strong working knowledge of Adult Learning Principals.&lt;/li&gt;
&lt;li&gt;You are knowledgeable about training evaluation techniques.&lt;/li&gt;
&lt;li&gt;You communicate effectively with customers and fellow Spring team members&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The target base salary range for this position is &lt;em&gt;&lt;strong&gt;60,000 - 69,000 GBP &lt;/strong&gt;&lt;/em&gt;Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually using&amp;nbsp;&lt;a href=&quot;https://springhealth.link/jd-2022-09-radfordcomp&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Radford Global Compensation Database&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;at minimum to ensure competitive and fair pay.&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Not sure if you meet every requirement?&lt;/strong&gt; &lt;a href=&quot;https://pubsonline.informs.org/doi/10.1287/mnsc.2023.4907&quot;&gt;Research shows&lt;/a&gt; that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to &lt;a href=&quot;https://www.springhealth.com/careers&quot;&gt;Thrive&lt;/a&gt;. If this role excites you, we encourage you to apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Ready to do the most impactful work of your life? Learn more about our values, what it’s like to work here, and how hypergrowth meets impact at Spring Health:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://drive.google.com/file/d/1TjOJ7_OtSkacBqhs5-jMsrMV6lySQXdw/view?usp=sharing&quot;&gt;&lt;strong&gt;Our Values&lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Our privacy policy:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;a href=&quot;https://springhealth.com/privacy-policy/&quot;&gt;&lt;strong&gt;&lt;em&gt;https://springhealth.com/privacy-policy/&lt;/em&gt;&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, pregnancy, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. If you have a disability or special need that requires accommodation, please let us know.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-london-spring-health/69d4821dc8e81216cd0c05f9</link><guid isPermaLink="true">http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-london-spring-health/69d4821dc8e81216cd0c05f9</guid><pubDate>Tue, 07 Apr 2026 04:03:41 GMT</pubDate><company>Spring Health</company><location>Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Program Manager, Global Clinical Training and Programming (EMEA) - Geneva]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our mission: to eliminate every barrier to mental health.&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology,&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://www.springhealth.com/our-approach&quot;&gt;&lt;strong&gt;Precision Mental Healthcare&lt;/strong&gt;&lt;/a&gt;, empowers us to deliver the right care at the right time—whether it’s therapy, coaching, medication, or beyond—tailored to each individual’s needs.&lt;/p&gt;
&lt;p&gt;We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we’ve been able to generate a &lt;a href=&quot;https://www.springhealth.com/news/first-net-roi-performance-guarantee-in-mental-health?utm_medium=DSMN8&amp;amp;utm_source=LinkedIn&quot;&gt;&lt;strong&gt;net positive ROI&lt;/strong&gt;&lt;/a&gt; for employers and we are the only company in our category to earn &lt;a href=&quot;https://www.springhealth.com/news/validation-institute-certifies-spring-health-delivers-net-savings-for-customers&quot;&gt;&lt;strong&gt;external validation&lt;/strong&gt;&lt;/a&gt; of net savings for customers.&lt;/p&gt;
&lt;p&gt;We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We’re just getting started—join us on our journey to make mental healthcare accessible to everyone, everywhere.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;Reporting to the Director of Clinical Training, the Senior Program Manager, Clinical Training and Global Programming will develop the strategy for Spring Health’s global training and programming, serve as the SME for global webinars/WellSprings, coordinate the logistics for training and programming, ensure quality member experience for the global population, meet with customers to develop customized training and programming for our larger global accounts. This is a full time remote position seated in Europe, Middle East, or Africa. Travel will be required up to 30% of the time for in person trainings.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you’ll do:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the primary Project Manager for Global (Non US) Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Serve as a SME on Global Clinical Training and Programming, including across time zones, cultures and languages&lt;/li&gt;
&lt;li&gt;Develop and implement a Global Clinical Training and Programming strategy that is sustainable for continued growth&lt;/li&gt;
&lt;li&gt;Coordinate logistics such as creating virtual events platforms, finding clinical providers, ensuring materials are prepared, tracking reporting and evaluation metrics&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Work closely with large Jumbo customers to consult on Training and Programming planning, including partnering with internal stakeholders to consult, manage and advise customers.&lt;/li&gt;
&lt;li&gt;Work closely with the Global team regarding strategy and implementation&lt;/li&gt;
&lt;li&gt;Partner with US Program Managers to plan and coordinate training and programming&lt;/li&gt;
&lt;li&gt;Ensure we are measuring training and program effectiveness&lt;/li&gt;
&lt;li&gt;If possible, involved in some delivery and/or producing of events&lt;/li&gt;
&lt;li&gt;Will take a leadership role in planning for global programming related to events such as World Mental Health Day&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What success looks like in this role:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and roll out a Global Training and Programming calendar, procedures and process to request and deliver clinical events globally&lt;/li&gt;
&lt;li&gt;Optimize efficiency for meeting customer needs related to Clinical Programming and Training&lt;/li&gt;
&lt;li&gt;Maintain customer satisfaction with training/programming as measured by average Kirkpatrick level 1 scores above 4.5 out of 5.0.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What you’ll bring:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Clinical license or equivalent in your country&lt;/li&gt;
&lt;li&gt;3-5 years of experience in facilitation and event planning&lt;/li&gt;
&lt;li&gt;You have complete knowledge and understanding of the unique global challenges, potential solutions, and Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Work on problems of diverse scope where analysis of information requires evaluation of identifiable factors. You build solutions based on limited information and precedent and adapt existing approaches to resolve issues.&lt;/li&gt;
&lt;li&gt;Enhance relationships with senior internal/external partners who are not familiar with the subject matter. You adapt style and messaging to varying audiences and often advise on difficult matters.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Program Management and data evaluation&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Google Suite, Zoom, and additional events platforms as needed&lt;/li&gt;
&lt;li&gt;You have a solid understanding of instructional design and content development, including strong working knowledge of Adult Learning Principals.&lt;/li&gt;
&lt;li&gt;You are knowledgeable about training evaluation techniques.&lt;/li&gt;
&lt;li&gt;You communicate effectively with customers and fellow Spring team members&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The target base salary range for this position is &lt;strong&gt;&lt;em&gt;123,200 -141,680 CHF.&lt;/em&gt; &lt;/strong&gt;Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually using&amp;nbsp;&lt;a href=&quot;https://springhealth.link/jd-2022-09-radfordcomp&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Radford Global Compensation Database&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;at minimum to ensure competitive and fair pay.&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Not sure if you meet every requirement?&lt;/strong&gt; &lt;a href=&quot;https://pubsonline.informs.org/doi/10.1287/mnsc.2023.4907&quot;&gt;Research shows&lt;/a&gt; that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to &lt;a href=&quot;https://www.springhealth.com/careers&quot;&gt;Thrive&lt;/a&gt;. If this role excites you, we encourage you to apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Ready to do the most impactful work of your life? Learn more about our values, what it’s like to work here, and how hypergrowth meets impact at Spring Health:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://drive.google.com/file/d/1TjOJ7_OtSkacBqhs5-jMsrMV6lySQXdw/view?usp=sharing&quot;&gt;&lt;strong&gt;Our Values&lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Our privacy policy:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;a href=&quot;https://springhealth.com/privacy-policy/&quot;&gt;&lt;strong&gt;&lt;em&gt;https://springhealth.com/privacy-policy/&lt;/em&gt;&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, pregnancy, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. If you have a disability or special need that requires accommodation, please let us know.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-geneva-spring-health/69d4821ac8e81216cd0c05f7</link><guid isPermaLink="true">http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-geneva-spring-health/69d4821ac8e81216cd0c05f7</guid><pubDate>Tue, 07 Apr 2026 04:03:39 GMT</pubDate><company>Spring Health</company><location>Remote</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Program Manager, Global Clinical Training and Programming (EMEA) - Cairo]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;&lt;strong&gt;Our mission: to eliminate every barrier to mental health.&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;At Spring Health, we’re on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help they need, when they need it. Our clinically validated technology,&lt;strong&gt; &lt;/strong&gt;&lt;a href=&quot;https://www.springhealth.com/our-approach&quot;&gt;&lt;strong&gt;Precision Mental Healthcare&lt;/strong&gt;&lt;/a&gt;, empowers us to deliver the right care at the right time—whether it’s therapy, coaching, medication, or beyond—tailored to each individual’s needs.&lt;/p&gt;
&lt;p&gt;We proudly partner with over 450 companies, from startups to multinational Fortune 500 corporations, as a leading provider of mental health service, providing care for 10 million people. Our clients include brands you use and know like Microsoft, Target, and Delta Airlines, all of whom trust us to deliver best-in-class outcomes for their employees globally. With our innovative platform, we’ve been able to generate a &lt;a href=&quot;https://www.springhealth.com/news/first-net-roi-performance-guarantee-in-mental-health?utm_medium=DSMN8&amp;amp;utm_source=LinkedIn&quot;&gt;&lt;strong&gt;net positive ROI&lt;/strong&gt;&lt;/a&gt; for employers and we are the only company in our category to earn &lt;a href=&quot;https://www.springhealth.com/news/validation-institute-certifies-spring-health-delivers-net-savings-for-customers&quot;&gt;&lt;strong&gt;external validation&lt;/strong&gt;&lt;/a&gt; of net savings for customers.&lt;/p&gt;
&lt;p&gt;We have raised capital from prominent investors including Generation Investment, Kinnevik, Tiger Global, Northzone, RRE Ventures, and many more. Thanks to their partnership and our latest Series E Funding, our current valuation has reached $3.3 billion. We’re just getting started—join us on our journey to make mental healthcare accessible to everyone, everywhere.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;Reporting to the Director of Clinical Training, the Senior Program Manager, Clinical Training and Global Programming will develop the strategy for Spring Health’s global training and programming, serve as the SME for global webinars/WellSprings, coordinate the logistics for training and programming, ensure quality member experience for the global population, meet with customers to develop customized training and programming for our larger global accounts. This is a full time remote position seated in Europe, Middle East, or Africa. Travel will be required up to 30% of the time for in person trainings.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What you’ll do:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the primary Project Manager for Global (Non US) Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Serve as a SME on Global Clinical Training and Programming, including across time zones, cultures and languages&lt;/li&gt;
&lt;li&gt;Develop and implement a Global Clinical Training and Programming strategy that is sustainable for continued growth&lt;/li&gt;
&lt;li&gt;Coordinate logistics such as creating virtual events platforms, finding clinical providers, ensuring materials are prepared, tracking reporting and evaluation metrics&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Work closely with large Jumbo customers to consult on Training and Programming planning, including partnering with internal stakeholders to consult, manage and advise customers.&lt;/li&gt;
&lt;li&gt;Work closely with the Global team regarding strategy and implementation&lt;/li&gt;
&lt;li&gt;Partner with US Program Managers to plan and coordinate training and programming&lt;/li&gt;
&lt;li&gt;Ensure we are measuring training and program effectiveness&lt;/li&gt;
&lt;li&gt;If possible, involved in some delivery and/or producing of events&lt;/li&gt;
&lt;li&gt;Will take a leadership role in planning for global programming related to events such as World Mental Health Day&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What success looks like in this role:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and roll out a Global Training and Programming calendar, procedures and process to request and deliver clinical events globally&lt;/li&gt;
&lt;li&gt;Optimize efficiency for meeting customer needs related to Clinical Programming and Training&lt;/li&gt;
&lt;li&gt;Maintain customer satisfaction with training/programming as measured by average Kirkpatrick level 1 scores above 4.5 out of 5.0.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What you’ll bring:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Clinical license or equivalent in your country&lt;/li&gt;
&lt;li&gt;3-5 years of experience in facilitation and event planning&lt;/li&gt;
&lt;li&gt;You have complete knowledge and understanding of the unique global challenges, potential solutions, and Clinical Training and Programming&lt;/li&gt;
&lt;li&gt;Work on problems of diverse scope where analysis of information requires evaluation of identifiable factors. You build solutions based on limited information and precedent and adapt existing approaches to resolve issues.&lt;/li&gt;
&lt;li&gt;Enhance relationships with senior internal/external partners who are not familiar with the subject matter. You adapt style and messaging to varying audiences and often advise on difficult matters.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Program Management and data evaluation&lt;/li&gt;
&lt;li&gt;You have complete knowledge of Google Suite, Zoom, and additional events platforms as needed&lt;/li&gt;
&lt;li&gt;You have a solid understanding of instructional design and content development, including strong working knowledge of Adult Learning Principals.&lt;/li&gt;
&lt;li&gt;You are knowledgeable about training evaluation techniques.&lt;/li&gt;
&lt;li&gt;You communicate effectively with customers and fellow Spring team members&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The target base salary range for this position is &lt;em&gt;&lt;strong&gt;789,600 - 908,040 EGP. &lt;/strong&gt;&lt;/em&gt;Individual pay may vary from the target range and is determined by a number of factors including experience, location, internal pay equity, and other relevant business considerations. We review all employee pay and compensation programs annually using&amp;nbsp;&lt;a href=&quot;https://springhealth.link/jd-2022-09-radfordcomp&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;Radford Global Compensation Database&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt; &lt;/strong&gt;at minimum to ensure competitive and fair pay.&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Not sure if you meet every requirement?&lt;/strong&gt; &lt;a href=&quot;https://pubsonline.informs.org/doi/10.1287/mnsc.2023.4907&quot;&gt;Research shows&lt;/a&gt; that women and people from historically underrepresented communities often hesitate to apply for roles unless they meet every qualification compared to other similarly-qualified candidates. At Spring Health, we are committed to fostering a workplace where everyone feels valued, empowered, and supported to &lt;a href=&quot;https://www.springhealth.com/careers&quot;&gt;Thrive&lt;/a&gt;. If this role excites you, we encourage you to apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Ready to do the most impactful work of your life? Learn more about our values, what it’s like to work here, and how hypergrowth meets impact at Spring Health:&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://drive.google.com/file/d/1TjOJ7_OtSkacBqhs5-jMsrMV6lySQXdw/view?usp=sharing&quot;&gt;&lt;strong&gt;Our Values&lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Our privacy policy:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;a href=&quot;https://springhealth.com/privacy-policy/&quot;&gt;&lt;strong&gt;&lt;em&gt;https://springhealth.com/privacy-policy/&lt;/em&gt;&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Spring Health is proud to be an equal opportunity employer. We do not discriminate in hiring or any employment decision based on race, color, religion, national origin, age, sex, marital status, ancestry, disability, genetic information, veteran status, gender identity or expression, sexual orientation, pregnancy, or other applicable legally protected characteristic. We also consider qualified applicants regardless of criminal histories, consistent with applicable legal requirements. Spring Health is also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans. If you have a disability or special need that requires accommodation, please let us know.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-cairo-spring-health/69d48218c8e81216cd0c05f6</link><guid isPermaLink="true">http://biotechroles.com/senior-program-manager-global-clinical-training-and-programming-(emea)-cairo-spring-health/69d48218c8e81216cd0c05f6</guid><pubDate>Tue, 07 Apr 2026 04:03:36 GMT</pubDate><company>Spring Health</company><location>Remote</location><salary>$85000-120000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Android Engineer (KMM)]]></title><description><![CDATA[<p><span style="font-size: 16px;">Eko builds AI and digital tools to enable every healthcare provider to more accurately detect heart and lung disease – the leading causes of death globally. Our FDA cleared, industry leading products are used by hundreds of thousands of clinicians on millions of patients around the world. With Eko, clinicians can detect cardiac and pulmonary disease with higher accuracy, diagnose with more confidence, manage treatment effectively, and ultimately give their patients the best care possible.</span></p>
<p><span style="font-size: 16px;">We have strong venture capital backing from investors like Artis Ventures, Questa Capital, Highland Capital, and Mayo Clinic Ventures.</span></p>
<p><span style="font-size: 16px;">Recognized by TIME magazine in 2025 as one of the world’s top healthcare technology companies, Eko is one of the fastest growing digital health companies with products used around the world at some of the most prestigious health systems.</span></p>
<p><span style="font-size: 16px;">We have more than 8 FDA clearances including novel AI algorithms, and we invest heavily in quality clinical research and R&amp;D to build and validate exceptional products for patients we care deeply about.</span></p>
<p><span style="font-size: 16px;">We’ve built a mission driven, high performing, talented, and diverse team of engineers, physicians, PhD’s, creatives, and technologists. We are committed to investing in each other and our mission to ensure all patients have access to high quality care.</span></p>
<p><span style="font-size: 16px;">We are headquartered in Emeryville, California and privately-held with world class investors and partners.</span></p><div><br></div><div>
<h3><strong>Role Summary</strong></h3>
<p>We are seeking an experienced Senior Android Engineer to join our team. In this role, you will be responsible for designing, developing, and maintaining high-quality Kotlin Multiplatform applications for both iOS and Android. You will work closely with cross-functional teams, including product managers, designers, and other engineers, to deliver exceptional mobile experiences. As a Senior Engineer, you will also contribute to the continuous improvement of our development processes.</p>
<p>This is a hybrid role with required onsite presence on Tue/Wed/Thu.</p>
</div></br><b>Essential Functions:</b></br><div>

<li>
<p>Design, develop, and maintain robust, scalable, and high-performance Mobile Kotlin Multiplatform applications</p>
</li>
<li>
<p>Collaborate with product managers, designers, and other engineers to define, design, and ship new features</p>
</li>
<li>
<p>Contribute to the overall architecture and design of the mobile platform</p>
</li>
<li>
<p>Collaborate with backend developers to define and integrate APIs</p>
</li>
<li>
<p>Ensure the performance, quality, and responsiveness of applications</p>
</li>
<li>
<p>Help maintain code quality, organization, and automation</p>
</li>
<li>
<p>Participate in code reviews and contribute to the development of best practices</p>
</li>
<li>
<p>Stay up-to-date with the latest industry trends and technologies to ensure our applications remain current and competitive</p>
</li>

<p><strong>Note:</strong> Job duties may change at any time with or without notice.</p>
</div></br><b>Required Qualifications:</b></br><div>

<li>
<p>Bachelor's degree in Computer Science, Engineering, or a related field, or equivalent experience.</p>
</li>
<li>
<p>6+ years of experience in Mobile development with a good understanding of the Android platform as well as cross-platform development with Kotlin (KMM)</p>
</li>
<li>
<p>Proven track record of delivering high-quality Mobile applications to the App Store</p>
</li>
<li>
<p>Deep understanding of mobile application architecture and design patterns</p>
</li>
<li>
<p>Experience with Jetpack Compose for building modern, declarative UIs</p>
</li>
<li>
<p>Familiarity with continuous integration and continuous deployment (CI/CD) processes</p>
</li>
<li>
<p>Strong problem-solving skills and ability to debug complex issues</p>
</li>
<li>
<p>Experience with performance and memory tuning with tools</p>
</li>
<li>
<p>Knowledge of UI/UX standards and guidelines for both iOS and Android</p>
</li>
<li>
<p>Excellent communication and collaboration skills</p>
</li>

</div></br><p><span style="font-size: 16px;">Compensation is market-based and reflects the cost of labor across different U.S. geographic locations. The specific salary is based on several factors, including market location, and may vary depending on job-related knowledge, skills, and experience.</span></p>
<p><span style="font-size: 16px;">Eko is proud to be an equal opportunity employer and welcome people of different backgrounds, experiences, abilities and perspectives. We are committed to building a diverse and inclusive team.</span></p>]]></description><link>http://biotechroles.com/senior-android-engineer-(kmm)-eko/69d48211c8e81216cd0c05f1</link><guid isPermaLink="true">http://biotechroles.com/senior-android-engineer-(kmm)-eko/69d48211c8e81216cd0c05f1</guid><pubDate>Tue, 07 Apr 2026 04:03:29 GMT</pubDate><company>Eko</company><location>2100 Powell Street, Suite 300, Emeryville, California</location><salary>$160000-240000</salary><type>Full Time</type></item><item><title><![CDATA[Manager, Training & Quality Assurance]]></title><description><![CDATA[<div>Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.</div>
<div>&nbsp;</div>
<div>Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents—earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.</div><div><br></div><div>
<p>At Ro, the care experience is at the heart of how we build trust with our patients. Every conversation, every resolved issue, and every moment of support shapes how people experience their healthcare - often during moments when they need it most.</p>
<p>As the <strong>Manager of Training &amp; Quality Assurance</strong>, you will define and lead the strategy for how we enable high-quality, consistent, and scalable support across Ro’s non-clinical Member Experience organization. This includes both our onshore (U.S.-based) teams and our BPO partners.</p>
<p>In this role, you will own the end-to-end learning ecosystem and quality assurance function- ensuring that every team member is set up to deliver exceptional patient experiences from day one and continues to grow over time. You’ll establish the frameworks, standards, and systems that drive quality, while building training programs that evolve alongside our products, policies, and patient needs.</p>
<p>You will partner closely with Operations, Product, Quality &amp; Safety, Legal, and BPO leadership to ensure alignment between training, quality standards, and the broader care experience. Your work will directly influence how we measure performance, coach teams, and continuously improve the patient journey.</p>
<p>This is a highly cross-functional and strategic role, focused on building scalable systems for learning, performance, and quality that support a growing, distributed care organization. This role is a people manager role with direct oversight of QA and training team members (including QA associates and team leadership), while also owning the broader training and QA roadmap. Success in this role requires balancing hands-on execution with strategic ownership, and driving alignment across internal and BPO teams through strong cross-functional influence.</p>
</div></br><b>What You'll Do:</b></br>
<li>Own and drive the Training and QA roadmap, balancing near-term operational needs with longer-term capability building across the organization</li>
<li>Own the end-to-end Training and Quality Assurance strategy for Ro’s non-clinical Member Experience organization across both onshore and BPO teams</li>
<li>Design and implement scalable onboarding programs, including curriculum development, certification frameworks, and role-based learning paths for new hires</li>
<li>Build and evolve continuous learning programs to support ongoing development, product education, policy updates, and performance improvement</li>
<li>Define and operationalize a centralized QA framework across all support channels (e.g., messaging, email, voice), including scorecards, audit methodologies, and calibration processes</li>
<li>Establish clear quality standards and ensure consistent application across internal teams and BPO partners</li>
<li>Partner with Operations and frontline leadership to translate QA insights into targeted coaching, training interventions, and performance improvements</li>
<li>Develop feedback loops between QA, training, and operations to identify systemic gaps and drive continuous improvement initiatives</li>
<li>Leverage data to identify trends in quality, knowledge gaps, and performance drivers, and translate insights into actionable programs</li>
<li>Partner cross-functionally with Product, Engineering, Legal, and Quality &amp; Safety to ensure training and QA frameworks reflect current workflows, policies, and compliance requirements</li>
<li>Serve as the primary point of contact for QA and training across BPO partners, ensuring alignment to Ro standards and consistency in patient experience</li>
<li>Lead vendor calibration sessions, quality reviews, and training audits to maintain high performance across outsourced teams<br>Introduce and scale tools, technologies, and best practices (including AI-enabled QA and learning tools) to improve efficiency and effectiveness</li>
<li>Support organizational change initiatives (e.g., new product launches, workflow updates, policy changes) by ensuring structured training, readiness, and adoption across teams</li>
</br><b>What You’ll Bring to the Team:</b></br>
<li>5+ years of experience in training, quality assurance, customer experience, or service operations, with increasing scope in complex, scaled environments</li>
<li>3+ years of leadership experience, including managing individual contributors or senior ICs</li>
<li>Proven experience building and scaling training programs and QA frameworks across distributed teams, including BPO environments</li>
<li>Strong understanding of quality assurance methodologies, calibration processes, and performance management in customer support or patient experience settings</li>
<li>Experience supporting omnichannel environments (e.g., chat, messaging, email, voice) with a focus on consistency and quality across channels</li>
<li>Strong data fluency, with experience analyzing QA results, performance trends, and learning outcomes to drive business decisions</li>
<li>Hands-on experience with CRM and support tooling (e.g., Zendesk), as well as familiarity with QA platforms, LMS tools, and AI-enabled solutions</li>
<li>Demonstrated ability to influence cross-functional stakeholders and translate business needs into scalable training and quality programs</li>
<li>Experience working in fast-paced, high-growth environments, with the ability to balance strategic thinking and execution</li>
</br><div>The target base salary for this position ranges from $106,300 - $128,000, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills and experience. These considerations may cause your compensation to vary.</div><div><br></div><div>Ro recognizes the power of in-person collaboration, while supporting the flexibility to work anywhere in the United States. For our Ro’ers in the tri-state (NY) area, you will join us at HQ on Tuesdays and Thursdays. For those outside of the tri-state area, you will be able to join in-person collaborations throughout the year (i.e., during team on-sites).</div>
<div>&nbsp;</div>
<div>At Ro, we believe that our diverse perspectives are our biggest strengths — and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law.</div>
<div>&nbsp;</div>
<div>Ro is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and interview process. If you require a reasonable accommodation in the application or interview process, please contact us at talent@ro.co.</div>
<div>&nbsp;</div>
<div>See our California Privacy Policy <span class="postings-link"><a href="https://ro.co/job-applicant-privacy-policy/">here</a></span>.</div>]]></description><link>http://biotechroles.com/manager-training-and-quality-assurance-ro/69d481d1c8e81216cd0c05e2</link><guid isPermaLink="true">http://biotechroles.com/manager-training-and-quality-assurance-ro/69d481d1c8e81216cd0c05e2</guid><pubDate>Tue, 07 Apr 2026 04:02:25 GMT</pubDate><company>Ro</company><location>New York, NY or Remote</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Backend Engineer Team Lead - Bloom]]></title><description><![CDATA[<div>At Sword, we’re building AI to heal billions and unlock humanity’s full potential. In doing so, we’re pioneering AI Care, a fundamentally new approach to healthcare built for medical reasoning, safety, and real-time treatment, not generic technology applied after the fact. As both a clinical-centric frontier AI lab and an applied AI platform, Sword is reimagining how care is delivered at scale, removing traditional barriers like appointments, waiting rooms, and stigma so more people can access the care they need—and ultimately get back to lives lived in full.<br><br>Since 2020, Sword has expanded across physical therapy, women’s health, cardiometabolic, and mental health, and is now moving beyond the session to a fully AI-native, 24/7 care program that brings physical activity, therapeutic exercise, psychotherapy, nutrition, and behavior change into one connected experience. More than 700,000 members across three continents have completed over 10 million AI sessions, helping 1,000+ enterprise clients avoid more than $1 billion in unnecessary healthcare costs. Backed by 42 clinical studies, 44+ patents, and more than $500 million raised from leading investors including Khosla Ventures, General Catalyst, and Founders Fund, Sword is defining a new standard for healthcare.</div><div><br></div><div>
<p>As a Backend Tech Lead, you will establish the technical vision and scale the AI-driven infrastructure powering Bloom’s real-time clinical care. You will lead and mentor a high-performance engineering team, ensuring excellence through automated pipelines, robust architecture, and continuous skill development. By partnering with Product and Infrastructure teams, you will drive the software lifecycles necessary to expand our care categories across every life stage. Your role balances hands-on technical leadership with a focus on team motivation, performance monitoring, and the recruitment of top-tier talent. Ultimately, you will bridge technical innovation with operational success to keep Bloom at the forefront of accessible health technology.</p>
<p>&nbsp;</p>
<p>Today, 1 in every 3 women suffer from a pelvic-health disorder and Bloom is here to change that.</p>
<p>Sword Health developed Bloom to connect millions of women with accessible pelvic-health care, using the most innovative technology available today. Bloom includes customized guidance from Pelvic Health Specialists, an intra-vaginal biofeedback device, and a mobile app to track real-time results and progress. Women meet with Pelvic Health Specialists remotely and progress through the program from the comfort of home, on their own time.</p>
<p>Starting with pelvic health and now expanding into menopause, fertility, pregnancy, and postpartum care, Bloom is powered by the same AI Care model driving Sword's platform: a continuous interaction between the member, an AI health specialist (Phoenix), and a human clinician.</p>
<p><br>To get to know more about our Tech Stack, check <a href="https://stackshare.io/sword-health/sword-health">here</a>.</p>
</div></br><b></b></br><div><strong>AI</strong>&nbsp;<strong>Proficiency at Sword Health</strong>
<p>AI fluency is a core expectation at Sword Health. Every candidate is assessed against our three-level framework — be ready to share real examples of how AI is already part of how you work.</p>

<li>
<p>Explorer (Level 1) — Uses AI daily to boost personal productivity</p>
</li>
<li>
<p>Builder (Level 2) — Creates workflows and tools that elevate the whole team</p>
</li>
<li>
<p>Integrator (Level 3) — Embeds AI into products and processes at scale</p>
</li>

<p>Every hire must demonstrate at least Level 1. The expected level will vary depending on the seniority of the role.</p>
</div></br><b>What you’ll be doing:</b></br>
<li>Lead a team, establishing a technical vision, resolving technical disagreements and ensuring the success of delivered solutions.</li>
<li>Oversee day-to-day operations, delegating tasks and set deadlines/goals.</li>
<li>Stay up to speed with all web technologies, software architecture principles and design patterns, investing in continual improvements.</li>
<li>Use appropriate engineering practices, such fully automated development pipelines and testing.</li>
<li>Understanding the current lifecycle and development of new lifecycles with emphasis on software quality processes.</li>
<li>Work closely with our infrastructure team and other tech leads to define and improve our software and infrastructure architecture.</li>
<li>Maintaining a productive and inspiring working environment for development teams, actively participating in the training/building skills, provide coach, monitoring performance, motivating the team, recognize high performance and reward accomplishments.</li>
<li>Together with the HR team and assisting Hiring Manager, help on R&amp;D process, motivation and retention of new members.</li>
</br><div><span data-sheets-root="1">*This range includes base, variable and equity<br><br>These compensation bands are just the starting point. Once someone joins and proves they’re outlier talent, we adjust quickly to ensure their compensation aligns with their impact.<br><br>Our job titles may span more than one career level. Actual pay is determined by skills, qualifications, experience, location, market demand, and other factors. Compensation details listed in this posting reflect the base salary and any potential variable, bonus or sales incentives, and the Company’s estimation of the value of private company stock options, if applicable. The pay range is subject to change, future value of company stock options is not guaranteed, and compensation may be modified in the future. In addition to our total compensation, Sword offers a number of benefits as listed below.</span></div>
<div>&nbsp;</div>
<div><strong>Portugal - Sword Benefits &amp; Perks:</strong></div>
<div>&nbsp;</div>
<div>• Health, dental and vision insurance</div>
<div>• Meal allowance</div>
<div>• Equity shares</div>
<div>• Remote work allowance</div>
<div>• Flexible working hours</div>
<div>• Work from home</div>
<div>• Discretionary vacation</div>
<div>• Snacks and beverages</div>
<div>&nbsp;</div>
<div><strong>Note:</strong>&nbsp;Please note that this position does not offer relocation assistance. Candidates must possess a valid EU visa and be based in Portugal.</div>
<div>&nbsp;</div>
<div>Sword Health complies with applicable Federal and State civil rights laws and does not discriminate on the basis of Age, Ancestry, Color, Citizenship, Gender, Gender expression, Gender identity, Gender information, Marital status, Medical condition, National origin, Physical or mental disability, Pregnancy, Race, Religion, Caste, Sexual orientation, and Veteran status.</div>]]></description><link>http://biotechroles.com/backend-engineer-team-lead-bloom-sword-health/69d481ccc8e81216cd0c05df</link><guid isPermaLink="true">http://biotechroles.com/backend-engineer-team-lead-bloom-sword-health/69d481ccc8e81216cd0c05df</guid><pubDate>Tue, 07 Apr 2026 04:02:20 GMT</pubDate><company>Sword Health</company><location></location><salary>$140000-190000</salary><type></type></item><item><title><![CDATA[Senior Manager / Director, People Operations]]></title><description><![CDATA[<div>
<h3><strong>About Osmind</strong></h3>
<p><a href="https://osmind.org/">Osmind</a>&nbsp;is a public benefit corporation advancing psychiatry through technology, services, and real-world evidence to bring innovative mental health treatments to patients in need. Osmind’s psychiatry-tailored software and services, used by leading psychiatry practices across the U.S., help improve patient outcomes while driving practice success. Osmind's network of over 1000 clinics comprises the country's largest network of interventional psychiatry practices. Simultaneously, Osmind's clinic network, point-of-care software, and real-world data support life sciences companies in developing and scaling access to cutting-edge treatments. Osmind is a 50-person, Series B-stage company and has raised funding from top investors such as DFJ Growth, Y Combinator, and General Catalyst.</p>
<p>&nbsp;</p>
<h3><span style="color: #000000;">The opportunity</span></h3>
<p>Osmind is hiring a Senior Manager / Director, People Operations to own day-to-day People Operations and report directly into the co-founder/CEO as we continue to scale. This role is the execution and accountability layer for core HR programs (performance, manager enablement, employee experience, compliance, and workforce planning), ensuring work is well-scoped, owners are clear, and follow-through is consistent. You’ll bring strong judgment, clear communication, and a practical, high-trust approach, helping leaders and teams do their best work without unnecessary bureaucracy.</p>
</div></br><b>Responsibilities</b></br><div>

<li><strong>Be the steady HR business partner in the moments that matter:</strong>&nbsp;coach managers through performance and team dynamics, navigate employee relations with care, and handle sensitive issues with consistency and sound judgment.</li>
<li><strong>Partner with the CEO to translate AI strategy into cultural change:</strong> design an industry-best program to upskill our employee base and drive positive cultural change around AI adoption.</li>
<li><strong>Contribute to workforce planning and hiring discipline:</strong> maintain headcount plans and scenarios, surface tradeoffs, and bring recommendations to the CEO &amp; VP Finance for decisions.</li>
<li><strong>Serve as an internal “emcee”, culture carrier, and steward of employee experience:</strong>&nbsp;partner with the CEO and leaders to shape and support key internal moments—bringing a clear, high-energy voice to energize and motivate our employee base. Build cultural programs that maintain our track record of strong employee retention.</li>
<li><strong>Run high-trust people programs end-to-end:</strong>&nbsp;deliver people initiatives ranging from performance cycles, offsite get-togethers, to benefits renewals. Ensure the initiatives are clear, fair, and lightweight so managers and teams know what “good” looks like.</li>
<li><strong>Ensure operational excellence and compliance:</strong>&nbsp;keep payroll, benefits/leave, and policies accurate and on time; own QA and escalation paths with vendors/legal.</li>
<li><strong>Lead recruiting operations and employee experience through the People team:</strong>&nbsp;manage our in-house recruiter, holding yourself accountable for talent outcomes. When times are busy, step in as talent partner for select roles, owning full-cycle recruiting: from sourcing, to recruiter screens, offer issuance, to overall pipeline movement.</li>
<li><strong>Own the SF in-office experience (2 days/week):</strong>&nbsp;run office operations and logistics so in-person time is consistent, productive, and genuinely worth showing up for.</li>

</div></br><b>What Success Looks Like</b></br><div>
<p>Success in this role looks like balancing the business's needs with cultivating strong employee experience. You bring real discipline to workforce management, giving leadership &amp; managers decision-ready options and keeping the company aligned on priorities and tradeoffs. You're on top of the latest workforce trends around AI adoption, and you're passionate about driving positive cultural change that benefits both employees and the company. And you help set an energizing, human company voice in key moments, building confidence that the organization is moving forward together.</p>
<p>TL;DR: We're a tight-knit, low-ego, mission-oriented team that cares not only about what impact we make, but&nbsp;<em>how</em>&nbsp;we make it. Your role is critical in supporting the company to reach its mission, while also creating the opportunity for our employees to have a career-defining experience working at Osmind.</p>
</div></br><div>
<p>Some candidates may see the list above and feel discouraged because they don't match all the items. Please apply anyway: there's a good chance you also have important skills we’ve missed! We are committed to diversity and building an equitable and inclusive environment for people of all backgrounds and experiences, and we're taking steps to meet that commitment. We especially encourage members of traditionally underrepresented communities to apply, including women, underrepresented people of color, LGBTQ+ people, veterans, and people with disabilities.</p>
<p>Osmind is a public benefit corporation and platform for clinicians and researchers advancing new life-saving mental health treatments. We recently published our first Public Benefit Report that chronicles how our team of scientists, technologists, and psychiatrists have been working to help solve the worldwide mental health crisis, advance responsible innovation and research, and help ensure robust access to care for patients of all backgrounds. Read the report here:&nbsp;<a href="https://www.osmind.org/pbc">https://www.osmind.org/pbc</a>.</p>
</div>]]></description><link>http://biotechroles.com/senior-manager-director-people-operations-osmind/69d481c7c8e81216cd0c05dd</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-director-people-operations-osmind/69d481c7c8e81216cd0c05dd</guid><pubDate>Tue, 07 Apr 2026 04:02:15 GMT</pubDate><company>Osmind</company><location>San Francisco, CA</location><salary>$160000-220000</salary><type></type></item><item><title><![CDATA[Patient Journey Partner (field-based HCP point of contact - Hemophilia)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><span>The Opportunity</span></b></p><p></p><p>As a <b>Patient Journey Partner (PJP)</b>, in this innovative role, you’ll move beyond traditional responsibilities to directly collaborate with healthcare providers, ecosystem stakeholders, and other key partners. You play a key role in transforming healthcare by directly engaging with stakeholders to improve patient outcomes. In this field based role, you will support the <b>Hemophilia area</b>, working closely with healthcare providers, ecosystem stakeholders and other key partners to address challenges and enhance the patient journey and experience. This role shifts Roche’s approach from simply providing medicines to actively partnering, innovating, and driving change within the healthcare ecosystem.</p><ul><li><p>Act as the primary point of contact (PPOC) between Roche and ecosystem stakeholders, building strong, trust-based relationships.</p></li><li><p>Understand and analyze patient journeys, identifying opportunities to remove barriers and optimize healthcare pathways.</p></li><li><p>Leverage Roche’s expertise, science, and capabilities to bring innovative solutions to healthcare stakeholders.</p></li><li><p>Co-create solutions with external partners that drive better patient outcomes and community health improvements.</p></li><li><p>Ensure seamless stakeholder engagement through omnichannel communication strategies.</p></li><li><p>Steward Roche’s products through their lifecycle and supporting their appropriate use, which includes sharing balanced, evidence-based and up-to-date information about Roche medicinal products with healthcare professionals (HCPs) in a truthful and balanced manner.</p></li><li><p>Capture insights and interactions in the CRM system to support continuous improvement and regulatory compliance.</p></li></ul><p></p><p><b>Who you are </b></p><ul><li><p>Mandatory qualifications for the role according to 3/2009 EüM direction 8. § 1. paragraph: University degree in medicine, dentistry, pharmacy, biology, chemistry or life sciences (nurse, dietitian, physiotherapist, ambulance office, midwife, voice, speech and swallowing therapist, occupational therapist, digital dental designer, public health supervisor, health visitor, dental hygienist, health care manager, medical diagnostic analyst, advanced practice nurse, health psychologist, health care manager, social worker in health care, clinical laboratory scientist, rehabilitationist, expert in public health, radiographer, advanced health visitor, nutritionist ) with experience in patient engagement, medical affairs, or healthcare-related roles are required.</p></li><li><p>Ability to work cross-functionally, lead discussions, and influence stakeholders effectively.</p></li><li><p>Comfortable using digital tools, data-driven decision-making, and omnichannel engagement strategies.</p></li><li><p>Willingness to adapt, experiment, and implement innovative solutions in an evolving healthcare environment.</p></li><li><p>Strong interpersonal, negotiation, and consulting skills to build lasting partnerships.</p></li><li><p>Fluent in local language and proficient in English, enabling seamless collaboration across teams.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/patient-journey-partner-field-based-hcp-point-of-contact-hemophilia-roche/69d3ed75c8e81216cd0bb0be</link><guid isPermaLink="true">http://biotechroles.com/patient-journey-partner-field-based-hcp-point-of-contact-hemophilia-roche/69d3ed75c8e81216cd0bb0be</guid><pubDate>Mon, 06 Apr 2026 17:29:25 GMT</pubDate><company>Roche</company><location>Budapest</location><salary>$55000-85000</salary><type>Full time</type></item><item><title><![CDATA[Patient Journey Partner Oncology]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><span>The Opportunity</span></b></p><p><span>Health care is changing: Radical innovation, increased openness to change, increasing patient empowerment, multiple sources of medical information, and pressure on public spending. As a result of all this, the needs of our stakeholders continue to evolve.</span></p><p></p><p>The Patient Journey Partner (PJP) is at the center of the new Roche organization, turning upside down the role we play in society - from mostly offering world-class medicines towards much more partnering, innovating and leading generative disruption. By doing so the PJP will be directly accountable to deliver better outcomes for patients, their community, the ecosystem and the organisation, faster.</p><p></p><p>The PJP is an empowered leader and the local face of Roche. She or he partners closely with all stakeholders directly touching the patient journey (in a given therapeutic or disease area), gaining a deep understanding of their needs in order to connect Roche’s capabilities to co-create meaningful solutions.</p><p></p><p>This role is locally embedded in the ecosystem, it is an integrated role, functionally agnostic, (i.e. it does not fit into the traditional concepts of Commercial/Sales or Medical Affairs)<br />It has no profitability, sales objectives or incentives</p><p><br /><b>Major Responsibilities</b></p><p>- Senior level role within the affiliate, with decision making authority to request resources of Roche (both within the affiliate and broader network) in order to have improved impact on the patient journey </p><p>- Focuses on the importance of bringing the outside in, working with partners to uncover all potential opportunities to transform outcomes for patients, faster. Brings the inside out, to bring Roche expertise, science and knowledge to the ecosystem.<br />- Acts as trusted partner and is the primary (but non-exclusive) point of contact between stakeholders and Roche; shares the patient and stakeholder community needs internally, prioritizes and secures resources, and drives solutions that deliver outcomes faster.<br />- Partners with patient journey stakeholders to remove roadblocks and unlock possibilities to deliver value for patients and the community.<br />- Stewards Roche’s products through their lifecycle and supports their appropriate use, which includes sharing their merits with HCPs in a truthful and balanced manner.<br />- By overseeing the patient journey in its entirety, acts as a system thinker with the ability to identify shared purpose among stakeholders and leverages this to co-create solutions with stakeholders in the ecosystem..</p><p><br /><b>Who You Are?</b></p><p>Required Education and Experience</p><p>- University degree (scientific, economic, or business degree). An advanced degree in Life science and/or MBA  is a plus.</p><p>- Deep understanding of patient journey(s) and related treatments in defined disease area(s), enabling engagement at the specialist level.<br />- Robust understanding of medical affairs strategies and tactics including clinical research</p><p>- Practical understanding of digital innovation methodologies</p><p>- Fluent in local language. Proficient in English to collaborate internally across the broader Roche enterprise is highly desired</p><p></p><p>Required Competencies and Skills</p><p>- System thinker and deep listener<br />- Excellent stakeholder engagement skills including partnering with TAE&#39;s and organizations is required. Experience partnering with PAGs is highly desired.<br />- Experience leading Cross-functional team is required. Experience in both formulating cross-functional strategies and orchestrating cross-functional teams is highly desired.<br />- Strong business acumen with desired expertise in commercialization, medical and customer experience excellence<br />- Able to understand and leverage digital means and tools is desired<br />- Deep experience in agile ways of working is desired</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/patient-journey-partner-oncology-roche/69d3ed75c8e81216cd0bb0bd</link><guid isPermaLink="true">http://biotechroles.com/patient-journey-partner-oncology-roche/69d3ed75c8e81216cd0bb0bd</guid><pubDate>Mon, 06 Apr 2026 17:29:25 GMT</pubDate><company>Roche</company><location>Morocco</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Especialista en Licitaciones]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Objetivo general del puesto</b>: Preparar y proporcionar información y documentación de los procesos de licitación y concursos gubernamentales y del sector privado con base en los requerimientos de éstos, políticas y procesos locales y globales con la finalidad de facilitar la participación de Roche en el mercado de diagnóstico clínico. Realizar algunas gestiones administrativas internas y externas para la celebración de contratos en los diversos canales de distribución (venta directa, indirecta, POC y/o qPCR/RTD), tanto en el sector privado como en gobierno.</p><p></p><p><b>La Oportunidad</b></p><p>1. Actualizar semanalmente la base de datos de licitaciones y/o procesos de compras directas de clientes.</p><p>2. Participar en reuniones con los canales de distribución internos y externos.</p><p>3. Entregar registros sanitarios, certificados de libre venta y de calidad, cartas de distribución y manuales de operación actualizados a los distribuidores y/o clientes para la participación en licitaciones y concursos dentro del sector público y/o privado.</p><p>4. Dar seguimiento a los requerimientos solicitados cuando se trate de concursos de participación directa para asegurar la exitosa participación de Roche en los distintos procesos de compra.</p><p></p><p><b>Quién eres</b></p><p>Escolaridad Indispensable: Licenciatura/ Ingeniería (Titulado con cédula profesional)</p><p>Experiencia laboral : 3 años en Área de Licitaciones en compañías de productos para la salud</p><p>Conocimientos Técnicos:</p><ul><li><p>Gestión de Licitaciones desde el Área Administrativa</p></li><li><p>Experiencia en utilización plataformas de compras gubernamentales (ej: Compras MX)</p></li><li><p>Conocimientos legales básicos, interpretación de las distintas leyes y normativas aplicables a los procesos de compras.</p></li><li><p>Experiencia técnica y administrativa en el ramo del diagnóstico.</p></li><li><p>Tener un mindset ágil, innovador, adaptable y colaborativo, centrado en el cliente.</p></li><li><p>Tener elevada motivación para trabajar bajo un esquema de marcos de trabajo Ágiles.</p></li></ul><p></p><p>Esta posición no incluye beneficios de relocación</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/especialista-en-licitaciones-roche/69d3ed74c8e81216cd0bb0bb</link><guid isPermaLink="true">http://biotechroles.com/especialista-en-licitaciones-roche/69d3ed74c8e81216cd0bb0bb</guid><pubDate>Mon, 06 Apr 2026 17:29:24 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Compliance Senior Manager]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span><span>The Compliance Manager will be responsible for designing, implementing, and supervising the Compliance Program at the local level in the Mexico affiliate. Their objective is to ensure that all company operations are conducted under the highest ethical standards and in total conformity with local laws, industry codes (e.g., CETIFARMA, IFPMA), and the company&#39;s global policies.</span></span></p><p></p><p><span><span><b>The Opportunity</b></span></span></p><ul><li><p><span><span>Lead the implementation and continuous execution of the Ethics and Compliance program at a local level.</span></span></p></li><li><p>Develop initiatives to foster a strong culture of corporate Ethics and Integrity among all employees.</p></li><li><p><span><span>Conduct periodic risk assessments to establish and adjust the company&#39;s internal controls.</span></span></p></li><li><p>Design and execute the annual monitoring plan.</p></li><li><p>Supervise and monitor high-risk procedures such as Payments to Healthcare Professionals, events, interactions with government officials, among others.</p></li><li><p><span><span>Act as a strategic business partner for internal areas, reviewing and approving activities and addressing regulatory compliance inquiries.</span></span></p></li><li><p>Provide advice and follow-up on the Due Diligence process for third parties and suppliers.</p></li><li><p><span><span>Ensure the update, localization (tropicalization), and implementation of policies, procedures (SOPs), and manuals, adapting them to national legislation and global requirements.</span></span></p></li><li><p>Ensure employee compliance with the Code of Conduct and the Declaration of Interests.</p></li><li><p><span><span>Address and investigate reports and inquiries of conflicts of interest received through the reporting channels.</span></span></p></li><li><p>Draft investigation reports and present cases to the corresponding Committee.</p></li><li><p>Establish and follow up on the corresponding remediation measures.</p></li><li><p><span><span>Develop materials and conduct periodic training and induction courses on topics of Compliance, Anti-Corruption, and Data Privacy.</span></span></p></li><li><p>Create communication campaigns to raise awareness about the importance of compliance.</p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p><span><span>University Degree: Law, Administration, Health Sciences, or related fields (with Cedula Profesional)</span></span></p></li><li><p><span><span>Postgraduate Degree: Specialization or Certification in Compliance is highly desired.</span></span></p></li><li><p><span><span>Experience: Minimum 3-5 years in compliance positions, preferably in the innovative pharmaceutical or medical device industry.</span></span></p></li><li><p><span><span>Knowledge of the pharmaceutical industry, Industry Codes, and local legislation on health and data privacy.</span></span></p></li><li><p><span><span>Languages: Fluent English, as the role will interact with global and/or regional structures.</span></span></p></li></ul><p></p><p><span><span>Soft Skills</span></span></p><ul><li><p><span><span>Mental Agility: Ability to adapt to changing business models (Omnichannel, pharmaceutical e-commerce).</span></span></p></li><li><p><span><span>Assertive Communication: Ability to say &#34;no&#34; when necessary, but offering compliance alternatives to achieve business objectives.</span></span></p></li><li><p><span><span>Analytical Thinking: Management of data analysis tools to proactively detect compliance anomalies.</span></span></p></li><li><p><span><span>High sense of responsibility.</span></span></p></li><li><p><span><span>High ethical solvency and congruence.</span></span></p></li></ul><p></p><p><span><span>This position does not include relocation benefits</span></span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/compliance-senior-manager-roche/69d3ed74c8e81216cd0bb0ba</link><guid isPermaLink="true">http://biotechroles.com/compliance-senior-manager-roche/69d3ed74c8e81216cd0bb0ba</guid><pubDate>Mon, 06 Apr 2026 17:29:24 GMT</pubDate><company>Roche</company><location>Mexico City</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Molecular Account Executive - GenMark - South Texas, Utah, New Mexico, Colorado, and Northern Arizona]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b>Molecular Account Executive - GenMark - </b>South Texas, Utah, New Mexico, Colorado, and Northern Arizona</p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</p><p></p><p><b>The Opportunity:</b></p><p>Are you an experienced sales professional with a talent for solving complex challenges? In this role, you&#39;ll use your expertise to navigate diverse issues and make strategic decisions that drive success. You&#39;ll manage medium to large accounts, exceeding sales targets while building lasting relationships with key decision-makers.</p><p></p><p>Your goal will be to expand your network, identify new opportunities, and present compelling value propositions. With a deep understanding of our product line, you&#39;ll serve as a trusted advisor, continuously improving our quality system through your daily actions. </p><p>As an Account Executive - GenMark, you will:</p><ul><li><p>be responsible for promoting GenMark’s products and services.</p></li><li><p>contact new and existing customers to meet and exceed sales objectives in targeted accounts, by developing new business, growing existing business, maintaining customer relationships and troubleshooting customer problems. This includes identifying and developing strategic account plans, developing and delivering the differentiating message and quantifiable economic value for products and services, selling the primary differentiation of Roche products, overcoming and managing objections, and negotiating to obtain sales.</p></li><li><p>generate demand and maximize product awareness by working with and providing education and information to customers.</p></li><li><p>implements strategic initiatives and plans to facilitate sales process and productivity.</p></li><li><p>work with others, as needed or required, to prepare proposals for assigned accounts. Presents all contract proposals to customers to maximize overall business and profitability, which may require some negotiation.</p></li><li><p>Conduct and organize necessary territory planning and routing for efficiency. Conducts business analysis and planning.</p></li><li><p>communicates competitive market information internally.</p></li><li><p>networks and interfaces with internal colleagues to share information and best practices while remaining actively involved in industry/customer organizations that impact business.</p></li></ul><p></p><p>This is a field-based role - the territory is South Texas, Utah, New Mexico, Colorado, and Northern Arizona. Ideal candidate would live in Texas, Colorado, or Utah within 25 miles of a major airport.</p><p></p><p>Travel expectation: 50% Overnight</p><p></p><p><b>Who You Are:</b></p><ul><li><p>Bachelor’s degree or equivalent experience</p></li><li><p>3&#43; years relevant sales or equivalent experience</p></li><li><p>Participation in an approved accelerated development, fellowship or rotational program may be considered in lieu of experience</p></li></ul><p></p><p><b>Preferred Requirements:</b></p><ul><li><p>Good oral and written communication skills, including making impactful presentations</p></li><li><p>Proven leadership abilities</p></li><li><p>Negotiation, contracting, and problem-solving skills</p></li><li><p>Ability to work in a regulated environment</p></li><li><p>Strategic planning and organizational skills</p></li></ul><p></p><p>Relocation benefits are not available for this job posting</p><p></p><p>The expected salary range for this position, based on the primary location of Texas is $86,700.00 - $169,00.00.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/molecular-account-executive-genmark-south-texas-utah-new-mexico-colorado-and-northern-arizona-roche/69d3ed74c8e81216cd0bb0b8</link><guid isPermaLink="true">http://biotechroles.com/molecular-account-executive-genmark-south-texas-utah-new-mexico-colorado-and-northern-arizona-roche/69d3ed74c8e81216cd0bb0b8</guid><pubDate>Mon, 06 Apr 2026 17:29:24 GMT</pubDate><company>Roche</company><location>San Antonio</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Associate Project Leader]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b>Associate Project Leader</b></p><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. </span></p><p></p><p><b>The Opportunity:</b></p><p><span>This role serves as the Associate Project Leader within cross-functional global teams and is a core member of the Life Cycle Team (LCT), responsible for guiding projects from initiation through Launch Decision. The candidate will provide strategic and operational leadership, ensuring alignment with LCT objectives while balancing time, cost, risk, and technical, regulatory, and business considerations.</span></p><p><span>The role will partner closely with Product Management to drive product lifecycle execution, including new product development and updates of medium business impact with varying levels of technical and regulatory complexity. Responsibilities include defining development pathways, enabling early-stage planning, and ensuring effective cross-functional collaboration and communication throughout the project lifecycle.</span></p><p><span>Additionally, the Project Leader is accountable for delivering projects on time, within scope, and on budget, while monitoring team performance and supporting team member development. The role also contributes to continuous improvement by implementing best practices, driving process enhancements, and supporting change management initiatives across the LCT to ensure high-quality outcomes.</span></p><p></p><p><b>Key Roles &amp; Responsibilities:</b></p><ul><li><p><span>Lead and, where applicable, manage direct reports (e.g., Associate Project Leaders) to ensure successful execution of product development strategies aligned with LCT objectives.</span></p></li><li><p><span>Provide end-to-end leadership of global project teams from project initiation through Launch Decision, setting clear direction and priorities.</span></p></li><li><p><span>Build and lead high-performing, cross-functional teams by ensuring the right expertise, alignment, accountability, and collaboration across all functions.</span></p></li><li><p><span>Establish and drive project goals, timelines, and best practices, fostering a culture of urgency, accountability, and continuous improvement.</span></p></li><li><p><span>Motivate and inspire team members while cultivating a transparent, trust-based, and collaborative team environment.</span></p></li><li><p><span>Guide the development of strategic options, including alternative pathways, through structured evaluation of cost, timeline, risk, and benefits.</span></p></li><li><p><span>Facilitate constructive debate and decision-making among cross-functional experts to ensure well-informed, data-driven project outcomes.</span></p></li><li><p><span>Oversee integrated project planning, including early-stage development strategy and transition planning across the product lifecycle.</span></p></li><li><p><span>Manage stakeholder communications, including providing regular updates on project status, risks, and strategic options to LCT, LCL, and collaborators.</span></p></li><li><p><span>Own project execution across scope, budget, and timelines, while coordinating resources, managing risks, resolving conflicts, and supporting process improvement and, where applicable, co-development and CDx partnership initiatives. </span></p></li></ul><p></p><p><b>Who You Are:</b></p><ul><li><p><span>Bachelor’s degree in science, engineering, or a related field required; advanced degree (Master’s or PhD) preferred.</span></p></li><li><p><span>Minimum of 9 years of relevant work experience, with advanced degrees potentially counting toward up to 3 years of this requirement.</span></p></li><li><p><span>At least 4 years of experience in the medical diagnostics industry.</span></p></li><li><p><span>Proven experience leading cross-functional, globally distributed teams within a matrix organization.</span></p></li><li><p><span>Demonstrated track record managing complex projects through product launch, including milestone-driven delivery in regulated environments.</span></p></li><li><p><span>Strong leadership and communication skills, with the ability to influence stakeholders and confidently challenge senior management on budget, data, and resource decisions.</span></p></li><li><p><span>Experience working with external partners and managing collaborations in co-development or partnership settings.</span></p></li><li><p><span>Ability to manage competing priorities, resolve conflicts, and adapt effectively in high-pressure, fast-paced environments.</span></p></li><li><p><span>Solid understanding of diagnostic development processes, including Design Control principles (preferred).</span></p></li><li><p><span>Knowledge of industry trends, customer needs, and the competitive and technology landscape within diagnostics (CDx or related experience preferred).</span></p></li></ul><p></p><p><span><b>Travel Requirements:</b> 25% Based on business needs.</span></p><p></p><p><b><span>Location: Tucson, AZ</span></b></p><p><b><span>Relocation benefits are not available for this job posting. </span></b></p><p></p><p><span>The expected salary range for this position based on the primary location of Tucson, AZ is $123,500- $229,300.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/associate-project-leader-roche/69d3ed73c8e81216cd0bb0b5</link><guid isPermaLink="true">http://biotechroles.com/associate-project-leader-roche/69d3ed73c8e81216cd0bb0b5</guid><pubDate>Mon, 06 Apr 2026 17:29:23 GMT</pubDate><company>Roche</company><location>Tucson</location><salary>$95000-130000</salary><type>Full time</type></item><item><title><![CDATA[Complaint Handling Engineer - Medical Software]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p style="text-align:inherit"></p><h3>The Position</h3><p></p><p>As a <b>Complaint Handling Engineer - Medical Software</b> you will be dealing with complaints concerning Digital Solutions quality and product performance of Hospital/Laboratory Information Systems (HIS/LIS), medical data networks, middleware solutions. data communication, apps algorithms. </p><p></p><p>As a member of the Digital Solutions Chapter, you will be working in a very transversal Software environment having the opportunity to work with cutting edge technologies and different programming languages for on-premise and cloud-based software. You need to be able to read and understand source code in order to find out the root cause/causal factor of a SW malfunction/SW issue, and also be able to learn about Software requirements, fixing bugs process (even if you will not fix them)  and general code maintenance, all of it in an Agile environment where you could contribute with your own ideas and proposals in a team continuously improving</p><p></p><p>At Roche, we offer a <b>hybrid work model</b> that combines flexibility with in-person collaboration. For now, we require our employees to be in our offices on average two days per week. The specific office days may vary depending on business needs, such as workshops, conferences, town halls, team meetings, and other collaborative events.</p><p></p><p><b>The Opportunity:</b><br /> </p><ul><li><p>Accountable for the timely handling of individual cases (Inquiry, Complaint, Potential Reportable and Safety issues) according to ISO Quality System requirements and regulations, and needs of the Country Organizations including creation, acceptance, classification, investigation, complete documentation, on-site trouble-shooting and resolution of cases.</p></li><li><p>Resolves cases in the assigned area, potentially requiring consultation with more senior team members on technical or process-related aspects.</p></li><li><p>Interface with Affiliates and assumes responsibility for timely communication of quality related information to the Country Organizations. Supports initiatives and measures to maintain enhanced interfaces with country organizations and regional representatives.</p></li><li><p>Analyzes data using statistical measures for determining a potential product performance issue.</p></li><li><p>Responsible for escalating cases which cannot be directly resolved to appropriate levels and initiating further investigation and communicating case derived information as appropriate.</p></li><li><p>Ensures cases are compliant and conform to established quality processes, standards, and regulations.</p></li></ul><p></p><p></p><p><b>Who you are:</b></p><ul><li><p>You own a degree in bioinformatics, computational biology, biomedical engineering, computer science,  or an IT related field. </p></li><li><p>Strong communication skills in <b>English</b> (written and spoken) are essential</p></li><li><p>Work experience in the area of Software related or bioinformatics and/or in support related functions is desired.</p></li><li><p>Experience reading source code </p></li><li><p>Understanding of cloud computing platforms as well as experience managing on premise infrastructure (including servers and high performance computing clusters) is desired.</p></li><li><p>You are able to read and or debug source code of different programming languages to understand the root cause of reported issues.</p></li></ul><p></p><p><b>Apply if you are:</b></p><ul><li><p>Looking for an opportunity to continue growing in your career while mixing both the technical (IT) and medical fields.</p></li><li><p>Quick technology learner.</p></li><li><p>A team player who truly believes that together we can go further.</p></li><li><p>Not afraid to fail and learn.</p></li><li><p>Comfortable with uncertainty.</p></li><li><p>Looking for a purpose where your work will have a real impact on patient lives. Your work is meaningful to you.</p></li><li><p>Passionate and naturally curious.</p></li><li><p>Looking for solving real-world problems and helping people.</p></li></ul><p></p><p></p><p>If you feel this offer suits a friend of yours, feel free to share it. </p><p></p><p>Want to know what it’s like to be a part of Roche first-hand?  Check out our blog!  <br /><b>https://careers.roche.com/global/en/we-are-roche</b><br /> </p><p><br /><i>he controller of your personal data is Roche Diagnostics Polska sp. z o.o., ul. Domaniewska 28, 02-672 Warsaw. The data is processed for the purpose of recruitment. You have the right to access data, rectify it, delete it, limit processing, transfer it and - if processing is based on your consent - withdraw this consent at any time. Contact the Data Protection Officer at: dia.daneosobowe&#64;roche.com. More information on the principles of processing your personal data by Roche at the link: https://www.roche.pl/privacy-policy-recruitment-dia-en.</i></p><p></p><p><i>Roche Diagnostics sp. z o.o.  operates in full compliance with the law and does not tolerate any violations. Roche Diagnostics sp. z o.o.  has implemented a Procedure for Reporting Violations of Law. If you wish to report any irregularities related to our activities, all necessary information regarding the reporting process can be found on our website: https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen.</i><br /> </p><p></p><h3><b>Compensation &amp; Benefits</b></h3>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Warsaw. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><p>Information about the compensation package for this position will be provided ahead of any interview</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/complaint-handling-engineer-medical-software-roche/69d3ed73c8e81216cd0bb0b3</link><guid isPermaLink="true">http://biotechroles.com/complaint-handling-engineer-medical-software-roche/69d3ed73c8e81216cd0bb0b3</guid><pubDate>Mon, 06 Apr 2026 17:29:23 GMT</pubDate><company>Roche</company><location>Warsaw</location><salary>$45000-70000</salary><type>Full time</type></item><item><title><![CDATA[Finance Partner]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span><b>The Opportunity</b></span></p><p></p><p><span>The Finance Center of Excellence (FiCoE) Finance Partner resides within the US Dia affiliate and plays a key role in support of Commercial activities.  In this role you will be a financial business partner for the Diabetes Care and other franchises, and will be a member of the Partnering community.  You will partner with your stakeholders and create valuable impact through this role.</span></p><p></p><p><span>Key Responsibilities:</span></p><ul><li><p><span>Provides excellent finance business partnership to stakeholders and cross-functional colleagues in Diabetes Care (and potentially other franchises).</span></p></li><li><p><span>Utilizes, synthesizes, and integrates data to form insights to influence decision making. </span></p></li><li><p><span>Leads and prepares complex financial and business related analyses and research in such areas as financial performance and return on investment. </span></p></li><li><p><span>Navigates networks &amp; matrixed organization to achieve results.</span></p></li><li><p><span>Investigates and communicates key insights, trends, and variances to leadership. </span></p></li><li><p><span>Utilizes strong financial acumen to analyze and communicate financial impact to stakeholders. </span></p></li><li><p><span>Supports a broad range of product, market, and financial analyses. </span></p></li><li><p><span>Supports financial closing and procurement activities. </span></p></li><li><p><span>Understands and lives the Finance Framework, mindset and behaviors.</span></p></li><li><p><span>Demonstrates excellent presentation skills evidenced by the ability to present large volumes of complex data succinctly to all levels of the organization, including senior leadership.</span></p></li><li><p><span>Coordinates forecast and budget process across multiple stakeholders to ensure timely and accurate submission.</span></p></li><li><p><span>Serves as the liaison between finance and internal partners to build long-term, strategic modeling of future years financials.</span></p></li><li><p><span>Collaborates with internal and global partners on sales, costs, and product analyses.</span></p></li></ul><p></p><p><span><b>Who You Are</b></span></p><ul><li><p><span>Bachelor’s degree in Accounting, Finance, or Business related field; Master’s degree, MBA, or CPA preferred</span></p></li><li><p><span>Minimum 8 years of related experience</span></p></li><li><p><span>Strong knowledge of finance and accounting principles, such as GAAP and/or IFRS</span></p></li><li><p><span>Excellent stakeholder management</span></p></li><li><p><span>Excellent analytical skills and experience</span></p></li><li><p><span>Excellent presentation and communication skills</span></p></li><li><p><span>Strong financial acumen and business knowledge</span></p></li><li><p><span>Demonstrates an ability to influence</span></p></li><li><p><span>Ability to work in a fast-paced environment and manage multiple priorities</span></p></li></ul><p></p><p>The expected salary range for this position based on the primary location of Indiana is $101,300 - $188,100.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><i><b>Benefits</b></i></a></p><p><br /><b>Relocation benefits are not available for this job posting.</b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/finance-partner-roche/69d3ed71c8e81216cd0bb0b0</link><guid isPermaLink="true">http://biotechroles.com/finance-partner-roche/69d3ed71c8e81216cd0bb0b0</guid><pubDate>Mon, 06 Apr 2026 17:29:21 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$110000-150000</salary><type>Full time</type></item><item><title><![CDATA[Hospital Marketing Lead 医院市场负责人]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Primary Purpose of Job</b><br />● Lead the team to build Xofluza SOC and No.1 patient share leadership AI category to achieve ambitious growth<br />● Develop Xofluza hospital strategies and build strong brand among HCPs for both core and outsourced hospitals with proven model</p><p></p><p><b>Principle Roles and Responsibilities / Accountabilities</b><br />● Based on patient journey, deep market insights, potential and opportunities, formulate professional strategy for both core and outsourced channel<br />● Develop and formulate professional strategy and plans based on channel/department specific insights and prioritization to achieve short term sales and long term share objectives<br />● Lead the team to develop marketing activity plan towards clear goal, KPI tracking and evaluation mechanism with SMART principle<br />● TAE development and develop NTAE/RTAE engagement plan with clear goal and adoption target<br />● Work with cross function team KA, CE and medical team to strengthen listing, advocacy and share goal target<br />● Develop effective proven business model in outsourced channel leveraging distributor resources in partnership with CE, sales and operation teams, etc.<br />● Develop differentiated and consistent brand message, tool, materials in collaboration with field force, PSMs and cross functions, ensure EXCELLENT Training and EXEXUTION in field<br />● Build and develop positive team culture and cohesion, and provide leadership, coaching, mentoring, direction to team, including hiring, manpower allocation, performance management, training, and professional development<br />● Lead team to work closely and collaboratively with cross functions to combine resources, and drive win-win solution<br />● Manage turnover, develop high potential employees and provide career development opportunities for person</p><p></p><p><b>Requirements</b></p><p>● Bachelor or above, Medical, marketing, commerce preferred</p><p>● &#43;10 years and above experience in marketing and/sales, &#43;5 years managerial experience<br />● &#43;5 years Pharmaceutical RX and preferably with OTC/primary care product experience<br />● Experience in managing distributor/external partners<br />● Innovate and highly self-motivated to drive results<br />● Strong learning agility<br />● Excellent communication and presentation skills in Chinese and English (oral and writing)<br />● Strong execution capability, cross-functional communication</p><p>● Strong leadership in driving high performance team dealing with complexity and ambiguity<br />● Cultivating team development in both professional and leadership skills</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/hospital-marketing-lead-roche/69d3ed71c8e81216cd0bb0af</link><guid isPermaLink="true">http://biotechroles.com/hospital-marketing-lead-roche/69d3ed71c8e81216cd0bb0af</guid><pubDate>Mon, 06 Apr 2026 17:29:21 GMT</pubDate><company>Roche</company><location>Shanghai</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Product Specialist - Roche Diagnostics Solutions]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p></p><h3>The Position</h3><p><span>We are seeking a dedicated </span><b>Product Specialist</b><span><b> </b>to join our team, supporting pre- and post-sales functions to deliver a premium customer service experience. Your primary responsibilities will include training and ongoing education on our product portfolio, troubleshooting instruments and products, overseeing instrument installation and commissioning, and providing customer training on user procedures. You will also handle manufacturer modifications and after-sales service issues, ensuring customer satisfaction in alignment with our organization&#39;s SOPs and policies.</span></p><p></p><p><b>What you will be working on:</b></p><p><span>In this dynamic role, you will provide exceptional technical support to both internal and external customers, adding value to Roche Diagnostics’ assigned squads. This position offers flexibility across Core Lab, Molecular, and Export Markets, adapting to business needs and your area of expertise. </span></p><p></p><p><span>Join us to make a meaningful impact by delivering expert technical guidance and outstanding customer experiences. Key responsibilities include but are not limited to:</span></p><p><i>Training</i></p><ul><li><p><span>Maintain competence in the RD Analytical Systems portfolio and ensure continuing education with updates.</span></p></li><li><p><span>Conduct cross-training for colleagues and complete mandatory training in a timely manner.</span></p></li></ul><p><i>Instrument Installation, Commissioning, and Customer Training</i></p><ul><li><p><span>Oversee timely installation and commissioning of analytical systems following established protocols.</span></p></li><li><p><span>Conduct comprehensive customer training to enhance competence and reduce future support needs.</span></p></li></ul><p><i>Modifications and Instrument Troubleshooting Support</i></p><ul><li><p><span>Provide efficient after-sales support, troubleshooting, and adherence to SLAs for response times.</span></p></li><li><p><span>Handle complaint documentation per Roche’s Quality System and ensure timely technical/software updates.</span></p></li></ul><p><i>Roche User Group / Community</i></p><ul><li><p><span>Develop and facilitate engaging User Group content/events to build attendee confidence and enhance customer relationships.</span></p></li></ul><p><i>Product &amp; Marketing Support</i></p><ul><li><p><span>Provide expert technical input during sales processes and tenders, while monitoring market intelligence and competitor activity.</span></p></li></ul><p><i>Administration</i></p><ul><li><p><span>Ensure accurate and timely documentation, stock management, and up-to-date CRM customer records.</span></p></li><li><p><span>Identify business opportunities and support account and service contract strategies.</span></p></li></ul><p><i>Health, Safety, and Environment</i></p><ul><li><p><span>Comply with Roche’s safety, health, and environmental policies to safeguard employees and visitors.</span></p></li></ul><p></p><p><b>Who you are:</b></p><p><span>You are:</span></p><ul><li><p><span>A role model in agility, embodying Roche’s Leadership Commitment, Operating Principles, and APAC Spirit with the right mindset, culture, and behaviors.</span></p></li><li><p><span>An outstanding communicator and networker with proven relationship-building skills.</span></p></li><li><p><span>A strategic thinker who develops effective plans and ensures execution through teamwork, collaboration, and continuous improvement.</span></p></li><li><p><span>Highly collaborative, with the ability to set ego aside and focus on achieving the best outcomes for the team and organization.</span></p></li><li><p><span>Open to feedback and confident in seeking and providing constructive input to foster personal and team growth.</span></p></li><li><p><span>Skilled in representing the company externally and building meaningful, long-term relationships with stakeholders.</span></p></li><li><p><span>Energized by working in complex environments, with flexibility to mobilize and deliver results.</span></p></li><li><p><span>Enthusiastic about learning, driving excellence, and becoming a subject matter expert on assigned product portfolios.</span></p></li><li><p><span>Equipped with a strong background in science and business (tertiary qualification desired) and a thorough understanding of diagnostic and research laboratories.</span></p></li><li><p><span>A licensed driver, ready to contribute both on-site and in the field.</span></p></li></ul><p></p><p><span>This role is only open to candidates that have </span><b>full eligibility to live and work in New Zealand. </b></p><p></p><p><span>We do not accept any unsolicited resumes or enquiries from recruitment agencies. Roche has a dedicated in-house Talent Acquisition team.</span><span> </span></p><p><b> </b></p><p><b> </b></p><h3></h3><h3>What we offer</h3><p style="text-align:left"><span>Roche offers rewarding growth opportunities, a competitive remuneration package and a collaborative culture where people are united in purpose and will stretch you to be brave, speak up and think differently. Feel empowered to deliver meaningful outcomes, supported by accessible and inspiring leaders. </span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche encourages a high-performance culture where you are empowered and trusted to make decisions. We strive for excellence and extraordinary results and take a genuine interest in our people and their well-being, and our patients.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Take pride in knowing you can make a difference to millions of patients worldwide in developing diagnostics and treatments for oncology, neuroscience, inflammation, immunology, ophthalmology, rare diseases, respiratory disease and diabetes.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>We are committed to providing an inclusive, safe, secure and healthy workplace, and to minimise any such impacts to our employees, customers and the community. We welcome applications from all people and encourage you to advise of any individual circumstances that may require consideration.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><h2></h2><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/product-specialist-roche-diagnostics-solutions-roche/69d3ed70c8e81216cd0bb0ae</link><guid isPermaLink="true">http://biotechroles.com/product-specialist-roche-diagnostics-solutions-roche/69d3ed70c8e81216cd0bb0ae</guid><pubDate>Mon, 06 Apr 2026 17:29:20 GMT</pubDate><company>Roche</company><location>New Zealand</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Intern - Direct Procurement]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p style="text-align:inherit"></p><h3>The Position</h3><h2></h2><p><span><b>Intern - Direct Procurement</b></span></p><p></p><p><span><b>Contract type: </b>Contract of mandate (umowa zlecenie) for 12 months</span></p><p><span><b>Availability: </b>5 days per week, 25 - 40 hours per week</span></p><p><b>Place of work: </b>Warsaw Office or Remote</p><p></p><p><span>Join our procurement team as an operational and administrative support specialist! This is an ideal opportunity for someone starting their career to learn procurement processes from the inside, gain experience working in <b>SAP</b>, and participate in the department&#39;s digital transformation. You will support us in ensuring supply continuity and building professional relationships with our suppliers.</span></p><p></p><p><b>The Opportunity:</b></p><p></p><p><u><span>Operational and Systems Support:</span></u></p><ul><li><p><span><b>SAP Order Management:</b> Support in creating and processing orders, as well as monitoring delivery deadlines to clients.</span></p></li><li><p><span><b>Vendor Database Management:</b> Setting up new vendors and unblocking existing accounts in the system.</span></p></li><li><p><span><b>Material Data Administration:</b> Creating new material indexes in the system and performing regular price list updates.</span></p></li></ul><p></p><p><span>P<u>rocess and Quality Support:</u></span></p><ul><li><p><span><b>Contractor Verification:</b> Conducting supplier <b>Due Diligence</b> to secure current business operations and updating the <b>Preferred Supplier List (LPD)</b>.</span></p></li><li><p><span><b>Documentation Oversight:</b> Managing specialized documentation related to medical devices (<b>IVD/MD</b>).</span></p></li><li><p><span><b>Fulfilment Monitoring:</b> Supervising the status of order fulfillment and informing partners about delivery schedules.</span></p></li></ul><p></p><p><u><span>Administrative Tasks and Innovation:</span></u></p><ul><li><p><span><b>Contract Workflow and Archiving:</b> Managing the signing process and circulation of documents with suppliers, and archiving documents within systems (<b>MyBuy</b>).</span></p></li><li><p><span><b>Communication and AI:</b> Maintaining the Procurement Intranet site and providing substantive oversight of materials for the <b>AI assistant</b>.</span></p></li></ul><p></p><p></p><p><b>Who you are: </b></p><ul><li><p>You own a University Degree or you are still studying</p></li><li><p><span>You are meticulous and accurate when working with data and IT systems. </span></p></li><li><p><span>You have strong time management skills and the ability to prioritize tasks.</span></p></li><li><p><span>You have great communication skills and a desire to work in a dynamic, modern environment.</span></p></li><li><p><span>You are proficient in Polish &amp; English</span></p></li></ul><p></p><p></p><p><span><b>What you get:</b></span></p><ul><li><p><span><b>Flexibility:</b> A contract of mandate (<i>umowa zlecenie</i>) that can easily be adjusted to your university schedule.</span></p></li><li><p><span><b>Modern Toolkit:</b> Opportunity to learn <b>SAP</b> and <b>MyBuy</b> tools within international structures.</span></p></li><li><p><span><b>Exposure to Innovation:</b> The chance to co-create solutions based on <b>Artificial Intelligence (AI)</b> in procurement.</span></p></li><li><p><span><b>Expert Development:</b> Working within a team of &#34;team players&#34; who focus on knowledge sharing and substantive support.</span></p></li></ul><p></p><p></p><p>If you feel this offer suits a friend of yours, feel free to share it. </p><p></p><p>Want to know what it’s like to be a part of Roche first-hand?  Check out our blog!  <br /><b>https://careers.roche.com/global/en/we-are-roche</b><br /> </p><p><br /><i>The controller of your personal data is Roche Diagnostics Polska sp. z o.o., ul. Domaniewska 28, 02-672 Warsaw. The data is processed for the purpose of recruitment. You have the right to access data, rectify it, delete it, limit processing, transfer it and - if processing is based on your consent - withdraw this consent at any time. Contact the Data Protection Officer at: dia.daneosobowe&#64;roche.com. More information on the principles of processing your personal data by Roche at the link: https://www.roche.pl/privacy-policy-recruitment-dia-en.</i></p><p></p><p><i>Roche Diagnostics sp. z o.o.  operates in full compliance with the law and does not tolerate any violations. Roche Diagnostics sp. z o.o.  has implemented a Procedure for Reporting Violations of Law. If you wish to report any irregularities related to our activities, all necessary information regarding the reporting process can be found on our website: https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen.</i></p><p></p><h3><b>Compensation &amp; Benefits</b></h3>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Warsaw. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><p>Information about the compensation package for this position will be provided ahead of any interview</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/intern-direct-procurement-roche/69d3ed6fc8e81216cd0bb0ad</link><guid isPermaLink="true">http://biotechroles.com/intern-direct-procurement-roche/69d3ed6fc8e81216cd0bb0ad</guid><pubDate>Mon, 06 Apr 2026 17:29:19 GMT</pubDate><company>Roche</company><location>Warsaw</location><salary>$12000-18000</salary><type>Full time</type></item><item><title><![CDATA[Specjalista / Specjalistka ds. Serwisu Technicznego (Service Engineer)]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p style="text-align:inherit"></p><h3>The Position</h3><p></p><p><b>Specjalista / Specjalistka ds. Serwisu Technicznego (Service Engineer) </b></p><p></p><p>W Roche Diagnostics skupiamy się na wprowadzaniu innowacyjnych rozwiązań w obszarze medycyny laboratoryjnej. W Polsce działamy od kilkudziesięciu lat i należymy do wiodących pracodawców na światowym rynku diagnostycznym. Opracowujemy i wdrażamy rozwiązania diagnostyczne, które odpowiadają dzisiejszym wyzwaniom i są przygotowane na przyszłe potrzeby.</p><p></p><p><u>Zatrudnienie przez zewnętrzną agencję na okres 18 miesięcy. </u></p><p></p><p><b>Do naszego zespołu poszukujemy Specjalisty lub Specjalistki ds. Serwisu Technicznego z województwa kujawsko-pomorskiego:</b></p><p></p><p><b>Zadania:</b></p><ul><li><p>Instalacje i wdrażanie aparatury laboratoryjnej</p></li><li><p>Naprawy gwarancyjne i pogwarancyjne sprzętu</p></li><li><p>Szkolenia klientów z obsługi aparatury i systemów laboratoryjnych</p></li><li><p>Pomoc techniczna dla klientów</p></li><li><p>Raportowanie wyników pracy</p></li></ul><p></p><p><b>O Tobie:</b></p><ul><li><p>Mieszkasz na terenie województwa kujawsko-pomorskiego</p></li><li><p>Posiadasz wyższe wykształcenie techniczne (preferowane: mechanika precyzyjna, elektronika lub pokrewne specjalności)</p></li><li><p>Z łatwością potrafisz zrozumieć potrzeby Klienta i efektywnie się komunikować</p></li><li><p>Posiadasz prawo jazdy kategorii B</p></li><li><p>Dobrze znasz język angielski (min. B2)</p></li><li><p>Umiesz priorytetyzować zadania i pracować pod presją czasu</p></li><li><p>Doświadczenie w pracy na podobnym stanowisku będzie dodatkowym atutem</p></li></ul><p></p><p><b>Oferujemy:</b></p><ul><li><p>Zatrudnienie na podstawie umowy o pracę tymczasową</p></li><li><p>Atrakcyjny pakiet benefitów</p></li><li><p>Pracę w przyjaznej atmosferze w międzynarodowym środowisku</p></li><li><p>Możliwość rozwoju zawodowego</p></li><li><p>Stanowisko z możliwością wdrażania własnych inicjatyw</p></li><li><p>Program szkoleniowy i wdrożeniowy</p></li></ul><p></p><p><b>Brzmi interesująco? Nie czekaj - aplikuj! </b></p><p></p><p><i>Administratorem danych osobowych jest spółka Roche Diagnostics Polska sp. z o.o. z siedzibą w Warszawie przy ul. Domaniewskiej 28 (02-672). Dane przetwarzane są w celu prowadzenia rekrutacji. Osobom, które zaaplikują przysługuje prawo dostępu do danych, ich sprostowania, usunięcia, ograniczenia przetwarzania, przenoszenia oraz – w sytuacji, gdy są one przetwarzane na podstawie udzielonej zgody – cofnięcia tejże zgody w dowolnym momencie. Kontakt do Inspektora Ochrony Danych: dia.daneosobowe&#64;roche.com. Więcej informacji o zasadach przetwarzania przez Roche danych osobowych pod linkiem: </i><a href="https://www.roche.pl/klauzula-informacyjna-rekrutacja-dia-pl" target="_blank"><i>https://www.roche.pl/klauzula-informacyjna-rekrutacja-dia-pl</i></a></p><p></p><p><i>Roche Diagnostics Polska sp. z o.o. działa w pełnej zgodności z przepisami prawa i nie toleruje żadnych naruszeń. W Roche Diagnostics Polska sp. z o.o.  obowiązuje Procedura zgłaszania naruszeń prawa. W przypadku chęci zgłoszenia nieprawidłowości związanych z naszą działalnością, wszelkie niezbędne informacje dotyczące zgłaszania naruszeń znajdują się na naszej stronie internetowej: </i><a href="https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen" target="_blank"><u>https://www.roche.pl/kontakt/ochrona-sygnalistow-zglaszanie-naruszen</u></a><i>.</i></p><p></p><h3><b>Compensation &amp; Benefits</b></h3>Where pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Poland. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process.<p></p><p>Information about the compensation package for this position will be provided ahead of any interview</p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/specjalista-specjalistka-ds-serwisu-technicznego-service-engineer-roche/69d3ed6fc8e81216cd0bb0ac</link><guid isPermaLink="true">http://biotechroles.com/specjalista-specjalistka-ds-serwisu-technicznego-service-engineer-roche/69d3ed6fc8e81216cd0bb0ac</guid><pubDate>Mon, 06 Apr 2026 17:29:19 GMT</pubDate><company>Roche</company><location>Poland</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Logistics Operations Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>We are looking for a </span><b>Logistics Operations Specialist </b><span>at Roche Diagnostics.</span></p><p></p><h2><b><b>About the Role</b></b></h2><p><span>At Roche Diagnostics Turkey, the </span>Logistics Operations Specialist<span> plays a strategic role in the end-to-end management of logistics processes.</span><br /><span>This position is responsible not only for executing daily operations but also for driving </span>efficiency, system accuracy, digital transformation, and a culture of continuous improvement<span>.</span></p><p><span>The role supports Roche’s operational excellence vision across </span>3PL management, SAP integration, inventory optimization, transportation non-conformance management, sustainability, and budget control<span>.</span></p><p></p><p></p><h3></h3><h2><b><b>Key Responsibilities:</b></b></h2><h2><b><b>Operational Excellence &amp; System Accuracy</b></b></h2><ul><li><p><span>Systematically monitor inbound and outbound operations, ensuring data accuracy between SAP and 3PL systems</span></p></li><li><p><span>Identify transportation or SAP-related issues, create tickets to the global support team, and manage resolution through IT or other stakeholders (e.g., e-invoice partners)</span></p></li><li><p><span>Analyze inventory discrepancies and manage return or disposal processes as required</span></p></li><li><p><span>Conduct monthly stock counts with 3PL, verify system accuracy for occupied and empty locations, and coordinate annual count preparations</span></p></li><li><p><span>Ensure full compliance of logistics operations with </span>GDP, SHE, environmental, and quality standards (Roche Global Standards &amp; MQMS)</p></li><li><p><span>Manage waste and disposal processes in line with Roche’s environmental sustainability principles</span><br /> </p></li></ul><p><b><b>Inventory &amp; Warehouse Management</b></b></p><ul><li><p>Analyze slow-moving inventory to maintain optimal stock levels and proactively manage shelf-life control and disposal planning</p></li><li><p><span>Perform stock corrections and improvement actions, ensuring location-based optimization in line with fluctuating sales volumes</span></p></li><li><p><span>Oversee physical destruction activities and coordinate the preparation of quarantined materials for disposal</span></p></li></ul><p></p><p><b><span>​</span></b><b><b>Transportation &amp; Network Optimization</b></b></p><ul><li><p><span>Collaborate closely with 3PL partners on vehicle capacity and network optimization to improve efficiency</span></p></li><li><p><span>Support the preparation of distribution plans and city-based delivery schedules</span></p></li><li><p><span>Enhance operational efficiency and cost effectiveness in transportation flows</span><br /> </p></li></ul><p><b><b>Digitalization &amp; Process Improvement</b></b></p><ul><li><p><span>Utilize digital tools such as </span>SAP, Power BI, and Tableau<span> to measure performance and identify improvement opportunities</span></p></li><li><p><span>Actively contribute to automation, data integrity, and system integration projects</span></p></li><li><p><span>Foster a continuous improvement mindset and support the implementation of </span>Lean<span> methodologies</span><br /> </p></li></ul><p><b><b>Collaboration &amp; Stakeholder Management</b></b></p><ul><li><p><span>Build strong cross-functional collaboration with global, regional, and local stakeholders (Order Management, Finance, Quality, IT, 3PL, etc.)</span></p></li><li><p><span>Support transparent information flow between global and local processes to ensure operational visibility</span></p></li><li><p><span>Actively participate in regional and global logistics projects (e.g., process harmonization, 3PL transition, SAP EWM rollout)</span></p></li></ul><p></p><p><b><b>Reporting, Analysis &amp; Performance Management</b></b></p><ul><li><p><span>Prepare monthly operational KPI reports and reconcile findings with 3PL data to identify gaps</span></p></li><li><p><span>Track logistics performance indicators (KPIs), perform root cause analyses, and develop improvement plans</span></p></li><li><p><span>Generate actionable insights from operational data to support strategic planning</span></p></li><li><p><span>Prepare stock level, disposal, and shipment reports, providing analytical support where needed</span><br /> </p></li></ul><p><b><b>Financial &amp; Budget Management</b></b></p><ul><li><p><span>Communicate material requirements to the procurement team via ERP (operational purchases, disposal, packaging, pallets, etc.)</span></p></li><li><p><span>Manage related logistics (OPEX) budgets and verify all service invoices for approval</span></p></li><li><p><span>Identify and report cost efficiency opportunities to management</span><br /> </p></li></ul><h2><b>Who You Are</b></h2><ul><li><p><span>Bachelor’s degree in a relevant field</span></p></li><li><p><span>Minimum </span>5 years of experience<span> in Supply Chain, Logistics Operations, or Inventory Control</span></p></li><li><p><span>Preferably experienced in </span>Diagnostics or Pharmaceutical distribution<span> sectors</span></p></li><li><p><span>Proficient in </span>SAP (MM &amp; E-WM)<span>, </span>Power BI<span>, </span>Tableau<span>, </span>Excel<span>, and </span>PowerPoint</p></li><li><p><span>Strong command of </span>English<span>, both written and spoken</span></p></li><li><p><span>Experienced in SAP interfaces, and capable of managing e-invoice and e-waybill integrations</span></p></li><li><p><span>Solid knowledge of warehouse operations (</span>3PL management experience is an asset<span>)</span></p></li><li><p><span>Analytical thinker with strong communication and problem-solving skills</span></p></li><li><p><span>Able to collaborate effectively across multiple departments within the supply chain</span><br /> </p></li></ul><p><b><span>Available to work </span><b>on-site 5 days per week at the Tuzla DHL Asya 1 facility</b></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/logistics-operations-specialist-roche/69d3ed6fc8e81216cd0bb0aa</link><guid isPermaLink="true">http://biotechroles.com/logistics-operations-specialist-roche/69d3ed6fc8e81216cd0bb0aa</guid><pubDate>Mon, 06 Apr 2026 17:29:19 GMT</pubDate><company>Roche</company><location>Istanbul</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[RDT Onsite Workplace Experience Specialist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span style="color:#333333"><span><b><span style="font-size:13.3px">About the position</span></b></span></span></p><p><b>About Roche Digital Technology</b></p><p><span></span></p><p>In Roche Digital Technology (RDT), we build on Roche&#39;s 125-year history as one of the world&#39;s largest biotech companies, globally recognized for providing transformative innovative solutions across major disease areas. We combine human capabilities with cutting-edge technological innovations to do now what our patients need next. Our commitment to our patients&#39; needs motivates us to deliver technology that evolves the practice of medicine.</p><p>Be part of our inclusive team at Roche Digital Technology, where we&#39;re driven by a shared passion for technological novelties and optimal IT solutions.</p><p><span></span></p><p><span></span></p><p>We now have an exciting opportunity open within our RDT team to bring increased productivity and consultancy services to our employees. </p><p><span></span></p><p><span style="font-size:14.7px">We’re seeking an innovative and proactive RDT Onsite Workplace Experience Specialist who’s passionate about enhancing the digital workplace and improving employee productivity. You bring strong consultancy skills, business acumen, and experience with enterprise applications and adoption. You can influence global initiatives, communicate technical topics in clear, practical terms, and build trusted relationships across teams. With empathy, a growth mindset, and strong collaboration skills, you’re connected to the local site environment, well-networked within global Roche Digital Technologies, and eager to drive the adoption of Roche IT standards while fostering a positive, knowledge-sharing culture.</span></p><p><span></span></p><p><span style="font-size:13.3px">Your key responsibilities</span></p><p><span></span></p><ul><li><p>Providing technical consultancy for enterprise and business applications to business colleagues</p></li><li><p>Adoption and Training to foster digital enablement</p></li><li><p>Providing consultancy for specific groups and work with them how to leverage the existing tool for their benefit</p></li><li><p>Proactively approaching business functions to understand their processes and suggest methods to increase productivity </p></li><li><p>Increasing the adoption of RDT services and solutions by promoting the use and features of IT services to connect end users with the appropriate tool for the job.</p></li><li><p>Embracing agility through process automation and increased focus on stakeholder management and digital employee experience</p></li><li><p>Keeping track of what changes are coming in the enterprise platforms and solutions and analyzing how it can affect employee productivity</p></li><li><p>Automating business processes based on analysis and consultancy with business representatives</p></li><li><p>You will act as a digital enabler for our business colleagues &amp; functions</p></li><li><p>You act as the owner of the digital employee experience  for the respective site</p></li><li><p>You drive employee productivity through consultancy, provide intimacy and site proximity at the sites,  and ensure a personalized Roche employee experience.</p></li><li><p>You leverage available data (e.g.: Nexthink, SNOW) for proactive support</p></li><li><p>You support and manage the Incident/ Request management processes to ensure SLA&#39;s are met and drive continuous improvement through trend analysis.</p></li><li><p>You manage IT hardware lifecycle management &amp; deskside support processes/managed services for the site </p></li><li><p>You provide support &amp; guidance for onsite services (e.g. events and meetings) by leveraging from internal and external providers. Drive the user experience and promote best practice.  </p></li><li><p>You drive and enable standard workplace infrastructure, global/local projects and deployments in collaboration with product teams. </p></li><li><p>You proactively address and follow through on process-improvement ideas</p></li><li><p>You support &amp; drive budgeting process related to the respective site</p></li><li><p>You support local audit, inspection and certification requirements</p></li><li><p>You support local Business Continuity and IT Disaster Recovery planning activities</p></li><li><p>You partner with our internal and external service providers</p></li></ul><p><span></span></p><p style="color:#333333 !important"><span style="color:#333333"><span style="font-size:13.3px">Your qualifications and experience</span></span></p><ul><li><p>Exhibits a Lean-Agile Mindset</p></li><li><p>Manages risks progressively and in a way that leads to opportunity</p></li><li><p>Enterprise mindset that can break down silos. Focus on delivery through collaboration, and bringing people together to work towards the same purpose across organizational boundaries.</p></li><li><p>Exhibits intellectual curiosity and integrity and has a strong passion for innovation</p></li><li><p>Understanding of Roche-supported operating systems, devices and applications,  including the Google Suite of Applications, O365, etc.</p></li><li><p>Experience with ticketing systems and troubleshooting hardware, software  and mobile devices. </p></li><li><p>Excellent working knowledge of the ITIL processes in an IT service delivery</p></li><li><p>Fluent in local language, solid written and oral communication skills in English.</p></li></ul><p><span></span></p><p style="color:#333333 !important"><span style="color:#333333"><span style="font-size:13.3px">Mindset</span></span></p><ul><li><p>Ability to ask the right questions in order to increase employee productivity</p></li><li><p>Consultancy skills on digital workplace tools and solutions</p></li><li><p>Enterprise Application, deployments, consulting and adoption</p></li><li><p>Business acumen</p></li><li><p>Deep connection to the site and understanding the environment and the context</p></li><li><p>Good knowledge about the IT processes &amp; good network within global Informatics and the local site</p></li><li><p>Passionate and knowledgeable about the digital workplace</p></li><li><p>Empathetic</p></li><li><p>Good knowledge of Roche IT (platform) standards and capability to drive adoption locally</p></li><li><p>Influencing global projects (face of the business)</p></li><li><p>Desire to learn </p></li><li><p>Agile mindset: the set of attitudes supporting an agile working environment. These include respect, collaboration, improvement and learning cycles, pride in ownership, focus on delivering value, and the ability to adapt to change.</p></li><li><p>Learning mindset: the habit of approaching experiences in your life in a way that allows you to learn from them. This involves formulating goals, practicing deliberately, and using feedback actively to process your experiences and learn from them. </p></li><li><p>Enterprise mindset: that can break down silos and promote cross-networks collaborations. Focus on delivery through collaboration, ability to bring people together to work towards the same purpose across organization boundaries.</p></li><li><p>Entrepreneurial mindset: is about being committed to your vision regardless of the challenges and obstacles along the way. It’s a way of thinking that enables you to overcome challenges, be decisive, and accept responsibility for your outcomes.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/rdt-onsite-workplace-experience-specialist-roche/69d3ed6ec8e81216cd0bb0a7</link><guid isPermaLink="true">http://biotechroles.com/rdt-onsite-workplace-experience-specialist-roche/69d3ed6ec8e81216cd0bb0a7</guid><pubDate>Mon, 06 Apr 2026 17:29:18 GMT</pubDate><company>Roche</company><location>Kyiv</location><salary>$35000-55000</salary><type>Full time</type></item><item><title><![CDATA[Business Pipelines and Project Management Manager]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b><b>Primary Purpose of Job (Job Summary) </b><b>主要工作目标&#xff08;岗位简介&#xff09;</b></b></p><ul><li><p><span>Support strategic planning for both in-line and new pipelines of CE-I2 development by leveraging relevant expertise to identify and cultivate emerging opportunities within this domain.</span></p></li><li><p><span>Collaborate with the Business Operational Excellence Manager to deliver timely, insightful, and integrated execution of CE-I2 strategic initiatives, including tracking business performance, identifying business opportunities, and assessing associated risks.</span></p></li></ul><p><b><span> </span></b></p><p><b><b>Principle Roles &amp; Responsibilities / Accountabilities </b><b>主要职责</b><b>/</b><b>责任</b><b> </b></b></p><p><b><b>(Major functions of the position) </b><b>&#xff08;职位的首要职能&#xff09;</b><br /><b>Lead</b></b></p><ul><li><p><span>Maintain effective communication with the global team and affiliates to support pre-launch activities for new pipelines in therapeutic disease areas at an early stage.</span></p></li><li><p><span>Ensure a smooth handover with the brand team before the new product is launched.</span></p></li><li><p><span>Integrate different sources of internal and external insight reports and be able to prioritize key findings that address critical business questions.</span></p></li><li><p><span>Tracking CE-I2 OBP, and strategic initiatives to ensure working by outcomes.</span></p></li><li><p><span>Develop business performance dashboard and report in collaboration with Business Operational Excellence Manager through cross functional teams.</span></p></li><li><p><span>Provide business insights to timely identify growth opportunities and pre-empt potential risks</span></p></li></ul><p><b><b>Support</b></b></p><ul><li><p><span>Assess I2 business growth opportunities to inform strategic decisions.</span></p></li><li><p><span>Provide insights to support pipelines and portfolio planning and high-level go-to-market strategy.</span></p></li><li><p><span>Develop and customize key content related to new products and support the development of learning and training materials to enhance understanding among I² teams and employees.</span></p></li><li><p><span>Ensure efficient project management regarding I2 market research and strategy projects.</span></p></li><li><p><span>Attend monthly or quarterly meetings and Market Access related taskforce meeting of immunology and anti-infectious.</span></p></li></ul><p></p><p><b><u>Education&amp; Qualifications教育背景与专业资格:</u></b></p><ul><li><p><span>Master’s degree or above in pharmacy or medicine</span></p></li><li><p><span>Consulting, strategic planning, new product planning/ strategic marketing preferred</span></p></li><li><p><span>Experience in launching multiple new products will be given priority.</span></p></li></ul><p></p><p><b><u>Leadership Competencies</u><u>领导者胜任力</u></b></p><ul><li><p><span>Strong system thinking and business acumen </span></p></li><li><p><span>Strong communication skills and cross-functional teamwork</span></p></li><li><p><span>Influencing skills</span></p></li><li><p><span>High learning agility</span></p></li><li><p><span>Accountability and self-motivation</span></p></li></ul><p></p><p><b><u>Job Required Competencies</u><u>岗位所需胜任力</u></b></p><ul><li><p><span>More than 3 years of experience in pipeline management or new product launch in pharmaceutical companies is preferred </span></p></li><li><p><span>In-depth understanding of pharmaceutical value chain, e.g. regulatory, supply chain, sales, marketing, channel, access etc. and disease knowledge</span></p></li><li><p><span>Proven record of business analytics and insights synthesis </span></p></li><li><p><span>Strong storyboard development, PPT and excel capabilities</span></p></li><li><p><span>Fluent in both written and spoken English</span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/business-pipelines-and-project-management-manager-roche/69d3ed6ec8e81216cd0bb0a5</link><guid isPermaLink="true">http://biotechroles.com/business-pipelines-and-project-management-manager-roche/69d3ed6ec8e81216cd0bb0a5</guid><pubDate>Mon, 06 Apr 2026 17:29:18 GMT</pubDate><company>Roche</company><location>Shanghai</location><salary>$65000-110000</salary><type>Full time</type></item><item><title><![CDATA[Director / Sr. Director Pharma Partnering Transactions]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>The Corporate Business Development organization supports Roche and Genentech partnerships worldwide, encompassing R&amp;D assets, technologies (both biotech and digital), and commercial deals. As a pioneer in healthcare, Roche is dedicated to driving groundbreaking science and technology that transforms patients&#39; lives, and external innovation is a cornerstone of its R&amp;D strategy, complementing its extensive internal pipeline.</span></p><p></p><p><span>The Partnering Transaction Group (PTG) is composed of highly experienced business development professionals in Basel and San Francisco with deep expertise in the execution of pharmaceutical licensing and collaboration deals. We are looking for an excellent candidate to join our group in Basel to ensure that negotiated outcomes of our deals clearly reflect desired partnership arrangements and align with our business objectives.</span></p><p></p><h3>The Opportunity</h3><p><span>As a member of the Partnering Transaction Group, you will be an integral part of deal teams to structure and negotiate high-impact deals, and shape the direction of our global partnerships through the following responsibilities:</span></p><ul><li><p><span>Act as a core member of the deal team to drive strategic partnerships and licensing projects across all therapeutic areas and drug development stages worldwide.</span></p></li><li><p><span>Lead or co-lead the preparation of offers (NBOs, term sheets) and negotiations with biopharma executive teams and external advisors.</span></p></li><li><p><span>Participate in briefings with senior management at key project junctures to drive business decisions.</span></p></li><li><p><span>Focus on all elements of deal strategy and execution, including proposed deal structures and financials based on valuation, risks, and diligence assessments.</span></p></li><li><p><span>Draft term sheets and deliver detailed comments on complex licensing agreements while driving the resolution of deal issues.</span></p></li><li><p><span>Highlight deviations from standards on financial and key licensing clauses, identifying resulting risks and possible mitigation strategies.</span></p></li><li><p><span>Take a lead in developing the transaction and negotiation skills of the organization by creating and delivering training materials.</span></p></li></ul><p></p><h3>Who You Are</h3><p><span>You are an energetic, results-driven self-starter with a strong executive presence and a track record of leading strategic projects in a complex deal environment, meeting the following requirements:</span></p><ul><li><p><span>Advanced degree in Science, Business, Finance, Law, or a related area.</span></p></li><li><p><span>A minimum of 10 years of experience in the pharma/biotech industry including professional services, advisory or law firm supporting biopharma clients.</span></p></li><li><p><span>A minimum of 5 years of specific pharma/biotech transactions-related experience.</span></p></li><li><p><span>Significant experience in negotiating complex licensing or M&amp;A deals, preferably as the lead negotiator in the biopharma space.</span></p></li><li><p><span>A thorough understanding of corporate functions, including finance, accounting, legal, and intellectual property (IP).</span></p></li><li><p><span>Proficient communication skills with a collaborative mindset and the ability to think strategically through advanced professional judgment.</span></p></li></ul><p></p><p><span>Ready for the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/director-sr-director-pharma-partnering-transactions-roche/69d3ed6dc8e81216cd0bb0a3</link><guid isPermaLink="true">http://biotechroles.com/director-sr-director-pharma-partnering-transactions-roche/69d3ed6dc8e81216cd0bb0a3</guid><pubDate>Mon, 06 Apr 2026 17:29:17 GMT</pubDate><company>Roche</company><location>Basel</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Product Care Engineer - 1 year FTC]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Purpose:</b></p><p>LumiraDx sensors are complex, highly regulated products that require precision manufacturing, supported by a detailed supply chain, and monitored closely for on-market issues.</p><p>The product care engineer will support the manufacturing, logistics, R&amp;D, and quality teams with material lifecycle management, on-market product support, and transfer of new products to manufacturing.</p><p>Product or material issues are reviewed through the operations Action Team. Engineering resources are assigned to contain and troubleshoot problems, using a structured and methodical approach. Communication is key, and the product care engineer will report progress to the Action Team and other management stakeholders.</p><p></p><p><b>Responsibilities:</b></p><ul><li><p><b>Technical supplier management</b> – Work with cross-functional teams across sensor manufacturing and packaging to manage and support material lifecycles as LumiraDx transfers products to Roche branding and IVDR registration.</p></li><li><p><b>On-market product support</b> – Join the Action Team and perform root-cause investigations into product performance and manufacturing issues. Support material change projects by testing and validating changes from suppliers.</p></li><li><p><b>Product design transfers </b>– Aid the design transfer teams by developing and validating manufacturing processes for new products. Characterise product attributes and processes through DOE and test method development.</p></li></ul><p></p><p></p><p><b>Profile:</b></p><p></p><p><b>Essential Education/ Qualifications:</b></p><ul><li><p>Degree qualified in relevant engineering or scientific discipline and/or proven experience working as an engineer within a regulated industry</p></li></ul><p></p><p><b>Requirements (incl. Key Skills):</b></p><ul><li><p>Hands-on engineer with experience in medical (or other regulated) industry</p></li><li><p>Experience working in a fast-paced, target driven and regulated environment.</p></li><li><p>Experience working on multiple projects in tandem, while meeting timelines.</p></li><li><p>Experience / awareness of equipment, product, and process development and optimisation.</p></li><li><p>Experience with, or willingness to learn, the use of metrology equipment to assess and characterise products and materials.</p></li><li><p>Knowledge of statistical process controls, capabilities, and analysis techniques.</p></li><li><p>Experience of writing and executing product and process verification protocols.</p></li><li><p>High level of computer literacy in MS Office.</p></li><li><p>Competent in documentation and report writing, specifically verification and validation protocols and reports.</p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/product-care-engineer-1-year-ftc-roche/69d3ed6dc8e81216cd0bb0a2</link><guid isPermaLink="true">http://biotechroles.com/product-care-engineer-1-year-ftc-roche/69d3ed6dc8e81216cd0bb0a2</guid><pubDate>Mon, 06 Apr 2026 17:29:17 GMT</pubDate><company>Roche</company><location>Motherwell</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Medical Director - Ophthalmology]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p style="text-align:inherit"></p><h3>The Position</h3><p><b><b>Medical Director, Ophthalmology</b></b></p><p><b><span>Based in Welwyn, UK</span></b></p><p></p><p>This position will be within the Early development Group of the Ophthalmology department in the Pharmaceutical Research and Early Development organization (pRED) at Roche.</p><p><br /><span>Roche has a strong pipeline of Ophthalmology medicines and is expanding its portfolio in retinal vascular diseases, dry age-related macular degeneration and front of the eye diseases. With global partnerships and collaborations, Roche offers ample opportunities for drug development and career growth in Ophthalmology.</span><br /><br /><span>The Ophthalmology unit of Roche is rapidly growing and innovating and therefore offers the position of a Medical Director.</span><br /><br /><b><span>The opportunity</span></b><br /><span>We are offering the opportunity to join our Ophthalmology medical team. Currently, we are a team of 5 Medical Directors (MDs) working in diseases like age-related macular degeneration, diabetic retinopathy, dry eye disease, and others. You will play a key role in translating breakthrough science into transformative medicines that address significant unmet needs in vision loss. You will lead the molecule&#39;s clinical strategy from the preclinical stage through proof-of-concept.  </span></p><p></p><p><b><b>Your roles &amp; responsibilities</b></b></p><ul><li><p><span>Act as a core member of the Ophthalmology Early Development Team and assigned study teams by contributing to project deliverables (pre-clinical and clinical stage ophthalmology programs) and the generation of robust scientific and clinical evidence from the medical perspective</span></p></li><li><p><span>Scientific Leadership: Serving as the internal and external Subject Matter Expert (SME) for a specific therapeutic area (i.e. Ophthalmology).</span></p></li><li><p><span>Strategic Planning: Aligning medical goals with business objectives to ensure the clinical value of a drug is recognized by physicians, payors, and regulators.</span></p></li><li><p><span>Compliance &amp; Ethics: Acting as the &#34;conscience&#34; of the company, ensuring all communications and trials meet rigorous ethical, legal, and safety standards (GCP/ICH guidelines).</span></p></li><li><p><span>KOL Engagement: Building peer-to-peer relationships with Key Opinion Leaders (KOLs) and leading researchers to gather insights and share data.</span></p></li><li><p><span>Lead the clinical expert team to produce high quality clinical deliverables on schedule</span></p></li><li><p><span>Oversight of all elements underpinning Clinical Study Execution</span></p></li><li><p><span>Protocol Design: Writing the &#34;blueprints&#34; for Phase I–II clinical trials.</span></p></li><li><p><span>Medical Monitoring: Reviewing real-time patient data to ensure participant safety and trial integrity.</span></p></li><li><p><span>Regulatory Submissions: Authoring and supervising the clinical sections of the New Drug Application (NDA) and defending data before regulatory bodies</span></p></li><li><p><span>Scientific Communications: content generation, oversight and accountability for conference presentations, manuscript publications, etc.</span></p></li></ul><p></p><p><b><b>Who you are:</b></b></p><ul><li><p><span>M.D. or M.D. Ph.D. in a relevant field (e.g., Ophthalmology, Molecular Biology, Biomedical Sciences or related discipline). Board certification in Ophthalmology is strongly preferred.</span></p></li><li><p><span>Strong experience in academic research, pharmaceutical industry or in a clinical setting, with a demonstrated track record of impactful contributions, supported by a strong scientific publication record.</span></p></li><li><p><span>Solid understanding of methodological and bioanalytical approaches, with the proficiency to contribute to the integration and interpretation of pre-clinical and clinical data to support proof of biology, efficacy, and safety assessments.</span></p></li><li><p><span>Expertise in the Ophthalmology field: deep understanding of ocular cell biology and physiology, including the etiopathological mechanisms of the most relevant ophthalmic conditions (e.g. nAMD, DME, DR, iAMD/GA). Experience in drug development for Ophthalmology is a plus.</span></p></li><li><p><span>You always put patients at the center of our operations and ensure everything we do will sustainably benefit patients.</span></p></li><li><p><span>Demonstrated scientific curiosity and passion to drive projects and innovate, with the ability to take initiative and suggest new ideas.</span></p></li><li><p><span>Proven experience working in cross-functional, matrix teams, with strong interpersonal and collaboration skills.</span></p></li><li><p><span>Goal-oriented and highly motivated, with an analytical mindset and the ability to distill complex issues into actionable solutions.</span></p></li><li><p><span>Outstanding organizational skills, with the ability to manage multiple priorities and meet tight deadlines in a fast-paced environment.</span></p></li><li><p><span>Excellent presentation and communication skills, with the ability to clearly articulate complex scientific ideas in a concise and accessible manner.</span></p></li><li><p><span>Fluent in English (both written and spoken). </span></p></li></ul><p></p><p><span>Your responsibilities will be tailored to your experience level.</span></p><p><span>The preferred start date of this role is June 2026 or upon availability. Please clearly indicate your preferred starting date on your motivation letter.</span></p><p><span>All applications need to include a CV and cover letter.</span></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.</span></p>]]></description><link>http://biotechroles.com/medical-director-ophthalmology-roche/69d3ed6dc8e81216cd0bb0a0</link><guid isPermaLink="true">http://biotechroles.com/medical-director-ophthalmology-roche/69d3ed6dc8e81216cd0bb0a0</guid><pubDate>Mon, 06 Apr 2026 17:29:17 GMT</pubDate><company>Roche</company><location>Welwyn</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Market Access Partner]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Affiliate: Roche Korea (Pharma)</b></p><p><b>Cluster: Access &amp; Policy</b></p><p><b>Work location: Seoul, South Korea</b></p><p></p><p><b>Your key responsibilities</b></p><p>- Roche Korea Products pricing &amp; reimbursement management</p><p>o Pricing &amp; reimbursement of new drug: Strategy and dossier development with</p><p>chapter lead.<br />o HIRA, NHIS, MoHW process to ensuring the P&amp;R (new P&amp;R listing, reimbursement<br />expansion, negotiation) of Roche products<br />o Post-management of listing drugs (Price-volume Negotiation etc.)</p><p>- Develop PE study or outcomes study for products to have best reimbursement guideline and<br />competitive MRP/net price.</p><p>- Review &amp; Analysis of relevant P&amp;R regulations, reimbursement guidelines to educate in-house<br />customers and support business impact minimization.</p><p>- Modulate to communicate with relevant stakeholders (MOHW/NHIS/HIRA/Academy) through cross-functional collaboration.</p><p></p><p><b>Who you are </b></p><p>1. Minimum 5 years experience in P&amp;R of pharmaceutical company.<br />2. Bachelor degree, or above majored in pharmacy. (Pharmacist is preferred.)<br />3. Filing experience for new drug P&amp;R listing and/or reimbursement expansion.<br />4. Knowledge of external environment, relevant government regulations.<br />5. Knowledge and experience of pharmaco-economic analysis and new drug P&amp;R listing.<br />6. Good analyze the Budget Impact of health insurance.<br />7. Good at communication, English and computer skills. (Excel, Powerpoint, Word etc.)</p><p></p><p><b>Submission</b></p><p>자유 양식의 국/영문 이력서 및 국/영문 자기소개서 (하나의 MS Word 혹은 PDF 파일로 제출)</p><p>※ 이력서 상단에 반드시 현재 연봉과 희망 연봉을 표기하시기 바랍니다. 누락 시 이력서가 검토되지 않습니다.</p><p>※ 이력서 내 이메일 주소와 서류전형 지원 사이트의 입력하시는 이메일 주소를 반드시 동일하게 작성해주시기 바랍니다. </p><p>※ 국가보훈대상 및 장애인은 관련 서류 제출시 관련 법규에 의거 우대합니다.</p><p>※ 이력서에 개인민감정보 (신체적 조건, 출신 지역, 혼인 여부, 가족관계 등)는 기재하지 말아주십시오.</p><p>※ 입사 지원 서류에 허위 사실이 발견될 경우, 채용 확정 이후 라도 채용이 취소될 수 있습니다.</p><p></p><p><b>Process</b></p><p>서류 전형▶ 면접 전형 ▶ 종합 심사 ▶ 최종 합격 통지</p><p>※ 면접은 서류전형 합격자에 한해 개별 통보합니다.</p><p>※ 면접 일정 안내 및 조율을 위해 해외 번호(중국)로 연락이 갈 수 있는 점 미리 안내드립니다.</p><p>※채용이 유력한 후보자에 대해서 이력 검증 및 평판 조회, 건강검진 등의 종합심사를 진행하여 최종 합격자를 선정합니다.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/market-access-partner-roche/69d3ed6cc8e81216cd0bb09e</link><guid isPermaLink="true">http://biotechroles.com/market-access-partner-roche/69d3ed6cc8e81216cd0bb09e</guid><pubDate>Mon, 06 Apr 2026 17:29:16 GMT</pubDate><company>Roche</company><location>Seoul</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Associate Field Engineering Specialist- Tissue Diagnostics-Memphis, TN]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>This is an exciting time to join Roche Support Network. If you are passionate about problem solving then this is the position for you! As a research-focused healthcare company, Roche discovers, develops and provides innovative diagnostics and therapeutic products and services that deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnostics, treatment and treatment monitoring. Roche is a successful company that can offer exciting career opportunities. We encourage and support your development in areas of your interest which will prepare you for the next level in your career path. We know that people are responsible for our success and we value our employees. Our commitment is to create a work environment where feeling valued, respected, and empowered is a daily experience.</span><br /><b><span> </span></b></p><p><b><b>The Opportunity: </b></b></p><p><br /><span>The Roche Support Network group is committed to providing industry-defining support to its customers. As an</span><b><span> Associate Field Engineering Specialist,</span></b><span> you will have the opportunity to travel and demonstrate your expertise as a technical repair and/or installation specialist for Roche assigned product lines, and provide valued service to your laboratory customers in an assigned territory.</span></p><ul><li><p><span>Responsible for ensuring and maximizing customer satisfaction with Roche equipment and related products. </span></p></li><li><p><span>Promotes effective, positive, and productive communication among teams to ensure and maximize the satisfaction of the customer base. </span></p></li><li><p><span>Manages customer accounts at a level that promotes goodwill, confidence, and credibility in order to exceed customer expectations in terms of product, service, and support quality.</span></p></li><li><p><span>Follows standard practices and procedures to install, maintain and repair Roche Diagnostics’ equipment.  Identifies and analyzes current problems and repairs where possible or escalates to higher levels when repairs are not possible.  Schedules and performs preventative maintenance per department policy.  Monitors customer equipment performance and is able to respond to and resolve most routine issues. Refers complex problems and issues to higher levels.</span></p></li><li><p><span>Identifies revenue-generating and cost-saving opportunities, implements the Roche Diagnostics service agreement policy and seeks out opportunities to market service contracts to existing customers.  </span></p></li><li><p><span>Provides routine technical support to existing customers, including operator troubleshooting training when needed.</span></p></li><li><p><span>Completes and documents all service and customer account-related reports, updates, and emails in a timely and professional manner, compliant with all quality procedures.</span></p></li><li><p><span>Maintains expenses within departmental guidelines and controls inventory and all company property</span></p></li></ul><p><br /><b><span> </span></b></p><p><b><b>Who you are: </b></b></p><ul><li><p><span>High school diploma and 2 years of technical school or equivalent military training or equivalent work  experience</span></p></li><li><p><span>2 years of experience repairing or servicing mechanical/system hardware and software, or networking/wireless networking or equivalent level of competency attained through appropriate training curriculum</span></p></li></ul><p></p><p><b><b>Preferred Requirements:</b></b></p><ul><li><p><span>Basic knowledge of electronics, electro-mechanical systems and information technology</span></p></li><li><p><span>Ability to develop in-depth technically related troubleshooting skills</span></p></li><li><p><span>Knowledge of basic chemistry</span></p></li><li><p><span>Effective customer service skills, which includes a positive attitude, helpful customer interaction, and maintenance of ongoing customer relationships</span></p></li><li><p><span>Experience documenting troubleshooting and resolution efforts in electronic case management system(s) according to quality and regulatory standards (ALCOA).</span></p></li><li><p><span>Bachelor degree in mechanical, electrical or biomedical engineering</span></p></li><li><p></p></li></ul><p><b><b>Relocation benefits are not available for this posting.</b></b></p><p><b><b>Travel:</b></b> <span>50 to 75% overnight travel</span></p><p><b><b>Territory: </b></b><span>Tennessee - the candidate must reside in<span> </span>Memphis, TN.</span></p><p></p><p><span>The expected salary range for this position based on the primary location of Memphis, TN is 55,900.00 - 103,700.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</span></p><p><b><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/associate-field-engineering-specialist-tissue-diagnostics-memphis-tn-roche/69d3ed6cc8e81216cd0bb09d</link><guid isPermaLink="true">http://biotechroles.com/associate-field-engineering-specialist-tissue-diagnostics-memphis-tn-roche/69d3ed6cc8e81216cd0bb09d</guid><pubDate>Mon, 06 Apr 2026 17:29:16 GMT</pubDate><company>Roche</company><location>Memphis</location><salary>$75000-95000</salary><type>Full time</type></item><item><title><![CDATA[Cybersecurity and Digital Solutions Lead]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>This role is part of the Legal and Compliance department in Diagnostics Division with matrix reporting lines. Your direct report is to Head of Legal and Compliance with dotted line managers Head of Marketing and Head of Professional Services also with direct access to executive directors (as legally required).</p><p></p><p><span>The Cybersecurity and Digital Solutions Lead is responsible for developing and implementing cybersecurity policies and protocols to protect Roche&#39;s products, information systems and technologies and managing the roadmap, governance, and value realization of key digital initiatives across the Czech Affiliate and its Diagnostics and Pharma businesses.</span> Using your expertise in Roche&#39;s products and environment, you will ensure systems comply with all security and regulatory standards. You will also apply your technical skills to manage and mitigate cyber threats.</p><p></p><p><b>The Opportunity</b></p><ul><li><p>Develop and oversee <span>cybersecurity framework, strategy, policies and procedures (eg. ISO 27001 implementation, NIS2 local implementation) to safeguard digital systems and sensitive information.</span></p></li><li><p><span>Manage the cybersecurity responsibilities across different teams in Roche Diagnostics and Pharma divisions and ensure cooperation throughout the organization and overall alignment with Roche&#39;s security objectives.</span></p></li><li><p><span>Ensure Regulatory Compliance with cybersecurity and data protection requirements.</span></p></li><li><p><span>Manage the Risk Framework and monitor risk management activities.</span></p></li><li><p><span>Perform risk assessments to identify potential cyber threats and establish and coordinate a risk management plan in the context of the organisation as well as individual installation cases.</span></p></li><li><p><span>Assess system vulnerabilities and implement security measures.</span></p></li><li><p><span>Monitor network and information security systems for potential breaches and intrusions.</span></p></li><li><p><span>Coordinate potential cyber security incidents.</span></p></li><li><p><span>Cooperate and coordinate the process of cybersecurity asset management. </span></p></li><li><p><span>Conduct regular security audits and compliance checks across all systems and applications and elaborate regular reports on cybersecurity risks and mitigation steps.</span></p></li><li><p><span>Liaise and communicate directly with the regulatory Authorities and relevant Bodies on topics of cybersecurity.  </span></p></li><li><p><span>Communicate directly and regularly with the management on the topics of cybersecurity, support Executive Management in cybersecurity-related decisions </span></p></li><li><p><span>Prepare Security Assessments and Reports for Leadership.</span></p></li><li><p><span>Maintain updated knowledge of cybersecurity trends, emerging threats, and technologies.</span></p></li><li><p><span>Collaborate with external IT and external business units (e.g. hospitals and laboratories, etc.) to ensure effective cybersecurity strategies are integrated into business processes.</span></p></li><li><p><span>Provide training and awareness programs on cybersecurity best practices for all staff.</span></p></li><li><p><span>Manage cybersecurity training and awareness programs across business functions.</span></p></li><li><p><span>Oversee third-party risk management and vendor cybersecurity compliance.</span></p></li><li><p><span>Define and maintain the digital portfolio roadmap for diagnostics, including connected devices, remote monitoring tools, and AI-driven decision support systems.</span></p></li><li><p><span>Work cross-functionally with Product Management, IT, and Legal, Compliance and Regulatory teams to ensure timely and compliant delivery.</span></p></li><li><p><span>Collaborate with all stakeholders (internal/ external) on development and implementation of Digital Products and Solutions strategy.</span></p></li></ul><p></p><p><b>Who You Are</b></p><ul><li><p><span>Master’s degree in Information Security, Computer Science, Engineering, or related field.</span></p></li><li><p><span>Certifications such as CISSP, CISM, or PMP are a plus.</span></p></li><li><p><span>Proven (7&#43; years) experience in digital product implementation and cybersecurity, preferably in pharma, medical devices, or healthcare sector.</span></p></li><li><p><span>Proven experience in managing digital portfolios or complex IT/digital projects in a regulated environment.</span></p></li><li><p><span>Strong understanding of cybersecurity frameworks, medical device software lifecycle, and data privacy regulations.</span></p></li><li><p><span>Analytical and detail-oriented.</span></p></li><li><p><span>Proactive and solutions-driven approach.</span></p></li><li><p><span>Excellent interpersonal and communication skills, enabling the individual to simplify complex topics and convey them in an understandable manner to diverse audiences.</span></p></li><li><p><span>Highly organized with the ability to manage multiple priorities.</span></p></li><li><p><span>Czech and English language proficiency.</span><span> </span></p></li></ul><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/cybersecurity-and-digital-solutions-lead-roche/69d3ed6bc8e81216cd0bb09b</link><guid isPermaLink="true">http://biotechroles.com/cybersecurity-and-digital-solutions-lead-roche/69d3ed6bc8e81216cd0bb09b</guid><pubDate>Mon, 06 Apr 2026 17:29:15 GMT</pubDate><company>Roche</company><location>Czech Republic</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Senior Scientist]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><span>For nearly 25 years, Roche has been at the forefront of innovating companion diagnostics (CDx) that hold the power to transform patients’ lives by providing essential information that informs clinical decision-making and guides personalized treatment strategies.</span></p><p></p><p><span>With a steady pipeline of high medical value predictive tests fueled by collaborations with over 85 pharmaceutical partners, we deliver diagnostic certainty through the broadest menu of immunohistochemistry/in situ hybridization (IHC/ISH) companion diagnostics available today.</span></p><p></p><p><span>We are seeking a highly motivated and experienced IHC senior scientist with a strong histology/pathology background to join our innovative research and development team. This is a technical position within our antibody development group, focused on developing high quality rabbit monoclonal antibodies against novel biomarkers for tissue applications.  </span></p><p></p><p><b><span>The Opportunity:</span></b></p><p></p><p><b>Antibody Discovery &amp; Development:</b></p><ul><li><p><span>Lead the IHC functional screening for novel rabbit monoclonal antibodies against emerging and clinically relevant biomarkers.</span></p></li><li><p><span>Apply deep knowledge of biomarker biology and histology/pathology to guide antibody selections.</span></p></li><li><p><span>Analyze biomarker expression patterns across tissues, cell types, and tumor models to ensure appropriate targeting and clinical relevance.</span></p></li><li><p><span>Interpret complex staining patterns and correlate with biological and pathological context.</span></p></li></ul><p></p><p><b>IHC Assay Development &amp; Optimization:</b></p><ul><li><p><span>Develop, optimize, and standardize IHC assays using FFPE samples.</span></p></li><li><p><span>Evaluate antibody performance across normal and diseased tissues, including diverse tumor types and cell lines.</span></p></li><li><p><span>Improve assay sensitivity, specificity, and reproducibility for diagnostic applications.</span></p></li></ul><p></p><p><b>Research Sample Testing &amp; Performance Improvement:</b></p><ul><li><p><span>Conduct IHC testing on research and preclinical samples to assess antibody performance.</span></p></li><li><p><span>Identify opportunities to enhance antibody productivity, stability, and sensitivity through iterative testing and optimization.</span></p></li><li><p><span>Troubleshoot technical challenges and implement solutions to improve assay robustness.</span></p></li></ul><p></p><p><b>Validation &amp; Documentation:</b></p><ul><li><p><span>Perform analytical validation including specificity, sensitivity, reproducibility, and robustness studies.</span></p></li><li><p><span>Utilize orthogonal methods (e.g., Western blot, ELISA, RNA ISH, IF) to confirm antibody performance.</span></p></li></ul><p></p><p><b>Leadership &amp; Collaboration:</b></p><ul><li><p><span>Provide scientific leadership and mentorship to junior scientists and research staff.</span></p></li><li><p><span>Collaborate cross-functionally with R&amp;D, pathology, operation, and regulatory teams.</span></p></li><li><p><span>Contribute to scientific strategy, publications, patents, and external collaborations.</span></p></li></ul><p></p><p><span>This is an onsite position based in Pleasanton, CA.</span><br /><span>Relocation benefits are not being offered. </span></p><p></p><p><b>Who You Are:<br />(Required)</b></p><p></p><ul><li><p><span>You have a Bachelor of Science in Biology (or related field) plus 10 years relevant experience; or a master’s degree in Biology (or related field) plus 6 years; or a PhD in Biology (or related field) and 4 years relevant experience.</span></p></li><li><p><span>You have 3&#43; years of experience with immunohistochemistry (IHC) based methods.</span></p></li><li><p><span>You have 3&#43; years of experience in a solid background in Pathology, Histology or Oncology</span></p></li><li><p><span>You have the ability to translate biological insights into practical assay development strategies.</span></p></li><li><p><span>You have strong analytical and critical thinking skills with attention to detail; you have the ability to manage multiple projects and drive results in a fast-paced environment; you have a collaborative mindset with demonstrated leadership capabilities.</span><br /> </p></li></ul><p><b>Technical Expertise:</b></p><p></p><ul><li><p><span>Deep understanding of histology, capable of recognizing different tissues and cell types on FFPE samples.</span></p></li><li><p><span>Understanding of biomarker expressions across tissues, cell types, and tumor cell lines.</span></p></li><li><p><span>Proven experience working with novel or poorly characterized biomarkers.</span></p></li><li><p><span>Strong background in antibody screening and optimization.</span></p></li><li><p><span>Expertise in IHC assay development, troubleshooting, and interpretation of complex staining patterns.</span></p></li><li><p><span>Experience improving antibody productivity, stability, and sensitivity. </span></p></li></ul><p></p><p><b>Preferred:</b></p><p></p><ul><li><p><span>You have an advanced degree in Biology (or related field)</span></p></li><li><p><span>You have de novo antibody development experience.</span></p></li><li><p><span>Familiarity with digital pathology and image analysis tools.</span></p></li><li><p><span>Prior experience with RNA ISH or immunofluorescence.</span></p></li><li><p><span>Prior experience in a regulated IVD or diagnostic development environment.</span></p></li><li><p><span>You have demonstrated Interpersonal skills: Strong verbal communication and influencing skills; can influence without authority and has proven experience building and cultivating relationships with key partners and stakeholders, both internally and externally </span><br /> </p></li></ul><p><span>The expected salary range for this position is based on the primary location of Pleasanton, CA  is $111,000 - $206,500. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance. </span></p><p></p><p><span>This position also qualifies for the benefits detailed at the link provided below.</span><br /><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/senior-scientist-roche/69d3ed6bc8e81216cd0bb09a</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-roche/69d3ed6bc8e81216cd0bb09a</guid><pubDate>Mon, 06 Apr 2026 17:29:15 GMT</pubDate><company>Roche</company><location>Pleasanton</location><salary>$140000-200000</salary><type>Full time</type></item><item><title><![CDATA[Field Application Specialist- Core Lab-Richmond Virginia]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>This is an exciting time to join the Roche Support Network. If you are passionate about problem solving then this is the position for you! As a research-focused healthcare company, Roche discovers, develops and provides innovative diagnostics and therapeutic products and services that deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnostics, treatment and treatment monitoring. Roche is a successful company that can offer exciting career opportunities. We encourage and support your development in areas of your interest which will prepare you for the next level in your career path. We know that people are responsible for our success and we value our employees. Our commitment is to create a work environment where feeling valued, respected, and empowered is a daily experience.</p><p></p><p><span>As a</span><b><span> </span><b>Field Applications Specialist</b><span>, </span></b><span>you will be a key member of our Customer Support team as the primary scientific and technical representative in Richmond, Virginia, for Roche systems in customer laboratories within the Core Lab space. You will be responsible for providing best-in-class on-site customer support, including activities such as application implementation, operator training, and troubleshooting for diagnostic instrumentation and assays throughout the entire product life cycle.</span></p><p></p><p><b><span>The Opportunity:</span></b></p><p></p><ul><li><p><span> </span><span>Build and maintain strong, collaborative relationships with customer stakeholders, ensuring a high level of customer satisfaction and creating value within the customer’s lab operations. Consult with customers on lab needs and act as a partner by supporting the customer throughout the product lifecycle which could include supporting product upgrades and other changes. </span></p></li><li><p><span>Perform and/or assist with the installation of complex diagnostic instruments, software, and reagent applications in customer laboratories. Validate system performance to ensure it meets manufacturer specifications. Ensure effective and cohesive application of the newly installed solutions.</span></p></li><li><p><span>Deliver and, in some cases, develop comprehensive on-site training to laboratory personnel on the proper use and maintenance of Roche systems, including theory of operation, workflow, quality control, and data interpretation.</span></p></li><li><p><span>Act as the primary on-site resource for resolving complex technical issues related to instrumentation, software, and assay performance. Perform root cause analysis and implement corrective actions to minimize instrument downtime. Partner with other Roche team members to implement and support total solutions, such as automation, digital tools, etc.</span></p></li><li><p><span>Provide scientific and applications expertise to laboratory stakeholders (this could include supervisors, managers, directors, technologists) and medical professionals (this could include pathologists, doctors), helping them ensure cohesive lab operations by optimizing workflows, implementing new assays, and interpreting results for Roche&#39;s portfolio.</span></p></li><li><p><span>Serve as the customer liaison and collect feedback from customers on product performance, features, and usability, and then relay this information back to support and commercial teams, maintaining a competitive advantage.</span></p></li><li><p><span>Partner with the sales team and leverage in-depth technical knowledge during pre-sales activities, including product demonstrations, technical consultations, menu optimization, and other post-sales, revenue-generating opportunities.</span></p></li><li><p><span>Ensure consistent customer experiences by following Roche protocols and procedures. Maintain accurate and timely records of all service activities, customer interactions, and technical issues using Roche’s CRM system. Complete all administrative duties, such as travel and expense reporting, as required.</span></p></li><li><p><span>Overnight travel within a designated territory, which can range from a specific state to a larger region. </span></p></li><li><p><b><b>This is a field-based role - the territory will cover the Northeast Area.  50% travel is expected for this position. The ideal candidate for this role will reside in the Richmond, Virginia region</b></b><span> </span></p></li></ul><p></p><p><b><b>Who you are</b><span>:</span></b></p><p></p><ul><li><p><span>Bachelor’s degree in Biology, Chemistry, Cell Biology, Biochemistry, Medical Technology, Clinical Laboratory, and/or relevant experience.</span></p></li><li><p><span>3 years of previous experience in a clinical laboratory or IT in a clinical lab environment (including internships, college, certification time, etc.)</span></p></li></ul><p></p><p><b><b>Preferred Qualifications:</b></b></p><p></p><ul><li><p><span> </span><span>Medical Laboratory Technologist/Scientist (ASCP/AMT) or equivalent clinical laboratory experience in a clinical environment. </span></p></li><li><p><span>Experience working in a clinical environment with a demonstrated knowledge of clinical chemistry and immunoassay. </span></p></li><li><p><span>Ability to learn Roche solutions for applicable franchises (i.e. chemistry, immunology, life sciences, IT solutions), and stay current with industry trends.</span></p></li><li><p><span>Diagnose and solve technical problems efficiently and effectively.</span></p></li><li><p><span>Experience implementing new instrumentation or methodologies in a clinical or research laboratory environment</span></p></li><li><p><span>Effective written/verbal communication skills as well as project and stakeholder management experience.</span></p></li><li><p><span>Effective customer consultative skills which includes advanced scientific knowledge and analysis, training, exceptional customer engagement, and fostering of strong customer relationships.  </span></p></li><li><p><span>Demonstrated ability to coach and mentor junior staff and lead by example.</span></p></li><li><p><span>Ability to work as a field based individual contributor with independence and autonomy.</span><span> </span><br /> </p></li></ul><h2><b><b>Additional Information:</b></b></h2><p></p><ul><li><p><b><span>This is a remote, field-based position.  </span></b><span> </span><span>Overnight travel is expected &gt; 50% of the time, with variations based on business and customer support requirements.</span><span> </span></p></li><li><p><b><span>A company car is provided with this position.</span></b></p></li><li><p><b><span>No relocation benefits available for this job posting</span></b></p></li></ul><p></p><p>The expected salary range for this position based on the primary location of Richmond, VA is 63,800.00 - 118,400.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/field-application-specialist-core-lab-richmond-virginia-roche/69d3ed6bc8e81216cd0bb099</link><guid isPermaLink="true">http://biotechroles.com/field-application-specialist-core-lab-richmond-virginia-roche/69d3ed6bc8e81216cd0bb099</guid><pubDate>Mon, 06 Apr 2026 17:29:15 GMT</pubDate><company>Roche</company><location>Virginia</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Field Application Specialist- Core Lab-West Texas Region]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>This is an exciting time to join the Roche Support Network. If you are passionate about problem solving then this is the position for you! As a research-focused healthcare company, Roche discovers, develops and provides innovative diagnostics and therapeutic products and services that deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnostics, treatment and treatment monitoring. Roche is a successful company that can offer exciting career opportunities. We encourage and support your development in areas of your interest which will prepare you for the next level in your career path. We know that people are responsible for our success and we value our employees. Our commitment is to create a work environment where feeling valued, respected, and empowered is a daily experience.</p><p></p><p><span>As a </span><b><b>Field Applications Specialist</b><span>,</span></b><span> you will be a key member of our Customer Support team as the primary scientific and technical representative in  West Texas (Lubbock/Midland)for Roche systems in customer laboratories within the Core Lab space. You will be responsible for providing best-in-class on-site customer support, including activities such as, application implementation, operator training, and troubleshooting for diagnostic instrumentation and assays throughout the entire product life cycle.</span></p><p></p><p><b><span>The Opportunity:</span></b></p><p></p><ul><li><p><span> </span><span>Build and maintain strong, collaborative relationships with customer stakeholders, ensuring a high level of customer satisfaction and creating value within the customer’s lab operations. Consult with customers on lab needs and act as a partner by supporting the customer throughout the product lifecycle which could include supporting product upgrades and other changes. </span></p></li><li><p><span>Perform and/or assist with the installation of complex diagnostic instruments, software, and reagent applications in customer laboratories. Validate system performance to ensure it meets manufacturer specifications. Ensure effective and cohesive application of the newly installed solutions.</span></p></li><li><p><span>Deliver and, in some cases develop, comprehensive on-site training to laboratory personnel on the proper use and maintenance of Roche systems, including theory of operation, workflow, quality control, and data interpretation.</span></p></li><li><p><span>Act as the primary on-site resource for resolving complex technical issues related to instrumentation, software, and assay performance. Perform root cause analysis and implement corrective actions to minimize instrument downtime. Partner with other Roche team members to implement and support total solutions, such as automation, digital tools, etc.</span></p></li><li><p><span>Provide scientific and applications expertise to laboratory stakeholders (this could include supervisors, managers, directors, technologists) and medical professionals (this could include pathologists, doctors), helping them ensure cohesive lab operations by optimizing workflows, implementing new assays, and interpreting results for Roche&#39;s portfolio.</span></p></li><li><p><span>Serve as the customer liaison and collect feedback from customers on product performance, features, and usability, and then relay this information back to support and commercial teams, maintaining a competitive advantage.</span></p></li><li><p><span>Partner with the sales team and leverage in-depth technical knowledge during pre-sales activities, including product demonstrations, technical consultations, menu optimization, and other post-sales, revenue-generating opportunities.</span></p></li><li><p><span>Ensure consistent customer experiences by following Roche protocols and procedures. Maintain accurate and timely records of all service activities, customer interactions, and technical issues using Roche’s CRM system. Complete all administrative duties, such as travel and expense reporting, as required.</span></p></li><li><p><span>Overnight travel within a designated territory, which can range from a specific state to a larger region. </span></p></li><li><p><b>This is a field-based role - the territory will cover the Southwest Area.  50% travel is expected for this position. The ideal candidate for this role will reside in the West Texas region<span> </span></b></p></li></ul><p></p><p><b><b>Who you are</b><span>:</span></b></p><p></p><ul><li><p><span>Bachelor’s degree in Biology, Chemistry, Cell Biology, Biochemistry, Medical Technology, Clinical Laboratory, and/or relevant experience.</span></p></li><li><p><span>3 years of previous experience in a clinical laboratory or IT in a clinical lab environment (including internships, college, certification time, etc.)</span></p></li></ul><p></p><p><b><b>Preferred Qualifications:</b></b></p><p></p><ul><li><p><span> </span><span>Medical Laboratory Technologist/Scientist (ASCP/AMT) or equivalent clinical laboratory experience in a clinical environment. </span></p></li><li><p><span>Experience working in a clinical environment with a demonstrated knowledge of clinical chemistry and immunoassay. </span></p></li><li><p><span>Ability to learn Roche solutions for applicable franchises (i.e. chemistry, immunology, life sciences, IT solutions), and stay current with industry trends.</span></p></li><li><p><span>Diagnose and solve technical problems efficiently and effectively.</span></p></li><li><p><span>Experience implementing new instrumentation or methodologies in a clinical or research laboratory environment</span></p></li><li><p><span>Effective written/verbal communication skills as well as project and stakeholder management experience.</span></p></li><li><p><span>Effective customer consultative skills which includes advanced scientific knowledge and analysis, training, exceptional customer engagement, and fostering of strong customer relationships.  </span></p></li><li><p><span>Demonstrated ability to coach and mentor junior staff and lead by example.</span></p></li><li><p><span>Ability to work as a field based individual contributor with independence and autonomy.</span><span> </span><br /> </p></li></ul><h2><b><b>Additional Information:</b></b></h2><p></p><ul><li><p><span> </span><span><b>This is a remote, field-based position.</b>  Overnight travel is expected &gt; 50% of the time, with variations based on business and customer support requirements.</span></p></li><li><p><b><span>A company car is provided with this position.</span></b></p></li><li><p><b><span>No relocation benefits available for this job posting</span><span> </span></b></p></li></ul><p></p><p>The expected salary range for this position based on the primary location of West Texas is 63,800.00 - 118,400.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/field-application-specialist-core-lab-west-texas-region-roche/69d3ed6ac8e81216cd0bb098</link><guid isPermaLink="true">http://biotechroles.com/field-application-specialist-core-lab-west-texas-region-roche/69d3ed6ac8e81216cd0bb098</guid><pubDate>Mon, 06 Apr 2026 17:29:14 GMT</pubDate><company>Roche</company><location>Texas</location><salary>$85000-130000</salary><type>Full time</type></item><item><title><![CDATA[Field Application Specialist- Core Lab-South Texas Region]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><h2></h2><p>This is an exciting time to join the Roche Support Network. If you are passionate about problem solving then this is the position for you! As a research-focused healthcare company, Roche discovers, develops and provides innovative diagnostics and therapeutic products and services that deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnostics, treatment and treatment monitoring. Roche is a successful company that can offer exciting career opportunities. We encourage and support your development in areas of your interest which will prepare you for the next level in your career path. We know that people are responsible for our success and we value our employees. Our commitment is to create a work environment where feeling valued, respected, and empowered is a daily experience.</p><p></p><p><span>As a</span><b><span> </span><b>Field Applications Specialist</b><span>, </span></b><span>you will be a key member of our Customer Support team as the primary scientific and technical representative in  South Texas (McAllen/Rio Grande Valley)for Roche systems in customer laboratories within the Core Lab space. You will be responsible for providing best-in-class on-site customer support, including activities such as, application implementation, operator training, and troubleshooting for diagnostic instrumentation and assays throughout the entire product life cycle.</span></p><p></p><p></p><p><b><span>The Opportunity:</span></b></p><ul><li><p><span> </span><span>Build and maintain strong, collaborative relationships with customer stakeholders, ensuring a high level of customer satisfaction and creating value within the customer’s lab operations. Consult with customers on lab needs and act as a partner by supporting the customer throughout the product lifecycle which could include supporting product upgrades and other changes. </span></p></li><li><p><span>Perform and/or assist with the installation of complex diagnostic instruments, software, and reagent applications in customer laboratories. Validate system performance to ensure it meets manufacturer specifications. Ensure effective and cohesive application of the newly installed solutions.</span></p></li><li><p><span>Deliver and, in some cases develop, comprehensive on-site training to laboratory personnel on the proper use and maintenance of Roche systems, including theory of operation, workflow, quality control, and data interpretation.</span></p></li><li><p><span>Act as the primary on-site resource for resolving complex technical issues related to instrumentation, software, and assay performance. Perform root cause analysis and implement corrective actions to minimize instrument downtime. Partner with other Roche team members to implement and support total solutions, such as automation, digital tools, etc.</span></p></li><li><p><span>Provide scientific and applications expertise to laboratory stakeholders (this could include supervisors, managers, directors, technologists) and medical professionals (this could include pathologists, doctors), helping them ensure cohesive lab operations by optimizing workflows, implementing new assays, and interpreting results for Roche&#39;s portfolio.</span></p></li><li><p><span>Serve as the customer liaison and collect feedback from customers on product performance, features, and usability, and then relay this information back to support and commercial teams, maintaining a competitive advantage.</span></p></li><li><p><span>Partner with the sales team and leverage in-depth technical knowledge during pre-sales activities, including product demonstrations, technical consultations, menu optimization, and other post-sales, revenue-generating opportunities.</span></p></li><li><p><span>Ensure consistent customer experiences by following Roche protocols and procedures. Maintain accurate and timely records of all service activities, customer interactions, and technical issues using Roche’s CRM system. Complete all administrative duties, such as travel and expense reporting, as required.</span></p></li><li><p><span>Overnight travel within a designated territory, which can range from a specific state to a larger region. </span></p></li><li><p><b>This is a field-based role - the territory will cover the Southwest Area.  50% travel is expected for this position. The ideal candidate for this role will reside in the South Texas region<span> </span></b></p></li></ul><p></p><p><b><b>Who you are</b><span>:</span></b></p><p></p><ul><li><p><span>Bachelor’s degree in Biology, Chemistry, Cell Biology, Biochemistry, Medical Technology, Clinical Laboratory, and/or relevant experience.</span></p></li><li><p><span>3 years of previous experience in a clinical laboratory or IT in a clinical lab environment (including internships, college, certification time, etc.)</span></p></li></ul><p></p><p><b><b>Preferred Qualifications:</b></b></p><p></p><ul><li><p><span> </span><span>Medical Laboratory Technologist/Scientist (ASCP/AMT) or equivalent clinical laboratory experience in a clinical environment. </span></p></li><li><p><span>Experience working in a clinical environment with a demonstrated knowledge of clinical chemistry and immunoassay. </span></p></li><li><p><span>Ability to learn Roche solutions for applicable franchises (i.e. chemistry, immunology, life sciences, IT solutions), and stay current with industry trends.</span></p></li><li><p><span>Diagnose and solve technical problems efficiently and effectively.</span></p></li><li><p><span>Experience implementing new instrumentation or methodologies in a clinical or research laboratory environment</span></p></li><li><p><span>Effective written/verbal communication skills as well as project and stakeholder management experience.</span></p></li><li><p><span>Effective customer consultative skills which includes advanced scientific knowledge and analysis, training, exceptional customer engagement, and fostering of strong customer relationships.  </span></p></li><li><p><span>Demonstrated ability to coach and mentor junior staff and lead by example.</span></p></li><li><p><span>Ability to work as a field based individual contributor with independence and autonomy.</span><br /><span> </span> </p></li></ul><h2><b><b>Additional Information:</b></b></h2><p></p><ul><li><p><span> </span><span><b>This is a remote, field-based position.</b>  Overnight travel is expected &gt; 50% of the time, with variations based on business and customer support requirements.</span></p></li><li><p><b><span>A company car is provided with this position.</span></b></p></li><li><p><b><span>No relocation benefits available for this job posting</span><span> </span></b></p></li></ul><p></p><p></p><p>The expected salary range for this position based on the primary location of South Texas is 63,800.00 - 118,400.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/field-application-specialist-core-lab-south-texas-region-roche/69d3ed6ac8e81216cd0bb097</link><guid isPermaLink="true">http://biotechroles.com/field-application-specialist-core-lab-south-texas-region-roche/69d3ed6ac8e81216cd0bb097</guid><pubDate>Mon, 06 Apr 2026 17:29:14 GMT</pubDate><company>Roche</company><location>Texas</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Intern - Medical Information]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Como Pasante de Información Médica, te sumarás a un equipo dinámico enfocado en generar un impacto positivo y real en los profesionales de la salud y los pacientes.</p><p></p><p><b>La Oportunidad:</b></p><ul><li><p>Aprendes y brindas soporte operativo al área de Información Médica, colaborando en la gestión de consultas de profesionales de la salud y pacientes bajo la supervisión del equipo.</p></li><li><p>Colaboras en la recepción y derivación de consultas que ingresan por teléfono, plataforma web y correo electrónico, utilizando las guías de procedimientos globales y locales.</p></li><li><p>Asistes en la búsqueda de información científica para responder consultas externas, garantizando en todo momento la calidad y la precisión de los datos brindados.</p></li><li><p>Identificas y das curso a los reportes de eventos adversos o reclamos de calidad, asegurando el estricto cumplimiento de los tiempos regulatorios establecidos.</p></li><li><p>Participas y ofreces soporte administrativo en las tareas de reconciliación de eventos en conjunto con las áreas de seguridad y calidad.</p></li><li><p>Brindas soporte administrativo y participas activamente en el Programa de Soporte a Pacientes, marcando una diferencia en su experiencia.</p></li><li><p>Registras meticulosamente las interacciones y consultas de nuestros clientes en los sistemas globales corporativos.</p></li><li><p>Colaboras en la gestión de artículos científicos mientras te familiarizas con las normativas de derechos de autor vigentes.</p></li></ul><p></p><p><b>Quién eres:</b></p><ul><li><p>Eres estudiante de carreras de grado relacionadas con la salud, tales como Farmacia, Bioquímica, Medicina, Biotecnología, Biología o disciplinas afines.</p></li><li><p>Cuentas con excelentes habilidades de comunicación y demuestras una gran capacidad de escucha activa.</p></li><li><p>Posees una fuerte empatía para el trato con los pacientes, complementada con una estricta atención al detalle.</p></li><li><p>Tienes un nivel de inglés intermedio o avanzado que te permite leer de manera fluida las guías globales y utilizar los sistemas informáticos.</p></li></ul><p></p><p>Los beneficios de reubicación no están disponibles para esta vacante.</p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/intern-medical-information-roche/69d3ed69c8e81216cd0bb093</link><guid isPermaLink="true">http://biotechroles.com/intern-medical-information-roche/69d3ed69c8e81216cd0bb093</guid><pubDate>Mon, 06 Apr 2026 17:29:13 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$0-1000</salary><type>Part time</type></item><item><title><![CDATA[Intern - Patient Services]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>Buscamos un estudiante con una fuerte vocación de servicio para formarse en nuestra área de Patient Services. El objetivo es que el pasante aprenda a acompañar a las personas en su tratamiento, funcionando como un facilitador entre el paciente, su médico y su cobertura de salud. Adicionalmente, aprenderás las tareas administrativas relacionadas a los servicios a pacientes.</p><p></p><p><b>La Oportunidad:</b></p><ul><li><p>Realizas el seguimiento telefónico de los pacientes, brindando escucha activa y resolviendo dudas relacionadas al área.</p></li><li><p>Explicas de forma sencilla el alcance de nuestras soluciones para educar y apoyar al paciente.</p></li><li><p>Orientas al paciente en sus trámites con obras sociales para gestionar y superar las barreras de acceso.</p></li><li><p>Colaboras en la identificación de las necesidades del paciente para asegurar su adherencia y cuidado continuo.</p></li><li><p>Coordinas el soporte al paciente integrando el trabajo de las áreas médicas, de acceso y operativas de la compañía.</p></li><li><p>Aprendes y ejecutas las tareas y circuitos administrativos vinculados a los servicios a pacientes.</p></li></ul><p></p><p><b>Quién eres:</b></p><ul><li><p>Eres estudiante de carreras de Salud (Enfermería, Farmacia, Psicología, Medicina, Nutrición) o Administración de Salud.</p></li><li><p>Te caracterizas por tu empatía, calidez y fuerte vocación de servicio.</p></li><li><p>Demuestras responsabilidad y compromiso para manejar información sensible y cuidar la continuidad del tratamiento del paciente.</p></li><li><p>Tienes ganas de aprender y un gran interés por desarrollarte en servicios que tienen al paciente como centro.</p></li><li><p>Cuentas con disponibilidad para cumplir uno de los siguientes horarios: de 9 a 13 hs o de 13 a 17 hs.</p></li></ul><p></p><p>No se ofrecen beneficios de reubicación para este puesto.</p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/intern-patient-services-roche/69d3ed69c8e81216cd0bb091</link><guid isPermaLink="true">http://biotechroles.com/intern-patient-services-roche/69d3ed69c8e81216cd0bb091</guid><pubDate>Mon, 06 Apr 2026 17:29:13 GMT</pubDate><company>Roche</company><location>Buenos Aires</location><salary>$0-1000</salary><type>Part time</type></item><item><title><![CDATA[Senior Data Scientist]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><b>Position title: Senior Data Scientist<br />Reporting to: Senior Manager – Data Science<br />Job Location: Hyderabad / Chennai</b></p><p></p><p>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. </p><p>That’s what makes us Roche.</p><p></p><p>Roche has established the Global Analytics and Technology Center of Excellence (GATE) to drive analytics- and technology-driven solutions by partnering with Roche affiliates across the globe. GATE enables data-led decision-making and innovation across healthcare and biotech operations.</p><p></p><p>As a <b>Senior Data Scientist</b>, you will lead and deliver high-impact data science projects that enable strategic decision-making within Roche’s healthcare and commercial ecosystem. Collaborating closely with cross-functional teams, your primary focus will be on Healthcare and Pharma Data Science and Marketing Mix Modeling (MMM) leveraging advanced statistical and machine-learning techniques to generate actionable insights and optimize business outcomes.</p><p>Exposure to GenAI, LLM, NLP, and ML Ops will be considered a strong advantage, supporting Roche’s future-ready analytics and AI roadmap.</p><p></p><p><b>Your Opportunity:</b></p><p><b>Project Leadership and Collaboration (Primary Focus):</b></p><ul><li><p>Lead and manage end-to-end data science projects from problem definition to model deployment ensuring alignment with business goals and timelines</p></li><li><p>Partner with cross-functional teams to define business requirements and deliver tailored analytics solutions</p></li><li><p>Develop and maintain key stakeholder relationships to ensure effective communication and collaboration throughout project lifecycles</p></li><li><p>Present analytical findings and strategic recommendations to business stakeholders, influencing data-driven decision making across multiple levels of the organization</p></li></ul><p></p><p><b>Advanced Analytics (Primary Focus):</b> </p><ul><li><p>Collect, clean, and prepare large and complex healthcare-related datasets (product performance, patient data, operational metrics, etc.) for analysis</p></li><li><p>Develop and implement statistical and machine learning models (e.g., multivariate regression, time-series analysis, XGBoost, clustering, classification, causal inference) to address complex business problems and uncover meaningful insights</p></li><li><p>Utilize advanced data analytics techniques to explore and identify patterns, trends, and root causes, applying methodologies such as clustering, classification, and causal inference</p></li></ul><p></p><p><b>Marketing and Experimental Analytics (Primary Focus):</b></p><ul><li><p>Build Econometric/market mix models (MMM), multi-touch attribution models (MTA), optimize marketing spend and come-up with implementable recommendations and strategy/plan</p></li><li><p>Lead the development and implementation of advanced Media Mix Models to inform and optimize marketing spend across multiple channels (e.g., TV, digital, print, radio)</p></li><li><p>Design and execute complex statistical analyses to evaluate the effectiveness of marketing strategies and optimize resource allocation</p></li><li><p>Apply experimental design and A/B testing methodologies to validate and measure marketing and operational initiatives</p></li></ul><p></p><p><b>GenAI, NLP, and Machine Learning Operations (Secondary / Emerging Focus):</b> </p><ul><li><p>Develop and implement GenAI models and tools to solve business problems</p></li><li><p>Deploy machine learning models in production environments, ensuring robust ML Ops practices for model monitoring, maintenance, and scaling</p></li><li><p>Collaborate with IT and DevOps teams to streamline the integration of ML models into existing systems and workflows</p></li><li><p>Enhance agent performance through experimentation with LLMs, prompt tuning, and advanced reasoning workflows</p></li></ul><p></p><p><b>Communication, Mentorship, and Governance (Primary Focus):</b></p><ul><li><p>Translate complex data insights into clear and actionable business strategies that address stakeholder needs and expectations</p></li><li><p>Mentor and guide junior data scientists, providing technical expertise and fostering an environment of continuous learning and improvement</p></li><li><p>Promote best practices in coding, data handling, and project management within the data science team, ensuring high-quality deliverables</p></li><li><p>Ensure adherence to Roche’s ethical AI standards and data privacy regulations</p></li></ul><p></p><p><b>Who you are:</b></p><ul><li><p>You hold a bachelor&#39;s degree in Technology or a relevant discipline, with a preference for Computer Science, Software, Statistics, Data Science, AI, Machine Learning, Data Engineering and related fields. Preferably, you have a Master&#39;s degree</p></li><li><p>Certifications in AI/ML, Data Science, or related technologies would be a plus</p></li><li><p>You have 5-8 years of hands-on experience in data science, with proven experience in leading data science projects within the pharma/biotech/healthcare domain</p></li><li><p>Strong proficiency in Python and SQL, with experience in data wrangling, feature engineering, and analytical model development</p></li><li><p>Experience working in cloud-based environments (AWS preferred), with practical knowledge of GitHub and cloud computing workflows for data science projects</p></li><li><p>Hands-on experience building models using algorithms and techniques such as multivariate regression, time series analysis, XGBoost, clustering, classification, OLS regression, Naïve Bayes, linear and time-decay attribution models, Markov chains, and Shapley value methods</p></li><li><p>Experience in Multi channel Marketing Mix Modeling (MMM), or related fields, with a track record of delivering impactful results</p></li><li><p>At least 4 years of strong experience with machine learning libraries and frameworks such as TensorFlow, PyTorch, scikit-learn, Keras, spaCy, NLTK, NumPy, pandas, and Spark</p></li><li><p>Basic understanding of pharmaceutical datasets (e.g., IQVIA, SHA, Patients data) and familiarity with US healthcare markets would be a plus</p></li><li><p>Strong analytical and problem-solving skills with a data-driven mindset</p></li></ul><p></p><p><b>Good to Have: </b></p><ul><li><p>Experience with modern deep learning architectures for NLP, including hands-on experience with transformers (e.g., Hugging Face, SBert, GPT-2/GPT-3) and the capability to build ML/DL pipelines for training/tuning models, including transfer learning</p></li><li><p>Proficiency with LLM APIs (e. g. , OpenAI, Claude, Gemini) and agent frameworks such as AutoGen, LangGraph, AgentBuilder, or CrewAI</p></li><li><p>Experience with prompt engineering or intelligent workflow automation</p></li><li><p>Bash/shell scripting is a plus, Experience with Docker, API development is advantageous</p></li></ul><p><br /><i><b>Note</b>: This job description is intended as a general guideline for the responsibilities and qualifications required for this position. It is not an exhaustive list, and responsibilities may evolve and change based on business needs.</i></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/senior-data-scientist-roche/69d3ed69c8e81216cd0bb08f</link><guid isPermaLink="true">http://biotechroles.com/senior-data-scientist-roche/69d3ed69c8e81216cd0bb08f</guid><pubDate>Mon, 06 Apr 2026 17:29:13 GMT</pubDate><company>Roche</company><location>Hyderabad</location><salary>$55000-95000</salary><type>Full time</type></item><item><title><![CDATA[People Support Solutions Lead (Recruitment Team Lead)]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>As a <b>PSS Global Chapter Services Recruitment Team Lead</b>, you will lead a team of specialists in the People Support Solutions (PSS) organization. The Global Chapter Services Team Lead is part of the IWS Recruitment chapter. Together with your team you will provide services and support in the Recruitment Area of Practice</p><p></p><p>Working closely with P&amp;C colleagues, you support an open and diverse work culture based on trust and performance. Your activities uphold Roche&#39;s reputation as an attractive employer – today and going forward. </p><p></p><p><b>Your Opportunity</b></p><p></p><p><b>Leadership, people and culture </b></p><ul><li><p>Responsible for all employment decisions for the team including resource planning, hiring, training, development, performance management and progressive disciplinary actions. </p></li><li><p>Responsible for engaging stakeholders, getting feedback and driving continued customer experience improvements </p></li><li><p>Escalation point for related topics to your area of responsibility </p></li><li><p>Lead, role model, and facilitate people processes in line with RocheLeadership commitments, People Practices and policies. </p></li><li><p>Through frequent check ins, ensure that ongoing dialog occurs on the topics of Career, Capabilities, Connections and Contributions. </p></li><li><p>Build an engaging culture to both attract and retain top talent. Coach team members regarding their individual development and career plan. </p></li><li><p>Responsible for team&#96;s compensation management, including yearly bonus distribution and salary increase. </p></li></ul><p></p><p><b>Outputs &amp; Deliverables </b></p><ul><li><p>High customer satisfaction through understanding of business requirements and providing high quality and end-to-end solutions with a sense of urgency o Successfully completion of cases or projects </p></li><li><p>complex senior vendor management </p></li><li><p>participating in/leading WPT on complex topics </p></li><li><p>High degree of employee satisfaction in your team </p></li></ul><p></p><p><b> Cross-Functional Collaboration </b></p><ul><li><p>Collaborate with peers within region and globally to ensure the PSS network provides consistent and effective services to our customers, including: ▪ PSS teams, network and communities </p></li></ul><ul><li><p> Other P&amp;C chapters and communities, especially the IWS and PR&amp;R Partner communities in the chapters including the chapters enabling teams   </p></li><li><p>Other enabling functions, e.g. Finance, Procurement, IT etc to ensure the solution implementation or improvement </p></li><li><p>PSS peers within region and global to ensure the PSS network  provides consistent and effective services to our customers</p></li><li><p> Achieve our PSS vision by driving global consistency through collaboration <br /> </p></li></ul><p><b>Business Acumen </b></p><ul><li><p>Use knowledge of business and P&amp;C insights, metrics, expertise, and decision principles to effectively deliver support on topics with a wide range of complexity.</p></li><li><p>Participate in global / regional squads for deployment of key P&amp;C initiatives or new system launches </p></li><li><p>Ensure alignment and execution of established policies, procedures and global P&amp;C initiatives. Ensure compliance of all P&amp;C practices within legislative requirements and established standards and guidelines by building a broad knowledge base on regional approaches and connecting with global P&amp;C colleagues. </p></li></ul><p></p><p><b>Leadership </b></p><ul><li><p>Be a trusted partner to leaders and partners in the chapters. </p></li><li><p>Be a trusted partner and lead others through complex P&amp;C topics by understanding the philosophies, approaches, global policies and systems-relevant configurations of topics such as (but not limited to) Recruiting, Talent Sourcing, Rewards, Compensation &amp; Benefits, Mobility </p></li><li><p>Ensure full ownership and leadership of incoming requests, prioritization and solution implementation to provide P&amp;C consultation to leaders with a connected and caring approach. </p></li><li><p>Partner with other Chapters, specifically PSS, IWS, PR&amp;R and Business Partnering to create value for the organization. </p></li><li><p>Strategic P&amp;C Insights &amp; Innovation </p></li><li><p>Oversees gathering and analysis of data and P&amp;C or business metrics to make critical decisions; shares insights with leaders and chapter Partners, recommends innovative solutions based on the P&amp;C decision principles that support the culture, strategic direction and resources. </p></li><li><p>Utilize data sources to review key metrics such as turnover, talent review-related information, on- and offboarding needs to sense and address organizational needs proactively. </p></li></ul><p></p><p> <b><u>Who you are </u></b></p><p></p><p>In this position, you will be leading a team of specialists focusing on an area of practice(s). You will be working with stakeholders from various functions and across levels within the organization. Strong leadership competencies and demonstrated success in change management are critical. </p><p></p><p>You bring the following skills and competencies: </p><p></p><p>- Passionate and knowledgeable P&amp;C professional with ability to work in a fast paced global and virtual environment. Demonstrated ability to navigate the P&amp;C system, leverage different Chapters for business impact and participate in work product teams to deliver on business and P&amp;C strategies. </p><p>- Demonstrated customer-centricity through day-to-day interactions, anticipating needs and showing cultural awareness and business </p><p> understanding. Demonstrated end-to-end ownership, engaging with leaders to ensure a successful outcome.</p><p>- Strong communication, coaching and influencing skills. Demonstrated ability and experience in effectively diagnosing short-term P&amp;C needs, and offering fit for purpose solutions to address them. </p><p>- Demonstrated negotiation skills and the ability to cope with time pressure in demanding situations. Demonstrated ability to influence with courageous authenticity and build trust with individuals at all levels within the organization. </p><p>- Demonstrated excellent situational assessment and objective evaluation skills, with an ability to comprehend and translate complex topics into </p><p> manageable pieces. </p><p>- Demonstrated ability to leverage data, technology and insights to find root causes, troubleshoot and inform innovative and compliant solutions </p><p></p><p>You are a role model for our Core Capabilities including: </p><ul><li><p>Living customer centricity through your day-to-day interactions (incl. needs anticipation, cultural awareness, managing one’s response) </p></li><li><p>Demonstrating end-to-end accountability (incl. big picture and impact understanding, engaging others to ensure a successful outcome) </p></li><li><p>Demonstrating problem-solving (incl. active listening, critical thinking, process improvements) </p></li><li><p>Having a growth mindset (incl. taking risks and experimenting, seeking new learning opportunities, asking and giving feedback) </p></li></ul><p></p><p>Further requirements </p><ul><li><p>University degree or equivalent, HR preferred </p></li><li><p><b>Mandarin speaking along with English</b> is must have for the position</p></li><li><p>5&#43; years of related experiences in Recruiting, Sourcing, Mobility </p></li><li><p>(International and US Domestic), Compensation, in multinational companies o Strong understanding of compensation/benefits practices and solutions or (Digital) Talent Management, Recruitment, Sourcing </p></li><li><p>3&#43; years people leadership experience strongly preferred </p></li><li><p>Proven experience handling projects involving different stakeholders and regions </p></li><li><p>Experience leading a geographically dispersed team preferred </p></li><li><p>Experiences with HR processes, functional expertise, and HR generalist know-how ) </p></li><li><p>Strong customer orientation with proven experiences, service delivery management, HR process design or employee administration   </p></li></ul><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/people-support-solutions-lead-recruitment-team-lead-roche/69d3ed68c8e81216cd0bb08d</link><guid isPermaLink="true">http://biotechroles.com/people-support-solutions-lead-recruitment-team-lead-roche/69d3ed68c8e81216cd0bb08d</guid><pubDate>Mon, 06 Apr 2026 17:29:12 GMT</pubDate><company>Roche</company><location>Petaling Jaya</location><salary>$65000-95000</salary><type>Full time</type></item><item><title><![CDATA[Healthcare Systems (Access) Partner (HSP) - 12 Months Fixed Term Contract]]></title><description><![CDATA[<p style="text-align:left">At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h2></h2><p></p><h3>The Position</h3><p><span>Join us in Auckland and take the lead in delivering meaningful change for patients across New Zealand. As a </span><b>Health System Partner (HSP)</b><span><b>,</b> you are the local face of Roche, working directly on the ground to navigate and shape the New Zealand healthcare ecosystem. In this hands-on role, you will focus on the &#34;how&#34;—executing the vital work of connecting with policy makers, regulators, and payers to remove barriers to patient care. Your mission is to move beyond theory and take practical action to co-create and implement solutions that deliver better health outcomes to more New Zealanders, faster.</span></p><p></p><p><b>What You Will Be Working On:</b></p><p><span>As a Health System Partner (HSP) you will:</span></p><ul><li><p><span>Actively partner with healthcare system stakeholders to identify shared goals and turn them into tangible projects.</span></p></li><li><p><span>Lead the development of all PHARMAC-related activities for the designated disease area to ensure best possible funding outcomes. </span></p></li><li><p><span>Lead the strategy and execution of new funding proposals, commercial proposals, contracts and tenders.</span></p></li><li><p><span>Engage with local and global colleagues in development of the pharmaco-economic analysis, pricing requests and reimbursement strategies.</span></p></li><li><p><span>Oversee product lifecycle processes such as new product introductions, pricing, divestments and discontinuations for your allocated squads.</span></p></li><li><p><span>Navigate the internal Roche network to pull in the specific technical expertise or tools needed to support local health initiatives.</span></p></li><li><p><span>Execute activities that support regulatory and reimbursement processes, ensuring our innovations reach the people who need them.</span></p></li><li><p><span>Manage the end-to-end delivery of complex health projects, staying focused on timelines, budgets, and practical results.</span></p></li><li><p><span>Use digital tools and health data to track the progress of your initiatives and demonstrate real-world impact to stakeholders.</span></p></li><li><p><span>Capture insights from your daily interactions and feed them back to the team to help refine our local approach.</span></p></li><li><p><span>Act as the &#34;glue&#34; between different Roche departments, ensuring everyone is aligned on the execution of your projects.</span></p></li><li><p><span>Ensure every action you take in the system is fully compliant with Roche’s high ethical standards and local regulations.</span></p></li></ul><p></p><p><b>Who Are You:</b></p><p><span>You have a deep passion for transforming healthcare and improving patient outcomes. You are a </span>natural collaborator and systems thinker<span>, skilled at connecting people and ideas to drive collective success. You have:</span></p><ul><li><p><span>A &#34;</span>roll up your sleeves<span>&#34; attitude as an action-oriented operator, thriving on the execution of projects rather than just designing high-level strategies.</span></p></li><li><p><span>A deep, practical understanding as a healthcare insider of how the </span>New Zealand healthcare system<span>, its governance, and its processes work on a daily basis.</span></p></li><li><p><span>A natural ability to build trust and rapport with diverse stakeholders and possess excellent </span>customer engagement<span> skills.</span></p></li><li><p><span>The skills of a system navigator, acting as a deep listener who can sense the needs of the system and respond with practical, effective solutions.</span></p></li><li><p><span>Highly developed organizational skills as a project manager, capable of managing the logistics of complex, cross-functional projects from start to finish.</span></p></li><li><p><span>The mindset of an agile learner, staying comfortable in fast-paced environments and pivoting quickly based on field feedback to get the job done.</span></p></li><li><p><span>Strong business acumen and the savvy to leverage digital tools to enhance the excellence of our customer experience.</span></p></li><li><p><span>A </span>university degree<span> in Scientific, Economic, Public Health or equivalent and are ready to apply your knowledge in a high-impact, hands-on professional role.</span></p></li></ul><p></p><p><span><b>Full eligibility to live and work in New Zealand</b> for the duration of the </span><b>12-month contract</b><span> is required.</span></p><p></p><p><span>We do not accept any unsolicited resumes or enquiries from recruitment agencies. Roche has a dedicated in-house Talent Acquisition team.</span><span> </span></p><p><b> </b></p><p><b> </b></p><h3></h3><h3>What we offer</h3><p style="text-align:left"><span>Roche offers rewarding growth opportunities, a competitive remuneration package and a collaborative culture where people are united in purpose and will stretch you to be brave, speak up and think differently. Feel empowered to deliver meaningful outcomes, supported by accessible and inspiring leaders. </span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche encourages a high-performance culture where you are empowered and trusted to make decisions. We strive for excellence and extraordinary results and take a genuine interest in our people and their well-being, and our patients.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Take pride in knowing you can make a difference to millions of patients worldwide in developing diagnostics and treatments for oncology, neuroscience, inflammation, immunology, ophthalmology, rare diseases, respiratory disease and diabetes.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>We are committed to providing an inclusive, safe, secure and healthy workplace, and to minimise any such impacts to our employees, customers and the community. We welcome applications from all people and encourage you to advise of any individual circumstances that may require consideration.</span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><h2></h2><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><div><div><div><div><div><div><div><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p></div></div></div></div></div></div></div>]]></description><link>http://biotechroles.com/healthcare-systems-access-partner-hsp-12-months-fixed-term-contract-roche/69d3ed67c8e81216cd0bb08b</link><guid isPermaLink="true">http://biotechroles.com/healthcare-systems-access-partner-hsp-12-months-fixed-term-contract-roche/69d3ed67c8e81216cd0bb08b</guid><pubDate>Mon, 06 Apr 2026 17:29:11 GMT</pubDate><company>Roche</company><location>Auckland</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Team Lead Engineering Enterprise IM Integrations & Automation]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>We’re looking for an <b>Engineering Manager </b>to lead our Enterprise IM Integrations &amp; Automation team —the growth engine of our Identity Governance (IGA) ecosystem. At its core, this role is about building scalable integration capabilities, empowering teams, and transforming how identity services are delivered across the enterprise. This team is responsible for onboarding applications into our SailPoint IIQ platform, enabling secure, compliant access for thousands of users across a complex, regulated environment.This is more than just integrations - you’ll help us build a scalable “onboarding factory”, driving standardization, automation, and innovation to move toward a Zero-Touch provisioning model.</span></p><p></p><p><b>Responsibilities:</b></p><p></p><ul><li><p><span>Lead, coach, and grow a high-performing engineering team, fostering a culture of ownership, innovation, and continuous improvement</span></p></li><li><p><span>Enable team members to shape their career paths while removing roadblocks and ensuring a sustainable pace</span></p></li><li><p><span>Drive end-to-end delivery of application integrations into SailPoint IIQ, ensuring quality, scalability, and compliance</span></p></li><li><p><span>Own and prioritize the integrations backlog, balancing new demand with platform stability</span></p></li><li><p><span>Define and enforce onboarding standards, templates, and best practices for consistent, secure integrations</span></p></li><li><p><span>Identify bottlenecks and drive automation to improve speed, quality, and efficiency (toward Zero-Touch provisioning)</span></p></li><li><p><span>Partner closely with Product, Security, SMEs, and support teams to ensure seamless delivery from intake to production</span></p></li><li><p><span>Act as the primary point of contact for stakeholders, managing demand, expectations, and priorities globally</span><br /> </p></li></ul><p><b><span> </span>What we’re looking for:</b></p><p></p><ul><li><p><span>5&#43; years of experience in people leadership, engineering management, or similar roles</span></p></li><li><p><span>Strong experience in Identity &amp; Access Management, ideally with SailPoint IIQ</span></p></li><li><p><span>Deep understanding of identity lifecycle (Joiner, Mover, Leaver) and access governance</span></p></li><li><p><span>Experience with modern integration patterns (REST APIs, SCIM, SOAP, LDAP, Active Directory, Entra ID)</span></p></li><li><p><span>Strong background in building scalable integrations and automation frameworks</span></p></li><li><p><span>Experience working in complex, global, and regulated environments (pharma/biotech is a plus)</span></p></li><li><p><span>Ability to manage stakeholders, prioritize effectively, and drive outcomes</span></p></li></ul><ul><li><p><span>Hands-on experience with SailPoint IIQ (workflows, rules, connectors, task definitions)</span></p></li><li><p><span>Expertise in onboarding standardization (templates, reusable integration patterns)</span></p></li><li><p><span>Familiarity with CI/CD, DevOps, and modern architecture (APIs, microservices, cloud)</span></p></li><li><p><span>Strong problem-solving skills using data, metrics, and root-cause analysis</span></p></li><li><p><span>Experience in pharmaceutical, biotech, or regulated healthcare environments</span><br /> </p></li></ul><p><b>Education</b></p><p></p><ul><li><p><span>Bachelor’s or Advanced degree in Computer Science, Cyber Security, Information Technology, or a related Engineering field.</span></p></li><li><p><span>Professional Information Security certifications (e.g., CISSP, CISM) are a plus.</span></p></li></ul><p></p><p><span>If you&#39;re ready to take on this exciting challenge and become a key driver of innovation and growth in our Identity Governance ecosystem, apply now to join our team and help shape the future of enterprise identity services!</span></p><p></p><p>#RDT2026<span> </span><span> </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/team-lead-engineering-enterprise-im-integrations-and-automation-roche/69d3ed67c8e81216cd0bb08a</link><guid isPermaLink="true">http://biotechroles.com/team-lead-engineering-enterprise-im-integrations-and-automation-roche/69d3ed67c8e81216cd0bb08a</guid><pubDate>Mon, 06 Apr 2026 17:29:11 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$85000-120000</salary><type>Full time</type></item><item><title><![CDATA[Materials Governance Coordinator]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p><span>The </span>Materials Governance Coordinator <span>is a temporary, dedicated resource supporting the execution of a high-priority remediation plan to restore operational integrity, visibility, and regulatory control over all promotional and non-promotional materials. This role involves a comprehensive &#34;clean-up&#34; of physical and digital archives, system reconciliation of the related system, and will support the implementation of a sustainable governance process to ensure inspection readiness and brand integrity.</span></p><p></p><p><b>Your role:</b></p><p><b>1. Archive Clean-up &amp; Physical Inventory:</b></p><ul><li><p><span>Conduct a full physical inventory and classification of the archive room, identifying obsolete supports for destruction.</span></p></li><li><p><span>Filter valid from expired promotional and non-promotional materials to ensure only current versions are in circulation.</span></p></li><li><p><span>Apply mandatory metadata and labeling to all validated physical materials to ensure findability and governance.</span></p></li><li><p><span>Assess the compliance of physical storage areas according to COREMAP standards.</span></p></li></ul><p></p><p><b>2. System Reconciliation &amp; Traceability:</b></p><ul><li><p><span>Verify and reconcile physical inventory against </span>system<span> approvals to identify and resolve potential mismatches.</span></p></li><li><p><span>Update and maintain a centralized tracker for all promotional assets, ensuring full traceability.</span></p></li><li><p><span>Identify, retrieve, and integrate external materials (e.g., banners and brochures held by field staff/PJPs) into the central tracking system.</span></p></li></ul><p></p><p><b>3. Compliance &amp; Lifecycle cycle management:</b></p><ul><li><p><span>Organize and document the formal destruction of obsolete materials in accordance with local SOPs and global directives.</span></p></li><li><p><span>Support the implementation of a structured, end-to-end (E2E) workflow for material reception, tracking, and eventual destruction to prevent future backlogs and ensure inspection readiness.</span></p></li><li><p><span>Serve as the local ambassador for promotional and non promotional material record management, ensuring all governance elements remain up-to-date.</span></p></li><li><p><span>Promptly identify and coordinate with the owner of physical and digital materials (e.g., intranets, gSites) that require withdrawal when the materials reach their expiry date or when a safety issue necessitates it.</span></p></li></ul><p></p><p><b>Who you are<span>:</span></b></p><ul><li><p>Education:<span> Fresh graduate profile, Scientific background is preferred .</span></p></li><li><p>Experience:<span> Previous experience in records management, document control, or clinical/medical affairs operations is preferred.</span></p></li><li><p>Technical Skills:<span>  Advanced Microsoft Office skills, particularly Excel for complex tracking and reconciliation. * Proficiency in system management  .</span></p></li><li><p>Competencies:<span> </span></p><ul><li><p><span>Ability to work independently on time-consuming, repetitive tasks with high accuracy.</span></p></li><li><p><span>Exceptional attention to detail and organizational skills.</span></p></li><li><p><span>Fluency in </span>French and English<span> (required for the global system management)</span></p></li></ul></li></ul><p><b>Duration:<span> Initial </span>3-month mandate<span>, with potential for renewal.</span></b></p><p></p><p></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/materials-governance-coordinator-roche/69d3ed67c8e81216cd0bb089</link><guid isPermaLink="true">http://biotechroles.com/materials-governance-coordinator-roche/69d3ed67c8e81216cd0bb089</guid><pubDate>Mon, 06 Apr 2026 17:29:11 GMT</pubDate><company>Roche</company><location>Algier</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Key Account Manager - Custom Biotech - N. California and Pacific Northwest]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p><b><b>Key Account Manager - Custom Biotech - Northern California and Pacific Northwest</b></b></p><p></p><p><span>A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.</span></p><p></p><p><b><b>The Opportunity:</b></b></p><p></p><p><span>Building on over 30 years of industry experience, Roche Custom Biotech uses the powerful multidisciplinary skills found in Roche facilities across the world. The team offers products and solutions for manufacturers in the diagnostics and pharma biotech industry, ranging from raw materials to system solutions for bioprocessing. Leveraging the unique know-how of Roche Diagnostics and Roche Pharmaceuticals, our Key Account Managers work to deliver high-quality raw materials, instrumentation, products, and services for the biopharmaceutical, cell therapy, or in vitro diagnostics business. </span></p><p></p><p><span>As a Key Account Manager, you will:</span></p><ul><li><p><span>Drive sales of Roche products and solutions by developing new business and expanding relationships within existing accounts.</span></p></li><li><p><span>Own and execute a strategic territory plan to achieve and exceed growth targets, including travel across assigned Pharma, Biotech, and IVD manufacturer accounts.</span></p></li><li><p><span>Proactively engage new and existing customers to build strong partnerships, identify opportunities, and deliver solutions that meet or exceed sales objectives.</span></p></li><li><p><span>Develop and execute strategic account plans that clearly articulate Roche’s differentiated value, including measurable economic impact, while effectively addressing objections and navigating complex negotiations.</span></p></li><li><p><span>Generate demand and increase product awareness by delivering impactful customer education, insights, and tailored solution positioning.</span></p></li><li><p><span>Collaborate cross-functionally to develop and present compelling proposals, ensuring alignment with customer needs and maximizing overall business value and profitability.</span></p></li><li><p><span>Plan and manage territory activities efficiently, optimizing routing and prioritization to maximize customer engagement and results.</span></p></li><li><p><span>Gather and translate market intelligence and competitive insights to inform strategy and strengthen Roche’s position in the market.</span></p></li><li><p><span>Lead negotiations for new and existing long-term agreements, ensuring mutually beneficial outcomes for customers and Roche.</span></p></li></ul><p></p><p><span>This is a field-based position that includes up to 25% overnight travel. The territory includes Northern California, the Pacific Northwest, and surrounding areas.</span> A company vehicle will be provided.</p><p></p><p><b><b>Who You Are:</b></b></p><ul><li><p><span>Bachelor’s Degree or equivalent experience</span></p></li><li><p><span>7&#43; years relevant sales or equivalent experience</span></p></li></ul><p></p><p><b>Preferred Requirements:</b></p><ul><li><p><span>7&#43; years of B2B sales experience preferred</span></p></li><li><p><span>Excellent oral and written communication skills, including making impactful presentations</span></p></li><li><p><span>Proven leadership abilities</span></p></li><li><p><span>Negotiation, contracting, and problem-solving skills</span></p></li><li><p><span>Ability to work in a regulated environment</span></p></li><li><p><span>Strategic planning and organizational skills</span></p></li></ul><p></p><p><span>Relocation benefits are not available for this job posting</span></p><p></p><p><span>The expected salary range for this position based on the primary location of California is $135,700-$251,900.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.</span></p><p><a href="https://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><u>Benefits</u></a><span> </span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/key-account-manager-custom-biotech-n-california-and-pacific-northwest-roche/69d3ed66c8e81216cd0bb088</link><guid isPermaLink="true">http://biotechroles.com/key-account-manager-custom-biotech-n-california-and-pacific-northwest-roche/69d3ed66c8e81216cd0bb088</guid><pubDate>Mon, 06 Apr 2026 17:29:10 GMT</pubDate><company>Roche</company><location>Sacramento</location><salary>$120000-180000</salary><type>Full time</type></item><item><title><![CDATA[Medical Enabler (Medical Manager) - Oncology]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><p>The <b>Medical Enabler </b>is a trusted, externally focused, scientifically grounded partner within our customer engagement model. By building and maintaining deep and trusted connections with key customers over a meaningful period of time, the medical enabler will generate impact by anticipating and proactively optimizing medical practice, and ensure increased partnership value in our key disease areas. </p><p></p><p><b>What you will be working on:</b></p><p>The role of the medical enabler is designed to maximize local and cross-country medical and scientific activities to accelerate the delivery of our pipeline, differentiate our portfolio based on data, drive strategic advocacy, community engagement, medical practice adoption, and access to our portfolio. As a Medical Enabler you will contribute towards:</p><p></p><p><b>Offer Medical Expertise:</b></p><ul><li><p><span>Medical Expertise: responsible for proactively contributing strong scientific, medical, and therapeutic area expertise within the relevant diseases informing differentiation of our pipeline and portfolio. Acting as a medical expert for the pipeline and portfolio throughout the product life cycle.</span></p></li><li><p><span>Shape Strategy: Lead the medical part of the integrated strategy, shape a scientifically sound and differentiated value story locally and communicate Roche’s contributions across key disease areas, reflecting an end-to-end business perspective that pulls through the strategy with impact.</span></p></li></ul><p><b>Proactive Customer Engagement :</b></p><ul><li><p><span>Proactive Targeted Medical Engagement: As a medical function our ambition is to spend the majority of our time proactively engaging with external customers as partners in the integrated customer engagement strategy. The medical enabler serves as the scientific and medical expert, proactively engaging Therapeutic Area Experts, and other key stakeholders in full strategic and operational alignment with other in-field roles </span></p></li><li><p>Medical enablership &amp; Education: Establish and maintain effective peer-to-peer relationships with external stakeholders and identify/develop science-driven collaborations with TAEs. Provide current, high-quality Medical Education and differentiating scientific information to external customers, support the scientific training of internal teams and ensure continuous education on medical knowledge for PPoC roles. Conduct high-quality, non-promotional Scientific Exchanges to disseminate relevant data, foster physician confidence and clinical endorsement based on differentiating evidence and experience.</p></li><li><p><span>Insight Generation: Based on aligned goals of the team, the medical enabler should systematically collect, analyze, and translate external scientific and clinical practice insights (including patient perspectives) into strategic actionable and differentiating recommendations for the team. </span></p></li></ul><p><b>License to operate &amp; Operational Excellence :</b></p><ul><li><p><span>Adherence to Standards: Ensure all medical activities, including customer engagements, research projects, and material co-creation, are executed in line with company policies, procedures, and the highest compliance standards. This includes strict adherence to corporate policies, ethical behaviour,  local regulatory requirements as well as Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP).</span></p></li></ul><p><b>Evidence Generation (Module Evidence Generation):</b></p><ul><li><p><span>Integrated Evidence Planning: Contribute to the local integrated evidence plan (IEP), putting forward a comprehensive local evidence gap analysis of required value narratives for the diverse set of healthcare system stakeholders, patients and caregivers.</span></p></li><li><p><span>Evidence Strategy Implementation: Contribute directly to the local evidence strategy, proactively identifying local differentiating evidence gaps, and facilitating the development and implementation of differentiating tactics to address the prioritized gaps, specifically to ensure, maintain and broaden access to our portfolio. </span></p></li><li><p><span>Clinical Development Support: Collaborate closely with Clinical Operations and Legal/Regulatory teams to provide support for Phase I-IV clinical studies when needed. Ensure that key insights from investigators, study coordinators and nurses are brought into the strategic planning of “how to go to market” and the local IEP gap analysis</span></p></li></ul><p><b>Focusing on Patient Impact and Value Creation:</b></p><ul><li><p><span>Maximizing HTA Value: Contribute scientific and medical expertise to local Health Technology Assessment (HTA) submissions and interactions, ensuring critical appraisal mindset on our data packages with good statistical understanding and by discussing the evidence for its transferability to the real-world healthcare setting. The medical enabler will support market access to articulate the differentiating value story of our innovations in the local context to secure patient access. </span></p></li><li><p>The medical enabler ensures early insights are used to generate local IEP/local gap analysis so data generation initiatives support the HTA value package locally.The medical enabler validates the data&#39;s scientific integrity and, through additional stakeholder exchange (TAEs/societies), ensures the HTA submission is clinically relevant and credible.</p></li></ul><p><b>Pipeline Product Strategic Contribution / Shaping:</b></p><ul><li><p><span>Providing insight and recommended actions linking to the highest value propositions (VP’s) for the affiliate pipeline products and/or new indications</span></p></li></ul><p><b>Regulatory Support:</b></p><ul><li><p>Contribute scientific and medical expertise to local Health Authority submissions and interactions to obtain, maintain, and develop product licenses, in close alignment with the local Regulatory Affairs team.</p></li></ul><p></p><p><b>Who you are:</b></p><p>You are a qualified medical professional who focusses efforts on the value creation, sustainability, and impact brought to patients, customers, and society within the ecosystems, by considering all actions and decisions through the customer and patient lens<b>. </b>You have:</p><ul><li>Completed Medical, Pharmaceutical, or Natural Sciences degree (e.g., MD, PharmD, PhD, or equivalent).</li><li><p>Prior experience in Medical Affairs, Clinical Research, or equivalent scientific/clinical expertise in a relevant Disease Area.</p></li><li><p>Fluency in English is essential for global collaboration</p></li><li><p>Customer Focus: Prioritizes the needs of patients and customers (HCPs/TAEs), ensuring all actions drive value and satisfaction.</p></li><li><p>Strategic Acumen: Ability to think strategically, act with autonomy, and thrive in complex, cross-functional team environments.</p></li><li><p>Digital: Basic level of AI literacy and learner mindset that proactively integrates digital tools in day-to-day work. Possesses the knowledge and skills to ensure human in the loop oversight of AI (i.e.  large language models) derived content for internal or external use.</p></li><li><p>Collaborative Networker: Collaborates effectively showing leadership, self-motivation and accountability as part of a multi-skilled team (squad) and proactively  shares expertise across the organisation and across countries to remove silos.</p></li><li><p>Growth Mindset &amp; Curiosity: Demonstrates enthusiasm for continuous learning, self awareness and showing leadership when building a feedback culture. The medical enabler should be comfortable navigating ambiguity, collaborate and show a strong solution finding mindset.</p></li><li><p>Assertive Communication: Excellent ability to articulate complex medical and scientific context, inform medical guidelines by contextualizing our data, build trust, and have conversations in a direct and respectful manner with key stakeholders externally and internally on peer to peer level.</p></li><li><p>Entrepreneurial mindset: Takes calculated risks, challenges the status quo, and proposes pragmatic, value adding solutions. The medical enabler is able to maintain a holistic view of patient, business, and ecosystem needs and does not compromise Roche’s license to operate.</p></li></ul><p></p><p><span>This role is exclusively available to candidates who possess </span><b>full eligibility to live and work in the Philippines.</b></p><p></p><p><span>We do not accept any unsolicited resumes or enquiries from recruitment agencies. Roche has a dedicated in-house Talent Acquisition team.</span></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/medical-enabler-medical-manager-oncology-roche/69d3ed66c8e81216cd0bb087</link><guid isPermaLink="true">http://biotechroles.com/medical-enabler-medical-manager-oncology-roche/69d3ed66c8e81216cd0bb087</guid><pubDate>Mon, 06 Apr 2026 17:29:10 GMT</pubDate><company>Roche</company><location>Taguig City</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Senior Talent Acquisition Partner]]></title><description><![CDATA[<p>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</p><h3></h3><p></p><h3>The Position</h3><div><h2></h2><p><span>As a senior team member within the Talent Acquisition group, you will foster a team environment and demonstrate collaborative leadership. You will partner with TA colleagues, Human Resource Business Partners, clients and Talent Acquisition Management to develop and implement staffing plans and strategies.</span></p><div></div><p><b>The Opportunity:</b></p><p></p><p><span>As a Senior Talent Partner, you will partner with hiring managers and senior management in the full lifecycle recruitment of talent in the Americas- individually managing a portfolio of requisitions and focusing on meeting and exceeding hiring manager&#39;s expectations and ensuring a positive candidate experience. <span> </span></span></p><p><span><b>Your responsibilities include:</b></span></p><ul><li><p><span><b><span>Recruitment Execution:</span></b><span> Recruit and support open requisitions by sourcing talent, reviewing applications, screening candidates, and processing offers in Workday. </span></span></p><div></div></li><li><p><span><b><span>Stakeholder Management:</span></b><span> Manage expectations of hiring managers and candidates, identifying and resolving issues while coaching managers on feedback and competency determination. </span></span></p><div></div></li><li><p><span><b><span>Strategic Partnership:</span></b><span> Partner with HR Business Partners and Talent Acquisition Management to develop and implement complex staffing plans and strategies. </span></span></p></li><li><p><span><span><b>Process Improvement: </b>Contribute to the development of staffing process improvements and projects to ensure solutions are consistent with corporate Talent Acquisition objectives.</span></span></p></li><li><p><span><span><b>Data &amp; Compliance: </b> Act as a point person for providing staffing reports and metrics while ensuring compliance with internal processes and maintaining the ATS and CRM.</span></span></p></li><li><p><span><b><span>Talent Management:</span></b><span> Partner with Client Groups on internal talent management, including succession planning and internal candidate movement. </span></span>​</p></li><li><p><span><b><span>External Engagement:</span></b><span> Attend job fairs, conferences, and networking events to proactively manage the escalation process related to all requisition activity. </span></span></p></li></ul><p></p><p></p><p><b>Who you are:</b></p><ul><li><p><span><span>You hold a Bachelor’s degree in Human Resources, Business, Life Science, or equivalent work experience. </span></span></p></li><li><p><span>You bring <b>5&#43; years of recruiting experience</b> in a corporate or Shared Services environment; </span><span><span><b>Pharma Industry</b> experience is a plus. </span></span></p></li><li><p><span>You possess a high level of social competence and are <b>fluent</b> in both <b>Spanish and English; </b></span><span><span><b>French</b> or <b>Portuguese </b>is a plus. </span></span></p></li><li><p>​<span><span>You are characterized by a growth mindset, end-to-end accountability, and a customer-centric approach in a multicultural, matrixed environment. </span></span></p></li><li><p><span><span>You have a strong understanding of behavioral interviewing techniques and the ability to translate business needs into recruitment strategies.</span></span></p></li><li><p>​<span><span>You are well known for your independent, yet collaborative working style and your ability to challenge the status quo to drive continuous improvement. </span></span></p></li></ul><p></p><p><b>Preferred:</b></p><ul><li><p><span><span>Experience with ATS systems (Workday) and progressive sourcing options such as Web 2.0 tools and direct sourcing. </span></span></p></li><li><p>​<span><span>Experience recruiting for different regions across the Americas (US, Canada, Latin, or Central America). </span></span></p></li></ul><p></p><p><b><span><span>Relocation benefits are not available for this posting. </span></span></b></p><div></div><p></p></div><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><b>Roche is an Equal Opportunity Employer.</b></p>]]></description><link>http://biotechroles.com/senior-talent-acquisition-partner-roche/69d3ed66c8e81216cd0bb086</link><guid isPermaLink="true">http://biotechroles.com/senior-talent-acquisition-partner-roche/69d3ed66c8e81216cd0bb086</guid><pubDate>Mon, 06 Apr 2026 17:29:10 GMT</pubDate><company>Roche</company><location>San Jose, Costa Rica</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Field Service Installation Representative - Nationwide]]></title><description><![CDATA[<p style="text-align:left"><span>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.</span></p><h3></h3><p></p><h3>The Position</h3><p>This is an exciting time to join the Roche Support Network. If you are passionate about problem solving then this is the position for you! As a research-focused healthcare company, Roche discovers, develops and provides innovative diagnostics and therapeutic products and services that deliver significant benefits to patients and healthcare professionals - from early detection and prevention of diseases to diagnostics, treatment and treatment monitoring.</p><p></p><p>The<b> Field Service Installation Representative</b> travel to customer sites across the US to install Roche analyzers and instruments. To be successful in this senior position, you will need to be highly proficient in installing or repairing Roche analyzers/instruments.</p><p></p><p><b>The Opportunity</b></p><ul><li><p>Install equipment as assigned.</p></li><li><p>Perform site surveys, installations and approved modifications with minimum assistance/supervision.</p></li><li><p>Install connectivity solutions as part of completing instrument installations.</p></li><li><p>Schedule modifications as indicated in the TSB and per policies during installations.</p></li><li><p>Identify, analyze and resolve IT product problems during installations and escalated service calls.</p></li><li><p>Monitor communication devices during all scheduled times.</p></li><li><p>Work with local FES teams to ensure installations are completed while ensuring customers are fully satisfied.</p></li><li><p>Support technical issues during the installation process to ensure installations are completed successfully.</p></li><li><p>Act as crew team lead to ensure and maximize efficient completion of installations.</p></li><li><p>Document all service related activities (inventory, service activity cases, expense reports, etc.)</p></li><li><p>Process service activity close-outs at the end of each customer site visit. Able to manage day to day administrative activities. </p></li></ul><p></p><p><b>Who you are</b></p><ul><li><p>High school diploma and 2 years of technical school or equivalent military training OR equivalent work experience,<b> AND</b></p></li><li><p>2 years progressive experience repairing or servicing mechanical/system hardware and software, or networking/wireless networking OR equivalent military experience</p></li></ul><p></p><p><b>Preferred Requirements</b></p><ul><li><p>Able and willing to travel 95%, including overnight travel</p></li><li><p>Resides within 50 miles of a major metropolitan airport</p></li><li><p>2 years prior experience installing or repairing Roche analyzers/instruments</p></li><li><p>Advanced knowledge of electronics, electro-mechanical systems, and information technology </p></li><li><p>Knowledge of basic chemistry</p></li><li><p>Effective customer service skills, which includes a positive attitude, helpful customer interaction, and maintenance of ongoing customer relationships</p></li><li><p>Effective time-management, organization and prioritization skills</p></li><li><p>Good written/verbal communication skills</p></li><li><p>Ability to work after hours, provide weekend and holiday support on a rotated basis within an assigned territory and/or geographic region and be on call 24/7 during rotation</p></li></ul><p></p><p><b>Additional Information</b></p><ul><li><p>This is a remote, field-based position.</p></li><li><p>Company car is provided with this position.</p></li></ul><p></p><p><b>Relocation benefits are not available for this position.</b></p><p></p><p>The expected salary range for this position based on the primary location of Indiana is 56,300.00 - 104,500.00 USD Annual.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.</p><p><a href="http://roche.ehr.com/default.ashx?CLASSNAME&#61;splash" target="_blank"><b><u>Benefits</u></b></a></p><p></p><p><b>Are you ready to apply?</b></p><p><b> </b></p><p><b> </b></p><p></p><h3>Who we are</h3><p style="text-align:left">A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.</p><p style="text-align:left"><br />Let’s build a healthier future, together.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company&#39;s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.</span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form <a href="https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform" target="_blank">Accommodations for Applicants</a>.</span></p>]]></description><link>http://biotechroles.com/field-service-installation-representative-nationwide-roche/69d3ed65c8e81216cd0bb085</link><guid isPermaLink="true">http://biotechroles.com/field-service-installation-representative-nationwide-roche/69d3ed65c8e81216cd0bb085</guid><pubDate>Mon, 06 Apr 2026 17:29:09 GMT</pubDate><company>Roche</company><location>Indianapolis</location><salary>$55000-75000</salary><type>Full time</type></item><item><title><![CDATA[Senior Expert Science & Technology – Downstream Process Modelling]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Basel, Switzerland #onsite <br><br>Role Purpose:<br>As a Senior Expert Science &amp; Technology in Downstream Process Development, you will play a key role in advancing model‑based development and decision making for biologics purification processes. You will develop, apply, and deploy mechanistic and hybrid models with a strong focus on chromatography, while also covering other downstream unit operations and their interconnection into integrated process flows.<br>This role combines deep scientific expertise, hands‑on experimental work, and digital implementation. You will work closely with project teams, process development scientists, data scientists, and manufacturing stakeholders, and you will be an active member of a global modelling community shaping the future of downstream development at Novartis.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>In this role, you will:</b></p><ul><li>Develop and apply downstream process models for biologics, with a strong emphasis on</li><li>chromatography (e.g. IEX, HIC, MMC, affinity) and their underlying physicochemical principles.</li><li>Extend modelling approaches to other downstream unit operations (e.g. filtration, UF/DF, viral inactivation) and connect individual steps into integrated DSP models to support process understanding and optimization.</li><li>Design, plan, and execute laboratory experiments to generate high‑quality data for model development, calibration, and validation, working hands‑on in the lab when required.</li><li>Use modelling to support process design, scale‑up, troubleshooting, robustness studies, and decision making across early and late development.</li><li>Implement and deploy models using Python, including development of user‑friendly tools or apps that enable broader adoption by project teams and stakeholders.</li><li>Translate complex modelling results into clear, actionable insights for multidisciplinary audiences, including process scientists, project leaders, and management.</li><li>Collaborate and communicate effectively with internal and external stakeholders, ensuring alignment between modelling activities, experimental work, and project objectives.</li><li>Actively contribute to and help shape the global modelling community, sharing best practices, methodologies, and innovations across sites and functions.</li><li>Contribute to scientific documentation, technical reports, and regulatory‑relevant deliverables as required.</li></ul><p></p><h2>What you will bring</h2><p><b>Education &amp; experience</b></p><ul><li>MSc, PhD, or equivalent experience in Biotechnology, Chemical Engineering, Biochemistry, or a related field.</li><li>Several years of experience in biologics downstream process development, with demonstrated focus on process modelling.</li><li>Strong, hands‑on expertise in chromatography, including mechanistic understanding of separation phenomena.</li></ul><p></p><h2>Technical expertise</h2><ul><li>Proven experience in downstream process modelling, ideally including chromatography modelling, parameter estimation, scale‑down/scale‑up concepts, and integration of multiple unit operations.</li><li>Ability to design and run experiments to support model development and validation.</li><li>Strong programming skills in Python, with experience in building reusable tools, workflows, or applications for broader user groups.</li><li>Familiarity with data analysis, visualization, and model deployment concepts is a strong advantage.</li></ul><p></p><p><span>Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams&#39; representative of the patients and communities we serve.</span><br /><br /><span><span>Accessibility and accommodation</span><br /><span>Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></span><br /> </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/senior-expert-science-and-technology-downstream-process-modelling-novartis/69d3ecbac8e81216cd0bafeb</link><guid isPermaLink="true">http://biotechroles.com/senior-expert-science-and-technology-downstream-process-modelling-novartis/69d3ecbac8e81216cd0bafeb</guid><pubDate>Mon, 06 Apr 2026 17:26:18 GMT</pubDate><company>Novartis</company><location>Basel (City)</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Principal Scientist - Translational Intestinal Immunology (80-100%*)]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Basel, Switzerland<br>Full time, onsite, #LI-Onsite<br><br>In the Immunology group in Biomedical Research,  We are developing the next generation of medicines for inflammatory bowel disease with the ambition to transform the lives of patients. This is an opportunity for you to bring your scientific talent and curiosity into a highly collaborative, interdisciplinary environment, where your work will turn complex human data into actionable therapy-relevant insights in a competitive and dynamic field.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>The Translational Inflammatory Bowel Disease (IBD) lab is integrated in the Immunology Research Disease Area and will accelerate target discovery and positioning of therapeutic compounds for IBD (Ulcerative Colitis, Crohn’s disease). To lead the lab research activities, we are looking for a scientist who has a strong background in mechanistic translational research in mucosal immunology. If you are passionate about the molecular basis of IBD and compound mode of action at the interface of preclinical and clinical research, we want you on our team. </p><p></p><p><b>Key Responsibilities</b></p><ul><li><p><b>Design and execute mechanistic experiments hands-on</b>, to link human disease biology to druggable targets within and beyond the immune system, and to accelerate preclinical compound development, strengthen understanding of drug modes of action, differentiate novel drugs to standard-of care treatment.</p></li><li><p><b>Leverage human biosamples</b> (e.g. blood, intestinal biopsies) to generate decision-making data and <b>position candidate molecules for clinical trials</b> (target validation, MoA studies, biomarker strategy).</p></li><li><p><b>Partner closely with early clinical teams</b> (Biomarker Development, Translational Medicine) to test clinical hypotheses for early clinical strategies (e.g. patient stratification).</p></li><li><p><b>Champion data-driven target discovery</b>, in collaboration with data scientists, in vivo biology labs and other groups in Novartis Biomedical Research to connect quantitative methods (e.g. ex vivo analyses, transcriptomics) to patient heterogeneity and outcomes.</p></li><li><p><b>Drive a culture of collaboration</b>, talent development and integrity.</p></li></ul><p></p><p><b>Minimum Requirements</b></p><ul><li><p><b>Ideally PhD or MD qualified in Mucosal Immunology, Gastroenterology, Barrier Immunology (skin/lung/intestine), or a related field</b> with a strong track record of peer-reviewed publications.</p></li><li><p><b>At least 3 years of relevant translational research expertise </b>in an interdisciplinary setting in academia or industry, bridging clinical and preclinical evidence</p></li><li><p>Hands-on mastery of routine <b>immunological/ cell biology/ molecular biology assays</b> (e.g. multi-parametric flow cytometry) and <b>in vitro human models</b> relevant to IBD and mucosal immunity (e.g. primary immune/epithelial cells, slice cultures).</p></li><li><p>Proven ability to conduct experiments using <b>in vitro human systems</b> <b>and biosamples</b> (e.g., PBMCs, primary immune/epithelial cells, tissue explants), including sample-tracking best practices and consent/ethics).</p></li><li><p><b>Experienced in collaboration with data scientists</b>, ensuring high quality experimental design and reproducibility.</p></li><li><p><b>Proven track record of completing projects on schedule in view of narrow timelines</b></p></li></ul><p></p><p><b>Additional Requirements</b></p><ul><li><p>Prior <b>experience mentoring junior researchers would be an advantage</b></p></li><li><p><b>Experience contributing to drug discovery programs </b>in biotech/pharma or translational academic/clinical setting (e.g. in vitro pharmacology, biomarker studies) is a plus.</p></li><li><p><b>Data Science literacy</b> and confidence in interpreting multi‑omic outputs and statistical analyses is an additional asset.</p></li></ul><p></p><p>*Restrictions on flexible working requirements may apply and can be discussed at interview stages as necessary</p><p></p><p><b>Accessibility and accommodation:</b><br />Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Gastroenterology, Gastrointestinal Disease, Inflammatory Bowel Diseases]]></description><link>http://biotechroles.com/principal-scientist-translational-intestinal-immunology-80-100percent-novartis/69d3ecbac8e81216cd0bafea</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-translational-intestinal-immunology-80-100percent-novartis/69d3ecbac8e81216cd0bafea</guid><pubDate>Mon, 06 Apr 2026 17:26:18 GMT</pubDate><company>Novartis</company><location>Basel (City)</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Director International Medical Affairs, Immunology]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Basel, Switzerland #LI-Hybrid<br><br>Purpose of the role:<br>The International Medical Affairs (IMA) team represents the voice of the International markets, with a focus on our top priority markets and addresses their needs across pre-launch, launch, life-cycle management and in-market.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p>We are seeking a Medical Affairs Director Immunology, to provide aligned input from the top priority International markets into IEP and is responsible for the implementation of the scientific communications and medical education strategy, as well as relevant medical standards in these markets.<br />This role will support the planning and execution at International for the medical/scientific engagement strategy (MSL/ Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development) addressing and delivering strategic pre-launch and launch medical activities needs for patient, clinical, access and value to health care systems.</p><p></p><p>Acting as a subject matter expert in the development of overarching International strategies, you will provide input during program design and throughout end to end execution. You will also serve as a strategic partner to International Commercial, International Value and Access, Global, Regional and US Medical Affairs, and Development.</p><p></p><p>This is a full-time position based in Basel, Switzerland. If you are driven by a commitment to making a difference in the lives of patients and possess the expertise to lead a dynamic team, we would love to hear from you. This role reports into the Head International Medical Affairs Immunology.</p><p></p><p></p><p><b>Major Accountabilities </b></p><ul><li><p>Lead the International Medical Affairs strategy for priority Immunology assets and indications, ensuring international market needs are reflected in medical priorities and plans.</p></li><li><p>Represent and translate the perspectives of priority international markets into actionable medical strategies, evidence requirements, and execution plans that enhance readiness and impact.</p></li><li><p>Shape integrated evidence plans and evidence‑generation priorities to ensure timely availability of data supporting scientific exchange, clinical adoption, and access-related decision-making.</p></li><li><p>Provide strategic input into field medical and medical engagement priorities, ensuring country insights and scientific requirements inform high‑quality, market‑relevant plans.</p></li><li><p>Drive external scientific engagement and communication strategies, including medical education, major congress activities, symposia, and other high-impact key scientific exchange initiatives.</p></li><li><p>Build and strengthen strategic relationships with healthcare professionals, scientific societies, and other stakeholders to advance scientific leadership and medical impact in Immunology.</p></li><li><p>Serve as a strategic medical partner to International Commercial, International Value &amp; Access, Global, Regional, and Country Medical Affairs, Development, and other cross‑functional teams to ensure aligned, high‑quality plans and execution.</p></li><li><p>Provide proactive medical leadership for lifecycle management and future therapeutic opportunities, identifying where medical strategy, evidence and stakeholder engagement can drive the greatest value and impact.</p></li><li><p>Ensure all International Medical Affairs activities meet the highest standards of medical quality, ethics, and compliance, including appropriate support for access‑related and patient‑focused initiatives.</p></li></ul><p></p><p><b>Essential Requirements</b></p><ul><li><p>Advanced scientific degree (MD, PhD, or PharmD) in Health or Life Sciences</p></li><li><p>Full professional proficiency in English</p></li><li><p>In depth experience in the pharmaceutical industry, in Medical Affairs or Clinical Development</p></li><li><p>Deep understanding of health care systems and key external stakeholders</p></li><li><p>Experience working in matrix organizations and leading cross-functional medical projects, with the ability to influence and collaborate across functions and geographies</p></li><li><p>Strong track record of leading complex medical affairs initiatives with clear impact on timelines, quality, and strategic outcomes</p></li><li><p>Additional training, certification or experience in Dermatology and/or Rheumatology is a plus</p></li></ul><p></p><p><b>Desirable Requirements</b></p><ul><li><p>Significant medical affairs pre-launch and launch experience in a major International market </p></li><li><p>Significant medical affairs pre-launch and launch experience in Immunology or Immuno-oncology</p></li><li><p>Experience in developing and executing “Best in Class” processes at scale</p></li></ul><p></p><p></p><p><b>Why Novartis?</b></p><p>Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that</p><p>change patients’ lives. Ready to create a brighter future together? <a href="https://www.novartis.com/about/strategy/people-and-culture" target="_blank">https://www.novartis.com/about/strategy/people-and-culture</a></p><p></p><p>Disclaimer*: Some restrictions on flexible working options may apply and will be discussed during interview if applicable</p><p></p><p><b>Benefits and Rewards:</b></p><p>Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: <a href="https://www.novartis.com/careers/benefits-rewards" target="_blank">https://www.novartis.com/careers/benefits-rewards</a></p><p></p><p><b>Commitment to Diversity and Inclusion / EEO:</b></p><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.</p><p></p><p><b>Accessibility and accommodation: </b></p><p>Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch&#64;novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</p><p></p><p><b>Join our Novartis Network</b>:  </p><p>If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network</p><p></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>]]></description><link>http://biotechroles.com/director-international-medical-affairs-immunology-novartis/69d3ecb9c8e81216cd0bafe8</link><guid isPermaLink="true">http://biotechroles.com/director-international-medical-affairs-immunology-novartis/69d3ecb9c8e81216cd0bafe8</guid><pubDate>Mon, 06 Apr 2026 17:26:17 GMT</pubDate><company>Novartis</company><location>Basel (City)</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[GSOC Senior Analyst]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>Location: Hyderabad<br>#LI-Onsite <br>Job title: GSOC Senior Analyst<br><br>Join our Global Security Operations Centre (GSOC) team to safeguard Novartis’ people and assets worldwide. As a Senior Analyst, you will transform real-time threat intelligence into actionable insights, enabling informed decisions and proactive risk mitigation. This role is critical to maintaining operational resilience and supporting secure travel, executive protection, and emergency communications.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities: </b></p><ul><li>Monitor global threat intelligence and security systems to identify and assess risks impacting Novartis operations.</li><li>Deliver timely, accurate alerts, threat assessments, and incident reports to support business continuity and decision-making.</li><li>Coordinate emergency notifications and crisis response workflows using approved platforms.</li><li>Provide secure travel support by evaluating itineraries against geopolitical risks and recommending mitigation strategies.</li><li>Ensure compliance with ISO 27001 and EN 50518 standards through structured documentation and audit readiness.</li><li>Maintain continuity of operations via comprehensive shift handovers and accurate incident logging.</li><li>Support executive protection helpline and manage sensitive communications with discretion.</li><li>Collaborate with internal and external stakeholders during critical events to ensure effective multi-agency coordination.</li></ul><p></p><p><b>Minimum Requirements:</b></p><ul><li>Bachelor’s degree in Security Management, Risk Analysis, Information Security, or related field (or equivalent experience).</li><li>Minimum 3–5 years of experience in GSOC operations, threat intelligence, or security monitoring.</li><li>Strong knowledge of ISO 27001 Annex A controls and EN 50518 standards.</li><li>Proficiency in security systems (CCTV/VMS, GPS tracking, alarm monitoring) and emergency communication platforms.</li><li>Excellent analytical, communication, and decision-making skills under time-sensitive conditions.</li><li>Ability to work in a 24x7 rotational shift environment and maintain strict confidentiality.</li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Knowledge Of Core Work Processes, Knowledge Of Relevant Tools And Systems]]></description><link>http://biotechroles.com/gsoc-senior-analyst-novartis/69d3ecb8c8e81216cd0bafe5</link><guid isPermaLink="true">http://biotechroles.com/gsoc-senior-analyst-novartis/69d3ecb8c8e81216cd0bafe5</guid><pubDate>Mon, 06 Apr 2026 17:26:16 GMT</pubDate><company>Novartis</company><location>Hyderabad (Office)</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Clinical Sciences Trial Leader, Translational Medicine]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>The Clinical Sciences Trial Leader contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, Contributes to operational excellence through process improvement and knowledge sharing<br><br>#LI-Hybrid<br>Internal Title: Clinical Sciences Trial Leader<br>Location: Cambridge<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><ul></ul><p><b>Key Responsibilities: </b></p><ul><li><p>Study Leader <span>and/or</span> Clinical Scientist for predominantly low complexity, global studies and may provide additional Clinical Sciences support to high complexity, global studies.</p></li><li><p>Lead or support the clinical protocol development process in collaboration with the Medical Lead and other line functions; responsible author for clinical protocols, amendments, etc.; contribute to the medical/scientific input given for the development of study-related documents and processes which reside in other line functions; contribute to the development of clinical sections of study-level regulatory documents.</p></li><li><p>Support development of strategic and scientific input into study concept, feasibility, and ability to execute; develops and implements study-level operational execution plan in partnership with key cross functional partners, if applicable.</p></li><li><p>Collaborate with key cross functional partners to identify and select strategic and high performing sites to ensure recruitment commitments are met.</p></li><li><p>Lead or support a global cross functional CTT to ensure all trial deliverables are met; sets stretch goals, promotes realistic planning and timelines, and presents actionable alternatives to accelerate timelines.</p></li><li><p>Partner with line functions to gain input and alignment and manages internal and external stakeholder expectations.</p></li><li><p>Lead or support the ongoing medical/scientific review of clinical trial data across assigned studies in collaboration with the medical expert and key line functions, and partners on data analysis and data interpretation, including safety trend analysis, signal detection, development of first interpretable results, reporting clinical study results in CSR, and internal/external publications.</p></li><li><p>Prepare, lead or support dose escalation meetings with investigators. Coordinate the real time availability of quality clinical trial data, to provide consolidated information for dose escalation meetings and Phase II data reviews with relevant stakeholders.</p></li><li><p>Proactively lead or support risk mitigation discussions, risk management and implementation at the trial level.</p></li><li><p>Responsible and accountable for forecasting and managing overall study budget(s) in collaboration with key partners.</p></li><li><p>Collaborate with key partners to set vendor strategy and timelines for assigned studies.</p></li><li><p>Responsible for implementation of best practices and standards for trial management, including sharing lessons learned. Represent group on initiatives; may serve as Subject Matter Expert.</p></li><li><p>Contribute to talent and career development of staff. In collaboration with the relevant manager, contributes to hiring/interview/onboarding and mentoring process for new hires.</p></li></ul><p></p><p><b><span>Essential Requirements: </span></b></p><ul><li><p>Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/PharmD/ Masters).</p></li><li><p>1&#43; years’ highly relevant experience within pharma clinical trial management/operations and demonstrated accountability in leading clinical trial aspects, coupled with a good knowledge of the drug development field.</p></li><li><p>Proficient in clinical trial methodology with an emphasis in early clinical development. Operational project management experience including excellent planning, prioritization, problem solving and organizational skills.</p></li><li><p>Track record of successfully managing multiple clinical trials concurrently. Used to managing multiple priorities.</p></li><li><p>Demonstrated capability to interpret, discuss and represent trial level data.</p></li><li><p>Working knowledge of clinical finance principles to manage efficient expenditure to minimize variance between actual and forecasted spend.</p></li><li><p>Maintain good knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies.</p></li></ul><p></p><p><b><span>Desirable Requirements: </span></b></p><ul><li><p>Pharm D highly desirable</p></li><li><p>1&#43; year experience in early phase clinical trial operations preferred.</p></li></ul><p></p><p>The salary for this position is expected to range between $119,700 and $222,300 per year.</p><p>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</p><p>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</p><p>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</p><p>To learn more about the culture, rewards and benefits we offer our people click <a href="https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf" target="_blank">here</a>.</p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$119,700.00 - $222,300.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Auditing, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Data Auditing, Data Management, Health Sciences, Lifesciences, Project Planning, Vendor Management, Waterfall Model]]></description><link>http://biotechroles.com/clinical-sciences-trial-leader-translational-medicine-novartis/69d3ecb7c8e81216cd0bafe4</link><guid isPermaLink="true">http://biotechroles.com/clinical-sciences-trial-leader-translational-medicine-novartis/69d3ecb7c8e81216cd0bafe4</guid><pubDate>Mon, 06 Apr 2026 17:26:15 GMT</pubDate><company>Novartis</company><location>Cambridge (USA)</location><salary>$120000-160000</salary><type>Full time</type></item><item><title><![CDATA[Executive Director, Channel Strategy & Account Management]]></title><description><![CDATA[<p style="text-align:left"><b>Job Description Summary</b></p>#LI-Remote <br><br>This position can be based remotely anywhere in the U.S. (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager.<br><br>The Executive Director, Channel Strategy &amp; Management serves as the enterprise strategic lead for Trade, Wholesale, Specialty Distribution, and Group Purchasing Organization (GPO) engagement, representing 100% of the US business with over $30B in gross sales. This role owns the integrated pricing and channel strategy across in-line, launch, and pipeline products within assigned portfolio, ensuring alignment with evolving customer models, sites of care, and access pathways.<br><br>The Executive Director leads negotiation and implementation of customer pricing and contract programs while synthesizing field and customer intelligence to inform enterprise access strategies. This position is accountable for developing scalable, forward-looking channel architectures that address increasing complexity in care delivery, reimbursement, and distribution while balancing patient access, customer sustainability, and business objectives. The role operates as a senior thought partner to executive leadership and a cross-functional integrator across Sales, Marketing, Medical, Finance, Patient Services and Market Access.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Key Responsibilities: </b></p><ul><li>Responsible for complete business ownership of integrated Channel Strategy for in-line and pipeline brands.  Develops portfolio Channel contract strategies in line with Business Unit sales goals and customer needs; aligns Channel strategy with other key Sales, Marketing, Medical and Managed Care functions and ensures cross-functional support</li><li>Manages a team of Directors and Associate Directors and provides constant feedback and motivation to team members to drive towards common access and sales goals for the US business</li><li>Creates and implements contract strategies designed to build long-term relationships with assigned accounts, based on deep understanding of the customer organization, structure, business strategy and priorities</li><li>Builds senior level relationships with large accounts and stakeholders; interfaces with key customer to understand their needs, perspective, and issues while recruiting customer sources to deliver competitive intelligence and customer insights in order to effectively guide and design effective customer strategies</li><li>Leads the pricing and contracting function for assigned new and in-line products focusing on the full commercialization continuum to develop pricing, contracting and Channel strategies for optimal patient access and profitability</li><li>Develops contracting and channel strategies leading the negotiation and implementation of customer contract/pricing programs with distribution entities. </li><li>Works closely with Market Access Strategy team, brand teams and pipeline colleagues to effectively prepare organization for new product launches in all relevant customer segments</li><li>Contributes to Channel Strategy leadership team to contribute to team objectives, accomplish priorities, and execute market access functional strategy.</li></ul><p></p><p><b>Essential Requirements: </b></p><ul><li><b>Education: </b>Bachelor’s degree required. MBA or equivalent preferred</li><li>A minimum of 9 years of pharmaceutical industry experience or consulting with significant experience in at least 2 of the following areas: Channel Strategy, Finance, Pricing, or Market Access</li><li>Proficiency or ability to become proficient with emerging technologies, specifically ethical and responsible use of artificial intelligence.</li><li>Thorough understanding, knowledge of and experience with US healthcare economics and the drivers of pharmaceutical demand, including pricing and reimbursement</li><li>Extensive experience in healthcare contracting and critical understanding of PBM, National and Regional Health Plan business, Medicare Part D, Medicare Part B and changing market landscape</li><li>Ability to design, build and analyze financial data for business cases, consider sensitivities and present to executive leadership</li><li>Demonstrated prioritization, organizational and analytical skills as well as the ability to create solutions for complex processes and procedures</li><li>Ability to lead, develop, and manage a high-performing team</li><li>Ability to navigate and lead others through a complex business, legal, and operational environment.</li></ul><p></p><p><b>Novartis Compensation Summary:</b></p><p><span>The salary for this position is expected to range between</span> <span><span>$248,500 and $461,500 per year.</span></span></p><p></p><p><span>The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.</span></p><p></p><p><span>Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.</span></p><p></p><p><span>US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.</span></p><p style="text-align:inherit"><br /> </p><p><b>EEO Statement:</b></p><p></p><p>The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. </p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Accessibility and reasonable accommodations</b></p><p style="text-align:inherit"></p><p style="text-align:left"><span>The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to <span class="WIO0">us.reasonableaccommodations&#64;novartis.com</span> or call &#43;1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</span></p><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Salary Range</b></p>$248,500.00 - $461,500.00<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Agility, Agility, Business Acumen, Business Strategy, Channel Strategy, Cross-Functional Collaboration, Cross-Functional Team Leadership, Customer-Centric Mindset, Employee Development, External Orientation, Global Value Chain (Gvc), Go-To-Market Strategy, Healthcare Sector Understanding, Health Economics, Health Policy, Health Technology Assessment (HTA), Influencing Skills, Innovation, Inspirational Leadership, Lcm Strategy, Market Access Strategy, Negotiation Skills, Patient Care, People Management, Pricing Strategy {+ 12 more}]]></description><link>http://biotechroles.com/executive-director-channel-strategy-and-account-management-novartis/69d3ecb6c8e81216cd0bafe3</link><guid isPermaLink="true">http://biotechroles.com/executive-director-channel-strategy-and-account-management-novartis/69d3ecb6c8e81216cd0bafe3</guid><pubDate>Mon, 06 Apr 2026 17:26:14 GMT</pubDate><company>Novartis</company><location>Remote Position (USA)</location><salary>$180000-280000</salary><type>Full time</type></item><item><title><![CDATA[Global Development Product Lead (Sr Director)]]></title><description><![CDATA[<p><span><b>JOB SUMMARY</b></span></p><p><span> </span></p><p>·         Leads multiple (~1-3) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages, at which point molecule may be handed to the late-stage Oncology Development team for post-POC (typically phase 3) development</p><p>·         In close collaboration with functional experts on the product teams, drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan and ensures delivery of data-driven milestones through successful risk identification and mitigation.</p><p>·         Support clinical trials and the development strategy for early development assets and lead development programs across multiple functions within Pfizer Oncology, as well as represent the program with the external clinical community.</p><p>·         Develop clinical development plan from first in human clinical trial to proof-of-concept, including assessment of appropriate combinations, as well as evaluation of potential predictive and pharmacodynamics biomarker plans.</p><p>·         To ensure the clinical components of the clinical plans and clinical expertise are provided to project teams, including medical monitoring of clinical trials. </p><p></p><p></p><p></p><p><span><b>JOB RESPONSIBILITIES</b></span></p><p></p><ul><li>Lead, develop and execute strategic development for early development assets. Lead cross-functional teams in collaboration with line function experts on the Global Product Teams (GPTs) to develop and drive an integrated product plan that addresses near-term technical uncertainties and ensures alignment with future pivotal development and commercialization success.</li><li>Ensure timely execution and delivery of product milestones within budget.</li><li>Communicate with executive management and governance committees to address program needs and provide recommendations. Ensure clear and effective product presentations and communications.</li><li>Collaborate with partners on co-development programs to deliver a shared global product strategy, when applicable.</li><li>Lead the team to set objectives, prioritize tasks, and ensure adherence to the plan and strategy</li><li>  Manage risk by proactively identifying and resolving issues and developing contingency plans</li><li>Oversee early development assets’ development broadly within a specific indication or group of indications. Typically, work on at least two clinical programs and support the development and provide consultation regarding multiple research projects.</li><li>Work across the organization and on multifunctional teams responsible for the development of early development assets (including Product Team, Global Development Team, and Study team).</li><li>Oversee the development and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents.</li><li>Provide leadership to early stage clinical scientists on the clinical study team for Early Development Assets, working in a matrix team environment with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet regularly with Pfizer Oncology group leaders/surrogates across functions to increase mutual awareness and influence of emerging program targets, priorities and status.</li><li>Implementation of PK-guided dose escalation, early combination strategies and emerging innovations on all Oncology R&amp;D first-in-human clinical trials with input from Pfizer Oncology’s Oncology Research Unit, Regulatory Strategy, Clinical Pharmacology and Precision Medicine, Clinical Development and Operations, Pharm Sci and Product Teams.</li><li>Oversee the evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies for early development assets.</li><li>Oversee manuscripts, abstracts and presentations for scientific meetings and advisory boards.</li><li>Conduct literature reviews and prepare summaries to support clinical development programs.</li><li>Medical resource for design and interpretation of clinical and preclinical programs to support existing and new development candidates.</li><li>Coordinate regular (at least quarterly and as needed) interactions with preferred clinical trials network and KOL advisory board to objectively consider and implement feedback.</li><li>Drive innovations in early clinical development, and the application of translational oncology and precision medicine approaches.</li><li>Collaborates with cross-functional leaders and teams to translate early preclinical discovery research into therapeutic candidates.</li><li>Coordinates with business development to establish strategic external collaborations and foster new research projects and programs.</li><li>Contribute to broader organizational excellence as a member of the OESD department. Create a positive team environment that fosters trust, encourages the sharing of disconfirming information, and promotes clear and transparent communication to align the team around the overall goal and vision for the product.</li></ul><p></p><p><span><b>QUALIFICATIONS / SKILLS</b></span></p><p></p><ul><li>MD or MD-PhD with 5&#43; years of industry experience required.</li><li>Oncology drug development experience, track record in oncology clinical research including early phase drug development is preferred.</li><li>Clinical oncology experience: Board certification in oncology preferred.</li><li>Significant industry leadership experience in clinical, translational or basic research in biomedical sciences or one of the disciplines related to drug development.</li><li>Understanding of related disciplines (e.g., biostatistics, regulatory, pre-clinical pharmacology, pharmaceutical sciences). </li><li>Demonstrated scientific productivity (publications, abstracts, etc.).</li><li>Proven scientific writing skills and good communication skills.</li><li>Proven leadership skills with ability to defend the clinical plan at governance meetings is essential.</li><li>Capacity to adapt to a fast-paced and changing environment.</li><li>Demonstrated history of effective leadership; including cross functional and matrixed teams, managing direct reports when applicable, and experience in seeking and maintaining alignment with cross-functional leaders</li><li>Demonstrates a passion for helping patients with cancer and for the science of oncology.</li><li>A proactive and strategic thinker, with strong data-driven decision-making skills</li><li>Ability to focus and motivate a team in a matrix organization with multiple stakeholders</li><li>Strong verbal, written, and presentation communication skills</li><li>Experience in staff management with effective mentoring experience and skills</li><li>Highly collaborative with outstanding relationship building skills with internal company leadership, external development partners and investigators/medical professionals</li><li>Has a strong leadership presence and the ability to work effectively with other leaders.</li><li>Is a team player, works well in a team environment both as a leader and a key contributor.</li><li>Has a global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures, backgrounds, and geographies</li></ul><p></p><p><span><b>ORGANIZATIONAL RELATIONSHIPS</b></span></p><p>Early stage clinical scientists on the clinical study team for Early Development Assets, clinicians, statisticians, clinical pharmacologists, translational biologists, regulatory specialists, pharmaceutical sciences, commercial strategy representatives, and other Pfizer Oncology group leaders/surrogates across functions. In addition, chairs of strategic oversight committees (head of oncology early stage development &#43; line function leaders on governance bodies), direct line managers of line function experts assigned to cross-functional molecule teams, governance committees and molecule development teams of contractual external development partners, and BD team including due diligence teams.</p><p></p><p></p><p><span><b>RESOURCES MANAGED</b></span></p><p></p><p>-          Manges individual product team annual clinical trial budget and projected operational plans for the coming years: $20-100M</p><p>-          This position does not manage direct reports</p><p></p><p></p><p> <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p><br />Relocation support may be available</p><p></p><p><b>Work Location Assignment:  </b><b>This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.</b></p>&amp;#xa;The annual base salary for this position ranges from $274,500.00 to $457,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Medical&amp;#xa;]]></description><link>http://biotechroles.com/global-development-product-lead-sr-director-pfizer/69d3eb27c8e81216cd0baead</link><guid isPermaLink="true">http://biotechroles.com/global-development-product-lead-sr-director-pfizer/69d3eb27c8e81216cd0baead</guid><pubDate>Mon, 06 Apr 2026 17:19:35 GMT</pubDate><company>Pfizer</company><location>United States - Washington – Bothell</location><salary>$220000-350000</salary><type>Full time</type></item><item><title><![CDATA[Comirnaty Brand Performance and Planning Director]]></title><description><![CDATA[<p>Vaccines is the only place in Pfizer where you can contribute to patients in a way like no other – you can prevent sickness and disease. This is at the heart of what drives us every day and it brings us great #Joy. It is a remarkable time to be part of Pfizer’s US Vaccines business as it expands on its mission of preventing disease and improving public health.</p><p></p><p>Join the team that contributed to ending the COVID-19 pandemic. Our efforts not only brought hope and healing to millions but also forged a path for a safer future. Now, we embark on the mission to build the COVID-19 immunization market post-pandemic as we remain vigilant against the mutating virus. Come and craft a legacy of enduring impact as we shape a healthier world.</p><p></p><p>Reporting to the Senior Director, US Comirnaty Strategy and Performance Lead, the Comirnaty Brand Performance and Planning Director will lead annual planning &amp; forecasting cycles, monitor brand performance, and execute on strategic project to improve performance.</p><p></p><p>The ideal candidate demonstrates a strong work ethic, highly analytical mindset, strong organizational skills, and an ability to create clarity in a highly dynamic, cross-functional environment. Prior experience within retail pharmacy setting is a plus.</p><p></p><p><b>ROLE RESPONSIBILITIES</b></p><ul><li><p>Analyze and interpret retail and non-retail performance data to identify trends, gaps, and opportunities. Connect reporting insights to provide recommendations</p></li><li><p>Test hypotheses to understand root causes behind performance gaps as well as performance drivers</p></li><li><p>Support retail and non-retail channel pull-through strategy development based on analytical assessment of the environment and opportunities available</p></li><li><p>As part of a cross functional team, ideate around potential solutions to address consumer vaccination barriers and design special projects to close gaps</p></li><li><p>Support spend optimization to drive greatest impact within annual budget</p></li><li><p>Monitor operating expense budget to ensure overall brand execution within budget</p></li><li><p>Engage cross functional ecosystem to represent US perspective in COVID strain selection activities</p></li><li><p>Lead annual brand planning cycle including forecasting, operating plan, and brand strategy</p></li><li><p>Plan and prioritize brand access &amp; reimbursement confidence activities ahead of in-season execution</p></li><li><p>Plan brand working sessions to support strategy development</p></li></ul><p><b> </b></p><p><b>BASIC QUALIFICATIONS (Required)</b></p><ul><li><p>BA or BS required</p></li><li><p>8&#43; years of relevant experience with U.S. pharmaceutical, biotechnology, or healthcare</p></li><li><p>MBA preferred with 7&#43; years of relevant experience with U.S. pharmaceutical, biotechnology, or healthcare</p></li><li><p>Demonstrated strategic, analytical, and problem‑solving skills</p></li><li><p>Proven retail pharmacy acumen</p></li><li><p>Strong collaboration, communication, and influence capabilities across complex matrix environments</p></li><li><p>Ability to operate effectively in ambiguity and manage multiple priorities in a fast‑paced environment</p></li></ul><p><b> </b></p><p><b>PREFERRED QUALIFICATIONS</b></p><ul><li><p>Strong business acumen and demonstrated flexibility</p></li><li><p>MBA or advanced degree preferred</p></li><li><p>Comfortable with ambiguity and able to adapt and operate successfully</p></li></ul><p></p><p> <b>PHYSICAL / MENTAL REQUIREMENTS</b></p><ul><li><p>Strong business acumen and demonstrated flexibility </p></li><li><p>Prolonged periods of sitting at a desk and working on a computer</p></li><li><p>Occasional travel may be required (e.g., for conferences and off-site meetings)</p></li><li><p>In-person attendance is expected for high-impact strategic meetings, workshops, or planning sessions; particularly those led or facilitated by the Director</p></li><li><p>Travel may include attendance at NY HQs meetings, and conferences</p></li></ul><p>  <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.<br /> </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p></p><ul><li><p>Strong business acumen and demonstrated flexibility </p></li><li><p>Prolonged periods of sitting at a desk and working on a computer</p></li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><ul><li><p>Occasional travel may be required (e.g., for conferences and off-site meetings)</p></li><li><p>In-person attendance is expected for high-impact strategic meetings, workshops, or planning sessions; particularly those led or facilitated by the Director</p></li><li><p>Travel may include attendance at NY HQs meetings, and conferences</p></li></ul><p></p><p>Other Job Details:</p><ul><li><p>Last day to apply: April 10, 2026</p></li><li><p>Work Location Assignment: On Premise</p></li></ul>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/comirnaty-brand-performance-and-planning-director-pfizer/69d3eb27c8e81216cd0baeac</link><guid isPermaLink="true">http://biotechroles.com/comirnaty-brand-performance-and-planning-director-pfizer/69d3eb27c8e81216cd0baeac</guid><pubDate>Mon, 06 Apr 2026 17:19:35 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$160000-220000</salary><type>Full time</type></item><item><title><![CDATA[Automation Technician U-05  - 2nd Shift]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability,</p><p>engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative</p><p>engineering team, you&#39;ll help bring medicines to the world even faster by imagining what’s possible and taking action.</p><p></p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li>Working with Pfizer’s dynamic engineering team, you will play a critical part in managing the Automation engineering activities involving the install, design, program, maintenance, and repair of Automation systems.</li><li>This position maintains and repairs all Automation, Manufacturing, Packaging/Inspection, and Utility systems/equipment with a focus on the maintenance and repair of the control system and associated equipment to ensure operation in compliance with cGMP requirements and the</li><li>Occupational Health and Safety Act and OSHA standards. Responsible to troubleshooting, diagnostics, disassembly, assembly, repair, identifying and replacing parts and a proactive maintenance of systems and electrical equipment in a cost-effective manner.</li><li>You are recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment.</li><li>You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements.</li><li>You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.</li><li>It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.</li></ul><p></p><p><b><u>Preventive Maintenance:</u></b></p><ul><li>Performs Preventive and Predictive Maintenance of electrical and controls systems, following the established guidelines for the CMMS system, operational procedures, site and Manufacturer recommended maintenance practices.</li><li>Reports opportunities identified during Preventive Maintenance execution.</li><li>Review and provides recommendations for Preventive Maintenance task improvements.</li><li>Follow the maintenance plan and alerts when there might be a risk of not complying with the schedule.</li><li>Generates Maintenance work order to report and coordinate repairs for task out of the scope of the Preventive Maintenance.</li><li>Installs, repairs, inspects, test, replace and maintains control systems/components.</li></ul><p></p><p><b><u>Equipment Troubleshooting:</u></b></p><ul><li>Manages all functions of the Qualified Building Management System and Building Management System (QBMS/BMS) and is responsible for wiring diagrams, backups, and Automation reports (i.e., alarms, trending, etc).</li><li>Maintaining all control systems (programmable logic controllers (PLC), etc).</li><li>Implement program (i.e., PLC, HMI, SCADA, BMS/QBMS, Historian, Robots, SQL, etc.) modifications.</li><li>Automation system software installation, troubleshooting and configuration.</li><li>Install, maintain, and inspect Automation control system, workstation (HMI/OIT), VFDs, devices.</li><li>Install, maintain, inspect and replace electrical and communication (ethernet) wiring.</li><li>Interface daily with computers\servers, performing data entry and data (i.e., trend report, alarm reports) retrieval.</li><li>Install, replace and troubleshooting variable frequency drives, encoders, motor, computerized vision system.</li><li>Responsible for Automation Disaster Recovery task (system and data backups, restores, archives, migration and export).</li><li>Responsible for the Automation SDLC documentation (i.e., URS, SIA, DDS, FDS, SCR, Backup Forms) reports.</li><li>Responsible for the Logical Security task (User Account Management) for the Automation System.</li><li>Monitor, investigate, communicate, document and address Automation Systems alarms in a daily basis.</li><li>Installs, inspects, troubleshoots, repairs, and maintains Automation system/devices.</li><li>Develop solutions to routine problems following established Pfizer policies and procedures.</li><li>Utilizes tools (multimeters, power tools), equipment, ladders, lifts, etc., in safe manner per plant safety procedures. Maintains a clean and safe jobsite at all times.</li><li>Participates in safety training programs.</li></ul><p></p><p><b><u>Projects:</u></b></p><p>Provides support for Capital projects which includes but not limited to Installation, commissioning, and qualification, (I/O, alarm, drawing, startup, and shutdown sequence, verification, etc.) and/or functional testing.</p><p></p><p><b><u>Documentation Responsibilities:</u></b></p><ul><li>Follows Good Documentation Practices per compliance requirements (i.e. 21 CFR Part 11, Data Integrity).</li><li>Completes documentation required for maintenance work and logbooks.</li></ul><p></p><p><b><u>Training, SOP’s and GMP:</u></b></p><ul><li>Reads and follows SOPs, Job Aids, PMs, work orders and other required documents and procedures.</li><li>Must be able to complete sterile garb training and work aseptically in manufacturing areas.</li><li>Complete trainings in PLS and assists in training of new colleagues as required.</li><li>Recommends changes to Maintenance tasks and/or SOP&#34;s.</li></ul><p></p><p><b><u>EHS:</u></b></p><ul><li>Follows EHS procedures, recommended practices, job safety analysis and safe work permit.</li><li>Report any abnormal situation that can impact environment, health and or safety of the colleague.</li></ul><p></p><p><b><u>General / Other Responsibilities:</u></b></p><ul><li>Assists other trades when necessary and or perform other duties as instructed.</li><li>Ability to learn how to operate Power trucks / Power lift and elevated platforms.</li><li>Housekeeping – Responsible for keeping assigned areas, as well as general areas clean and organized.</li><li>Escort Contractors.</li><li>May perform any other Engineering or Maintenance duty as requested by management.</li></ul><p></p><p><b>Here Is What You Need</b> (Minimum Requirements)</p><ul><li>Applicant must have a high school diploma and/or general education degree (GED).</li><li>3&#43; years of experience of Industrial PLC, Controls, electrical or automation maintenance, repair and troubleshooting experience.</li><li>Ability and experience reading, modifying, troubleshooting Programmable Logic Controllers, HMIs and PLCs.</li><li>Knowledge of programming languages (Ladder, Sequential Function Chart, Structural Test, Function block).</li><li>Demonstrated aptitude/understanding in Automation, electrical and instrumentation skills.</li><li>Knowledge of industry practices and standards.</li><li>Knowledge of basic mathematics.</li><li>Well-developed time management and problem-solving skills.</li><li>Excellent communication skills and strong work ethic.</li><li>OEM trained and certified in industrial automation systems (Eg: Rockwell (PLC/HMI/SCADA/BMS), Fanuc, Network Architecture, Systech vision systems).</li></ul><p></p><p><b>Bonus Points If You Have </b>(Preferred Requirements):</p><ul><li>Licensed electrician from the State of Michigan (i.e. Journeyman or higher).</li><li>OEM trained and certified in industrial electrical systems (NFPA-70E).</li><li>GMP Maintenance experience in a pharmaceutical manufacturing.</li></ul><p></p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p></p><p>This position is in a Penicillin Facility. The candidate must NOT be allergic to Penicillin.</p><p></p><p>This position requires the ability to:</p><ul><li>Make precisely coordinated movements.</li><li>Lift, push, pull, or carry objects.</li><li>Work at heights on ladders.</li><li>Lift up to 40 lbs.</li><li>Use of PPE (including but not limited to: eye protection, hearing protection,“Arc Flash”protection and foot safety wear).</li></ul><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><ul><li><u>This is a 2nd shift position with core hours from 3:00pm to 11:30 pm Monday through Friday with overtime required as needed</u>.</li><li>The candidate will be required to work off-shift and weekends to support production schedule as needed.</li><li>This is a union position; membership in union is required after 30 days.</li><li>At different times of the year, this position will work long hours for scheduled manufacturing shutdown periods.</li><li>Must be able to complete sterile garb training and work aseptically in manufacturing areas.</li></ul><p></p><p><b>OTHER JOB DETAILS</b></p><p></p><p><b>Last Date to Apply for Job: 4/9/26</b></p><p><b>Work Location Assignment: On site</b></p><p><b>Salary: $49.57</b></p><p><br /> </p>&amp;#xa;The salary for this position ranges from $0,00 to $0,00 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided applies only to the United States - Michigan - Rochester location.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Engineering&amp;#xa;]]></description><link>http://biotechroles.com/automation-technician-u-05-2nd-shift-pfizer/69d3eb26c8e81216cd0baeab</link><guid isPermaLink="true">http://biotechroles.com/automation-technician-u-05-2nd-shift-pfizer/69d3eb26c8e81216cd0baeab</guid><pubDate>Mon, 06 Apr 2026 17:19:34 GMT</pubDate><company>Pfizer</company><location>United States - Michigan - Rochester</location><salary>$65000-85000</salary><type>Full time</type></item><item><title><![CDATA[Director, Data Governance & Insights Enablement]]></title><description><![CDATA[<p><b>Role Summary</b></p><p></p><p>Patient Solution Insights &amp; Analytics, part of Pfizer Patient Services (PPS), harnesses the power of data to drive robust analytics and insight development that inform Pfizer&#39;s most critical business questions. The Patient Solution Insights and Analytics team&#39;s rigorous analytical expertise is depended on as the compass and decision support for the enterprise. Our dynamic, exciting team of subject-matter experts comes from diverse backgrounds and experiences, including data science, digital analytics, finance, market research, and consulting. As a team, we collaborate to turn data into meaningful insights that will have a direct impact on patient&#39;s lives and the future of Pfizer, as a data-driven organization.</p><p></p><p>The Director, Data Governance &amp; Insights Enablement is a senior leadership role within Pfizer Patient Services (PPS) Insights &amp; Analytics, accountable for establishing and sustaining a robust data governance foundation that enables trusted, compliant, and decision-ready patient services analytics across the enterprise.</p><p></p><p><b>Role Responsibilities</b></p><p>This role serves as the central owner of PPS data governance, including metric definitions, business rules, data quality controls, access guardrails, and cross-enterprise alignment with Digital, Legal, Compliance, and external data partners. The Director will address current fragmentation in data ownership, inconsistent measurement across brands, and manual data remediation by building scalable governance processes that support standardized reporting, advanced analytics, and end-to-end patient journey measurement.</p><p></p><p><b>Enterprise Data Governance Leadership</b></p><ul><li>Establish and operationalize a formal PPS data governance framework, defining clear ownership, stewardship, and decision rights across data domains, brands, and business units.</li><li>Own and maintain standardized business rules, metric definitions, and KPI frameworks to ensure consistency of patient services measurement across Specialty Care, Oncology, and Primary Care.</li><li>Serve as the single point of accountability for PPS data governance decisions, escalation paths, and governance forums.</li></ul><p></p><p><b>Data Quality, Controls &amp; Compliance</b></p><ul><li>Define and enforce data quality standards, validation rules, and QC processes to prevent data integrity issues.</li><li>Partner with Legal, Compliance, Privacy, and Digital to establish clear data access guardrails, usage policies, and approval workflows.</li><li>Lead development of SOPs and training related to data access, reporting, and analytics.</li></ul><p></p><p><b>Data Architecture &amp; Aggregation Enablement</b></p><ul><li>Partner with Digital and data architecture teams to support a fit-for-purpose data aggregation and reporting ecosystem.</li><li>Guide governance requirements for vendor platforms, data feeds, and analytics solutions</li><li>Reduce manual data cleansing through upstream standardization and automation.</li></ul><p></p><p><b>Vendor &amp; External Partner Oversight</b></p><ul><li>Define governance expectations for external data partners and vendors.</li><li>Evaluate vendor data quality, adherence to business rules, and delivery against governance standards.</li><li>Support RFPs, contract language, and SLAs related to data quality and transparency.</li></ul><p></p><p><b>Insights Enablement &amp; Leadership Partnership</b></p><ul><li>Partner with PPS Insights &amp; Analytics leaders to ensure governance enables timely insight generation.</li><li>Support leadership discussions by clarifying metric meaning, interpretation, and limitations.</li></ul><ul><li>Maintain comprehensive, and detailed, data governance standards to ensure consistency and clarity in program metrics / business rule implementation over time</li><li>Proactively work across the enterprise to push novel analytic methodologies, co-create solutions and oversee implementation of solutions with stakeholders</li><li>Identify efficiencies and future-forward ways to accelerate the timeliness of analytics / insights delivery</li><li>Work with and empower a high-performing team of insights professionals, responsible for delivering integrated insights, program measurement analytics, reporting, and launch support for each BU</li></ul><p></p><p><b>Basic Qualifications</b></p><p></p><p>Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><ul><li>Bachelor&#39;s degree required</li><li>8&#43; years’ experience required in Biopharma, analytics, strategic consulting, business, or related area</li><li>Experience with the pharma ecosystem and datasets including physician-level prescribing, institutional sales data, payer-prescriber-level data, formulary data, Rebates, Symphony claims, Copay claims</li><li>Prior experience with the operational monitoring and impact assessment of patient services programs, including specific programmatic components, spanning: Affordability Programs (e.g., Copay, eVoucher), Field Access Support, Hub / Prior Authorization Support, Pharmacy / Distribution Workflows (i.e., retail, specialty pharmacy, and buy-and-bill)</li><li>Demonstrated analytical capabilities and critical thinking skills</li><li>Strong project management and organizational skills with cross-functional teams of diverse colleagues;</li><li>Exceptional written and verbal communication skills, and prior experience in presenting to functional leaders</li><li>Demonstrated expertise in data governance, business rules, and data quality management.</li></ul><p></p><p><b>Other Job Details:</b></p><ul><li><b>Last Date to Apply for Job: April 19th, 2026.</b></li><li>Ability to travel based on business needs</li><li>NOT eligible for Relocation Package</li><li>This position is hybrid and requires working onsite 2 to 3 days per week</li></ul><p></p><p>#LI-PFE</p>&amp;#xa;The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/director-data-governance-and-insights-enablement-pfizer/69d3eb26c8e81216cd0baeaa</link><guid isPermaLink="true">http://biotechroles.com/director-data-governance-and-insights-enablement-pfizer/69d3eb26c8e81216cd0baeaa</guid><pubDate>Mon, 06 Apr 2026 17:19:34 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$180000-250000</salary><type>Full time</type></item><item><title><![CDATA[Associate Scientist Early Antigen Development]]></title><description><![CDATA[<p><b><u>Role Summary</u></b></p><p></p><p>We are seeking a dedicated Associate Scientist to support early antigen and assay development through the application of molecular, microbiological, and cell culture methods. The successful candidate is excited about preclinical research and will have the opportunity to help advance multiple bacterial vaccine programs. The Associate will be familiar with a BSL-2 environment and can work independently and as part of a cross-functional team.</p><p></p><p><b><u>Role Responsibilities</u></b></p><ul><li><p>Work in a BSL-2 environment to perform preclinical experiments aimed at developing and optimize vaccine candidates. Perform functional assays to assess vaccine candidates.</p></li><li><p>Build team skills and collaborate within the team as well as across groups to support vaccine development efforts.</p></li><li><p>Adhere to schedule and perform other activities as assigned.</p></li><li><p>Analyze data and present experimental results in meetings.</p></li><li><p>Document all work in electronic notebooks and write progress reports as required.</p></li><li><p>Stay current on all departmental and corporate training.</p></li><li><p>Perform other duties as assigned.</p></li></ul><p></p><p><b><u>Qualifications</u></b></p><p></p><p><b>Must Have:</b></p><ul><li><p>BS with 0 - 2 years of laboratory experience in a microbiology or biological discipline (Microbiology, Biotechnology, Biochemistry, or equivalent)</p></li><li><p>Experience working with bacteria in a BSL-2 environment.</p></li><li><p>Motivated, flexible, and willing to learn new skill sets.</p></li><li><p>Ability to work independently and collaboratively as part of a team.</p></li><li><p>Attention to detail and ability to follow instructions while confident in problem solving.</p></li><li><p>Excellent organizational and time management skills to meet deadlines.</p></li><li><p>Strong written and verbal communication skills.</p></li><li><p>Computer literacy and Microsoft Windows/Office 365 experience. Experience using PRISM and bioinformatics software for cloning and genome analysis preferred.</p></li></ul><p></p><p><b>Nice-To-Have:</b></p><ul><li><p>Experience in recombinant protein purification.</p></li><li><p>Experience with cloning and bacterial strain manipulation/engineering.</p></li><li><p>Familiar with performing preclinical functional assays.</p></li><li><p>Experience with mammalian cell culture systems.</p></li></ul><p>  <br /> </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p></p><p>Sitting, standing, walking, and repetitive procedures, light lifting; ability to analyze data and design experiments and present scientific concepts to colleagues. </p><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p></p><ul><li><p>Local travel, adherence to all safe work practices and working within defined biosafety requirements.</p></li><li><p>Flexibility to work late hours/weekends if needed.</p></li></ul><p><br />Work Location Assignment: On Premise</p>&amp;#xa;The annual base salary for this position ranges from $60,200.00 to $100,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Research and Development&amp;#xa;]]></description><link>http://biotechroles.com/associate-scientist-early-antigen-development-pfizer/69d3eb25c8e81216cd0baea9</link><guid isPermaLink="true">http://biotechroles.com/associate-scientist-early-antigen-development-pfizer/69d3eb25c8e81216cd0baea9</guid><pubDate>Mon, 06 Apr 2026 17:19:33 GMT</pubDate><company>Pfizer</company><location>United States - New York - Pearl River</location><salary>$85000-110000</salary><type>Full time</type></item><item><title><![CDATA[Associate Director, Commercial Data Strategy & Governance]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:15pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;"><span style="white-space:pre-wrap;">The Associate Director, Data Strategy &amp; Governance is a business-led data leader responsible for defining, governing, and scaling the organization’s end-to-end data ecosystem. This role sits within Enterprise Analytics &amp; Operations. It ensures that data strategies, architecture, and governance frameworks are aligned with evolving business needs and enable high-quality, decision-ready insights across the enterprise.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;"><span style="white-space:pre-wrap;">This role positions data as a strategic asset, integrating internal (Creto), third-party, Salesforce CRM, and omnichannel engagement data into a unified, governed ecosystem. The individual will ensure that all commercial data assets are structured, connected, and accessible to drive execution, insights, and growth.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;"><span style="white-space:pre-wrap;">The ideal candidate combines strategic thinking with hands-on execution, with the ability to design scalable data ecosystems, enforce governance standards, and proactively anticipate future data needs</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Commercial Data Strategy &amp; Architecture</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and steer the commercial data strategy in alignment with organizational goals, ensuring both successful launch readiness and sustained implementation. &nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish a scalable data architecture integrating:</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Salesforce CRM and commercial platforms</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Omnichannel engagement, marketing systems</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Consent and identify systems</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Internal Product and Patient HUB data sources</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment of data models, schemas, and standards across all systems and business functions.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Data Management &amp; Governance</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Design and implement data governance frameworks, including:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">o</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Data ownership and stewardship models</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">o</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Data quality standards and monitoring</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">o</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Metadata, lineage, and auditability</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure consistent definitions and usage of key data assets across CRM, omnichannel, analytics, and reporting environments.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Proactively identify and resolve data gaps, inconsistencies, and risks across the ecosystem.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Master Data Management (MDM)</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Establish and oversee MDM strategy across key commercial entities (e.g., HCP, HCO, accounts, affiliations).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure a unified and trusted “golden record” across Salesforce CRM, data warehouse, and downstream systems.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Implement stewardship processes to maintain data integrity and consistency at scale.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Salesforce CRM &amp; Commercial Data Integration</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure Salesforce CRM is effectively integrated as a core system within the broader data ecosystem (not siloed).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Define how CRM data structures align with enterprise data models and governance standards.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Enable seamless data flow between CRM, marketing platforms, analytics tools, and external data sources.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Partner with business teams to ensure CRM captures high-quality, decision-relevant data.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Omnichannel Data &amp; Engagement Ecosystem</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Define and manage the omnichannel data strategy across all engagement channels (e.g., field, digital, email, events).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Integrate engagement data from platforms such as marketing automation, digital channels, and CRM into a unified data model.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure consistent tracking, attribution, and measurement of customer interactions across channels.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Enable a 360° view of customer engagement to support targeting, personalization, and performance tracking.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Data Ecosystem &amp; Third-Party Data Management</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Own integration and management of third-party commercial data sources (e.g., claims, prescription, promotional, and engagement data).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure internal (Creto) and external datasets are harmonized into a consistent, analytics-ready structure.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Define standardized schemas and data models to support interoperability and scalability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Data Accessibility &amp; Analytics Enablement</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure high-quality, well-structured data is readily available for analytics, reporting, and decision-making.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Partner with analytics and business stakeholders to align data structures with reporting and insight needs.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Enable scalable access to trusted data across stakeholders, from leadership to field teams.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Data Privacy, Compliance &amp; Risk Management</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Establish and enforce data privacy and compliance standards (e.g., HIPAA, GDPR).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Ensure appropriate data access controls, consent management, and secure data handling practices across CRM and omnichannel systems.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Translate regulatory and policy requirements into practical, scalable data governance processes.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Proactive Data Operations &amp; Continuous Improvement</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Lead implementation sprints and prioritize work based on business impact.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Monitor and continuously improve data quality, availability, and usability across all data assets.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Identify opportunities to enhance data integration, governance, and ecosystem performance proactively.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Build and maintain a forward-looking data roadmap aligned with business priorities and growth.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">-</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="white-space:pre-wrap;">Establish repeatable processes that scale as the commercial footprint grows.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelors degree required</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">8+ years of experience in data strategy, data management, or enterprise data architecture roles.</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Proven experience designing and implementing:</span></li><li style="font-size:12pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Data warehouse and governance frameworks</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Master data management (MDM) solutions</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Enterprise data ecosystems integrating CRM and omnichannel data</span></li></ul></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;"> Strong experience with:</span></li><li style="font-size:12pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Salesforce CRM data structures and integration</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Omnichannel engagement data (marketing, digital, field interactions)</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Third-party commercial data sources</span></li></ul></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Deep understanding of data architecture, schema design, and data lifecycle management.</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Experience enabling analytics and BI through well-structured, governed data.</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Familiarity with data privacy and regulatory requirements (HIPAA, GDPR).</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2025 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/associate-director-commercial-data-strategy-and-governance-cg-oncology/69d3c3e6c8e81216cd0b96a4</link><guid isPermaLink="true">http://biotechroles.com/associate-director-commercial-data-strategy-and-governance-cg-oncology/69d3c3e6c8e81216cd0b96a4</guid><pubDate>Mon, 06 Apr 2026 14:32:05 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$150000-210000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Program Advisor - (Bilingual)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">What You Will Do</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:11pt;white-space:pre-wrap;">Business Development</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Identify and qualify inbound leads, as well as engage in outbound prospecting activities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Drive confidence through digital, voice, and video interactions positioning Fountain Life brand and services.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Promote longevity services, provide education, and establish relationships to facilitate member onboarding.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Actively listen to prospects to tailor solutions to their specific health needs and goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Follow up with prospects at various stages in the sales cycle to nurture and maintain engagement.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Document activity in CRM software for full visibility with internal and external team members.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Member Experience</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Guide the member and potential member down the path of a defined Customer Experience Journey and participate in the continuous improvement process.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Develop and maintain strong relationships with potential and current members, fostering trust and credibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Provide exceptional customer service by promptly responding to inquiries, delivering accurate information, and personalized touches.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Collaboration</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Collaborate with team members and leadership to optimize efficiency in lead outreach and relations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Coordinate with the marketing team to align messaging, campaigns, and lead generation efforts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Provide feedback on customer requests and preferences.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Communicate with the Fountain Life operations team, to ensure a seamless member-experience.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">What We Offer</strong></b><br><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:rgb(26,46,53);font-size:11pt;white-space:pre-wrap;">We believe the people who help us grow deserve every bit as much investment as our members. Here's what you can expect when you join Fountain Life:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">Competitive base salary commensurate with experience</span></li><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">Comprehensive health, dental, and vision benefits — because we mean it when we say we care about your wellbeing</span></li><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">Generous PTO and company holidays — we believe rest is part of performance</span></li><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">401(k)&nbsp;</span></li><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">A front-row seat at one of the most exciting companies in preventive health — your work here matters</span></li><li style="color:rgb(32,32,34);font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(32,32,34);font-size:11pt;white-space:pre-wrap;">A culture that values builders, doers, and people who take ownership</span></li></ul>]]></description><link>http://biotechroles.com/program-advisor-(bilingual)-fountain-life/69d3c3c5c8e81216cd0b969f</link><guid isPermaLink="true">http://biotechroles.com/program-advisor-(bilingual)-fountain-life/69d3c3c5c8e81216cd0b969f</guid><pubDate>Mon, 06 Apr 2026 14:31:33 GMT</pubDate><company>Fountain Life</company><location>Naples, FL</location><salary>$55000-75000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Member Experience Coordinator]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:16pt;white-space:pre-wrap;">Fountain Life Member Experience Specialist</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">About Fountain Life</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Fountain Life brings together the world’s most renowned medical and health experts to boost longevity and performance – putting the health back in healthcare. We do this by utilizing cutting-edge Artificial Intelligence (AI) to collect data and gain insights into the human body that have never been possible before. Our data-driven approach enables us to find illnesses including cancer, cardiac, metabolic, neurodegenerative disease early, before they can cause harm. As a result, our members operate at peak performance throughout their life; ultimately feeling as healthy and vibrant at 100 as they were at 60.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">What’s in it for you?</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Fountain Life is a group of innovators led by Dr. Robert Hariri, Tony Robbins and Dr. Peter Diamandis. This unique </span><span style="color:black;white-space:pre-wrap;">opportunity allows you the chance </span><span style="white-space:pre-wrap;">to be a part of this disruptive health care environment and change the way medicine is done forever. As an employee you will also receive Fountain Health Insurance, which enables you to utilize many of the proactive health features Fountain Life has to offer.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">Fountain Life lives by the following customer experience promises:</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will always strive to surprise and delight our members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will over deliver and exceed members expectations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will always consider a member’s emotional journey, the goal is for every member to feel safe, empowered, and educated.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will always be respectful of our member’s time and strive for a seamless experience.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will strive to make the testing day educational and understandable.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will ensure that all results are simple to understand, data driven, and actionable.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will remember that Fountain Life membership is exclusive and global. As such, our members will demand a 21</span><sup style="color:black;white-space:pre-wrap;"><span>st</span></sup><span style="color:black;white-space:pre-wrap;">century experience.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will ask for feedback and always strive to be better.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:black;white-space:pre-wrap;">I will create memorable experiences.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">What is the opportunity?</strong></b><span style="color:black;white-space:pre-wrap;">&nbsp;The Fountain Life Member Experience Specialist will report to the Center Director. They will act as the ‘face of Fountain Life’ and be responsible for delivering the 21st century experience our clients expect from our revolutionary practice. This important role involves overdelivering to provide an exceptional experience in the Center. The Member Experience Specialist must be able to ‘surprise &amp; delight’ every client that walks through our doors, while ensuring each client leaves with a clear understanding of what will happen next in their journey.</span><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">Come join our team of highly trained, innovative healthcare experts!&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">What will you do?</strong></b><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">This position is an integral part of Fountain Life’s overall mission to transform healthcare. The hostess will be tasked with delivering unique, personalized service, in ways that inspire, reflect trust and credibility to our clients, and ensure membership success and loyalty.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><b><strong style="color:black;white-space:pre-wrap;">Deliver exceptional customer service</strong></b><span style="color:black;white-space:pre-wrap;"> by greeting clients, addressing inquiries and processing payments, all while consistently exceeding expectations with a ‘surprise &amp; delight’ approach.</span><span style="white-space:pre-wrap;">&nbsp; </span><span style="color:black;white-space:pre-wrap;">Anticipating needs of the client while in the Center and providing a fond farewell.</span><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Preparing suites (clothes, tables settings, TV agendas created, etc)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Ordering food, preparing and delivering to suites</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Setting and clearing the suites of dishes / waters / coffees</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Resetting the suites at the end of day</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Reviewing schedules to see who is coming in to create Agendas (TVs)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Check out at the end of day to collect payment on any outstanding balances</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><span style="color:black;white-space:pre-wrap;">Answering phones and forwarding messages to appropriate people</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><b><strong style="color:black;white-space:pre-wrap;">Provide a memorable and special experience </strong></b><span style="color:black;white-space:pre-wrap;">for our clients on their testing day, and ensuring client satisfaction.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><b><strong style="color:black;white-space:pre-wrap;">Maximize client satisfaction and operational efficiency</strong></b><span style="color:black;white-space:pre-wrap;"> by clearly explaining to the client what will happen next in their journey thus providing clarity and setting client </span><span style="white-space:pre-wrap;">&nbsp;</span><span style="color:black;white-space:pre-wrap;">expectations.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><b><strong style="color:black;white-space:pre-wrap;">Safeguard client rights</strong></b><span style="color:black;white-space:pre-wrap;"> by strictly maintaining the confidentiality of personal and financial information.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">·</span><span style="font-size:7pt;white-space:pre-wrap;">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </span><b><strong style="color:black;white-space:pre-wrap;">Support senior management</strong></b><span style="color:black;white-space:pre-wrap;"> in showcasing Fountain Life’s vision by ensuring the facility meets the highest standards of cleanliness and presentation. Greeting arriving client in lobby</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor inventory, update system with inventory counts, and resupply as needed, ensuring needed product quantities and proper timing of deliveries</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Generate purchase orders as needed and ensure purchase order fulfillment</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor supplier performance and resolve any issues and concerns.&nbsp; Apply performance&nbsp; metrics as needed, if possible.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Set up new vendors in accounting and payments systems</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assist Care team as needed</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Arrange for client transportation</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">What do you need to succeed?</strong></b><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">To ensure success, our Fountain Life Member Experience Specialist must have a passion for health and wellness and be dedicated to helping our clients achieve their goals.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">Must-Have’s:</strong></b><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· A self-starter with the ability to multitask successfully</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Able to prepare coffee and other food and beverage offerings for client</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Capacity to maintain a calm and enthusiastic demeanor&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Have a passion for health, wellness and self-improvement&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Basic knowledge of Microsoft Office applications&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Must be reliable and aligned with Fountain Life’s common vision&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">&nbsp;</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">Nice-to-Have’s:</strong></b><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· Prior Experience working in a Medical Clinic environment&nbsp;and/or Hospitality industry</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">· First Aid/CPR certification&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">Job Type: Full-time&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Inclusion and Equal Opportunity Employment</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">Fountain Life provides&nbsp;equal&nbsp;employment opportunities to all employees and applicants in all company facilities without regard to race (including hair texture and hairstyles), color, religious creed, sex, national origin, ancestry, citizenship status, pregnancy, childbirth, (or related medical conditions, including, but not limited to lactation), physical disability, mental and/or intellectual disability, age, military status or status as a Vietnam-era or special disabled veteran, marital status, registered domestic partner or civil union status, gender (including sex stereotyping and gender identity or expression), medical condition (including, but not limited to, cancer related or HIV/AIDS related), genetic information, or sexual orientation in accordance with applicable federal, state and local laws.</span></p>]]></description><link>http://biotechroles.com/member-experience-coordinator-fountain-life/69d3c3c0c8e81216cd0b9699</link><guid isPermaLink="true">http://biotechroles.com/member-experience-coordinator-fountain-life/69d3c3c0c8e81216cd0b9699</guid><pubDate>Mon, 06 Apr 2026 14:31:28 GMT</pubDate><company>Fountain Life</company><location>Naples, FL</location><salary>$45000-60000</salary><type>HOURLY_FT</type></item><item><title><![CDATA[PRN Radiologic Technologist]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">Responsibilities include</strong></b><span style="color:black;white-space:pre-wrap;">:&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Address all members, staff, and visitors in a friendly, courteous and professional manner&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provides personal protective equipment in accordance with safely standards and policies/procedures/protocols set in place by Fountain Life and CDC guidelines&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assists with quality control duties and assignments as required.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Operates Cat Scan, DEXA and diagnostic Xray equipment</span><span style="color:red;white-space:pre-wrap;"> </span><span style="white-space:pre-wrap;">in accordance with established organizational policy&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Prepares and positions patients for CT scanning, DEXA and radiographic procedures; ensures patient modesty, confidentiality, and privacy&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Prepares IV solution sets and contrast agents for administration as ordered.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Perform complex tasks associated with the operation of high field strength magnets and related equipment to produce special radiographic images of specific body parts &nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Position patients for MR scans using immobilization and protective equipment to comply with government regulations and to ensure the safety of patients and staff</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Screen patients for MR safety prior to procedure performance &nbsp;&nbsp; &nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Evaluate MR scans for technical quality, collate processed images and sequence of exposure and label appropriately &nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Explains proper preparation to patients prior to procedure. Obtain patient signature and technologist initials on history form.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Contributes to and maintains good working rapport with all members, personnel, and providers to ensure that the organization’s objectives can effectively meet the needs of members&nbsp;and providers.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assures that patient rights to fair and equitable treatment, self-determination, individuality, privacy, and civil rights are maintained.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Contributes to an atmosphere of warmth, personal interest, and positive emphasis throughout the organization.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Reports all unsafe, hazardous conditions, defective equipment, etc. to supervisor immediately.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assures that work and/or assignment areas are maintained in a neat, safe, clean, and orderly fashion.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assists with training new employees as needed.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Handle stressful and emergency situations with a calm rational demeanor.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrate the ability to set priorities and maintain a clean and organized work area.&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintains and compiles records and reports as necessary.&nbsp;</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">What do you need to succeed?</strong></b><span style="color:black;white-space:pre-wrap;"> &nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">To ensure success, the Radiologic Technologist should be detail-oriented with the ability to deliver care in a compassionate manner, thus always ensuring absolute comfort of members. They will collaborate effectively with other members of the medical team in either the New York, Texas, or Florida locations on the status of members and the delivery of high-quality care.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="color:black;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:black;white-space:pre-wrap;">Requirements: </strong></b><span style="color:black;white-space:pre-wrap;"> &nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Graduate of an accredited Radiologic Technology Program or equivalent hospital-based program&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Possess a current ARRT certification and State license for specified location in which you are applying with IV injection permission&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ARRT Certification eligible in MRI or Cat Scan and/or Bone Densitometry (Experience in Cardiac CTA helpful)&nbsp;</span></li><li style="color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">BLS certification&nbsp;</span></li></ul>]]></description><link>http://biotechroles.com/prn-radiologic-technologist-fountain-life/69d3c3b3c8e81216cd0b9697</link><guid isPermaLink="true">http://biotechroles.com/prn-radiologic-technologist-fountain-life/69d3c3b3c8e81216cd0b9697</guid><pubDate>Mon, 06 Apr 2026 14:31:15 GMT</pubDate><company>Fountain Life</company><location>The Colony, TX</location><salary>$0-0</salary><type>HOURLY_FT</type></item><item><title><![CDATA[Manager, Talent Development]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">The Manager of Talent Development plays a critical administration and execution role in scaling CG Oncology’s people capability during a period of growth. Reporting to and partnering closely with the Director of Organizational &amp; Talent Development, this role translates strategy into consistent, repeatable, high-quality development programs at the tactical level that strengthen leadership effectiveness, employee capability and strengthening the modeling of Values and culture of the organization. This role is execution-focused with increasing program ownership over time. Success requires strong organization skills and operational discipline, facilitation strength, systems thinking, and strong cross-functional partnership. The Manager ensures development initiatives become systematized and embedded into operating rhythms (not standalone one-time initiatives)with measurable outcomes, leadership and executive visibility, and long-term sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:15pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Talent Development Program Execution</span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute and support organizational and talent development initiatives, ensuring programs are delivered consistently, on time, and on budget, and with clear outcomes.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish repeatable program cadences, timelines, and documentation to support sustainability and scale.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Partner with the Director of Organizational &amp; Talent Development to ensure clear ownership, coordination, and follow-through across initiatives. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assist with budgeting and tracking costs associated with the Org and Talent Development Initiatives. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Career Growth Connect &amp; Development Facilitation </span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Co-facilitate Career Growth Connect, a monthly employee forum focused on awareness and utilization of CG Oncology’s development resources. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support planning, facilitation, and follow-up for Career Growth Connect sessions. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Co-facilitate development trainings and enablement sessions, including, but not limited Culture Amp Develop and Coaching Habit.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Progress from co-facilitation to increased ownership of select development sessions over time.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Help administer the Culture Amp Develop platform to increase utility and utilization.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Culture Champion Program Support</span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, administer, and consolidate Cultural surveys and distill into actionable insights.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assist with the rollout and ongoing coordination of the Culture Champion program. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support logistics, communication, and follow-up to ensure consistent execution and alignment with broader culture priorities</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Program Tracking &amp; Leadership Visibility</span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain centralized tracking for assigned people programs, commitments, and milestones. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop clear, executive-ready summaries and dashboards highlighting progress, risks, and next steps.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Capture decisions and action items from meetings and ensure timely follow-through. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Role Clarity, Job Architecture &amp; HRBP Partnership</span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support the creation of and updates to job descriptions and role scopes driven by growth or organizational change. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Prepare documentation supporting promotions, salary adjustments, and leveling discussions. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Partner with HR Business Partners and Talent Acquisition to ensure alignment between role expectations, compensation, and hiring decisions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">May be assigned as an HRBP for a discrete client group for development. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Hiring &amp; Talent Process Enablement</span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support Performance-Based Hiring processes across assigned roles. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Complete Performance-Based Hiring certification.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Assist in integrating structured hiring insights into development and performance conversations as appropriate.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;"> Participate in Talent Debriefs to ensure quality of hire.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Help to assimilate the Harrisson WPQ with the PBH process for seamless utilization. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Capability Building &amp; Readiness to Scale </span></li><li style="list-style:none;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrate sound judgment, systems thinking, and prioritization in complex situations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Progress from program support to partial ownership of selected initiatives within the first 12 months. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build credibility and trust through reliable execution and thoughtful partnership.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor’s degree required in Organizational Development, Human Resources, Business, or related field preferred</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Seven (7) years of progressive experience in HR Business Partner, Talent Development, Organizational Development, or related people-focused roles </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated experience translating strategy into scalable program execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience facilitating development sessions or learning forums.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience operating in a fast-paced, scaling organization</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong facilitation and presentation skills </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">High operational discipline and follow-through</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to build dashboards and executive-ready reporting.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong cross-functional collaboration skills</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Comfort working in ambiguity and growth-stage environments.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2025 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/manager-talent-development-cg-oncology/69d3c39cc8e81216cd0b9691</link><guid isPermaLink="true">http://biotechroles.com/manager-talent-development-cg-oncology/69d3c39cc8e81216cd0b9691</guid><pubDate>Mon, 06 Apr 2026 14:30:51 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$110000-150000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Senior Medical Writer & Evidence Analyst]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">To author, review regulatory &amp; other medical writing deliverables</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">independently or with other Sr Medical Writer as per high-quality standards (internal &amp; external) and within expected timelines. Support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Position Responsibilities/</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:11pt;white-space:pre-wrap;">Accountabilities:</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Authoring &amp; review of patient narratives, CSRs, Protocol, IB, &amp; other regulatory submission documents (excluding CTD modules) for US FDA, EMEA and rest of the world.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Independent authoring and review of manuscripts, abstracts, posters, evidence synthesis projects and other techno-commercial documents as needed.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Author deliverables with scientific accuracy, based on facts from available sources and meeting quality standards (including grammar and editorial requirements).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Follow all internal and client processes and adhere to various ICH / regulatory guidelines and other industry best practices (e.g. GPP).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Undertake quality control (QC, scientific reviews and/or proofreading of the above-mentioned deliverables.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Showcase flexibility in terms of timelines and writing style based on client needs and/or therapeutic area requirements across various domains.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support audit readiness of the department overall. Contribute to development of the SOPs, work-instructions and other documentation.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support individual and department development goals for larger business needs.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Education:</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:11pt;white-space:pre-wrap;">Experience:</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">At least 3-5 years of experience in medical writing or flair for writing with proven academic standards. Fair understanding of industry standards and global trends in drug development and medical device domains. Highly proficient in MS Office and other software for authoring and data handling/interpretation. Basic understanding and comfort for use of automation platforms</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Required Certifications</strong></b><span style="white-space:pre-wrap;">:&nbsp; Relevant certification is preferable but not</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">mandatory</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proficient with Microsoft Office Suite. Mid to Advance level expertise for MS WORD features.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Excellent written and oral communication skills.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Excellent presentation skills.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong organizational, problem-solving, and analytical skills.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to manage priorities and workflow.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Versatility, flexibility, and a willingness to work within constantly changing priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven ability to handle multiple projects and meet deadlines.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong interpersonal skills.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to deal effectively with a diversity of individuals at all organizational levels.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to deal effectively with a diversity of individuals at all organizational levels.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Commitment to excellence and high standards.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Creative, flexible, and innovative team player.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to work independently and as a member of various teams and committees.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Good judgement with the ability to make timely and sound</span><span style="font-size:11pt;white-space:pre-wrap;"> decisions</span></li></ul>]]></description><link>http://biotechroles.com/senior-medical-writer-and-evidence-analyst-catalystcr/69d3c389c8e81216cd0b968c</link><guid isPermaLink="true">http://biotechroles.com/senior-medical-writer-and-evidence-analyst-catalystcr/69d3c389c8e81216cd0b968c</guid><pubDate>Mon, 06 Apr 2026 14:30:33 GMT</pubDate><company>Catalystcr</company><location>Thiruvananthapuram, India</location><salary>$12000-22000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (West)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, West is a remote, field-based leadership role covering the West region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">Los Angeles, CA, San Francisco CA, or Phoenix, AZ,</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Employee Value Proposition </strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Join CG Oncology at a pivotal moment as the company prepares for a major oncology launch. This role offers the opportunity to shape regional strategy, influence national commercialization efforts, and build meaningful partnerships with physicians and healthcare systems treating NMIBC patients.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (West) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(west)-cg-oncology/69d3c372c8e81216cd0b9687</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(west)-cg-oncology/69d3c372c8e81216cd0b9687</guid><pubDate>Mon, 06 Apr 2026 14:30:10 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$180000-250000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (Southwest)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, Southwest is a remote, field-based leadership role covering the Southwest region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">Dallas, TX, Houston, TX, or Denver, CO</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Employee Value Proposition </strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Join CG Oncology at a pivotal moment as the company prepares for a major oncology launch. This role offers the opportunity to shape regional strategy, influence national commercialization efforts, and build meaningful partnerships with physicians and healthcare systems treating NMIBC patients.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (Southwest) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(southwest)-cg-oncology/69d3c36cc8e81216cd0b9686</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(southwest)-cg-oncology/69d3c36cc8e81216cd0b9686</guid><pubDate>Mon, 06 Apr 2026 14:30:03 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$160000-220000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (Southeast)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, Southeast is a remote, field-based leadership role covering the Southeast region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">Orlando, FL, Miami, FL, or Atlanta, GA</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (Southeast) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(southeast)-cg-oncology/69d3c365c8e81216cd0b9685</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(southeast)-cg-oncology/69d3c365c8e81216cd0b9685</guid><pubDate>Mon, 06 Apr 2026 14:29:57 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$160000-220000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Clinical Trial Systems & Process Manager]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">The Clinical Trial Systems &amp; Process Manager is accountable for the strategic ownership, optimization, and governance of clinical trial systems and operational processes that enable high-quality, compliant, and inspection-ready execution of clinical development programs. This role ensures systems are scalable, inspection-ready, and aligned to CG Oncology’s late-stage development, BLA timelines, and future commercialization objectives. Ownership of CTMS and eTMF platforms is required, with Veeva Vault experience strongly preferred.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Own and manage clinical trial systems including CTMS, eTMF, and related platforms, Veeva Vault strongly preferred.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Define and maintain the clinical systems roadmap aligned to Phase 3 programs and rolling BLA milestones.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead system implementation, configuration, validation, upgrades, and lifecycle governance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Design and standardize end-to-end clinical trial operational workflows.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop SOPs, templates, and training materials to support adoption and compliance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with GCP, ICH guidelines, 21 CFR Part 11, and computer system validation requirements.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Oversee data integrity, audit trails, user access controls, and validation documentation.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Partner cross-functionally with Clinical Operations, Data Management, Regulatory, Quality, IT, and CRO partners.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain TMF completeness metrics and continuous inspection readiness dashboards.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Define KPIs and reporting dashboards to monitor operational health and risk.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support internal audits and regulatory inspections.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Manage system vendors to ensure alignment with CG Oncology quality standards</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor’s degree required, preferably in life sciences, Clinical Research, Biomedical Sciences, Health Sciences, Data Management, or related scientific discipline. Advanced degree preferred.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Six (6) years of progressive experience in clinical operations, clinical systems ownership, or process management in a regulated biotech or pharmaceutical environment</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Hands-on experience with CTMS and eTMF systems required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience supporting late-stage trials and inspection readiness preferred.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/clinical-trial-systems-and-process-manager-cg-oncology/69d3c364c8e81216cd0b9684</link><guid isPermaLink="true">http://biotechroles.com/clinical-trial-systems-and-process-manager-cg-oncology/69d3c364c8e81216cd0b9684</guid><pubDate>Mon, 06 Apr 2026 14:29:56 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$120000-165000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (Northeast)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, Northeast is a remote, field-based leadership role covering the Northeast region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">New York City, New York; Boston, Massachusetts; or Newark, New Jersey</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Employee Value Proposition </strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Join CG Oncology at a pivotal moment as the company prepares for a major oncology launch. This role offers the opportunity to shape regional strategy, influence national commercialization efforts, and build meaningful partnerships with physicians and healthcare systems treating NMIBC patients.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (Northeast) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(northeast)-cg-oncology/69d3c35fc8e81216cd0b9682</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(northeast)-cg-oncology/69d3c35fc8e81216cd0b9682</guid><pubDate>Mon, 06 Apr 2026 14:29:50 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$180000-250000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Sr Manager, Corporate Communications & Patient Advocacy]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">The Senior Manager, Corporate Communications and Patient Advocacy will play a central role in shaping and executing CG Oncology’s integrated communications and patient advocacy strategy as the company advances its immunotherapy platform in bladder cancer. Reporting to and partnering closely with the Vice President of Communications and Patient Advocacy, this individual will help drive communications strategy for key corporate reputation initiatives and lead campaigns that build measurable awareness of CG Oncology’s strategy, pipeline, products, and culture. This role will lead the development of differentiated narratives and content across external and internal channels, support executive visibility through thought leadership and media engagement, and help protect and strengthen CG Oncology’s reputation with patients, healthcare stakeholders, investors, and employees. The position requires strong content strategy capabilities, experience supporting patient-facing initiatives, disciplined media engagement, and digital activation expertise informed by data and emerging AI capabilities. This is a high-visibility role operating within a publicly traded, pre-commercial biotech environment and requires sound judgment, regulatory fluency, and consistent execution amid evolving business conditions.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Corporate Communications &amp; Reputation Management</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive and support communications strategy for key corporate reputation initiatives, leading campaigns that build awareness of CG Oncology’s strategy, pipeline, products, and culture among priority stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Craft differentiated narratives, messaging frameworks, and content that translate complex scientific, clinical, and corporate information into clear, audience-appropriate communications.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure consistent message implementation across programs and channels, including press, digital, social, executive communications, and internal platforms. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor news, industry trends, and public sentiment; proactively identify and help manage emerging issues to protect and strengthen company reputation </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Media Relations &amp; Executive Visibility </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support proactive and reactive media engagement efforts designed to enhance corporate reputation. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain relationships with healthcare, biotech, and business journalists and industry organizations; pitch proactive stories and manage inbound media inquiries.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support executive visibility through thought leadership initiatives, traditional and social media engagement, and speaking opportunities aligned with corporate priorities. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Content Development &amp; Channel Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, manage, and maintain corporate and public relations materials including press releases, executive presentations, talking points, Q&amp;A documents, website content, digital assets, and internal communications.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Launch and help lead new social media channels, supporting channel governance, content strategy, and ongoing optimization.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support thought leadership initiatives through short-form and long-form content tailored to investors, healthcare providers, advocacy communities, and employees.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Use internal communications to strengthen employee engagement and understanding of business priorities, strategy, and milestones. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Patient Advocacy &amp; Stakeholder Engagement</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support engagement with key advocacy stakeholders including patients, caregivers, healthcare providers, and bladder cancer advocacy organizations aligned to shared objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Contribute to building and sustaining compliant relationships with national and regional advocacy groups and support patient ambassador initiatives and advocacy-driven programs in accordance with ethical and regulatory standards. Monitor advocacy landscapes, patient sentiment, and competitor positioning within urologic oncology. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Compliance, Cross-Functional Collaboration &amp; Analytics</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure communications comply with applicable SEC regulations, Regulation FD disclosure requirements, and FDA promotional guidance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Partner closely with Legal, Regulatory, Medical Affairs, Commercial, and Investor Relations to ensure scientific accuracy, compliance, and alignment. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Leverage data analytics to measure the impact of communications strategies and campaigns; track performance metrics and support preparation of executive-level reports summarizing communication impact and program milestones. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with cross-functional leadership and agency partners to ensure message consistency, efficient resource utilization, and high-quality execution.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Own defined workstreams supporting both external and internal communications initiatives and prepare progress updates for executive leadership.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor’s degree in communications, Public Relations, Journalism, Public Health, or related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">8+ years of experience in biotechnology or pharmaceutical communications.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience within a publicly traded company and/or agency supporting biotech/pharma clients.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Direct experience developing and executing corporate communications programs. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong understanding of SEC regulations, disclosure requirements, and FDA communication guidance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Excellent written and verbal communication skills</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated ability to simplify complex scientific information for diverse audiences.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience with advocacy engagement principles and industry best practices.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven success in proactive and reactive communications execution.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience working with external agency partners.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience with vendor management including contracting</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/sr-manager-corporate-communications-and-patient-advocacy-cg-oncology/69d3c35ec8e81216cd0b9681</link><guid isPermaLink="true">http://biotechroles.com/sr-manager-corporate-communications-and-patient-advocacy-cg-oncology/69d3c35ec8e81216cd0b9681</guid><pubDate>Mon, 06 Apr 2026 14:29:49 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$140000-180000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (Mid Atlantic)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, Mid Atlantic is a remote, field-based leadership role covering the Mid Atlantic region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">Baltimore, MD/DC, Charlotte, NC, or Philadelphia, PA</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="white-space:pre-wrap;">Employee Value Proposition </strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">Join CG Oncology at a pivotal moment as the company prepares for a major oncology launch. This role offers the opportunity to shape regional strategy, influence national commercialization efforts, and build meaningful partnerships with physicians and healthcare systems treating NMIBC patients.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (Mid Atlantic) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2025 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(mid-atlantic)-cg-oncology/69d3c357c8e81216cd0b9680</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(mid-atlantic)-cg-oncology/69d3c357c8e81216cd0b9680</guid><pubDate>Mon, 06 Apr 2026 14:29:43 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$160000-220000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Regional Business Director (Great Lakes)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Regional Business Director, (Great Lakes) is a remote, field-based leadership role covering the Great Lakes region. The preferred candidate must reside within reasonable driving distance of a major metropolitan hub such as </span><b><strong style="font-size:12pt;white-space:pre-wrap;">Chicago, IL, Detroit, MI, or Indianapolis, IN</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> to support efficient access to key accounts, field team oversight, and regional travel</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">CG Oncology is seeking a high-impact Regional Business Director to lead regional commercialization efforts and drive launch excellence for Cretostimogene. This leader will build, develop, and hold accountable a high performing team of Key Account Managers to deliver regional revenue objectives and achieve incentive compensation plan targets in alignment with national strategy. The Regional Business Director operates as a regional commercial operator — accountable for sales performance, strategic account execution, cross-functional enterprise alignment, and disciplined resource stewardship. This role requires deep expertise in complex healthcare ecosystems, including IDNs, private equity-backed networks, large physician groups, and buy-and-bill environments. Reporting to the Associate Vice President of Sales, the RBD will design and execute regional business plans, mobilize enterprise stakeholders to accelerate market adoption, and ensure compliant, patient-centric commercialization. This is a critical leadership role responsible for delivering launch performance, strengthening strategic customer partnerships, and building sustainable regional growth in a high-visibility, first-commercial-launch environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="color:rgb(0,0,0);background-color:rgb(255,255,255);font-size:15pt;white-space:pre-wrap;"> </strong></b><b><strong style="font-size:15pt;white-space:pre-wrap;">Location: </strong></b><span style="white-space:pre-wrap;">Remote (Great Lakes Region) </span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Essential Functions</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">I. Commercial Performance &amp; Incentive Accountability</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve Launch Excellence as defined by the Launch Scorecard.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve or exceed annual regional sales goals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Achieve regional incentive compensation plan targets and drive balanced quota attainment across all Key Account Managers (KAMs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure disciplined execution of quarterly and annual incentive plans aligned to national strategy and ethical commercialization standards. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Monitor performance analytics, pipeline strength, and territory execution to proactively mitigate underperformance.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participate in the development and implementation of national and regional sales strategy and tactics.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform the organization of market trends, competitive intelligence, risks, and opportunities impacting launch success.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">II. Strategic Account &amp; Market Leadership </span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop, present, and execute quarterly regional business plans with clear, measurable objectives aligned to national priorities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate with HSDs to develop and execute Private Equity, IDN, VA/DoD, and Top LUGPA strategic account plans.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Align enterprise account strategies with local market execution and leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead and mobilize pull-through execution meetings with market stakeholders to ensure strategic alignment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Facilitate strategic engagement between CG Oncology ELT/senior stakeholders and key regional accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inform and influence Key Opinion Leaders (KOLs).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop customer-specific segmentation, strategic roadmaps, and account plans for all targeted accounts.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Build and maintain strong, long-term customer partnerships that drive sustainable regional growth.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">III. Talent Acquisition, Development &amp; Performance Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Recruit, hire, onboard, and develop a high-performing team of Key Account Managers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish clear roles, responsibilities, performance metrics, and expectations consistent with regional and national objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provide ongoing coaching, performance assessments, and structured feedback to optimize team effectiveness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute disciplined performance management, including differentiation of high and low performers.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead responsible compensation planning, including merit increases, salary adjustments, promotions, and incentive payout governance. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Plan and execute Regional Sales Meetings to reinforce strategy, culture, and execution discipline.</span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">IV. Cross-Functional Enterprise Collaboration</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure strong collaboration and partnership with HSDs, FAMs, Market Access, Marketing, Operations, and other enterprise stakeholders. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drive alignment between regional execution and national commercial objectives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Establish and maintain effective regional communication channels. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Influence cross-functional partners to accelerate launch adoption and remove execution barriers. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">V. Financial &amp; Operational Stewardship</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develop and manage the assigned regional operational budget.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Optimize resource allocation to maximize return on investment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain disciplined territory planning and operational execution. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensure compliance with all financial, regulatory, and company policies. </span></li></ul></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">VI. Values-Based &amp; Compliant Leadership</span></li><li style="font-size:11pt;list-style:none;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><ul data-pattern="discCircleSquare" data-depth="2" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin-left:0px;margin-right:0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:circle;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serve as a role model for compliant behavior consistent with CG Oncology’s mission, vision, and values.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Model high-touch, influential relationship management for team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Inspire and motivate individuals and teams around a shared launch vision. </span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Lead through change and ambiguity with resilience and accountability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Uphold the highest standards of ethical commercialization and patient-centric engagement.</span></li></ul></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor's Degree in related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Minimum of 10 years of pharmaceutical sales experience is necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Must be willing to travel up to 50% inclusive of overnights to meet with customers, internal stakeholders, relevant conferences, and other CG specific events.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Candidates should possess at least five years of notable experience in sales leadership.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Biotech or pharmaceutical US marketplace launch experience required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exhibit substantial expertise in overseeing and optimizing the management of regional accounts, ensuring strategic alignment and operational excellence across all levels</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated exceptional skills in achieving consensus and fostering strategic collaborations with stakeholders from multiple functions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven track record in cultivating talent and driving the professional advancement of team members through strategic mentorship and targeted development initiatives.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Demonstrated expertise in recruiting, attracting, and nurturing high-caliber sales professionals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Entrepreneurial mindset; resourceful, resilient, and motivated by working in a small-company environment with high visibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Exceptional communication and collaboration skills; able to flex between strategic framing and hands-on execution.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><u><i><b><strong style="text-decoration:underline;font-style:italic;white-space:pre-wrap;">Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.</strong></b></i></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HIGHLY COMPETITIVE SALARIES&nbsp;&nbsp;&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE/MERIT REVIEWS</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ANNUAL PERFORMANCE BONUSES</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">EQUITY</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">SPECIAL RECOGNITION</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="font-size:15pt;white-space:pre-wrap;">Well-Being Benefits</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to  meet the majority of the needs of our unique and growing workforce.&nbsp; These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Well-Being Benefits eligibility begins the 1st of the month after hire.&nbsp; While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">FULLY REMOTE WORK ENVIRONMENT</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HOLIDAYS –In 2026 we will observe 14 holidays</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">RETIREMENT – 401K with 100% company Safe Harbor match up to 4% of base salary</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH (MEDICAL, DENTAL, VISION) – PPO &amp; HDHP – Cigna/Principal</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ILLNESS &amp; DISABILITY PROTECTION – Company Paid LTD Coverage + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">LIFE INSURANCE – Company Paid 1 x base salary + Voluntary Plans</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">ADDITIONAL EXCLUSIVE BENEFITS – Voluntary Legal, Pet, Plus More</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">CG Oncology is an Equal Opportunity Employer</strong></b><span style="white-space:pre-wrap;">:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.&nbsp; At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p>]]></description><link>http://biotechroles.com/regional-business-director-(great-lakes)-cg-oncology/69d3c351c8e81216cd0b967f</link><guid isPermaLink="true">http://biotechroles.com/regional-business-director-(great-lakes)-cg-oncology/69d3c351c8e81216cd0b967f</guid><pubDate>Mon, 06 Apr 2026 14:29:37 GMT</pubDate><company>CG Oncology</company><location>Remote (United States)</location><salary>$140000-190000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Associate Director, Downstream Process Development]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Do</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serves&nbsp;as a strategic manager for the company’s downstream process development and production operations&nbsp;to drive program timelines.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Directs the strategic planning of downstream process development and manufacturing in support of all phases of clinical development including support of late clinical phase filings.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborates within cross-functional teams (Research, Development, Clinical, Quality, Regulatory), to define and execute development strategies for novel biotherapeutics and ADCs.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Leads project-specific efforts in process development, scale-up, production and tech transfer of processes within and between CMOs.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Participates in the development of RFP’s to solicit project specific bids from CMOs/CROs.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develops SOWs defining work to be performed and provide subsequent&nbsp;oversight of experiments and activities conducted at the CMO/CRO.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Develops highly productive manufacturing processes in a timely manner for novel antibody, multispecific and ADC therapeutics. Brings issues to the attention of appropriate personnel as necessary.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Designs, manages and supports process characterization studies and develops control strategies for process validation.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Authors technical documents and deliver presentations to technical and project groups.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Contributes to the preparation and submission of CMC portions of regulatory submissions and updates (IND and BLA).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Works directly with Analytic Sciences, Manufacturing Sciences and Technology and Quality teams to plan and implement execution of downstream process development and manufacturing operations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ensures that all developed processes are compatible with quality requirements including regulations, policies, applicable guidelines and procedures.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Serves&nbsp;as primary point of contact with contract manufacturing organizations (CMOs) and&nbsp;performs&nbsp;person-in-plant duties as needed to provide technical support for ongoing manufacturing.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Provides&nbsp;technical support for all CMC activities, including investigations, CAPAs, Change Controls, technology transfers, operation and lifecycle management of pre-clinical and cGMP manufacturing processes, ensuring all product delivery schedules are met.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Authors&nbsp;and reviews&nbsp;technical CMC documentation, including protocols, technical reports, manufacturing batch records, SOPs, change controls and deviations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Drives&nbsp;timely decisions and&nbsp;facilitates&nbsp;active communication and information flow between CMOs and&nbsp;Zymeworks&nbsp;team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Fosters&nbsp;strong, long-lasting cross-functional working relationships with internal and external CMC, Quality Assurance, Project Management, Clinical Operations, and external manufacturing entities to ensure successful development and manufacture of all products.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Promotes&nbsp;a culture of continuous improvement in product quality and productivity.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Works&nbsp;closely with all internal and external resources to ensure DS supply availability</span><b><strong style="font-size:13.5pt;white-space:pre-wrap;">.</strong></b></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:13.5pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Bring</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="--listitem-marker-color:black;font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">University degree&nbsp;in science or engineering and a minimum of </span><span style="color:black;white-space:pre-wrap;">8 years&nbsp;</span><span style="white-space:pre-wrap;">related experience in biopharmaceutical process development and GMP operations or an equivalent combination of education and experience.&nbsp;</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience working with contract manufacturing organizations.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team. Ability to establish and maintain effective working relationships.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Excellent organizational skills and the ability to work effectively in a high paced, fast changing environment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Consistent analytical reasoning ability.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Familiarity with QbD and Control Strategy Development or multivariate analysis and DoE approaches to process development a plus.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong background in the regulatory compliance requirements for the cGMP production of biologicals for clinical and commercial use.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Working knowledge of regulatory guidelines and expertise in CMC, PK or toxicology for the advancement of therapeutics through different phases of development.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Proficiency with cGMP and ICH guidelines.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br><span style="font-size:11pt;white-space:pre-wrap;">The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate’s location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">Our total rewards package that includes:&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Industry leading vacation and paid time off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Exceptional medical, dental and vision benefits by country</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Zymelife health and wellness benefits</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Matching RRSP / 401K / Pension program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Share Purchase Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Equity Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Paid time off to volunteer in your community</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">This role is not eligible for relocation or immigration support.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:11pt;white-space:pre-wrap;">NOTE TO AGENCIES:&nbsp;</strong></b><span style="font-size:11pt;white-space:pre-wrap;"> Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract. &nbsp;</span></p>]]></description><link>http://biotechroles.com/associate-director-downstream-process-development-zymeworks/69d3c32bc8e81216cd0b9676</link><guid isPermaLink="true">http://biotechroles.com/associate-director-downstream-process-development-zymeworks/69d3c32bc8e81216cd0b9676</guid><pubDate>Mon, 06 Apr 2026 14:28:59 GMT</pubDate><company>Zymeworks</company><location>Bellevue, WA</location><salary>$160000-220000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Senior IT Systems Administrator (G&A)]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Do</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Own and administer core G&amp;A enterprise applications, including NetSuite (ERP), Coupa (P2P), DocuSign, and other Finance, Legal, and HR systems.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Serve as the technical lead for configuration, optimization, and ongoing support of finance-related systems.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Design, build, and maintain system integrations between ERP, P2P, payroll, equity, and other internal platforms using middleware and ETL tools.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Perform hands-on configuration, workflows, role-based permissions, reporting, and system enhancements within NetSuite and related applications.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Troubleshoot complex application and integration issues across systems and vendors.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Manage system upgrades, patches, releases, and regression testing.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Develop and maintain technical documentation, data flows, and system architecture diagrams.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Support SOX ITGC controls related to financial systems, including access management, change management, and audit readiness.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Partner with Finance leadership to translate operational requirements into scalable technical solutions (without positioning as a relationship-only role).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Drive automation and process optimization across financial operations (GL, AP, procurement, reporting).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Support data extraction, transformation, and loading (ETL) processes for reporting and downstream systems.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Bring</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">8+ years of hands-on IT applications experience with strong focus on ERP and financial systems.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Deep experience with NetSuite (administration/configuration preferred).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Experience with Coupa or other P2P systems.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Strong background in system integrations and middleware platforms.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Demonstrated experience with ETL tools and financial data pipelines.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Experience supporting SOX ITGCs within ERP environments.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Experience in life sciences or regulated environments preferred.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Strong technical configuration and system administration skills (not just requirements gathering).</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Experience designing integrations across enterprise platforms.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Ability to troubleshoot system and data issues independently.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Strong understanding of financial system architecture and data structures.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Experience in high-growth environments where systems must scale quickly.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="color:rgb(22,22,22);font-size:11pt;white-space:pre-wrap;">Clear documentation and technical communication skills.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br><span style="font-size:11pt;white-space:pre-wrap;">The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate’s location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">Our total rewards package that includes:&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Industry leading vacation and paid time off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Exceptional medical, dental and vision benefits by country</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Zymelife health and wellness benefits</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Matching RRSP / 401K / Pension program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Share Purchase Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Equity Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Paid time off to volunteer in your community</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">This role is not eligible for relocation or immigration support.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:11pt;white-space:pre-wrap;">NOTE TO AGENCIES:&nbsp;</strong></b><span style="font-size:11pt;white-space:pre-wrap;"> Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract. &nbsp;</span></p>]]></description><link>http://biotechroles.com/senior-it-systems-administrator-(ganda)-zymeworks/69d3c326c8e81216cd0b9674</link><guid isPermaLink="true">http://biotechroles.com/senior-it-systems-administrator-(ganda)-zymeworks/69d3c326c8e81216cd0b9674</guid><pubDate>Mon, 06 Apr 2026 14:28:54 GMT</pubDate><company>Zymeworks</company><location>Vancouver, Canada</location><salary>$110000-150000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Investment Analyst]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Do</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Support the Investment team in managing the company’s buy-side investment pipeline, ensuring all active opportunities are tracked, organized, and progressed in a timely and disciplined manner.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Maintain and update the project database, including opportunity status, counterparty records, and transaction history, ensuring data integrity and accessibility.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Build, maintain, and refine financial models in Excel to support investment evaluation, including royalty, asset or business valuations using NPV and rNPV methodologies, deal structure modeling, and scenario and sensitivity analysis.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Conduct data analysis to support investment forecasting, competitive benchmarking, providing clear quantitative insights to inform decision-making.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Assist in conducting scientific and financial due diligence on prospective licensing and equity investment opportunities, synthesizing findings across technical, clinical, and financial dimensions to support investment decisions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Contribute to due diligence findings presentations by capturing key scientific, strategic, and financial considerations in a clear and concise format.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Develop and maintain high-quality presentation materials including investment presentations, opportunity assessments, and deal summaries to support the Investment team in internal reviews and Board-level communications.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Correspond and coordinate with relevant internal teams including Technical, Legal, Finance, and Operational as needed to support investment due diligence and transaction execution.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Monitor the competitive investment landscape, tracking deal activity, valuations, emerging platform technologies, and biotech financing trends, and compile regular briefings for the Investment team.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Assist with administrative aspects of the investment function, including scheduling, document management, and logistical coordination to support an efficient and well-organized deal process for Investment team members.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Take on additional analytical and project-based responsibilities as directed to support the growth and effectiveness of the company’s investment function.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">What You'll Bring</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">2-5 years of experience in investment banking, corporate development, private equity, venture capital, management consulting, or a comparable analytical role within life sciences or healthcare; recent graduates with exceptional academic backgrounds and relevant internship experience will also be considered.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Bachelor’s degree in a life sciences, finance, business, or quantitative discipline required.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Background in life sciences (biology, biochemistry, pharmacology, or related field) sufficient to understand the scientific and technical basis of drug development programs and investment opportunities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Exposure to equity investment, venture capital, private equity, or asset valuation processes within the biotechnology or life sciences sector is a strong asset.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Advanced financial modeling skills, including the ability to build, maintain, and interpret complex models supporting investment decisions.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Scientific literacy sufficient to critically evaluate drug development programs, understand biological mechanisms and therapeutic modalities, and engage meaningfully with R&amp;D teams during due diligence.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Strong project management skills, with demonstrated ability to manage multiple concurrent workstreams, meet deadlines, and maintain attention to detail in a fast-paced environment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Strong analytical and data analysis capabilities, with the ability to synthesize large volumes of scientific, financial, and market information into clear, actionable insights.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Excellent written and verbal communication skills, with demonstrated ability to produce clear, polished due diligence summaries, investment memos, and presentation materials for senior audiences.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Highly organized and detail-oriented, with strong project management instincts and the ability to keep multiple workstreams on track simultaneously with minimal oversight.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Collaborative and proactive communicator, comfortable coordinating with cross functional teams as needed to support investment due diligence and transaction processes.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Self-motivated with a strong work ethic and genuine intellectual curiosity about biotechnology, drug development, and the life sciences investment landscape.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Proficient with Excel, PowerPoint, and other Microsoft Office tools.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:13.5pt;white-space:pre-wrap;">Total Rewards</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br><span style="font-size:11pt;white-space:pre-wrap;">The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate’s location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">Our total rewards package that includes:&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Industry leading vacation and paid time off</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Exceptional medical, dental and vision benefits by country</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Zymelife health and wellness benefits</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Matching RRSP / 401K / Pension program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Share Purchase Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Employee Equity Program</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Paid time off to volunteer in your community</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:11pt;white-space:pre-wrap;">This role is not eligible for relocation or immigration support.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:11pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:11pt;white-space:pre-wrap;">NOTE TO AGENCIES:&nbsp;</strong></b><span style="font-size:11pt;white-space:pre-wrap;"> Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract. &nbsp;</span></p>]]></description><link>http://biotechroles.com/investment-analyst-zymeworks/69d3c31ec8e81216cd0b9671</link><guid isPermaLink="true">http://biotechroles.com/investment-analyst-zymeworks/69d3c31ec8e81216cd0b9671</guid><pubDate>Mon, 06 Apr 2026 14:28:44 GMT</pubDate><company>Zymeworks</company><location>New York, NY</location><salary>$85000-130000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Project Manager / Senior Project Manager]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;"><b><strong style="background-color:white;font-size:12pt;white-space:pre-wrap;">About Us</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;"><span style="background-color:white;font-size:12pt;white-space:pre-wrap;">Sapient is an early-stage fee for service, multi-omic contract research organization in San Diego, CA. Our focus is on accelerating drug development and transforming personalized medicine for our pharma and biotech clients. We are an agile, highly collaborative team of passionate scientists, committed to making innovations with scientific rigor, and executing in a timely manner in accordance with key regulatory standards. Combining state-of-the-art mass spectrometry technology with advanced biocomputational services and multifaceted human health data, we enable biomarker discovery at unprecedented speed and scale to provide a deeper understanding of human biology and effectively align biological targets, patients, and drug therapies in support of our clients.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><u><span style="text-decoration:underline;white-space:pre-wrap;">&nbsp;</span></u></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">About the Role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The Bioanalytical Project Manager / Senior Project Manager is responsible for the overall administration and successful delivery of projects within the Bioanalytical Laboratory for Metabolomics, Proteomics, biocomputational and mutli-omics workstreams. This includes both internal initiatives (e.g., equipment, systems, assay/panel validation) and external customer-facing qualification, validation, and sample analysis projects. This role ensures projects are delivered on time, within scope and budget, and in compliance with applicable quality and regulatory standards while meeting or exceeding customer expectations.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">The incumbent will implement and maintain robust project management and daily scheduling methodologies to optimize laboratory efficiency, proactively manage risk, and ensure high-quality execution across a fast-paced, regulated environment.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Key Responsibilities</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Project &amp; Program Management</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:7pt;white-space:pre-wrap;"> </span><span style="font-size:12pt;white-space:pre-wrap;">Oversee bioanalytical projects throughout the full lifecycle, including method development, validation, and sample analysis.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Develop, maintain, and adjust detailed project plans, schedules, and resource allocations in collaboration with Bioanalytical Principal Investigators (BPIs), Client Services, laboratory operations, and support teams.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Track and report project milestones, deliverables, budgets, and timelines; proactively identify risks and implement mitigation strategies using approved change management practices.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Monitor project progress against contractual scope, ensuring deliverables, reporting requirements, and timelines are met.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Identify changes in scope and ensure appropriate change orders are executed prior to additional work being performed.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Scheduling &amp; Resource Coordination</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Establish and communicate daily schedules for laboratory staff performing bench testing and support activities</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Continuously update schedules to address changes in resource availability, materials, or priorities.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Work closely with laboratory management to ensure appropriate staffing and resources are available to meet study timelines.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Client &amp; Stakeholder Communication</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Serve as a primary liaison between clients/sponsors and internal cross-functional teams (Business development reps, accounting, scientific staff, QC, QA, Data Management, and Study Management).</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Provide regular project status updates, forecasts, and risk communications to clients and internal leadership.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Lead and participate in client meetings, prepare agendas and meeting minutes, and ensure alignment on deliverables and expectations.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Coordinate and participate in onsite client visits as needed.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Quality, Compliance &amp; Documentation</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Perform quality reviews of project deliverables, including validation and bioanalytical reports, for completeness, accuracy, and compliance with SOPs and GxP regulations.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Review and approve analytical data, laboratory notebooks, and reports; initiate investigations and deviations as required.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Ensure adherence to Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), and applicable regulatory standards.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Ensure all project documentation is properly maintained and archived in accordance with SOPs and contractual requirements.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Process Improvement &amp; Leadership</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Lead and mentor project team members and stakeholders in the effective use of project management tools, standards, and methodologies.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Identify opportunities for process improvement to enhance efficiency, resource utilization, and on-time delivery.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Collaborate with Business Development and Finance teams to support new business opportunities, prepare quotes, and assist with invoicing, revenue recognition, and budget reconciliation.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Experience &amp; Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Bachelor’s degree in Business, Engineering, Life Sciences, Chemistry, or a related field; Master’s degree preferred.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Minimum of 3–5 years of experience managing projects in a CRO, pharmaceutical, biotechnology, or regulated bioanalytical laboratory environment.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Project management certification or completion of a recognized project management curriculum (or equivalent experience).</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Required training and hands-on experience with GLP and/or GCLP.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Experience managing projects and scheduling resources in a high-throughput, fast-paced laboratory environment.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Prior supervisory, mentoring, or team leadership experience is strongly preferred.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Knowledge, Skills &amp; Abilities</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Strong analytical and problem-solving skills with a structured, detail-oriented approach to project execution.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Working knowledge of bioanalytical assays, method development, validation, and sample analysis; familiarity with LC-MS/MS</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Intermediate knowledge of GLP/GCLP principles as applied to bioanalytical laboratories.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Excellent written, verbal, and interpersonal communication skills with the ability to communicate complex issues clearly and effectively</span><span style="font-size:7pt;white-space:pre-wrap;">.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Proven ability to lead cross-functional teams, establish accountability, and manage competing priorities.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Proficiency with MS Office (Excel, Word, PowerPoint); experience with enterprise project management and scheduling tools (e.g., MS Project, QuickBase, Smartsheet) strongly preferred.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Demonstrated professionalism, strong customer focus, and ability to work calmly and effectively under pressure.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Physical Demands</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Ability to communicate and exchange information effectively and utilize standard office equipment.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Ability to move about the office and laboratory environment as required.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Work Environment</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Primarily office-based with regular interaction with laboratory operations.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Onsite presence required as needed to support project execution and client interactions.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">--- This role offers the opportunity to work closely with scientific, operational, and client-facing teams to deliver high-impact bioanalytical projects in a regulated environment focused on quality, collaboration, and continuous improvement.</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Location</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> - San Diego, California (Sorrento Valley)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Type </strong></b><span style="font-size:12pt;white-space:pre-wrap;">-</span><b><strong style="font-size:12pt;white-space:pre-wrap;"> </strong></b><span style="font-size:12pt;white-space:pre-wrap;">Full-time,</span><b><strong style="font-size:12pt;white-space:pre-wrap;"> </strong></b><span style="font-size:12pt;white-space:pre-wrap;">On-site</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Compensation </strong></b><span style="white-space:pre-wrap;">– $85,000 – 115,000 final compensations will be based on qualification and experience)</span></p>]]></description><link>http://biotechroles.com/project-manager-senior-project-manager-sapient-bioanalytics/69d3c30ec8e81216cd0b966c</link><guid isPermaLink="true">http://biotechroles.com/project-manager-senior-project-manager-sapient-bioanalytics/69d3c30ec8e81216cd0b966c</guid><pubDate>Mon, 06 Apr 2026 14:28:29 GMT</pubDate><company>Sapient Bioanalytics</company><location>San Diego, CA</location><salary>$110000-160000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Data Scientist III]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">About The Role:</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">We are in search of a passionate Data Scientist to support Sapient’s biomarker discovery service offerings and R&amp;D effort with insights gained from analyzing clinical and multi-omics data.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">This role is within the data science team and working under the oversight and mentorship of Head of Data Science. This role will focus on solving structured biological/clinical problems and deriving insights from proteomics, metabolomics, and clinical data. The data scientist will have experiences using a variety of data mining and statistical analysis methods and platforms, building and implementing models, using and creating algorithms, and contributing to final insights on biomarker discoveries. The data scientist will work with a wide range of stakeholders and collaborate with chemists, biologists, clinicians, business associates within and outside of the Company, and will have a demonstrated ability to drive biomarker discovery with their data-based insights. This is a great opportunity to tackle a diverse set of problems while shaping the future of drug development and healthcare.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">Responsibilities:</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Work with supervision and guidance to analyze datasets, mine databases, and create code according to Company-defined good practice, to drive rigor, efficiency, and reproducibility within and across projects.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Apply statistical and machine learning methods with rigor to high-dimensional omics and clinical data, and think critically about biological/clinical questions to derive grounded and impactful insights.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Collaborate with scientists and clinicians internally and externally to investigate scientific and medical problems with rigorous analyses and critical thinking.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Communicate methods used, data insights, and scientific findings to collaborators and clients with clarity.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><b><strong style="white-space:pre-wrap;">Experience and Qualifications:</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">PhD in Biostatistics, Bioinformatics, Computational Biology, Bioengineering, Data Science, Applied Math, Physics, or Life Science related scientific field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">2+ years of hands-on experience in statistical analysis and data mining, as well as modeling and coding.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Deep knowledge and understanding of statistical methods and basic machine learning algorithms.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Life science domain knowledge and good intuition in applying appropriate data analysis approaches to best address questions given the scientific context.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Consistent use of git or other code management tools.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Proficiency in Python for product-level code development.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Strong use of clean code principles, testing principles, and understanding of CI/CD processes.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Experience with prompt engineering and major coding and scientific AI tools.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Experience with database query language (e.g. SQL) and cloud computing (e.g. AWS) is preferred.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Experience in clinical or epidemiological study data analysis is preferred.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Excellence in communicating findings by visualizing the results, composing presentation slides, and forming a scientific report.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Self-motivated, dedicated, and accountable.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Curious and eager to grow, thriving in a dynamic and intellectually challenging environment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:start;"><span style="white-space:pre-wrap;">Great team player.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Position Location – San Diego, California (Sorrento Valley)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Position Type – Full-time, on-site</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Compensation Range – $130K-$150K</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:start;"><span style="white-space:pre-wrap;">Sapient is an equal opportunity employer. We value diversity, inclusivity and belonging of all people from different cultures socioeconomic backgrounds. We do not discriminate based on race, ethnicity, gender, age, sex, disability or any other secondary biases</span></p>]]></description><link>http://biotechroles.com/data-scientist-iii-sapient-bioanalytics/69d3c309c8e81216cd0b966a</link><guid isPermaLink="true">http://biotechroles.com/data-scientist-iii-sapient-bioanalytics/69d3c309c8e81216cd0b966a</guid><pubDate>Mon, 06 Apr 2026 14:28:24 GMT</pubDate><company>Sapient Bioanalytics</company><location>San Diego, CA</location><salary>$120000-160000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Research Scientist III / Senior Research Scientist]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">About the Role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">We are in search of a Research Scientist II|/Senior Research Scientist with expertise primarily in proteomics workflows for complex matrices (e.g., biosamples) to join our interdisciplinary bioanalytical team here at Sapient. As an RSIII/SRS, you will be responsible for performing laboratory experiments such as the preparation of clinical and biological samples for global/targeted proteomics analyses using medium to high throughput liquid chromatography mass spectrometry instrumentation.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">What we’re looking for</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">For </strong></b><span style="font-size:12pt;white-space:pre-wrap;">RSIII/SRS</span><b><strong style="font-size:12pt;white-space:pre-wrap;">:</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Experience with size exclusion chromatography, nanoparticle and other proteomics enrichment preparations, BCA and SPE techniques.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Familiarity with mass spectrometry techniques (preferably untargeted LC-MS, however targeted LC-MS is also favorable) and working in a BSL2/BSL2+ environment.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Experience with custom data workflows and data analysis required (i.e., Skyline, Specronaut, mzmine)</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Bachelor's degree in biology, Biochemistry, Chemistry, or a related Life Science field and 3+ years of related work experience or a master’s degree with 1 year of related work experience.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Responsibilities/Skills</strong></b><b><strong style="white-space:pre-wrap;">&nbsp;</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Technical Duties</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Prepares samples using techniques such as size exclusion chromatography, nanoparticle enrichment and solid phase extraction</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Prepares protein samples from a wide range of specimens (e.g., cells, tissue, biofluids, recombinant proteins) for discovery and targeted proteomics analysis</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Conducts global proteome profiling by data-dependent (DDA) and data-independent (DIA) acquisition mass spectrometry, as well as experiments for post-translational modifications (e.g., phosphorylation, acetylation).</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Conducts relative and absolute quantitative analysis using Parallel Reaction Monitoring (PRM) mass spectrometry.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Uses key software tools for proteomics data analysis (e.g., Spectronaut, Skyline, MSFragger)</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Independently operates laboratory equipment and performs basic troubleshooting and routine maintenance on instruments (e.g., timsTOF Pro 2, Thermo Stellar)</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Assists with developing new methods for testing in the laboratory and maintains detailed records of development, interpretation and results.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Maintains clear and organized electronic laboratory notebook (ELN), documenting protocols, reagent preparation, and results of all experiments performed in real time.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Reviews and QCs analytical data using manual and automated pipelines and uses analytical abilities to make decisions regarding the accuracy of results.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Performs all responsibilities in adherence with regulatory principles and best laboratory practices such as GLP/GCP.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">General Duties</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">&nbsp;</span></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Performs all responsibilities in adherence with regulatory principles and best laboratory practices such as GLP/GCP.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Establishes excellent working relationships with key collaborators throughout the organization and communicates effectively through appropriate channels and tools.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Demonstrates the ability to complete projects in a communicative and timely manner under regulatory guidance.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Maintains safe and efficient procedures in the laboratory.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Supports the organization, tracking, and storing of specimens. </span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Supports management of lab consumables, including ordering, receiving, and storage of consumables.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Demonstrates the ability to learn complex tasks with instruction and to apply this to perform a variety of new techniques.</span></li><li style="font-size:7pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Other duties as assigned </span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Location</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> - San Diego, California (Sorrento Valley)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Type </strong></b><span style="font-size:12pt;white-space:pre-wrap;">-</span><b><strong style="font-size:12pt;white-space:pre-wrap;"> </strong></b><span style="font-size:12pt;white-space:pre-wrap;">Full-time,</span><b><strong style="font-size:12pt;white-space:pre-wrap;"> </strong></b><span style="font-size:12pt;white-space:pre-wrap;">On-site</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Compensation </strong></b><span style="white-space:pre-wrap;">– $85,000 – 115,000 final compensations will be based on qualification and experience)</span></p>]]></description><link>http://biotechroles.com/research-scientist-iii-senior-research-scientist-sapient-bioanalytics/69d3c302c8e81216cd0b9669</link><guid isPermaLink="true">http://biotechroles.com/research-scientist-iii-senior-research-scientist-sapient-bioanalytics/69d3c302c8e81216cd0b9669</guid><pubDate>Mon, 06 Apr 2026 14:28:18 GMT</pubDate><company>Sapient Bioanalytics</company><location>San Diego, CA</location><salary>$120000-160000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[(Director/Manager) Business Development]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">This Business Development&nbsp;role is critical to driving&nbsp;Sapient’s&nbsp;growth by&nbsp;identifying, developing, and closing new business opportunities across pharma and biotech partners.&nbsp;This individual&nbsp;serves as a trusted external representative of the organization, building deep client&nbsp;relationships&nbsp;and clearly articulating&nbsp;Sapient’s&nbsp;scientific and commercial value. Success in this role requires a passion for science, a strong understanding of complex drug development challenges, and a genuine desire to help clients answer high‑impact biological questions through innovative multi‑omic&nbsp;solutions.&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Job Description:&nbsp;</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Develop and execute plans to achieve sales targets and expand our customer base within specified key accounts and geographic markets.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Build and&nbsp;maintain&nbsp;strong, long-lasting client relationships by understanding their needs and offering tailored solutions.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Research and analyze market trends, strategic investments/partnerships, and competitor strategies to&nbsp;identify&nbsp;new business opportunities.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Prepare and deliver presentations and proposals to potential clients, effectively communicating the value proposition of our products and services.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Negotiate contracts and close agreements to maximize profits while ensuring clients' needs are met.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Collaborate with internal teams, including operations,&nbsp;marketing&nbsp;and product development, to align efforts and enhance our offerings.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Attend industry events, conferences, and trade shows to network and promote our brand.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Provide feedback and insights to the management team on market trends, customer challenges, and competitive activities.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Take an active role in support of sales process initiatives, maximizing sales effectiveness and&nbsp;assisting&nbsp;as needed in the development and mentoring of team members&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Maintain&nbsp;accurate&nbsp;records of activities, meetings, sales, and customer information within our CRM system.&nbsp;</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">&nbsp;</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Requirements:&nbsp;</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Extensive drug development commercial experience&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Deep customer relationships within pharma,&nbsp;biotech&nbsp;and emerging biopharma markets&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Demonstrated&nbsp;success in sales within the desired pharma markets in life science services or products.&nbsp;Keenly&nbsp;interested in those with multi-omic&nbsp;experience supporting metabolomics and/or proteomic services&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">High achiever who thrives working alongside other high performers&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">5 years’ prior experience preferred in pharmaceutical or biotech industries, with a preference for scientific service sales&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Excellent listening, presentation, and networking abilities&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Strong interpersonal skills for effective internal and external collaboration&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Self-motivated with a results-driven approach and proven&nbsp;track record&nbsp;of outperformance.&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Exceptional verbal and written communication skills&nbsp;</span></li><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;text-align:left;"><span style="font-size:12pt;white-space:pre-wrap;">Willingness to travel up to 50% of the time&nbsp;</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Skills Requires:</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Proven experience in&nbsp;marketing, sales support, or related field&nbsp;preferred.&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Proven knowledge of AI systems and agent training for outreach success&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Strong technical acumen with Mass&nbsp;Spectrometry, ‘omics, or both&nbsp;with specific experience in metabolomics&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Strong prospecting skills&nbsp;and&nbsp;capacity to cultivate client relationships.&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Strong communication&nbsp;skills, both written and verbal, with the ability to present complex information clearly.&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Strong understanding of market dynamics and competitive&nbsp;landscape.&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Ability to&nbsp;clearly present strategies, data, reports, etc. and&nbsp;influence stakeholders effectively.&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Familiarity with CRM software&nbsp;(Salesforce).&nbsp;</span></li></ul><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:12pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:12pt;white-space:pre-wrap;">Exceptional analytical skills with&nbsp;a keen&nbsp;attention to detail.&nbsp;</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">Experience and Education:</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="font-size:12pt;white-space:pre-wrap;">3+ years of relevant work experience in&nbsp;a technical role,&nbsp;business development, sales, sales support, or a related field, in the life sciences industry (e.g., biotechnology and/or biopharma) with prior “omics” or mass spectrometry.</span><span style="color:windowtext;background-color:rgb(255,255,255);font-size:12pt;white-space:pre-wrap;">&nbsp;</span><span style="font-size:12pt;white-space:pre-wrap;">BSc or higher&nbsp;in life&nbsp;sciences</span><span style="color:windowtext;background-color:rgb(255,255,255);font-size:12pt;white-space:pre-wrap;">&nbsp;.</span></p>]]></description><link>http://biotechroles.com/(directormanager)-business-development-sapient-bioanalytics/69d3c2fcc8e81216cd0b9667</link><guid isPermaLink="true">http://biotechroles.com/(directormanager)-business-development-sapient-bioanalytics/69d3c2fcc8e81216cd0b9667</guid><pubDate>Mon, 06 Apr 2026 14:28:11 GMT</pubDate><company>Sapient Bioanalytics</company><location>Remote (United States)</location><salary>$120000-180000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Staff Accountant / Senior Accountant]]></title><description><![CDATA[<meta><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:18pt;white-space:pre-wrap;">About the role</strong></b></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><span style="white-space:pre-wrap;">The Staff Accountant / Senior Accountant will be a core member of the accounting team and will own key operational accounting processes, including accounts payable, accounts receivable, prepaids, fixed assets, and other general accounting activities. This role is well suited for someone who thrives in a fast‑paced startup environment, works independently, and enjoys improving processes as the organization scales.</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:18pt;white-space:pre-wrap;">Key Responsibilities</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Own full‑cycle accounts payable, including processing vendor invoices and payment requests in Bill.com, managing corporate credit card transactions, and recording activity in the ERP system.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Own full‑cycle accounts receivable, including customer invoicing, cash applications, collections, and ERP posting.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Coordinate with internal stakeholders to ensure invoices and payment requests have appropriate approvals, accurately match purchase orders and receiving information, and resolve discrepancies.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Execute vendor payments, monitor due dates, and ensure timely and accurate payment processing.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Prepare and maintain account reconciliations, including bank, accounts receivable, accounts payable, fixed assets, accruals, and AP aging analysis.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Complete all assigned month‑end close activities accurately and in accordance with the close calendar and checklists.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Maintain accounting documentation and record retention in compliance with company policies and accepted accounting practices.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Collaborate effectively with accounting, finance, and cross‑functional teams.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Support audits, reviews, and other compliance activities.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Perform additional accounting and administrative duties as assigned.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:18pt;white-space:pre-wrap;">Required Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Bachelor’s degree in Accounting, Finance, or a related field.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Solid understanding of U.S. GAAP fundamentals.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Strong analytical, organizational, and problem‑solving skills.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">High attention to detail with the ability to manage multiple priorities and deadlines.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Ability to adapt to change in a scaling organizational environment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">High proficiency in Microsoft Excel, including VLOOKUPs and pivot tables.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Curious, proactive mindset with a desire to learn and improve processes.</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11.25pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:18pt;white-space:pre-wrap;">Preferred Qualifications</strong></b></p><ul data-pattern="discCircleSquare" data-depth="1" style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;"><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="white-space:pre-wrap;">Experience w</span><span style="font-size:11pt;white-space:pre-wrap;">ith NetSuite or other ERP systems and Bill.com.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">Prior experience in a startup or high‑growth company environment.</span></li><li style="font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;"><span style="font-size:11pt;white-space:pre-wrap;">CPA or interest in pursuing a CPA</span></li></ul><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Location:</strong></b><span style="font-size:11pt;white-space:pre-wrap;"> San Diego, California (Sorrento Valley)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Position Type:</strong></b><span style="font-size:11pt;white-space:pre-wrap;"> Full-time, On-site</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><b><strong style="font-size:12pt;white-space:pre-wrap;">Annual Base Compensation:</strong></b><span style="font-size:12pt;white-space:pre-wrap;"> </span><span style="font-size:11pt;white-space:pre-wrap;">$85,000 to $105,000 (final compensation will be based on qualifications and experience)</span></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p><p style="font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;"><br></p>]]></description><link>http://biotechroles.com/staff-accountant-senior-accountant-sapient-bioanalytics/69d3c2f8c8e81216cd0b9660</link><guid isPermaLink="true">http://biotechroles.com/staff-accountant-senior-accountant-sapient-bioanalytics/69d3c2f8c8e81216cd0b9660</guid><pubDate>Mon, 06 Apr 2026 14:28:07 GMT</pubDate><company>Sapient Bioanalytics</company><location>San Diego, CA</location><salary>$85000-120000</salary><type>SALARIED_FT</type></item><item><title><![CDATA[Principal Research Associate, Mass Spectrometry]]></title><description><![CDATA[<p>Our Culture: Why work with us?</p><p>At Foghorn Therapeutics, we believe in “People First, Mission Always.”</p><p>We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities. We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives.</p><p>We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of people with diseases including cancer and immune disorders.</p><p>Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop.</p><p><strong>Our Science:</strong></p><p>The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, autoimmune and inflammatory diseases, and impact millions of people. Targeting chromatin regulatory system may therefore provide innovative and potential therapeutics to treat those diseases.</p><p>Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way.</p><p><strong>Job Summary</strong></p><p>This role will support drug discovery efforts through research‑driven, MS–based analytical method development and deep scientific problem‑solving. It will contribute to advancing discovery programs through hands-on operation of instrumentation, development and execution of analytical workflows, and close collaboration with cross-functional scientists across research teams.</p><p><strong>Responsibilities</strong></p><ul><li>Perform mass spectrometry–based analyses (e.g., proteomics, intact MS) to characterize small molecules, protein interactions, and other targets relevant to drug discovery programs.</li><li>Operate, maintain, and troubleshoot analytical instrumentation, including LC-MS and related platforms.</li><li>Develop, optimize, and execute analytical methods and exploratory assays, to support compound characterization, screening activities, and project workflows.</li><li>Analyze and interpret experimental data, prepare summaries, and communicate results to cross-functional project teams.</li><li>Collaborate with scientists across chemistry, biology, and pharmacology to advance discovery programs and provide mass spectrometry expertise.</li><li>Contribute to experimental planning, documentation, reporting, and ownership of analytical workflows supporting research activities.</li></ul><p><strong>Requirements</strong></p><p><strong>Qualifications</strong></p><ul><li>Bachelor’s or Master’s degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.</li><li>3+ years of relevant laboratory experience in mass spectrometry, biochemistry, or analytical chemistry in a drug discovery, pharmaceutical, or biotechnology setting.</li><li>Experience operating LC-MS, LC-MS/MS, or related analytical instrumentation, with a strong interest in hands-on instrument operation, maintenance, and troubleshooting.</li><li>Demonstrated experience in research‑focused experimental work, such as assay development, method refinement, or troubleshooting complex datasets, beyond analytical testing.</li></ul><ul><li><strong>Preferred</strong></li><ul><li>Experience developing and optimizing LC‑MS analytical methods, including innovating new research assays, adapting techniques to novel targets, or working through complex, non‑routine analytical challenges.</li><li>Familiarity with intact MS, proteomics, or related mass spectrometry workflows.</li><li>Experience with software tools for MS data processing and analysis.</li></ul></ul><p><strong>Benefits</strong></p><p>Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:</p><ul> <li>Highly competitive and inclusive medical, dental and vision coverage options</li> <li>FSA and HSA for medical expenses and dependent care expenses</li> <li>Free premium access to fitness, nutrition, and mindfulness classes</li> <li>Unlimited paid time off policy</li> <li>Discretionary winter shut down</li> <li>Generous Paid Leave offerings, including 12 weeks of 100% paid parental leave</li> <li>Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options</li> <li>Free parking or subsidized commuter passes<br> </li> </ul><p>Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment.<br><br>Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.</p>]]></description><link>http://biotechroles.com/principal-research-associate-mass-spectrometry-foghorn-therapeutics/69d3c0f8c8e81216cd0b9576</link><guid isPermaLink="true">http://biotechroles.com/principal-research-associate-mass-spectrometry-foghorn-therapeutics/69d3c0f8c8e81216cd0b9576</guid><pubDate>Mon, 06 Apr 2026 14:19:35 GMT</pubDate><company>Foghorn Therapeutics</company><location>Watertown, United States</location><salary>$130000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Director, DMPK]]></title><description><![CDATA[<p><strong>Our Culture: Why work with us?</strong></p><p>At Foghorn Therapeutics, we believe in “People First, Mission Always.” </p><p>We put “People First” because we know our people are the key to everything we will accomplish. We value the diversity of background, ideas, perspectives and experiences that our team members bring to Foghorn Therapeutics – demonstrated by our community speaking more than 22 languages and representing over 24 nationalities. We value our teammates as people, not just as employees – validated by our actions that let our people know that we care about them, their families, and their lives. </p><p>We say “Mission Always” because we know a relentless commitment to our mission will make a difference in the lives of others. We believe our success will come from evaluating the data to follow the science. We work hard to develop a new class of therapies that could improve the lives of over 2.5 million people with cancer. </p><p>Our culture is focused on succeeding through the evaluation of data, not people. And in that, relationships can flourish and develop. </p><p><strong>Our Science:</strong></p><p>The groundbreaking science behind our therapies continues to yield vital insights into diseases that have confounded physicians and researchers. Our core scientific approach is centered on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.</p><p>Our proprietary Gene Traffic Control® platform is a powerful tool for understanding and modulating the chromatin regulatory system. We are pursuing multiple treatments for breakdowns in this system. We are the only company with the ability to study and target the chromatin regulatory system at scale, in context, and in an integrated way.</p><p><strong>The Role:</strong></p><p>This position offers an exciting opportunity to be a key part of a research and development organization that is pioneering a new class of medicines. The Director, DMPK project representative, will provide direct support to multiple project teams across the discovery and early clinical development portfolio.</p><p><strong>What you will be doing:</strong></p><ul> <li>Design and execute issue-driven ADME/PK studies to address critical discovery project needs, supporting program progression through lead optimization to early development</li> <li>Analyze and interpret preclinical ADME/PK data, communicating results and recommendations to project teams effectively</li> <li>Build and maintain strong collaborations with internal and external partners across chemistry, biology, pharmacology, CMC and other R&amp;D disciplines</li> <li>Partner with discovery and clinical groups to design preclinical studies that inform clinical dosing strategy</li> <li>Contribute to key decisions including candidate selection, development strategy, and clinical trial design</li> <li>Author and review preclinical study reports, including nonclinical toxicology, DMPK and biomarker sections of regulatory documents</li> <li>Design and interpret PK/PD, efficacy and toxicology studies in collaboration with cross-functional teams</li> <li>Stay current with DMPK scientific literature and emerging technologies to identify potential applications for ongoing programs</li> <li>Help finalize clinical study protocols and reports with focus on DMPK aspects</li> </ul><p><strong>Requirements</strong></p><p><strong>About You:</strong></p><ul> <li>PhD or equivalent in relevant field</li> <li>7+ years of experience in pharmaceutical/biotechnology setting</li> <li>Strong understanding of DMPK principles and ADME/PK assays in drug development</li> <li>Demonstrated expertise in human PK and dose projections</li> <li>Proven track record as DMPK project representative/leader on multiple project teams</li> <li>Up-to-date knowledge of regulatory guidance related to ADME/PK characterization, drug-drug interaction, and human ADME studies</li> <li>Experience with IND preparation and other regulatory documents</li> <li>Strong communication and collaboration skills with ability to effectively convey ADME/PK risks</li> <li>Experience with covalent modalities, PROTACs and parenteral delivery preferred</li> <li>Demonstrated ability to work effectively in cross-functional team environments</li> </ul><p><strong>Benefits</strong></p><ul><li><strong>Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:</strong></li><ul><li>Highly competitive and inclusive medical, dental and vision coverage options</li><ul><li>BCBS PPO and PPO HSA plans</li><li>BCBS Dental Plan</li><li>EyeMed Vision Plan</li></ul><li>FSA and HSA for medical expenses and dependent care expenses</li><li>401(k) Program via Fidelity with the company match</li><li>Corporate Wellness Program</li><li>Unlimited Paid Time Off policy</li><li>Winter shut down</li><li>12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.</li><li>Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options</li><li>Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work</li><li>Company lunches on Wednesdays</li></ul><li>Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment.<br> </li><li>Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.</li><li>Base salary range for this position: $200,000–$240,000 per year</li></ul>]]></description><link>http://biotechroles.com/director-dmpk-foghorn-therapeutics/69d3c0f4c8e81216cd0b9575</link><guid isPermaLink="true">http://biotechroles.com/director-dmpk-foghorn-therapeutics/69d3c0f4c8e81216cd0b9575</guid><pubDate>Mon, 06 Apr 2026 14:19:31 GMT</pubDate><company>Foghorn Therapeutics</company><location>Watertown, United States</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager - HRIS, Benefits & Compensation]]></title><description><![CDATA[<p>The Senior Manager, HRIS, Benefits &amp; Compensation is responsible for leading the strategy, administration, and continuous improvement of the company’s Human Resources Information Systems and employee benefits programs. This role serves as the primary owner of HR systems infrastructure and benefits operations, ensuring data integrity, system optimization, regulatory compliance, and an exceptional employee experience.</p><p>As the organization continues to scale, this role will partner closely with People &amp; Culture leadership, Finance, Payroll, IT, and external vendors to ensure HR systems and benefits programs support a growing and geographically distributed workforce.</p><p>This position combines strategic planning with hands-on operational ownership and is expected to drive process improvements, system enhancements, and data insights that support organizational growth.</p><p>This role reports to the Head of People &amp; Culture.</p><p>Open to candidates based in California or US remote.</p><p></p><h3>Key Responsibilities</h3><p><u><strong>HRIS Strategy, Governance, and System Administration</strong></u></p><p><strong>System Ownership:</strong> Serve as the primary administrator for the HRIS platform (currently ADP TotalSource) as well as the benefits (bSwift), compensation, performance review (Culture Amp), talent acquisition (Workable), learning and development platform (Veeva), and 401k platforms, overseeing configuration, integration between systems, workflows, and system settings.&nbsp;&nbsp;</p><ul><li>Continuously evaluate HR systems and benefits processes to identify opportunities for automation, efficiency, and improved employee experience.</li><li>Develop and maintain system documentation, standard operating procedures, and training resources.</li><li>Provide training and guidance to HR team members and managers on HRIS functionality and benefits processes.</li></ul><p><strong>Data Integrity &amp; Auditing:</strong> Own the accuracy of all employee transactions and system communications. Perform regular HRIS systems audits, validations, and data cleanup to ensure "audit-ready" status in alignment with internal control documents.</p><p><strong>Security &amp; Access:</strong> Manage user permissions, security roles, and system protocols to maintain data privacy and compliance.</p><p><strong>Optimization &amp; Support:</strong> Troubleshoot complex system issues, coordinate with vendor support, and stay current on new features and best practices to optimize system functionality.</p><p></p><p><u><strong>Benefits and Compensation</strong></u></p><p><strong>Benefits Oversight:</strong> Manage the full lifecycle of employee benefits programs, including open enrollment, vendor management, and ensuring seamless integration between the HRIS and external providers.</p><ul><li>Ensure compliance with all applicable federal, state, and local regulations related to benefits administration and HR data management including ERISA, ACA, HIPAA, COBRA, and state leave programs.</li><li>Maintain compliance with California-specific employment and benefits regulations including leave programs, pay transparency requirements, and reporting obligations. </li><li>Conduct audits and reporting requirements related to benefits programs.</li><li>Maintain accurate plan documentation and required regulatory filings.</li></ul><p><strong>Compensation Administration:</strong> Support the Head of People &amp; Culture in the administration of compensation structures, including base pay, bonuses, and equity.&nbsp; Responsible for carrying out year-end merit cycle.&nbsp;</p><p><strong>Market Benchmarking:</strong> Assist in conducting regular market salary surveys and benchmarking to ensure competitive and equitable pay scales.</p><p><strong>System Alignment:</strong> Ensure all compensation and benefits data is accurately reflected in the HRIS for payroll processing and financial reporting.</p><p><strong>Leave of Absence Administration:</strong> Oversee administration of employee leave programs including FMLA, CFRA, Pregnancy Disability Leave (PDL), California Paid Family Leave (PFL), ADA accommodations, and workers’ compensation coordination, partnering with third-party administrators and ensuring compliance with California and federal regulations while supporting employees and managers throughout the leave lifecycle.</p><p><strong>Employee Handbook Maintenance:</strong> Responsible for annual review and updates to employee handbook.</p><p><strong>Reporting &amp; Data Analytics</strong></p><ul><li><strong>Insight Generation:</strong> Design, build, and maintain a library of standard and ad hoc reports for People &amp; Culture, Finance, and Executive leadership.</li></ul><ul><li><strong>Advanced Analytics:</strong> Deliver custom analytics regarding employee data, turnover trends, and benefit/compensation utilization to drive data-informed decision-making.</li></ul><p><strong>Compliance Reporting: </strong>Prepare and file required compliance reports (5500s, ACA reporting, non-discrimination testing).</p><p></p><p></p><p></p><p></p><p></p><p></p><p></p><p><strong>Requirements</strong></p><p><strong>Experience:</strong> 10+ years of experience in HRIS management and benefits administration; prior experience in a "Manager" or "Lead" capacity preferred.</p><p><strong>Technical Proficiency:</strong> Advanced expertise in ADP TotalSource (or similar Tier-1 HRIS like Workday or UKG) is required.</p><p><strong>Analytical Skills:</strong> High proficiency in Microsoft Excel (VLOOKUPs, Pivot Tables, Advanced Formulas) and the ability to interpret complex datasets.</p><p><strong>Education:</strong> Bachelor’s degree in Human Resources, Business Administration, Information Technology, or a related field.</p><p><strong>Compliance Knowledge:</strong> Strong understanding of ERISA, COBRA, HIPAA, FLSA, and FMLA regulations.</p><p><strong>Preferred Qualifications</strong></p><p><strong>Certifications:</strong> SHRM-CP/SCP, PHR/SPHR, or Certified Professional in HRIS (CPHRIS).</p><p><strong>Implementation Experience:</strong> Previous experience leading or assisting in a system implementation or migration.</p><p><strong>Communication:</strong> Proven ability to translate technical system language into clear, actionable information for non-technical stakeholders.</p><p></p><p><strong>Compensation</strong></p><p>For candidates based in the SF Bay Area, the expected base salary range for this role is $170,000 - 205,000</p><p>For candidates based outside the SF Bay Area, the expected base salary range for this role is 150,000 - 180,000</p><p>The actual base pay offered will depend on factors such as experience, skills, and location. Employees in this role are also eligible to participate in our annual bonus and stock option program.</p><p></p><p><strong>Benefits</strong></p><ul><li>Comprehensive benefits package, including competitive employer premium contributions</li><li>Meaningful stock option grants</li><li>PTO, sick time, and holiday pay</li><li>Generous Parental Leave program</li><li>Pre-tax medical and dependent care programs</li><li>STD, LTD, Life and AD&amp;D</li><li>Professional development opportunities</li><li>Team-building events</li><li>Fully stocked kitchen</li><li>Fitness center at our SF office</li></ul><p></p><p>Employees (and their families) may obtain medical, dental, vision and basic life insurance benefits through the company and enroll in our company's 401k plan. Employees will also accrue vacation time off and paid sick time off and may become eligible for paid parental leave. Employees will also enjoy designated paid holidays throughout the calendar year. </p><p>Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages.</p><p>If you need assistance or an accommodation due to a disability, you may call us at +1 650-491-0272.</p><p></p>]]></description><link>http://biotechroles.com/senior-manager-hris-benefits-and-compensation-encoded-therapeutics/69d3c0efc8e81216cd0b956c</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-hris-benefits-and-compensation-encoded-therapeutics/69d3c0efc8e81216cd0b956c</guid><pubDate>Mon, 06 Apr 2026 14:19:26 GMT</pubDate><company>Encoded Therapeutics</company><location>South San Francisco, United States</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, US Medical Affairs]]></title><description><![CDATA[<p>Encoded Therapeutics is a biotechnology company combining the precision of gene regulation with the versatility of gene therapies to create breakthrough treatments for individuals living with severe genetic diseases. For more information, please visit www.Encoded.com. </p><p>Reporting to the VP Clinical/Medical Affairs, the Senior Director of US Medical Affairs is a high-impact leadership role responsible for building and executing the US Medical Affairs strategy as Encoded prepares for BLA and commercial launch. </p><p>This individual will provide critical input across the product lifecycle and must be a creative thinker capable of producing and executing rapid, high-quality strategic plans. Collaborating closely with cross-functional teams, this is a highly visible internal and externally-facing position to ensure appropriate education, insights, and launch excellence.</p><p><strong>Responsibilities:</strong></p><p><strong>US Launch Strategy &amp; Execution</strong></p><ul><li>Drive the development and execution of the integrated US Medical Affairs strategy, ensuring alignment between clinical development and commercial launch requirements.</li><li>Design US Field Medical strategy and planning, defining engagement models and territory mapping across US treatment centers, as well as performing field-based engagement and research, as needed.</li><li>Remain at the forefront of gene therapy science and the competitive landscape to inform internal strategy and external positioning. Provide clinical and competitive insights to shape launch needs and market entry.</li></ul><p><strong>External Engagement &amp; Execution</strong></p><ul><li>Cultivate and maintain deep professional relationships with US Key Opinion Leaders (KOLs), healthcare professionals, and industry experts to exchange scientific knowledge, identify clinical trial opportunities, and understand commercial needs.</li><li>Represent Encoded at major medical congresses, advisory boards, and investigator meetings, presenting complex data with clarity</li></ul><p><strong>Cross-Functional Collaboration</strong></p><ul><li>Collaborate closely with Scientific Communications to ensure medical messages, publication plans, and educational materials are scientifically rigorous and strategically aligned with US regulatory standards.</li><li>Work in lockstep with Patient Advocacy to ensure the patient voice is integrated into clinical trial design and commercial planning.</li><li>Support development of a comprehensive US HEOR and outcomes research plan to support market access, PBM negotiations, and reimbursement.</li><li>Partner with Clinical and HEOR teams to design evidence generation activities, including Investigator Sponsored Studies (ISS) and observational research to support regulatory approval and endpoint validation.</li><li>Partner with Commercial, Regulatory, and Clinical to ensure a seamless transition from development to market. </li><li>Lead US-specific initiatives, including payer/HTA research and value messaging, launch roadmaps, and center of excellence and patient journey mapping to ensure development of approaches that address the unique opportunities and challenges of gene therapy.</li><li>Develop and manage long-range budget forecasts and oversee vendors to ensure timely delivery of US medical materials.</li></ul><p></p><p><strong>Requirements</strong></p><ul><li>Educational Background: MD, PhD, PharmD or MD/PhD.</li></ul><ul><li>Experience: A minimum of 10–12 years in Medical Affairs, including at least 3–5 years specifically supporting Phase 1–3 clinical development and a proven track record in US pre-commercial planning and building US Medical Affairs functions.</li></ul><ul><li>Strong familiarity with US payer and/or PBM requirements for value demonstration and reimbursement. </li><li>Prior expertise in gene therapy (ATMPs), neuroscience (e.g., epilepsy/CNS), and/or pediatric rare diseases.</li><li>Deep understanding of FDA guidelines, OIG compliance, and US-specific requirements for scientific exchange.</li><li>Strategic thinker while maintaining tactical execution excellence; a self-starter who can produce complex plans and adapt rapidly. Exemplary organizational skills.</li><li>Exceptional ability to build collaborative partnerships in a matrixed, small-team environment, and to forge strong external relationships with external subject matter experts.</li><li>Strong skills in interpreting scientific/clinical research and translating it into actionable medical strategy to support treatment access and adoption.</li><li>Proven success in a startup environment, with the ability to build functions from the ground up and manage multiple complex projects simultaneously.</li><li>Direct experience identifying, managing, and maintaining relationships with high-performing external consultants and partner agencies.</li><li>Travel: Ability to travel up to 40%, including international trips for conferences and KOL engagements.</li></ul><p></p><p>For candidates based in the SFBA area, the salary range for this position is: $258,000 to $280,000.</p><p>For candidates based outside the SFBA area, the salary range is 233,000 to 263,000.</p><p></p><p>Encoded considers a variety of factors when determining base compensation, including experience, qualifications, internal equity and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package.</p><p><strong>Benefits</strong></p><ul><li>Comprehensive benefits package, including competitive employer premium contributions</li><li>Meaningful stock option grants</li><li>PTO, sick time, and holiday pay</li><li>Generous Parental Leave program</li><li>Pre-tax medical and dependent care programs</li><li>STD, LTD, Life and AD&amp;D</li><li>Professional development opportunities</li><li>Team-building events</li><li>Fully stocked kitchen</li><li>Fitness center at our San Francisco office</li></ul><p></p><p>Employees (and their families) may obtain medical, dental, vision and basic life insurance benefits through the company and enroll in our company's 401k plan. Employees will also accrue vacation time off and paid sick time off and may become eligible for paid parental leave. Employees will also enjoy designated paid holidays throughout the calendar year. </p><p>Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages.</p><p>If you need assistance or an accommodation due to a disability, you may call us at +1 650-491-0272.</p><p>#LI-CD</p>]]></description><link>http://biotechroles.com/senior-director-us-medical-affairs-encoded-therapeutics/69d3c0eac8e81216cd0b9569</link><guid isPermaLink="true">http://biotechroles.com/senior-director-us-medical-affairs-encoded-therapeutics/69d3c0eac8e81216cd0b9569</guid><pubDate>Mon, 06 Apr 2026 14:19:22 GMT</pubDate><company>Encoded Therapeutics</company><location>South San Francisco, United States</location><salary>$220000-300000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Global HEOR and Evidence Generation]]></title><description><![CDATA[<p>Encoded Therapeutics is a biotechnology company combining the precision of gene regulation with the versatility of gene therapies to create breakthrough treatments for individuals living with severe genetic diseases. For more information, please visit <a href="http://www.Encoded.com" rel="nofollow noreferrer noopener" class="external">www.Encoded.com</a>.</p><p>Reporting to the VP Medical Affairs, the Senior Director, Global HEOR and Evidence Generation is a senior member of the Medical and Patient Affairs (MPA) team who will serve as a critical cross-functional bridge to support regulatory and commercial evidence generation needs. This individual will be the primary architect and owner of the HEOR and value evidence strategy for ETX101, the first gene therapy for Dravet syndrome. </p><p>ETX101 is a single-administration, potentially transformative intervention. As such, this individual understands global evidence needs and will be responsible for developing a sophisticated, long-term value evidence package for global stakeholders, and for designing and implementing effective solutions that optimize value and access discussions. This is a high-impact role for an individual who thrives on translating vision into execution within a fast-evolving and innovative environment.</p><p><strong>Responsibilities:</strong></p><ul><li>Strategic planning and implementation: Define and lead the global HEOR roadmap for ETX101, ensuring that strategies drive creation of a strong value story for ETX101 to optimize payer and HTA engagement in alignment with clinical, regulatory and commercial readiness timelines and plans.</li><li>Integrated evidence generation: Serve as a key internal expert supporting design of Encoded’s clinical development program to maximize their utility both for regulatory authorities and payers. Design and execute specific studies, including burden-of-illness (BOI; clinical, humanistic, economic), real-world evidence, and patient preference studies. Support development and/or validation of clinically meaningful outcome measures. Oversee development of cost-utility analyses and budget impact modelling.</li><li>Stakeholder engagement: Partner with clinical experts, the patient community, HTA bodies/payers, and other external collaborators to disseminate accurate information across channels, including publications, congresses, and symposia.</li><li>Operational excellence: Manage vendor selection, budgets, and resource allocation for complex HEOR projects, ensuring timely completion and, in concert with Scientific Communications, high-impact delivery of abstracts, posters, and manuscripts.</li><li>Cross-functional support: Contribute to or lead other cross-functional initiatives, as needed, including Medical Affairs, Market Access and Commercial activities (e.g. payer/HTA research, value messaging, launch roadmaps, and CoE and patient journey mapping) to ensure development of innovative approaches that address the unique opportunities and challenges of gene therapy.</li><li>Travel domestically and internationally, as required.</li></ul><p><strong>Requirements</strong></p><ul><li>Education: PhD, PharmD, or MD with 10–12+ years of experience in HEOR within the biotech/pharma industry.</li></ul><ul><li>Deep technical knowledge of the unique value drivers for high-cost, one-time therapies and the global HTA landscape (e.g., ICER, NICE, G-BA, JCA).</li></ul><ul><li>Understanding of medical terminology, statistical concepts, and the ability to oversee complex observational research studies and cost-effectiveness modelling.</li><li>Exceptional written and verbal communication skills, capable of presenting technical data to payers, investors, and clinical experts.</li><li>Strong project management, and proven success managing multiple complex projects simultaneously in a fast-paced environment</li><li>Direct experience of identifying and managing consultants, agencies, or other vendors</li><li>Excellent written and verbal communication, negotiation, and presentation skills</li><li>Strong interpersonal skills and ability to communicate across all levels of the organization</li><li>Familiarity with gene therapy, rare diseases, or CNS indications preferred</li><li>Proven understanding of medical terminology and statistical concepts</li></ul><p><strong>Preferred Qualifications:</strong></p><ul><li>Proven success in a startup environment, with the ability to build functions from the ground up and manage multiple complex projects simultaneously.</li><li>Experience in rare/orphan diseases, epilepsy or CNS indications, and direct management of high-performing external consultants or agencies.</li></ul><p></p><p>For candidates based in the SFBA area, the salary range for this position is: $250,000 to $280,000.</p><p>For candidates based outside the SFBA area, the salary range is $233,000 to $263,000.</p><p>Encoded considers a variety of factors when determining base compensation, including experience, qualifications, internal equity and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package.</p><p><strong>Benefits</strong></p><ul><li>Comprehensive benefits package, including competitive employer premium contributions</li><li>Meaningful stock option grants</li><li>PTO, sick time, and holiday pay</li><li>Generous Parental Leave program</li><li>Pre-tax medical and dependent care programs</li><li>STD, LTD, Life and AD&amp;D</li><li>Professional development opportunities</li><li>Team-building events</li><li>Fully stocked kitchen</li><li>Fitness center at our SF office</li></ul><p></p><p>Employees (and their families) may obtain medical, dental, vision and basic life insurance benefits through the company and enroll in our company's 401k plan. Employees will also accrue vacation time off and paid sick time off and may become eligible for paid parental leave. Employees will also enjoy designated paid holidays throughout the calendar year. </p><p>Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages.</p><p>If you need assistance or an accommodation due to a disability, you may call us at +1 650-491-0272.</p><p>#LI-CD</p>]]></description><link>http://biotechroles.com/senior-director-global-heor-and-evidence-generation-encoded-therapeutics/69d3c0e5c8e81216cd0b9566</link><guid isPermaLink="true">http://biotechroles.com/senior-director-global-heor-and-evidence-generation-encoded-therapeutics/69d3c0e5c8e81216cd0b9566</guid><pubDate>Mon, 06 Apr 2026 14:19:16 GMT</pubDate><company>Encoded Therapeutics</company><location>South San Francisco, United States</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Health Representative - Karachi]]></title><description><![CDATA[<ul><li><p>Responsible for making professional &amp; skillful presentations to targeted doctors of his/her assigned territory for business generation.</p><p>o   Required to ensure adequate knowledge of his/her products and their competition to establish the net gains to customers/users with our products.</p><p>o   Updates doctors/chemists contact records list as &amp; when needed with the consent of his/her Health Rep Manager and maintains all call records accordingly through VeeVa/PforceRx system.</p><p>o   Prepares his/her weekly and monthly call plans and properly follows it to improve coverage of A, B &amp; C class customers as per defined KPIs.</p><p>o   Submits his/her call reports through VeeVa/PforceRx application as per scheduled time of submission of these.</p><p>o   Keep track of competitive activities in his/her geographical area and provide feedback to his/her HRM for onward communication to marketing for rebuttal strategies.</p><p></p><p><b><u>PART II: Principal Responsibilities:</u></b></p><p>o   Representative is responsible for calling on practicing physicians, hospitals, and other health-related organizations/personnel within an assigned territory.</p><p>o   Makes professional presentations using selling skills to listed doctors on the approved indications of Pfizer products with a view to increase prescriptions.</p></li><li><p></p><p> Submits reports regarding calls made to doctors and chemists to his/her Health Rep Manager through VeeVa/PforceRx application as per defined KPIs</p></li><li><p>Follows the approved tour program, makes planned calls accordingly and presents the coverage of A, B &amp; C class customers.</p></li><li><p> Adopt ethical practices while promoting his/her products to customers and the desired information should be passed on about benefits offered by the product.</p></li><li><p>Arranges Product Group Meetings with the doctors to discuss one or two products in detail.</p></li><li><p>Updates knowledge on own &amp; competitive products.</p></li><li><p>Collects and reports information on promotional and marketing moves of the competition.</p></li><li><p>Provides periodic feedback to his/her manager and the marketing group on these promotional activities.</p></li><li><p>Ensures stock availability of major promotable products at retail level in his/her territory for honoring the prescriptions generated by his/her customers.</p></li><li><p>Follows the plans to achieve assigned objectives for increased prescription flow from identified doctors and reports his/her findings periodically to his/her Health Representative Manager.</p></li><li><p>Forwards technical queries raised by his/her doctors to the Medical Division for clarification with intimation to the Health Representative Manager.</p></li><li><p>Ensures proper dressing; attire &amp; maintenance of records / detailing kit and vehicle provided to him/her.</p></li><li><p>Submits his/her expenses and leave plans as per the deadlines.</p><p></p><p><b><u>Qualification:</u></b> Science graduate, preferably Pharm D</p></li><li><p></p><p><b><u>Work Experience</u>:</b> Min 1 Year, max up to 6 years of pharmaceutical sales experience</p><p>  <br />Work Location Assignment: Remote - Field Based (Karachi)</p><p>  </p></li></ul>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;Remote - Field Based<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/health-representative-karachi-pfizer/69d3bf86c8e81216cd0b93e9</link><guid isPermaLink="true">http://biotechroles.com/health-representative-karachi-pfizer/69d3bf86c8e81216cd0b93e9</guid><pubDate>Mon, 06 Apr 2026 14:13:25 GMT</pubDate><company>Pfizer</company><location>Pakistan - Remote</location><salary>$12000-20000</salary><type>Full time</type></item><item><title><![CDATA[VR B&P Statistician]]></title><description><![CDATA[<p><b>&#xff11;&#xff0e;主な職務における成果責任/ Description of Primary Role &amp; Responsibility</b></p><p><span>ワクチンプロジェクトにおける臨床試験および承認申請資料に関する統計業務を行います。</span><br /><span>ワクチンプロジェクトに特化し&#xff0c;臨床試験の治験総括報告書を含む承認申請資料全般に関わる統計業務を提供するため、統計解析計画書の作成およびその品質管理を行います。また、統計担当者として、開発計画やプロトコール作成について統計的な助言を行います。さらに必要に応じてプログラミング業務もサポートします。</span><br /><span>グローバルワクチン・リサーチへのダイレクトレポートの特色を生かし、グローバルとのコミュニケーション&#xff08;電話&#xff0c;メール&#xff09;を活用しつつ、Development</span> <span>Japan&#xff08;DJ&#xff09;の一員として協働し業務を行います。</span></p><p></p><p><b>&#xff12;&#xff0e;応募資格/ Qualifications</b></p><p><b>【資格・能力要件/ Desired Behavioral and Technical Skills】</b></p><p>【資格・能力要件】<br /><span>英語力&#xff08;読解および文書作成&#xff1a;中級レベル、会話&#xff1a;中級レベル&#xff09;、TOEIC</span> 600点以上<br /><span>SAS/Rプログラミングスキル、生物統計トレーニング&#xff08;BioS等&#xff09;</span><br /><br />【職務経験】<br /><span>臨床開発における統計業務経験歴&#xff08;統計解析計画書作成含む&#xff09;&#xff15;年以上</span><br /><span>特にワクチンの開発経験、意欲があることが望ましい。</span></p>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;Hybrid<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>]]></description><link>http://biotechroles.com/vr-bandp-statistician-pfizer/69d3bf84c8e81216cd0b93e6</link><guid isPermaLink="true">http://biotechroles.com/vr-bandp-statistician-pfizer/69d3bf84c8e81216cd0b93e6</guid><pubDate>Mon, 06 Apr 2026 14:13:24 GMT</pubDate><company>Pfizer</company><location>Japan - Tokyo</location><salary>$110000-160000</salary><type>Full time</type></item><item><title><![CDATA[Coordenador Planejamento Financeiro | Financial Planning Coordinator (Sede: São Paulo/SP)]]></title><description><![CDATA[<h2><b>Use Your Power for Purpose</b></h2><h2>At Pfizer, we believe that every team member has the power to make a significant impact on improving patients&#39; lives. You will be at the forefront of our Finance division, driving initiatives that support our mission to deliver breakthroughs that change patients&#39; lives. Your role will be pivotal in ensuring financial accuracy and strategic planning, ultimately contributing to the well-being of patients worldwide.</h2><h2></h2><h2><b>What You Will Achieve</b></h2><h2>In this role, you will:</h2><ul><li><h2>Manage projects and set objectives, leading people, technology, and financial resources.</h2></li><li><h2>Identify and implement potential improvements in processes, develop innovative concepts, and take calculated risks to achieve desired results.</h2></li><li><h2>Create opportunities for colleagues and manage the performance of both direct and indirect reports.</h2></li><li><h2>Coordinate the completion of standard and ad hoc Finance requests, lead cross-business unit continuous improvement projects, and assist in delivering complex analysis and reporting requests.</h2></li><li><h2>Review financial reports and analyses for completeness and accuracy, lead and participate in meetings and cross-functional projects with finance colleagues.</h2></li><li><h2>Support the migration of management reports related to integration activities.</h2></li></ul><h2></h2><h2><b>Here Is What You Need </b>(Minimum Requirements)</h2><ul><li><h2>High school diploma (or equivalent) with 8&#43; years of experience or associate’s degree with 6&#43; years of experience or BA/BS with 2&#43; years of experience or MBA/MS with any years of relevant experience  </h2></li><li><h2>Proficiency in Microsoft Office Suite, and skilled in data manipulation and financial systems</h2></li><li><h2>Strong analytical skills with the ability to interpret complex financial data</h2></li><li><h2>Excellent communication skills, both written and verbal</h2></li><li><h2>Proven ability to manage multiple projects and meet deadlines</h2></li><li><h2>Experience in leading and developing teams</h2></li></ul><h2></h2><h2><b>Bonus Points If You Have </b>(Preferred Requirements)</h2><ul><li><h2>Demonstrated expertise in Commercial and/or operational Financial Planning &amp; Analysis, including management reporting, analysis, planning, budgeting, and forecasting</h2></li><li><h2>Familiarity with Generally Accepted Accounting Principles (GAAP) and International Financial Reporting Standards (IFRS) is essential</h2></li><li><h2>Proven experience in Management Reporting &amp; Analysis</h2></li><li><h2>Prior experience with financial systems like SAP BI and Hyperion Planning</h2></li><li><h2>Strong leadership skills with the ability to influence and motivate others</h2></li><li><h2>Excellent problem-solving skills with a proactive approach to identifying and implementing solutions</h2></li><li><h2>Ability to work collaboratively with cross-functional teams</h2></li><li><h2>Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use</h2></li></ul><h2>  </h2><h2><b>Other Job Details</b></h2><ul><li><h2><span>Work Location Assignment: On-site 2-3x/week or as needed by the business</span></h2></li><li><h2><span>Last day to apply for job: April 17, 2026</span></h2></li></ul><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p><p style="text-align:left"><b>EEO (Equal Employment Opportunity) &amp; Employment Eligibility </b></p><p style="text-align:inherit"></p><p style="text-align:left">Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.</p>Finance &amp; Accounting<p style="text-align:inherit"></p><p style="text-align:inherit"></p>]]></description><link>http://biotechroles.com/coordenador-planejamento-financeiro-or-financial-planning-coordinator-sede-sao-paulosp-pfizer/69d3bf81c8e81216cd0b93e3</link><guid isPermaLink="true">http://biotechroles.com/coordenador-planejamento-financeiro-or-financial-planning-coordinator-sede-sao-paulosp-pfizer/69d3bf81c8e81216cd0b93e3</guid><pubDate>Mon, 06 Apr 2026 14:13:21 GMT</pubDate><company>Pfizer</company><location>Brazil - São Paulo</location><salary>$45000-75000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Manager Training Compliance]]></title><description><![CDATA[<p>The Senior Manager, Training Compliance provides leadership and oversight of training compliance for the Vaccines organization, ensuring colleagues, contractors, and external partners maintain compliant, accurate, and inspection ready training records. This role serves as the Vaccines training compliance subject matter expert, overseeing and designing role-based curricula, learning management (LMS/PLA) governance, on-the-job (OJT) and retraining frameworks, management of a train the trainer function, and training documentation standards, reporting to Director of Quality Records and Training Compliance.</p><p></p><p>The Senior Manager partners closely with QIDO QA, Quality, and business stakeholders to drive standardization, continuous improvement, and sustained inspection readiness.</p><p></p><p><b>Key Responsibilities:</b></p><ul><li><p>Lead Vaccines training compliance strategy in alignment with Vaccines SOPs, enterprise quality systems, and GxP requirements (namely GCLP, GLP, GCP).</p></li><li><p>Defines and drives the Vaccines Train‑the‑Trainer strategy, partnering with Quality and business stakeholders to ensure qualified trainers, standardized delivery, and sustained inspection readiness.</p></li><li><p>Govern role-based curricula, job roles, training documentation, OJT, retraining, and training waivers across Vaccines.</p></li><li><p>Serve as SME for Vaccines training compliance processes, including PLA administration, curricula management, and training record archival.</p></li><li><p>Partner with Quality and business stakeholders to assess procedural changes, manage compliance impact, and implement scalable solutions.</p></li><li><p>Drive continuous improvement and standardization of Vaccines training compliance processes and tools.</p></li><li><p>Lead and develop Training Compliance staff within QRT; provide escalation support for complex compliance issues.</p></li><li><p>Monitor training compliance risks and trends; lead corrective and preventive actions as needed.</p></li><li><p>Large scale innovative projects, like adoption of electronic systems for OJT and similar manual functions.</p></li><li><p>Communicate training compliance status, risks, and expectations to Vaccines leadership and stakeholders.</p></li></ul><p></p><p><b>Education &amp; Experience:</b></p><ul><li><p>Bachelor’s degree in life sciences, quality, education, technology, or related discipline and 6&#43; years’ experience OR MS with 5&#43; years’ experience</p></li><li><p>Extensive experience in training compliance or quality systems within a regulated pharma/biotech environment.</p></li><li><p>Hands-on experience with LMS platforms (e.g., PLA), role-based curricula, and training governance.</p></li><li><p>Experience supporting audits, inspections, and cross functional initiatives.</p></li></ul><p></p><p><b>Skills &amp; Competencies</b></p><ul><li><p>Strong GxP training and compliance expertise</p></li><li><p>Proven people leadership and stakeholder influence</p></li><li><p>Clear, effective written and verbal communication</p></li><li><p>Analytical, risk based decision making</p></li><li><p>Ability to manage complexity and drive standardization across Vaccines</p></li></ul><p>  <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.<br /> </p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p></p><p>Office based</p><p><br />Work Location Assignment:  <span><b>This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week or more as needed.</b></span></p>&amp;#xa;The annual base salary for this position ranges from $124,400.00 to $207,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States.</span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Quality Assurance and Control&amp;#xa;]]></description><link>http://biotechroles.com/sr-manager-training-compliance-pfizer/69d3bf80c8e81216cd0b93e2</link><guid isPermaLink="true">http://biotechroles.com/sr-manager-training-compliance-pfizer/69d3bf80c8e81216cd0b93e2</guid><pubDate>Mon, 06 Apr 2026 14:13:20 GMT</pubDate><company>Pfizer</company><location>United States - New York - Pearl River</location><salary>$130000-170000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Institutional Customer Marketing, Platforms, Portfolio & Brand]]></title><description><![CDATA[<p><b>What You Will Achieve</b></p><p></p><p>The US Commercial organization, which is in the Global Hospital &amp; Biosimilars organization, is comprised of over 200 products, spanning more than 10 therapeutic areas, with annual revenue of over $2.5B.</p><p></p><p>The Senior Manager, Institutional Customer Marketing, is responsible for execution of marketing tactics for the U.S. Hospital &amp; Biosimilar portfolio. In this role, the colleague will support the Directors of Customer Marketing (Brands, Platforms and Portfolio) and partner with internal and agency partners to create and maintain product sales and marketing assets and digital platforms that effectively reach and drive awareness among key sterile injectable, biosimilar and surgical customer audiences including hospital clinicians/pharmacy, Group Purchasing Organizations (GPOs) and Integrated Delivery Networks (IDNs). This role is part of the US Hospital Marketing and Communications Team, which supports the promotional marketing and customer communications strategy and implementation for the US Hospital &amp; Biosimilar business. </p><p></p><p>The role will involve working cross functionally with key stakeholders in Portfolio, Sales, Account Management, Medical, Legal, Regulatory and PGS, among others, internal marketing team members, and external agency partners.</p><p></p><p>The Senior Manager, Institutional Customer Marketing, Platforms &amp; Brands, reports directly to the Customer Marketing and Communications Lead.</p><p></p><p><b>How You Will Achieve It </b></p><ul><li><p>This role will be responsible for driving tactical implementation and execution of marketing strategy throughout the Hospital and Biosimilar portfolio.</p></li><li><p>Lead the development of sales tools and marketing assets—including Digital Sales Presentations (DSPs), Rep-Triggered Emails (RTEs), HQ Emails, Print Leave-Behinds, Digital Ads, and more.</p></li><li><p>Manage marketing development and approval processes and timelines, working closely with external agency partners and internal reviewers.</p></li><li><p>Maintain and update content on Pfizer Hospital website, in partnership with agency and Pfizer development partners.</p></li><li><p>Manage print resource utilization and distribution to support field force needs.</p></li><li><p>Prepare field force implementation guides and related resources to support customer-facing colleague use of marketing assets.</p></li><li><p>Monitor marketing tactical performance. Regularly solicit qualitative field force, customer and other key stakeholder input on marketing materials alongside quantitative key trends including utilization, customer engagement data, and industry/competitive trends to identify continuous improvement and optimization opportunities.</p></li><li><p>Monitor Pfizer Digital Readiness Team (DRT) Guidelines to ensure that all sterile injectable digital assets are compliant with the latest guidelines. Coordinate with Regulatory on required updates, as needed.</p></li><li><p>In collaboration with Medical colleagues, monitor USPI label changes and ensure appropriate and compliant updates to marketing resources on an as needed basis.</p></li><li><p>Support development of marketing strategies and product launch plans, leveraging effective omnichannel approaches to drive effective customer communication and engagement, in partnership with Director, Institutional Customer Marketing, Platforms and Director, Institutional Customer Marketing, Brands.</p></li><li><p>Support content development at relevant sterile injectables conventions and congresses.</p></li><li><p>Collaborate with Marketing and Communication colleagues to drive adoption of implementation of omnichannel marketing best practices and CMO standards (Adobe AEM, Adobe Franklin, etc.)</p></li><li><p>Effectively partner with Marketing and Communications colleagues to drive internal awareness and utilization of marketing assets and ensure effective and complementary customer communication regarding platform and brand product availability and supply status.</p></li></ul><p></p><p><b>Here Is What You Need (Basic Requirements)</b></p><ul><li><p>Undergraduate degree in marketing, business, or related area.</p></li><li><p>7&#43; years’ experience in pharmaceutical marketing and/or sales.</p></li></ul><p></p><p><b>Bonus Points If You Have (Preferred Requirments)</b></p><ul><li><p>Experience developing marketing assets and content; website management or development experience preferred.</p></li><li><p>Strong project management experience; track record of reliable and timely marketing planning and execution. </p></li><li><p>Demonstrated understanding of how marketing strategy and tactics advance business results.</p></li><li><p>Overall marketing skills including marketing strategy; customer targeting; tactical planning; marketing piece creation; digital advertising and social media; measurement and reporting. Experience working with agency partners preferred.</p></li><li><p>Strong knowledge of healthcare and biopharmaceuticals industries.Preferred knowledge of hospital generics / sterile injectables market. Preferred experience supporting sales teams (knowledge of sales tools, sales cycle, customer profiles, etc.).</p></li><li><p>Proven ability to work effectively and inclusively in teams with diverse internal and external stakeholders, including senior leaders; influence, negotiation and stakeholder management skills.</p></li><li><p>Excellent written and oral communications skills, including presentation/PowerPoint skills.</p></li><li><p>Able to work to tight deadlines, manage multiple projects at once and maintain professionalism under pressure.</p></li><li><p>Proactive self-starter, and able to work independently. Team player. Entrepreneurial mindset.</p></li><li><p>Sterile Injectable, Surgical and/or Biosimilar experience preferred</p></li></ul><ul><li><p>MBA preferred.</p></li></ul><p> <br />Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.</p><p><br />Work Location Assignment: Hybrid</p><p><b>Last Date To Apply: </b>April 13, 2026</p>&amp;#xa;The annual base salary for this position ranges from $124,400.00 to $207,400.00.* In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;* The annual base salary for this position in Tampa, FL ranges from $111,900.00 to $186,500.00.&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Marketing and Market Research&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-institutional-customer-marketing-platforms-portfolio-and-brand-pfizer/69d3bf7fc8e81216cd0b93e1</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-institutional-customer-marketing-platforms-portfolio-and-brand-pfizer/69d3bf7fc8e81216cd0b93e1</guid><pubDate>Mon, 06 Apr 2026 14:13:19 GMT</pubDate><company>Pfizer</company><location>United States - New York - New York City</location><salary>$150000-220000</salary><type>Full time</type></item><item><title><![CDATA[Senior Manager, Document Quality Reviewer, Vaccines]]></title><description><![CDATA[<p><b>Why Patients Need You</b></p><p>Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.</p><p></p><p><b>What You Will Achieve</b></p><p>As a <b>Senior Manager, Document Quality Reviewer</b>, you will manage projects and conduct document quality review (DQR) on the clinical components of documents authored by Vaccine Clinical Research (VCR) across VCR global sites.  DQR includes clinical data checking/consistency checking, clinical editing, checking for uniformity and compliance with Pfizer and clinical guidelines.  Day-to-day goals and priorities are guided by Vaccine Clinical Research objectives and priorities.</p><p></p><p><b>How You Will Achieve It</b></p><ul><li><p>Independently performs DQR of clinical components of assigned documents (e.g., protocols, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, etc.).  Formally documents quality review findings for assigned documents.  Identifies and immediately escalates any significant findings. </p></li><li><p>Participates in resolution of findings with the document authors, clinicians and other team members, if necessary. </p></li><li><p>Manages DQR document archival processes and procedures.</p></li><li><p>Independently produces style guides, manuals, and quality review work guides for Vaccine programs and documents, coordinating agreement on style issues within and across projects.</p></li><li><p>Leads and/or manages the completion of complex tasks by applying technical skills and specialized knowledge to communicate initial findings.</p></li><li><p>Analyzes DQR findings to identify root causes of errors and discrepancies and participate in corrective action planning.  Leads the compilation and analysis of data quality metrics to ensure consistency of reviews.</p></li><li><p>As Subject Matter Expert (SME) of DQR/QC of clinical documents, leads quality activities, setting the standard for enhanced collaboration, delivery of project commitments, and customer satisfaction.</p></li><li><p>Participates on project teams, task forces, and/or working groups and develops recommendations for cross-Pfizer processes to ensure alignment with quality goals and other groups performing the same function.</p></li><li><p>Evaluates routine processes and procedures to identify areas that can be eliminated or streamlined. Makes recommendations on process improvements that could reduce recurring errors in documents.  </p></li></ul><p></p><p><b>Basic Qualifications</b><br /> </p><ul><li><p>BS/BA degree (preferably in English/journalism/communications or biological science). </p></li><li><p>7&#43; years of experience in medical writing and/or DQR/QC of clinical documents in the pharmaceutical/healthcare industry. </p></li><li><p>A thorough understanding of scientific principles, knowledge of medical terminology and familiarity with the AMA Manual.</p></li><li><p>The ability to edit for clarity is required, as are strong verbal, written, and interpersonal communication skills, and the ability to pay rigorous attention to detail while working rapidly and accurately. </p></li></ul><p></p><p><b>Preferred Qualifications</b></p><ul><li><p>An advanced degree with relevant medical editing or document quality review experience is preferred.</p></li><li><p>Prior experience preparing clinical regulatory documents in a clinical setting, at a pharmaceutical company, or at a CRO is helpful.</p></li></ul><p></p><p><b>Technical Skills</b></p><ul><li><p>Analytical skills and statistical aptitude</p></li><li><p>Clinical knowledge and expertise</p></li><li><p>Editing skills</p></li><li><p>Project and process management</p></li><li><p>Quality review skills</p></li><li><p>Strategic thinking</p></li><li><p>Technical learning</p></li><li><p>Priority setting</p></li><li><p>Problem solving</p></li></ul><p></p><p><b>PHYSICAL/MENTAL REQUIREMENTS</b></p><p>Work is performed at a desk, primarily with laptop, monitor, and keyboard. </p><p></p><p><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS </b></p><p>Work schedule is a 40-hour week during core business hours, Monday through Friday.  Project priorities occasionally necessitate work beyond regular work hours, including evenings and weekends.  </p><p>  <br />Work Location Assignment: Remote</p>&amp;#xa;The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.  Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.&amp;#xa;&amp;#xa;&amp;#xa;&amp;#xa;<p style="text-align:left">Relocation assistance may be available based on business needs and/or eligibility.</p>&amp;#xa;<p>Candidates must be authorized to be employed in the U.S. by any employer.</p><p>U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.</p>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>Sunshine Act</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.</span></span></span></p></div></div></div></div></div></div></div></div>&amp;#xa;<div><div><div><div><div><div><div><div><p style="text-align:left"><span><span><span><b>EEO &amp; Employment Eligibility</b></span></span></span></p><p style="text-align:left"><span><span><span>Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  This position requires permanent work authorization in the United States. </span></span></span></p><p style="text-align:inherit"></p><p style="text-align:left"><span>Pfizer endeavors to make<span> </span></span><a href="http://www.pfizer.com/careers" target="_blank"><span><span class="WKM0">www.pfizer.com/careers</span></span></a><span><span> </span>accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email<span> </span></span><a href="mailto:disabilityrecruitment&#64;pfizer.com" target="_blank"><span><span class="WKM0">disabilityrecruitment&#64;pfizer.com</span></span></a><span>. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.</span></p></div></div></div></div></div></div></div></div>&amp;#xa;Medical&amp;#xa;]]></description><link>http://biotechroles.com/senior-manager-document-quality-reviewer-vaccines-pfizer/69d3bf7ec8e81216cd0b93df</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-document-quality-reviewer-vaccines-pfizer/69d3bf7ec8e81216cd0b93df</guid><pubDate>Mon, 06 Apr 2026 14:13:17 GMT</pubDate><company>Pfizer</company><location>United States - Pennsylvania - Collegeville</location><salary>$130000-170000</salary><type>Full time</type></item><item><title><![CDATA[Health Representative Oncology]]></title><description><![CDATA[<p><b>Health Representative- (Riyadh ) </b></p><p>Oncology Team</p><p></p><p><b>Position Summary:</b></p><p>Responsible for maximizing Pfizer brand growth through the different promotional activities and being a business enabler through becoming a territory owner within certain geography.</p><p></p><p><b>Primary Tasks</b></p><p><b>Product Promotion:</b></p><p>Promote products to designated customers in order to achieve territory plan</p><p>objectives Implement value added programs across the territory</p><p></p><p><b>Key Activities:</b></p><ul><li>Visiting physicians to promote Pfizer products</li><li>Conducting marketing activities/literatures to HCPs.</li><li>Providing approved information to HCPs on Pfizer products</li><li>Reporting visits and other activities using proper channels.</li></ul><p></p><p><b>Customer Relations:</b></p><ul><li>Build relationships with target customers to enhance territory knowledge</li><li>Ensure that accurate, timely and relevant customer knowledge is captured and shared with colleagues using agreed processes e.g. VCC, RTEs &amp; F2F visits.</li><li>Segment and target high potential customers.</li><li>Visiting physicians with focus on target KOL and selected physicians in a given geography to promote Pfizer products and build strong relationship with them.</li><li>Providing feedback to manager on customer requests, responses to promotions and product access and competitive activities.</li></ul><p></p><p><b>Territory Planning &amp; Management:</b></p><ul><li>Diagnosis of the territory situation e.g. local market drivers and initiatives leading to subsequent design and implementation of territory action plan to achieve business objectives.</li><li>Develop and execute territory business plan.</li><li>Involved in Pfizer community awareness programs</li><li>Attending seminars and participate in setting up promotional demonstrations and exhibitions</li><li>Organizing AV activities in his/her area, Initiate &amp; Participate in the nomination and selection of the local speakers in his/her territory</li><li>Preparing POA for his/ her territory and products.</li><li>Presenting reports according to Management recommendations and market needs.</li><li>Planning and organizing regular value-added programs.</li></ul><p></p><p><b>Market Intelligence:</b></p><p>Feedback to Team, Managers &amp; cross functions colleagues of relevant competitor ctivity or local issues to ensure appropriate actions</p><p></p><p><b>Teamwork:</b></p><p>Liaise with team members to share information, motivate and support team</p><p>members and therefore contribute to the generation and delivery of the territory</p><p>plan.</p><p></p><p><b>Administrative Systems</b>:</p><ul><li>Ensure territory and administrative systems/processes are maintained and updated to ensure an accurate record of territory is always available.</li><li>Timely update of records and systems</li><li>Produce reports, as requested by managers</li><li>Understand and work in compliance with company’s SOPs</li></ul><p></p><p><b>Self Development:</b></p><ul><li>Proactively implement/update personal development plans in order to develop self within current role</li><li>Actively seek feedback</li><li>Develop, own and implement IDP</li></ul><p></p><p><b>Additional Assignments:</b></p><p>As agreed with line manager, undertake additional assignments, ensuring</p><p>objectives are met and outputs delivered to the brief given</p><p></p><p><b>Criteria for applying:</b></p><ul><li>Holding of Bachelor Degree in Pharma</li><li>Experience as a Medical Representative in a multinational organization is a plus</li><li>Experience in Oncology therapeutic area is a plus</li><li>Good command of English language, speaking, writing, listening and pronunciation</li><li>Example of living Pfizer Values &amp; core competencies:</li><li>Change Agile</li><li>Acts Decisively</li><li>Peer relationship</li><li>Seizes Accountability</li><li>Commits to one Pfizer</li><li>Grows Self</li></ul><p>  </p><p></p><p>#LI-PFE</p>  <br />Work Location Assignment: On Premise<br />&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/health-representative-oncology-pfizer/69d3bf7dc8e81216cd0b93de</link><guid isPermaLink="true">http://biotechroles.com/health-representative-oncology-pfizer/69d3bf7dc8e81216cd0b93de</guid><pubDate>Mon, 06 Apr 2026 14:13:17 GMT</pubDate><company>Pfizer</company><location>Saudi Arabia - Riyadh</location><salary>$45000-65000</salary><type>Full time</type></item><item><title><![CDATA[Area Medical Advisor]]></title><description><![CDATA[<p><b>Job Purpose</b></p><ul><li><p>Provide scientific expertise, build knowledge and activity based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer’s image in the scientific community.</p></li><li><p>To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors.</p></li><li><p>To provide high quality and timely service in the areas of Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training,  and business support in the areas of New Product Development, Regulatory Affairs, Quality Standards, and Business Technology</p></li></ul><p>The role will act as a critical interface with identified scientific leaders and will build regional, national or international relationships to contribute to understanding of diseases, research and scientific trends, clinical practice guidelines, treatment patterns in areas relevant to our business.</p><p></p><p><b>Position Responsibilities</b></p><p></p><p>Strategic/Policy</p><ul><li><p>With support from the mentor or Line manager, provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed</p></li></ul><p>Operational</p><ul><li><p>Key Opinion Leader / Key Organization Engagement</p></li></ul><ul><li><p>KOLs include generalists, specialists and superspecialists as well as non-traditional external stakeholders such as hospital administrators, govt. health authorities (state and national health programs)</p></li><li><p>Work in alignment with the concerned medical affairs colleagues to support them in implementing the medical activities relevant to the brand plan strategies for specific products and therapy areas as appropriate.</p></li><li><p>Develop and customize presentations when required and relevant to specific programs/regional requests from KOLs. Ensure approval by concerned Medical Advisor before roll out of the same.</p></li><li><p>Work closely with Regional Business Manager, District Managers and PSO’s to identify and establish relationships with key opinion leaders/organizations in select therapeutic area within the region to support their clinical and research activities by understanding their needs and offering appropriate research projects, continuing medical education programs, clinical/educational grants.</p></li><li><p>Participate/facilitate/conduct customized promotional/educational interactions with Health Care Professionals (HCPs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, etc, by working in close coordination with Therapy Area Specialists and PSOs (as applicable).</p></li><li><p>Focus on stage shifting for KOLs (Stage I: Initiate, Stage II: Develop, Stage III: Partner, Stage IV: Impact) numbers as mentioned in the BU specific objectives.</p></li></ul><ul><li><p>Clinical Research:</p></li></ul><ul><li><p>Support efforts to identify new investigators and institutions for Clinical Research in order to expand research base.</p></li><li><p>Provide medical support for local studies on request from clinical operations, including need-based visits to study sites</p></li><li><p>Assist in review/interpret data generated; Assist in writing final reports for locally sponsored studies as required</p></li><li><p>Develop and execute publication plan; assist in review/write manuscripts for publication of locally sponsored studies</p></li><li><p>Develop and execute Information Dissemination Plan/Program</p></li></ul><ul><li><p>Business (Marketing and Sales) Support:</p></li></ul><ul><li><p>Facilitate Marketing/Sales Force access to KOLs where appropriate.</p></li><li><p>Support / Lead marketing and sales initiated projects that align with therapeutic area requirements and involve KOLs in the region</p></li><li><p>Provide scientific and medical support to institutional sales initiatives.</p></li><li><p>Field medical support for various access initiatives</p></li></ul><ul><li><p>Medical Initiatives:</p></li></ul><ul><li><p>Participate in and provide medical inputs for key opinion leader meetings / advisory boards, Customer Launch Meeting (CLMs).</p></li><li><p>Driving adult vaccination stewardship (AVS) at the hospitals</p></li><li><p>Conduct/facilitate round table meetings/group discussions in coordination with concerned medical advisor for assigned therapy area/product as appropriate.</p></li><li><p>Conduct CMEs as a speaker/moderator for assigned therapy area as per requirement and in coordination with the concerned medical advisor.</p></li></ul><ul><li><p>Medical Information:</p></li></ul><ul><li><p>Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies</p></li></ul><ul><li><p>Sales Force Training:</p></li></ul><ul><li><p>Provide medical training to new sales staff on basic sciences/assigned Therapy Areas/assigned products.</p></li><li><p>Provide refresher training to sales staff through ongoing training initiatives.</p></li><li><p>Assist in pre-launch and launch training to sales staff for new products.</p></li></ul><ul><li><p>Technology</p></li></ul><ul><li><p>Liaison with the Business Technology functions in areas such as databases, websites, interactive systems, product and health information, etc.</p></li><li><p>Identify technology solutions for enabling better information availability</p></li></ul><ul><li><p>Values and Behaviors:</p></li></ul><p>Consistently adhere to/demonstrate all Pfizer Values/Leader Behaviors, with special focus on excellence, equity, courage and joy. Work in harmony with internal and external stakeholders.</p><p> <br />Work Location Assignment: Remote - Field Based</p><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>]]></description><link>http://biotechroles.com/area-medical-advisor-pfizer/69d3bf7bc8e81216cd0b93dd</link><guid isPermaLink="true">http://biotechroles.com/area-medical-advisor-pfizer/69d3bf7bc8e81216cd0b93dd</guid><pubDate>Mon, 06 Apr 2026 14:13:15 GMT</pubDate><company>Pfizer</company><location>India - Mumbai</location><salary>$80000-150000</salary><type>Full time</type></item><item><title><![CDATA[Heathcare Executive]]></title><description><![CDATA[<p><b><span style="font-size:inherit">Strategic/ Policy</span></b></p><ul><li><p><span style="font-size:inherit">Ensure achievement of Sales budgets for the assigned geographical territory</span></p></li><li><p><span style="font-size:inherit">Develop a clear understanding of his/her role as a responsible Officer of the Company and apply the knowledge, experience and skills to achieve the defined objectives for the position and the team.   </span></p></li><li><p><span style="font-size:inherit">Review and discuss his/her plans for the achievement of territory’s sales budget each month (overall and product wise). Seek the assistance of the District Manager in formulating sales strategy.</span></p></li><li><p><span style="font-size:inherit">Conduct sales analytics to identify areas / stakeholders to be focused upon for driving business growth in the territory</span></p></li><li><p><span style="font-size:inherit">Provide inputs to the District Manager to help him validate the sales forecast or the rolling sales plan as per the defined frequency</span></p></li><li><p><span style="font-size:inherit">Provide inputs to the District Manager to help him manage salvage net to maintain it at an acceptable level</span></p></li><li><p><span style="font-size:inherit">Jointly with the District Manager, classify the medical practitioners in his/her territory in three categories A, B and C in the descending order of importance, A being the most important and C the least.</span></p></li><li><p><span style="font-size:inherit">Schedule the frequency of calls on the doctors depending on their criticality with respect to achievement of the sales targets for the district</span></p></li><li><p><span style="font-size:inherit">Deliver promotional messages tailored to each customer’s need so as to maximize sales</span></p></li><li><p><span style="font-size:inherit">Strictly adhere to coverage plans and frequency</span></p></li><li><p><span style="font-size:inherit">Strictly adhere to all applicable Pfizer policies and procedures. </span></p></li></ul><p> </p><p><b><span style="font-size:inherit">Operational / Process</span></b></p><ul><li><p><span style="font-size:inherit">Regularly visit chemists in the area to ensure sale of Pfizer’s products, collect information on the sales of competitor’s products and regularly update the team about this data</span></p></li><li><p><span style="font-size:inherit">Stay updated on the competitors’ activities through personal visits to wholesalers and retailers. Maintain regular contacts with medical practitioners, consultants, chemists and wholesalers.</span></p></li><li><p><span style="font-size:inherit">Book orders from the retailers to ensure adequate availability of products to meet the market demand. Also, ensure display of point-of-sale promotion material display in retailers’ stores in line with the promotion plan</span></p></li><li><p><span style="font-size:inherit">Ensure thorough pre-call planning and ask for the assistance of the District Manager wherever necessary.</span></p></li><li><p><span style="font-size:inherit">Prepare and implement special schedule for doctors’ visits/calls at the time of new product launch or sales campaign etc. using special presentation and promotional materials in line with the sales strategy</span></p></li><li><p><span style="font-size:inherit">Carry meticulous one-to-one detailing of the product bringing to the doctor’s attention the special features/benefits of the product, its proven efficacy, new research and clinical findings etc.</span></p></li><li><p><span style="font-size:inherit">Follow the approved tour program.</span></p></li><li><p><span style="font-size:inherit">Prepare and send daily reports as per the defined process on his/her day to day activities mentioning in detail about the calls made on the doctors clinics and hospitals.</span></p></li><li><p><span style="font-size:inherit">Maintain contacts with nursing homes, clinics and hospitals in his/her territory. Collect the data on annual budget for medicines with respect to each of the hospitals, their mode of purchase, rate contract, and drug committee members</span></p></li><li><p><span style="font-size:inherit">Forward adverse events and product complaints reported by customers and consumers in the appropriate format in a timely manner as described in the relevant SOPs</span></p></li><li><p><span style="font-size:inherit">Conduct taxi tours to meet the customers in micro-interiors and generate business for the products</span></p></li><li><p><span style="font-size:inherit">Conduct group meetings, speaker programs, and round table meetings for the doctors and chemists to create awareness around product benefits</span></p></li><li><p><span style="font-size:inherit">Build relationships with and manage Key Opinion Leaders (KOLs) and key customers</span></p></li><li><p><span style="font-size:inherit">Coordinate with CFA for inventory management</span></p></li><li><p><span style="font-size:inherit">Execute the product promotion campaigns for new and existing products for the territory</span></p></li><li><p><span style="font-size:inherit">Track the hospital purchase trend for the territory  </span></p></li><li><p><span style="font-size:inherit">Conceive, plan and organize Continuing Medical Education (CME) programs with help from HODs, Consultants and hospital admin department </span></p></li></ul><p> </p><p><b><span style="font-size:inherit">People</span></b></p><ul><li><p><span style="font-size:inherit">Trainee PSOs or other field trainees as may be assigned as mentees</span></p></li><li><p><span style="font-size:inherit">Share learning from experience with team colleagues  </span></p></li><li><p><span style="font-size:inherit">Demonstrate and promote Pfizer global values in all interactions.</span></p></li><li><p><span style="font-size:inherit">Demonstrate team spirit and cooperation towards achievement of individual and team objectives</span></p></li><li><p><span style="font-size:inherit">Adhere to proposed training calendar for the year for self</span></p></li><li><p><span style="font-size:inherit">Act as the custodian of all compliance related matters for the territory</span></p></li></ul><p><b><span style="font-size:inherit">Financial</span></b></p><ul><li><p><span style="font-size:inherit">Ensure achievement of Sales budgets</span></p></li><li><p><span style="font-size:inherit">Assist in the collection of receivables, where required</span></p></li><li><p><span style="font-size:inherit">Ensure proper utilisation of product samples, detailing aids and other promotional material.</span></p></li><li><p><span style="font-size:inherit">Ensure proper accounting and reporting of expenses </span></p></li></ul><p> </p><p><b><span style="font-size:inherit">Technology</span></b></p><ul><li><p><span style="font-size:inherit">Use technology solutions for enabling better information availability</span></p></li><li><p><span style="font-size:inherit">Use technology developments for effective field operations .</span></p></li></ul><p><span style="font-size:inherit"> </span></p><p><span style="font-size:inherit"> </span><br /><span style="font-size:inherit">Work Location Assignment: Flexible</span></p><p> </p>&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Sales<p></p><p></p>]]></description><link>http://biotechroles.com/heathcare-executive-pfizer/69d3bf79c8e81216cd0b93db</link><guid isPermaLink="true">http://biotechroles.com/heathcare-executive-pfizer/69d3bf79c8e81216cd0b93db</guid><pubDate>Mon, 06 Apr 2026 14:13:13 GMT</pubDate><company>Pfizer</company><location>India - Delhi</location><salary>$65000-120000</salary><type>Full time</type></item><item><title><![CDATA[Senior Associate, Senior Central Testing Analyst, Central Services]]></title><description><![CDATA[<p><b>Use Your Power for Purpose</b></p><p>Our mission is straightforward: support healthcare decisions that ensure the safe and effective use of medications. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.</p><p> </p><p><b>What You Will Achieve</b></p><p>In this role, you will:</p><ul><li><p><b>ROLE RESPONSIBILITIES </b>Provides technical skills and knowledge to assigned work to achieve and perform activities, including but not limited to:  the testing of CRF design, Database building, Acquisition &amp; Processing of electronic data, such as external eData, Lab Data and PK/PD Data; Data extraction and listing for quality review, Data Visualization; Data and Documentation Processing, CRF and Database edit checks/validation and outputs. </p></li><li><p>Accountable for high quality and on time delivery for assigned deliverables. </p></li><li><p>Participate in initial DM meetings with Clinical Data Scientist (CDS) to understand the expectation and scope of the study. </p></li><li><p>Ensure work carried out in accordance with applicable SOPs and working practices. </p></li><li><p>Understand the Protocol and provide input to Study Team on Database Design and Edit Check Specification as appropriate. </p></li><li><p>Based on Study Data Specification (SDS) the Screen UAT has to be executed and compare the Schedule of Assessment from Protocol with Database and Provide Suggestions. </p></li><li><p>Review the Edit Check Specification, write UAT test scripts. </p></li><li><p>Execute the scripts and log the issues in UAT tracker and provide feedback to Study Team </p></li><li><p>May perform peer review on programming of edit checks  </p></li><li><p>May perform check on metadata listing </p></li><li><p>Participate in UAT feedback meetings  </p></li><li><p>Streamline/Standardize the Scripts for Standard Forms/Edit Checks  </p></li><li><p>Validation of Manual queries/Listings (Standards/Therapeutic Specific)  </p></li><li><p>Able to understand the Postproduction Changes in Database during conduct and provide clinical/technical suggestion. </p></li><li><p>Communicates effectively to study team about suggestion and changes to database. </p></li><li><p>Track the lessons learned and share the knowledge across the team. </p></li><li><p>Complete all the documentation related to study and share it with study team. </p></li><li><p>Perform testing of reports and document the same. </p></li><li><p>Maintain a high customer satisfaction level and work with global study teams to meet objectives/timelines. </p></li><li><p>Able to resolve conflicts, influence and communicate with key stakeholders and customers. </p></li><li><p>Organizes own work to time to meet agreed milestones and targets; develops plans for short-term work activities on own assignments (timelines, work plans, deliverables). </p></li><li><p>Learns and applies basic team effectiveness skills (e.g., commitment, feedback, consensus management). </p></li><li><p><b>QUALIFICATIONS </b>Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP </p></li><li><p>Demonstrated knowledge of data management processes and principles in area of responsibility. </p></li><li><p>Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review </p></li><li><p>Demonstrates strong verbal and written communication skills including ability to communicate remotely  </p></li><li><p>Minimum 7 years of relevant experience required </p></li><li><p>Working knowledge of clinical research, FDA &amp; ICH, GCP, GCDMP, and related regulatory requirements  </p></li><li><p>Proficient experience using commercial clinical data management systems and/or EDC products (e.g., Inform preferred)  </p></li><li><p>Experience using data visualization tools (e.g. Spotfire, J-Review) preferred </p></li><li><p>Familiarity with MedDRA/WHO-Drug  </p></li><li><p>Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) </p></li><li><p>Bachelor’s degree minimum requirement.  </p></li><li><p>Experience of project management skill in terms of resource management and timeline and quality control preferred. </p></li><li><p>Experience performing testing of database and/or leading a team of testers performing the UAT activities. </p></li></ul>&nbsp;&nbsp;<br>Work Location Assignment:&nbsp;On Premise<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>]]></description><link>http://biotechroles.com/senior-associate-senior-central-testing-analyst-central-services-pfizer/69d3bf77c8e81216cd0b93da</link><guid isPermaLink="true">http://biotechroles.com/senior-associate-senior-central-testing-analyst-central-services-pfizer/69d3bf77c8e81216cd0b93da</guid><pubDate>Mon, 06 Apr 2026 14:13:11 GMT</pubDate><company>Pfizer</company><location>India - Chennai</location><salary>$25000-45000</salary><type>Full time</type></item><item><title><![CDATA[Sr. Director, US Quality Assurance]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Scholar Rock is seeking an experienced and motivated Senior Director of US Quality Assurance. Reporting to the Head of Global Quality, this position provides strategic and operational leadership for US Quality Assurance with a strong focus on external partner governance, quality risk management, and scalable quality infrastructure to support development through commercialization.</div></br><b>Position Responsibilities</b></br>
<li>Lead the US Quality Assurance function for external GxP biologics operations, including oversight of CMOs, contract laboratories, and other critical service providers.</li>
<li>Provide QA oversight for external manufacturing, testing, release support, deviations, investigations, CAPAs, change controls, product impact assessments, and disposition-related decisions.</li>
<li>Design and maintain a robust, scalable product disposition program for clinical trial material as well as commercial products across multiple markets.</li>
<li>Ensure continuous inspection readiness across outsourced operations and support health authority inspections, partner inspections, and due diligence activities.</li>
<li>Monitor partner quality performance through defined metrics, scorecards, and governance forums; identify trends and proactively escalate compliance or execution risks.</li>
<li>Partner cross-functionally to assess quality risk associated with process changes, deviations, investigations, comparability activities, tech transfer, and supply continuity issues.</li>
<li>Provide strategic guidance on quality requirements for product lifecycle activities, including clinical supply, commercial readiness, distribution, complaints, and post-approval changes.</li>
<li>Build and develop internal QA capabilities, processes, and team structure appropriate for a virtual biotech operating model.</li>
<li>Drive a culture of quality, accountability, and proactive issue identification across internal stakeholders and external partners.</li>
<li>Collaborate with the Head of Quality and site leadership to ensure alignment with corporate goals, customer expectations, and regulatory obligations (FDA, EU, and other global regulators).</li>
</br><b>Candidate Requirements</b></br>
<li>BS/MS degree in a scientific discipline.</li>
<li>15+ years of experience in the pharmaceutical/biotech industry (including meaningful experience in outsourced/virtual operating models), with 7+ years in leadership roles within Quality or related functions</li>
<li>Deep knowledge of GMP/GxP requirements, FDA/EMA expectations, ICH guidance, and risk-based quality management principles.</li>
<li>Demonstrated success overseeing external manufacturers, testing laboratories, suppliers, and quality service providers.&nbsp;</li>
<li>Experience supporting biologics products across development stages; commercial and launch readiness experience strongly preferred.</li>
<li>Strong judgment, executive presence, and the ability to balance strategic thinking with hands-on execution.</li>
<li>Highly proactive, decisive, and capable of independently managing key initiatives.</li>
<li>Engaged people manager committed to building culture as well as mentorship and talent development&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/sr.-director-us-quality-assurance-scholar-rock/69d3be1ec8e81216cd0b920b</link><guid isPermaLink="true">http://biotechroles.com/sr.-director-us-quality-assurance-scholar-rock/69d3be1ec8e81216cd0b920b</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$200000-280000</salary><type>Full-Time</type></item><item><title><![CDATA[Sr. Medical Director, Drug Safety & Pharmacovigilance]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 11pt;">The Sr. Medical Director, Drug Safety &amp; Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines &amp; with high quality.</span></div></br><b>Position Responsibilities: </b></br>
<li>Lead and support development of pharmacovigilance strategies for products within Therapeutic area, to ensure compliance with&nbsp;corporate clinical development and commercial goals.</li>
<li>Oversight and conducting of signal detection activities include monitoring, evaluation, interpretation, management and&nbsp;communication of safety information.</li>
<li>Responsible for oversight and conduct of Product Safety Committee (PSC) meeting(s) to evaluate risk-benefit for the&nbsp;compounds with support from cross-functional teams. Escalate and present safety issues to&nbsp;the Executive Safety Committee.</li>
<li>Medical safety review including causality assessment of all available safety data generated from various&nbsp;sources (e.g. pre-clinical, clinical trial data, post-marketing and literature) throughout the development&nbsp;process for assigned compounds/projects.</li>
<li>Provides medical expert safety review input into all critical documents for products in clinical&nbsp;development (e.g., INDs/NDA/BLA submissions, protocols and amendments, ICFs, IBs, and clinical&nbsp;research reports (CSR))</li>
<li>Oversight of aggregate reports and signal evaluation reports for assigned projects.</li>
<li>Responsible for the Clinical content of responses to inquiries from regulatory authorities related to&nbsp;Safety topics.</li>
<li>Provide leadership and support to Contract Research Organization (CRO) staff to ensure overall&nbsp;delivery of services. Ensures vendor oversight of outsourced Medical activities, as applicable.</li>
<li>Oversee and collaborate with internal safety scientists within TA</li>
<li>Assist with the writing and development of SOPs as required to ensure compliance to regulations and local laws.</li>
<li>Lead high quality planning and execution of external meetings and internal stakeholder meetings (e.g., DMCs, Vendor oversight meetings, etc.)</li>
<li>Demonstrated ability to build effective working relationships, influence, negotiate, and drive organizational engagement. Ability to be flexible and adapt quickly to the changing needs of the organization.</li>
<li>Support process improvement and functional training at departmental &amp; company level</li>
<li>Ensure that the highest quality, ethical &amp; professional values are demonstrated in all aspects of work.</li>
<li>Ensures compliance with corporate policies and procedures, as well as all related healthcare laws and regulations</li>
</br><b>Candidate Requirements: </b></br>
<li>MD or MBBS or MD-PhD or equivalent medical degree</li>
<li>5 or more years of pharmaceutical experience in Drug Safety &amp; Pharmacovigilance.</li>
<li>Strong understanding of pharmacovigilance regulations in the US and EU.</li>
<li>Experience in supporting drug safety activities in registrational clinical studies</li>
<li>High level of medical competence, with an ability to balance this with industry standards to achieve business goals</li>
<li>Demonstrated skills in scientific analysis and reasoning.</li>
<li>Sound knowledge of overall drug development process from discovery to registration and post marketing requirements &amp; surveillance.</li>
<li>Prior IND, as well as NDA/BLA (filing/submission) and other regulatory interaction experience is highly desirable</li>
<li>Strong track record of delivering results through effective team and peer leadership in matrix</li>
<li>Excellent leadership &amp; organizational skills, analytical skills, presentation skills, and strong experience in translating important data into clinical strategies.</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/sr.-medical-director-drug-safety-and-pharmacovigilance-scholar-rock/69d3be1ec8e81216cd0b920d</link><guid isPermaLink="true">http://biotechroles.com/sr.-medical-director-drug-safety-and-pharmacovigilance-scholar-rock/69d3be1ec8e81216cd0b920d</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Vice President, Global Head of Communications]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>
<p>We are seeking a strategic, and highly collaborative Vice President &amp; Global Head of Communications to lead our global communications function. The leader will shape and drive all enterprise, executive and business communications strategies and efforts to strengthen our reputation, engage stakeholders, and advance our business and brand across internal and external audiences.<br><br>The ideal candidate will bring a bold communications vision, deep experience and &nbsp;perspective to a diverse range of topics and issues, a track record of influencing and enabling business strategy, and the ability to be agile and lead through complexity, change, and opportunity. This position reports to the Chief Operating Officer and will partner closely with the CEO, the entire executive team and key business leaders to ensure communications are aligned, forward-looking, and aligned with our mission to bring medicine to the communities we serve and become the next great commercial biotech company globally.</p>
<p>&nbsp;</p>
<p>&nbsp;</p>
<h3>Position Responsibilities:&nbsp;</h3>
</div></br><b>Strategic Communications Leadership</b></br>
<li>Develop and execute a comprehensive, global communications strategy that supports business priorities, enhances reputation, and drives stakeholder trust.</li>
<li>Architect the corporate re-branding including mission, vision, values, and corporate narrative with the COO, CEO, and executive team.</li>
<li>Evolve the company’s communications platform and messaging to align with the company’s strategic priorities and brand. &nbsp;</li>
<li>Act as a strategic communications advisor to the COO, CEO and executive team and lead all matters of corporate narrative, media positioning, and communications risks.</li>
<li>Serve as steward of the company’s voice, ensuring consistency, clarity, and mission-driven across channels and audiences.</li>
</br><b>Executive Communications</b></br>
<li>Partner with the COO, CEO and business leaders to craft impactful narratives that reinforce vision, performance, and values. Shape and oversee all executive messaging, visibility, and thought-leadership.&nbsp;</li>
<li>Work with COO and CEO on internal and external communications, including speaking opportunities, internal employee forums, board communications, media, etc.</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/vice-president-global-head-of-communications-scholar-rock/69d3be1fc8e81216cd0b920e</link><guid isPermaLink="true">http://biotechroles.com/vice-president-global-head-of-communications-scholar-rock/69d3be1fc8e81216cd0b920e</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$280000-450000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Director, HCP Marketing (US)]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Senior Director, HCP Marketing (US) will play a critical leadership role in the preparation for and execution of Scholar Rock’s first U.S. commercial launch. This role will be accountable for developing and driving the U.S. healthcare professional (HCP) marketing strategy and tactical execution for apitegromab, the first and only muscle-targeted therapy for spinal muscular atrophy (SMA).</div>
<div>This individual will own the U.S. HCP brand strategy from launch through commercialization, ensuring clear differentiation, compelling scientific communication, and flawless execution across channels. The role will work closely with U.S. commercial, medical, market access, and patient services teams to deliver an integrated launch.</div>
<div>&nbsp;</div>
<div>In addition to U.S. leadership responsibilities, this role will provide limited ex-U.S. support (~10%), focused on strategic alignment, communication, and knowledge sharing with regional and local teams to ensure consistency of core HCP strategy while respecting local needs.</div>
<div>&nbsp;</div>
<div>This is a high-impact, high-visibility role within a fast-growing organization and an opportunity to shape the commercial foundation of Scholar Rock’s first marketed product.</div>
<div>&nbsp;</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Position Responsibilities:</strong></div></br><b>U.S. HCP Strategy & Launch Execution</b></br>
<li>Lead the development of the U.S. HCP brand strategy for apitegromab, grounded in deep understanding of the SMA landscape, unmet need, and clinical data.</li>
<li>Own U.S. HCP launch planning, including positioning, messaging, segmentation, targeting, and channel strategy.</li>
<li>Translate strategy into high-quality, compliant HCP promotional tactics across personal and non-personal channels.</li>
<li>Partner with Sales leadership to ensure strong integration between HCP marketing strategy and field execution.</li>
<li>Oversee agency partners and vendors to deliver best-in-class creative and execution.</li>
</br><b>Cross-Functional Leadership</b></br>
<li>Serve as a core member of the U.S. Marketing Team, collaborating closely with Medical Affairs, Market Access, Patient Services, Regulatory, Legal, and Compliance.</li>
<li>Ensure HCP strategy is aligned with scientific narrative, access considerations, and patient support offerings.</li>
<li>Provide strategic input into competitive readiness and scenario planning for current and future competitors as well as pipeline considerations.&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/senior-director-hcp-marketing-(us)-scholar-rock/69d3be1ec8e81216cd0b9209</link><guid isPermaLink="true">http://biotechroles.com/senior-director-hcp-marketing-(us)-scholar-rock/69d3be1ec8e81216cd0b9209</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-320000</salary><type>Full-Time</type></item><item><title><![CDATA[Sr. Director, Global Quality Control]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Scholar Rock is seeking an experienced and motivated Senior Director of Global Quality Control. Reporting to the Head of Global Quality, this position is the senior QC leader responsible for establishing and maintaining a phase-appropriate, scalable, and inspection-ready global QC strategy for a fully outsourced development and manufacturing network. This role provides strategic and technical leadership for Quality Control activities executed through external contract laboratories, CMOs, and other testing partners supporting drug substance, drug product, raw materials, in-process, release, and stability programs.</div></br><b>Position Responsibilities</b></br>
<li>Lead the company’s global QC function across a fully outsourced model, with end-to-end oversight of external QC laboratories, CMOs, and contract partners supporting clinical and commercial programs.</li>
<li>Define and execute the global QC strategy, serving as the internal QC subject matter expert across analytical control strategy, compendial compliance, specification lifecycle management, and stability.</li>
<li>Provide strategic oversight of stability programs, including protocol design, pull schedule governance, data review and trending, shelf-life support, comparability assessments, and post-approval stability commitments.</li>
<li>Oversee post-approval specification management, including revision strategy, change assessment, comparability impacts, commitment tracking, and implementation through external partners.</li>
<li>Ensure effective method qualification, validation, transfer, verification, and lifecycle management across outsourced laboratories, including technical troubleshooting and issue escalation.</li>
<li>Partner with Analytical Development and CMC teams to support method readiness, control strategy development, and phase-appropriate analytical plans for new programs, process changes, and commercialization activities.</li>
<li>Provide QC leadership for investigations involving OOS, OOT, non-conforming results.</li>
<li>Establish and monitor quality and operational performance expectations for external testing partners through governance forums, metrics, trend reviews, and business process oversight.</li>
<li>Author, review, and approve QC-related controlled documents, including specifications, protocols, reports, SOPs, method transfer plans, stability documents, and technical assessments as applicable.</li>
<li>Build fit-for-purpose QC systems, governance, and internal capabilities appropriate for a virtual biotech environment, with a focus on compliance, technical rigor, and scalability.</li>
<li>Collaborate with the Head of Quality and site leadership to ensure alignment with corporate goals, customer expectations, and regulatory obligations (FDA, EU, and other global regulators).</li>
</br><b>Candidate Requirements</b></br>
<li>BS/MS degree in a scientific discipline; advanced degree (MS or PhD) preferred</li>
<li>15+ years of progressive Quality Control and/or Analytical Sciences experience in biotech/pharma industry (including outsourced operating models), with 7+ years in leadership roles</li>
<li>Deep technical expertise in analytical methods supporting biologics and/or other advanced therapeutic modalities, including release, stability, and characterization testing.</li>
<li>Strong working knowledge of USP, EP, and JP pharmacopeial requirements, and cGMP, ICH guidance, global regulatory requirements, and inspection readiness for outsourced QC operations.</li>
<li>Demonstrated success leading global stability programs, including shelf-life support, data trending, protocol governance, and regulatory commitment execution.</li>
<li>Proven experience in specification development, justification, and lifecycle management, including post-approval specification revisions and change implementation.</li>
<li>Extensive experience with method transfer, qualification, validation, verification, and troubleshooting across contract testing laboratories and manufacturing partners.&nbsp;</li>
<li>Proven ability to lead through influence in a matrixed organization and manage complex external technical relationships with appropriate rigor and accountability.</li>
<li>Strong executive presence, sound scientific judgment, and the ability to balance strategic leadership with practical execution.</li>
<li>Highly proactive, decisive, and capable of independently managing key initiatives.</li>
<li>Engaged people manager committed to building culture as well as mentorship and talent development&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/sr.-director-global-quality-control-scholar-rock/69d3be1ec8e81216cd0b920a</link><guid isPermaLink="true">http://biotechroles.com/sr.-director-global-quality-control-scholar-rock/69d3be1ec8e81216cd0b920a</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-320000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Director, Patient Marketing (US)]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Senior Director, Patient Marketing (US) will play a critical leadership role in the preparation for and execution of Scholar Rock’s first U.S. commercial launch. This role will be accountable for developing and driving the U.S. patient and caregiver marketing strategy and tactical execution for apitegromab, the first and only muscle-targeted therapy for spinal muscular atrophy (SMA).</div><div><br></div><div>This individual will own the U.S. patient brand strategy from launch through commercialization, ensuring a deeply patient-centric approach across education, engagement, and community presence. The role will lead the development of integrated, compliant, multi-channel patient programs designed to support awareness, understanding, and empowerment throughout the patient journey.</div><div><br></div><div>As a senior leader on the U.S. Marketing Team, this role will work closely with Patient Services, Medical Affairs, Advocacy, Market Access, Legal, Regulatory, and Compliance to ensure a cohesive, high-quality experience for patients and caregivers. This is a high-impact, high-visibility role with the opportunity to shape how Scholar Rock engages with the SMA community as it brings its first therapy to patients.</div><div><br></div><div><br></div><div><br></div><div><b style="font-size: 18px">Position Responsibilities:</b></div></br><b>U.S. Patient Strategy & Launch Execution</b></br><li>Lead the development of the U.S. patient and caregiver brand strategy for apitegromab, grounded in a deep understanding of the SMA community, patient journey, and unmet needs.</li><li>Own U.S. patient launch planning, including strategy, messaging, channel mix, and executional roadmap.</li><li>Translate strategy into high-quality, compliant patient-facing tactics across digital, community, advocacy-aligned, and experiential channels.</li><li>Ensure consistency and excellence across all patient touchpoints while maintaining a strong, authentic patient-centric lens.</li></br><b>Patient Engagement & Community Leadership</b></br><li>Build and maintain strong, trusted relationships within the SMA patient and caregiver community.</li><li>Lead the patient ambassador and engagement programs, including long-term retention and stewardship strategies.</li><li>Own the U.S. patient conference and event strategy, elevating Scholar Rock’s presence and impact at key national, regional, and local meetings.</li><li>Champion innovation in patient engagement, continuously evolving approaches to improve the patient experience across the journey.</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/senior-director-patient-marketing-(us)-scholar-rock/69d3be1ec8e81216cd0b920c</link><guid isPermaLink="true">http://biotechroles.com/senior-director-patient-marketing-(us)-scholar-rock/69d3be1ec8e81216cd0b920c</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Regional Business Leader, Central]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Regional Business Leader is responsible for driving commercial success, shaping regional launch success, and developing strong relationships with key stakeholders within the rare disease ecosystem—with a specific and initial focus on Spinal Muscular Atrophy (SMA). The role combines high engagement field presence and strategic account management, ensuring timely and appropriate access to innovative therapies for patients living with SMA.</div><div><br></div></br><b>Position Responsibilities</b></br><li>Execute territory and account-based sales plans to achieve commercial goals in the SMA therapeutic area, including identifying key accounts, prioritizing centers of excellence, and managing physician relationships.&nbsp;</li><li>Proactively prospect, develop and expand relationships with clinicians involved in SMA diagnosis and treatment (neurologists, pediatric neurologists, clinical geneticists, hospitals).&nbsp;</li><li>Deliver product presentations, educational conversations, and scientific discussions in a compliant manner, tailored to varying HCP needs.&nbsp;</li><li>Manage complex sales cycles, ensuring strong presence and consistent follow-up in academic and hospital environments.</li><li>Provide expertise in national and/or regional market access related matters</li><li>Raise awareness about SMA, diagnostic pathways, genetic testing, early intervention, and treatment value—aligned with the company’s overall value proposition and story&nbsp;</li><li>Develop deep, trusted relationships with neuromuscular KOLs, SMA centers, and hospital pharmacists&nbsp;</li><li>Represent the organization at congresses, regional neurology events, peer to peer and scientific meetings.&nbsp;</li><li>Work closely with Medical Affairs, Market Access, Marketing, and Patient Support Programs to ensure cohesive support for HCPs and patients&nbsp;</li><li>Communicate market insights, treatment barriers, and customer feedback to inform strategy and operational planning.&nbsp;</li><li>Comply with German regulatory standards (AMG, HWG), promotional codes, and company policies</li><li>Ensure transparent and ethical interactions with HCPs.</li></br><b>Candidate Requirements</b></br><li>Bachelor’s or Master’s degree in Life Sciences, Health Sciences, Business, or related field.</li><li>7+ years of commercial experience in biotech/pharmaceutical field sales, </li><li>Proven track record in rare disease, neurology, or SMA/specialty care markets.</li><li>Strong experience working with KOLs, hospital structures, and complex patient pathways in Germany</li><li>Experience in the &nbsp;development of the German rare disease/SMA ecosystem</li><li>Demonstrated success in product launches, national and regional Market Access activities, market development, and regional P&amp;L leadership is a plus.</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/regional-business-leader-central-scholar-rock/69d3be1ec8e81216cd0b9204</link><guid isPermaLink="true">http://biotechroles.com/regional-business-leader-central-scholar-rock/69d3be1ec8e81216cd0b9204</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Giessen</location><salary>$180000-280000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Director, Drug Product External Manufacturing]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Scholar Rock is seeking a highly experienced and technically strong Senior Director of Drug Product External Manufacturing to lead drug product external manufacturing for our portfolio of biologics, including monoclonal antibodies, fusion proteins, and bispecifics. In this role you will lead and oversee all drug product manufacturing operations managed through external contract manufacturing organizations (CMOs). This role is critical in ensuring the seamless production, quality, and delivery of clinical and commercial products, aligning with company goals and regulatory standards. The ideal candidate will possess deep expertise in biopharmaceutical manufacturing, strategic leadership, and a strong ability to manage complex global operations.</div></br><b>Position Responsibilities</b></br>
<li>Develop and execute manufacturing strategies to support drug product manufacturing needs.&nbsp;</li>
<li>Lead end-to-end management of external drug product manufacturing, including planning, production, and delivery as well as execution of new projects.&nbsp;</li>
<li>Interface closely with each drug product CMO as the Scholar Rock primary contact, providing direction to and partnering with the CMO program manager, site leadership and business lead as appropriate. &nbsp;</li>
<li>Ensure CMOs meet production timelines, cost targets, and regulatory and quality standards.&nbsp;</li>
<li>Establish and manage partnerships with CMOs to ensure capacity, capability, and compliance with company standards (e.g., FDA, EMA, ICH guidelines).&nbsp;</li>
<li>Coordinate and manage CMO governance meetings, in partnership with CMO program manager and/or business lead.&nbsp;&nbsp;</li>
<li>Maintain financial responsibility for CMO spend, managing the budget allocation, negotiating work statements, ensuring purchase requisitions are raised, and PO’s are reconciled . &nbsp;</li>
<li>Establish alignment of objectives and priorities in close coordination with CMC team, supply chain, quality, regulatory CMC, and other functions as needed, representing the CMO(s) in strategic decisions. &nbsp;</li>
<li>Drive continuous improvement initiatives across external manufacturing operations to optimize efficiency and cost-effectiveness.&nbsp;</li>
<li>Partner with quality teams to address deviations, CAPAs, and other quality-related issues.&nbsp;</li>
<li>Oversee CMO due diligence during new CMO selection to vet capabilities, risks and investments required.&nbsp;</li>
<li>Engage, as needed, in contract negotiation and review. After execution of a contract, act as contract monitor, ensuring both Scholar Rock and the CMO comply with commitments.&nbsp;&nbsp;</li>
</br><b>Candidate Requirements</b></br>
<li>Bachelor’s degree in engineering, life science or related field with 15 years of relevant work experience, or advanced degree and a minimum of 12 years of work experience, and at least 8 years in a leadership role overseeing manufacturing operations with vendors and/or CMOs.&nbsp;</li>
<li>Strong understanding of quality and regulatory requirements for drug product biopharmaceutical manufacturing (e.g., GMP, FDA, EMA).&nbsp;</li>
<li>Strong leadership and an innate ability to collaborate and build relationships is critical. &nbsp;</li>
<li>Ability to influence senior management both internally and externally. &nbsp;</li>
<li>Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view. Ability to execute and follow-through to completion.&nbsp;</li>
<li>Ability to establish and monitor vendor performance metrics and implement corrective actions, as needed.&nbsp;</li>
<li>Can foster a culture of collaboration, accountability, and excellence within the team.&nbsp;</li>
<li>Can develop and manage budgets for external manufacturing operations.&nbsp;</li>
<li>This position may require up to 20% travel to CMO sites as necessary.&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/senior-director-drug-product-external-manufacturing-scholar-rock/69d3be1ec8e81216cd0b9205</link><guid isPermaLink="true">http://biotechroles.com/senior-director-drug-product-external-manufacturing-scholar-rock/69d3be1ec8e81216cd0b9205</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-320000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Director, Global Quality Systems and Compliance]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 11pt;">Scholar Rock is seeking an experienced and motivated Director of Quality Systems and GxP Compliance. Reporting to the Head of Quality, this position will oversee all aspects of quality systems and regulatory compliance across commercial, clinical, and development activities. The Director will lead the implementation and maintenance of an effective Quality Management System (QMS) to ensure compliance with global regulatory requirements.</span></div></br><b>Position Responsibilities</b></br>
<li>Serve as the Quality Lead for systems and compliance operations across the organization.</li>
<li>Provide strategic guidance to the quality function on Quality Systems and GxP compliance.</li>
<li>Oversee and manage GxP training, document control, and QMS operations—including change controls, deviations, CAPAs, complaints, audits, and supplier management activities.</li>
<li>Monitor the lifecycle of quality system records to preserve the integrity and compliance of Scholar Rock’s QMS.</li>
<li>Manage the intake and triage of product complaints, ensure accurate documentation, timely escalation, and alignment across systems and departments.</li>
<li>Assign and manage GxP training in the learning management system, track compliance, and generate completion reports as needed.</li>
<li>Participate in validation efforts for new or updated GxP IT systems, including documentation review, test script execution, and change control support.</li>
<li>Oversee the supplier management program, including supplier evaluations and audits.</li>
<li>Provide metrics and reports on QMS and supplier performance during periodic quality reviews.</li>
<li>Lead and implement Scholar Rock’s internal audit program.</li>
<li>Drive continuous improvement initiatives to maintain compliance and enhance QMS efficiency.</li>
<li>Support inspection readiness activities.</li>
<li>Contribute to regulatory submissions such as annual reports, IND/CTA updates, and marketing authorizations.</li>
<li>Lead and manage the Quality Systems and Compliance team, including direct reports.</li>
<li>Collaborate with the Head of Quality and site leadership to ensure alignment with corporate goals, customer expectations, and regulatory obligations (FDA, EU, and other global regulators).</li>
</br><b>Candidate Requirements</b></br>
<li>BS/MS degree in a scientific discipline.</li>
<li>15+ years of experience in the pharmaceutical/biotech industry, with 10+ years in leadership roles within Quality or related functions.&nbsp;&nbsp;</li>
<li>Deep understanding of GxP and Quality System requirements (US and EU) for pharmaceutical/biotech manufacturing and development.</li>
<li>Experience leading regulatory inspections and interfacing with global health authorities.</li>
<li>Strong knowledge of electronic Quality Management Systems, Document Management Systems, and Learning Management Systems.</li>
<li>Hands-on experience with systems such as Veeva Vault is preferred.</li>
<li>Highly proactive, decisive, and capable of independently managing key initiatives.</li>
<li>Engaged people manager committed to building culture as well as mentorship and talent development.</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/senior-director-global-quality-systems-and-compliance-scholar-rock/69d3be1ec8e81216cd0b9206</link><guid isPermaLink="true">http://biotechroles.com/senior-director-global-quality-systems-and-compliance-scholar-rock/69d3be1ec8e81216cd0b9206</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-320000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Director of Global Facilities]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Scholar Rock is entering a defining chapter as we prepare to launch our first commercial product. We are seeking a Director of Global Facilities who can lead our facilities function with a strategic, enterprise-wide perspective while remaining deeply engaged in day-to-day operations.&nbsp; This is not a purely administrative role. We need a builder — someone who understands what it takes to scale infrastructure in a growing biotech organization and is equally comfortable shaping long-term facility strategy as they are resolving operational issues in real time.</div>
<div>&nbsp;</div>
<div>With facilities across the globe and ready for future expansion, this leader will ensure our environments are safe, compliant, efficient, and built to support both research and commercial readiness.&nbsp; If you are a self-motivated individual who enjoys the challenges and opportunities that come with a growing, transformative organization, this is an excellent opportunity to apply yourself, learn, and make an impact. You thrive in environments where you are involved in both strategic planning (the bigger picture) and execution. As a catalyst for the organization, you value proactive collaboration, communication, and teamwork as essential for success.&nbsp; &nbsp;&nbsp;</div>
<div>&nbsp;</div></br><b>Position Responsibilities</b></br>
<li>Provide end-to-end operational oversight of Scholar Rock’s facilities, and serve as the primary liaison to property management, contractors, vendors, and personnel across several global locations (US, EU and Asia)</li>
<li>Oversee laboratory operations including instrument preventative maintenance (PM), repairs &amp; calibration, glass wash, autoclave workflows, chemical and biological inventory tracking, receiving and efficient dispersion of incoming materials, and more</li>
<li>Lead EH&amp;S programs across all sites, including policies &amp; procedures, training, maintaining safety data sheets (SDS), incident reporting/tracking, ergonomics, and more.&nbsp;</li>
<li>Oversee facility planning, design, and execution, including reconfiguration and expansion; Work with research leaders to organize and manage the current and future state of Scholar Rock’s lab space and resources, including allocating freezer/ refrigerator/ liquid nitrogen space, etc.</li>
<li>Implement and support processes that increase the operational efficiency of the facility and lab operations.</li>
<li>Monitor and maintain core building functions, including lighting, HVAC, backup power, life safety, and all other building support functions</li>
<li>Collaborate with the finance and legal teams to obtain contract bids and negotiate contracts</li>
<li>Interface with Federal, State, County, and City agencies as required for ongoing operations and maintaining compliance with relevant codes</li>
<li>Develop and maintain effective vendor relationships&nbsp;</li>
<li>Hire and manage facilities personnel &amp; outsourced services such as janitorial, day porter, and shipping services at all local facilities</li>
<li>Lead 24-hour response team for facility and EH&amp;S issues and emergencies.</li>
<li>Order and maintain office &amp; food supplies for the office</li>
</br><b>Candidate Requirements</b></br>
<li>Bachelor's degree or equivalent years of experience in a similar function</li>
<li>7+ years of facilities management experience&nbsp;&nbsp;</li>
<li>EH&amp;S management experience</li>
<li>Prior experience in a biotech or pharma environment is a must.&nbsp; Exposure to GMP a plus&nbsp;&nbsp;</li>
<li>Demonstrated success in maintaining similar-sized and function facilities (50,000+ square feet, mix of lab and office), including build-outs, moves, renovations, and reconfigurations</li>
<li>Capability to communicate with all levels of employees, outside vendors, and contractors</li>
<li>Demonstrated strong collaborative skills with strong oral, writing, and interpersonal communication skills</li>
<li>Well organized and stays on schedule, able to function under pressure in a rapidly changing environment, emphasis on quality</li>
<li>Experience with tools and simple mechanical, plumbing, and electrical work. Able to supervise trades as necessary.</li>
<li>Able to lift and move up to 50 lbs</li>
<li>Experience maintaining autoclaves, laboratory dishwashers, DI systems, CDA, vacuum and other laboratory systems&nbsp;&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/senior-director-of-global-facilities-scholar-rock/69d3be1ec8e81216cd0b9208</link><guid isPermaLink="true">http://biotechroles.com/senior-director-of-global-facilities-scholar-rock/69d3be1ec8e81216cd0b9208</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Head of IP, Europe]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>We have an exciting opportunity for a qualified European patent attorney to join the Legal Department at Scholar Rock to support all aspects of the company’s global intellectual property portfolio.&nbsp;</div>
<div><br>Scholar Rock is a clinical-stage biopharmaceutical company dedicated to discovering, developing, and delivering therapies that create new possibilities for patients suffering from rare neuromuscular diseases. &nbsp;The company is preparing for potential FDA and EMA approval of apitegromab for the treatment of children and adults living with SMA.&nbsp;</div>
<div><br>Since its foundation in 2012, Scholar Rock has steadily built an extensive patent portfolio to protect its intellectual property. As a rare disease-focused company, Europe is a key jurisdiction, where strong IP protection can generate value to the company.&nbsp;</div>
<div><br>This is a highly visible position where you will build partnerships across the business to drive the IP strategy. The company is seeking a seasoned European patent attorney with extensive experience in EPO opposition practice to work from the company's Zug, Switzerland office.&nbsp;</div>
<div><br>You will lead EPO opposition matters and work cross-functionally to provide proactive support, harvest inventions, conduct FTO searches and analyses, from target to launch. Robust scientific curiosity, commitment to excellence, and the ability to do so through effective communication and collaboration are key elements for success for this position. This role reports into the SVP, Head of IP. Prior global patent litigation exposure preferred.</div></br><b>Position Responsibilities </b></br>
<li>You will be embedded within R&amp;D project teams and working collaboratively with other members of the Intellectual Property group to fully scope out opportunities, risks, breadth of inventions and prosecution strategies.</li>
<li>You will take a lead in EPO opposition matters and manage external legal counsel in these matters.</li>
<li>You will be involved in providing training/education to various business functions on the value of IP and driving IP strategies for multiple projects.</li>
<li>You will be expected to be comfortable with a level of autonomy with drafting and prosecuting patent applications, oppositions, due diligence, negotiating legal agreements with external parties, and proactively work towards risk assessment and risk mitigation.&nbsp;</li>
</br><b>Candidate Qualifications </b></br>
<li>Qualified Patent Attorney (EPA and/or CPA or equivalent national qualification).</li>
<li>Over 15 years experience working within the biopharmaceutical sector, with solid training in a law firm setting, as well as prior in-house experience.&nbsp;</li>
<li>Advanced degree in relevant disciplines, such as biology, biochemistry, immunology, etc.</li>
<li>Expertise in European opposition and UPC practice; additional litigation experience a plus.&nbsp;</li>
<li>Strong skills in formulating filing strategies and drafting and prosecuting biopharmaceutical patent applications.</li>
<li>Intellectual ability, integrity, a high level of commercial awareness and professionalism, and the drive to excel as an attorney.</li>
<li>A team player with strong interpersonal, communication, analytical and problem-solving skills.</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/head-of-ip-europe-scholar-rock/69d3be1ec8e81216cd0b9201</link><guid isPermaLink="true">http://biotechroles.com/head-of-ip-europe-scholar-rock/69d3be1ec8e81216cd0b9201</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Zug</location><salary>$180000-280000</salary><type>Full-Time</type></item><item><title><![CDATA[Medical Director, Clinical Research (Early-stage)]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Medical Director, reporting to the VP, Clinical Research, will be a member of the early development team, accountable for driving clinical development activities for product candidates from IND through Proof-of-Concept. The successful candidate will be responsible for providing medical leadership for clinical development activities of follow-on indication(s) for apitegromab as well as new product candidates, in alignment with corporate strategy. This position requires a highly motivated physician scientist with hands-on expertise in advancing product candidates to deliver life-changing medicines.</div></br><b>Position Responsibilities: </b></br><li>Deliver clinical development plan for assigned pipeline products from IND through Proof-of-Concept</li><li>Provide medical leadership for clinical development activities of pipeline product candidates, including new indication assessment</li><li>Collaborate with other members of the development and preclinical research teams to contribute to building a collaborative culture and improving effectiveness of the development team</li><li>Engage with external scientific and clinical trial experts, health authorities, and consultants, to develop scientifically robust development plans</li><li>Drive scientifically robust evaluation of new opportunities, including disease area assessment, landscape analysis, evaluation of development and regulatory pathways, and development of study concepts</li><li>Provide strategic guidance and support to the early development team, including hands-on authoring, for the development of clinical development plans, study protocols, investigator brochures, regulatory documents, publications, etc.</li><li>Provide medical leadership and input in cross-functional team activities, including business development activities, non-clinical development, quality assurance, clinical operations, biostatistics, regulatory affairs and drug safety</li><li>Responsible for medical oversight of clinical trials, including medical monitoring of studies, adverse event reporting, and patient safety for all clinical trials across a development program.&nbsp;</li><li>Provide medical and scientific leadership in data analysis and interpretation, maintaining integrity, scientific rigor, and transparency</li><li>Work within compliance to all applicable GCP/ ICH regulations</li></br><b>Candidate Requirements:</b></br><li>MD, MD/PhD, or equivalent, based in greater Boston</li><li>Strong critical thinking skills, with ability to synthesize complex information, and exceptional communication skills, both verbal and written </li><li>5+ years of experience in the biopharmaceutical clinical development function, with 3+ years of clinical development leadership experience; neuromuscular or rare disease experience preferred but not required</li><li>Highly organized, outcome-oriented, self-motivated team player with strong interpersonal skills and effective conflict management skills</li><li>Experience in innovative clinical study design, analysis of clinical data, publications, and working knowledge of biostatistics and pharmacokinetics/pharmacodynamics</li><li>Understanding of the drug development process from pre-IND through BLA</li><li>Experience interacting with health authorities in the US and EU</li><li>In-depth knowledge of ICH-GCP and other application regulatory guidelines</li><li>Ability to travel domestically and internationally (~15%)</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/medical-director-clinical-research-(early-stage)-scholar-rock/69d3be1ec8e81216cd0b9203</link><guid isPermaLink="true">http://biotechroles.com/medical-director-clinical-research-(early-stage)-scholar-rock/69d3be1ec8e81216cd0b9203</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Medical Director/Sr. Director, Clinical Research]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 11pt;">The Medical Director/Senior Director, reporting to the SVP, Clinical Research, will be a member of the late-stage development team, accountable for driving clinical development activities for product candidates from Proof-of-Concept through marketing approval and lifecycle management. The successful candidate will be responsible for providing medical leadership for clinical development activities for apitegromab as well as other product candidates entering late-stage development, in alignment with corporate strategy. This position requires a highly motivated physician scientist with hands-on expertise in advancing late-stage product candidates to deliver life-changing medicines.</span></div></br><b>Position Responsibilities</b></br><li>Deliver clinical development plan for pipeline products from Proof-of-Concept through marketing approval and lifecycle management</li><li>Provide medical leadership for clinical development activities of assigned pipeline products</li><li>Collaborate with other members of the development and preclinical research teams to contribute to building a collaborative culture and improving effectiveness of the development team</li><li>Engage with external scientific and clinical trial experts, health authorities, and consultants, to develop scientifically robust development plans</li><li>Provide strategic guidance and support to the late-stage development team, including hands-on authoring, of clinical development plans, study protocols, investigator brochures, regulatory documents, publications, etc.</li><li>Provide medical leadership and input in cross-functional team activities, including business development activities, non-clinical development, quality assurance, clinical operations, biostatistics, regulatory affairs and drug safety</li><li>Responsible for medical oversight of clinical trials, including medical monitoring of studies, adverse event reporting, and patient safety for all clinical trials across a development program.&nbsp;</li><li>Provide medical and scientific leadership in data analysis and interpretation, maintaining integrity, scientific rigor, and transparency</li><li>Work within compliance to all applicable GCP/ ICH regulations</li></br><b>Candidate Requirements</b></br><li>MD, MD/PhD, or equivalent</li><li>Based in greater Boston with ability to be present regularly in the Cambridge, MA office</li><li>Strong critical thinking skills, with ability to synthesize complex information, and exceptional communication skills, both verbal and written&nbsp;</li><li>5+ years of experience in the biopharmaceutical clinical development function, with 3+ years of clinical development leadership experience; neuromuscular or rare disease experience preferred but not required</li><li>Highly organized, outcome-oriented, self-motivated team player with strong interpersonal skills and effective conflict management skills</li><li>Experience in innovative clinical study design, analysis of clinical data, publications, and working knowledge of biostatistics and pharmacokinetics/pharmacodynamics</li><li>Understanding of the drug development process from pre-IND through BLA</li><li>Experience interacting with health authorities in the US and EU</li><li>In-depth knowledge of ICH-GCP and other application regulatory guidelines</li><li>Ability to travel domestically and internationally (~15%)</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/medical-directorsr.-director-clinical-research-scholar-rock/69d3be1ec8e81216cd0b9207</link><guid isPermaLink="true">http://biotechroles.com/medical-directorsr.-director-clinical-research-scholar-rock/69d3be1ec8e81216cd0b9207</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Financial Planning & Analysis Intern]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>
<p>The purpose of the internship is to provide real world exposure to FP&amp;A. The ideal candidate will have strong academic achievement, ability to multi-task in a demanding environment, and strong leadership potential.</p>
</div></br><b>Position Responsibilities</b></br><div>
<ul type="disc">
<li>Assist in preparing monthly and quarterly financial reporting</li>
<li>&nbsp;Build and maintain revenue models in Excel or similar tool</li>
<li>Support the budgeting and forecasting process</li>
<li>Work with cross-function teams to gather data to support analysis</li>
<li>Analyze financial data to identify key trends and variances</li>
<li>Maintain clear, accurate documentation of financial processes to ensure consistency, compliance, and effective knowledge sharing</li>
<li>Provide ad hoc financial analysis to support strategic projects and operational initiatives across the division</li>

</ul></div></br><b>Candidate Requirements</b></br><div>
<ul type="disc">
<li>Currently pursuing B.S. or Masters in Finance, Business, Economics, Accounting, or related field with a minimum of 2 years college complete.</li>
<li>Proficiency with Excel to conduct complex analysis that will support key decisions</li>
<li>Strong communication skills and comfort working in a collaborative environment</li>

</ul></div></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/financial-planning-and-analysis-intern-scholar-rock/69d3be1ec8e81216cd0b91ff</link><guid isPermaLink="true">http://biotechroles.com/financial-planning-and-analysis-intern-scholar-rock/69d3be1ec8e81216cd0b91ff</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$3000-5000</salary><type>Internship / Co-op</type></item><item><title><![CDATA[Head of Biomarker Development]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Scholar Rock is seeking a strategic and accomplished scientific leader to serve as Head of Biomarker Development. This individual will be responsible for shaping and executing the biomarker strategy across Scholar Rock’s pipeline to enable translation from discovery through clinical development in neuromuscular and rare diseases. Reporting to the Vice President, Head of Preclinical Sciences, this leader will design and implement fit-for-purpose biomarker approaches, oversee assay development and data generation, and serve as a key contributor to regulatory submissions, clinical protocols, and program strategy. This individual will be a member of the research leadership team.</div>
<div>&nbsp;</div>
<div>The successful candidate will integrate discovery, translational, and clinical perspectives to ensure biomarker strategies inform patient selection, target engagement, pharmacodynamics, and disease progression across stages of development.</div>
<div>&nbsp;</div>
<div>&nbsp;</div>
<div><strong style="font-size: 18px;">Position Responsibilities:</strong></div></br><b>Strategic Leadership & Vision</b></br>
<li>Define and drive the biomarker development strategy across preclinical and clinical programs, ensuring alignment with overall portfolio goals.</li>
<li>Serve as a translational science thought leader, integrating biomarker approaches into program strategy, clinical development plans, and indication expansion activities.</li>
<li>Represent Biomarker Development in cross-functional governance and portfolio planning forums.</li>
</br><b>Functional & Scientific Oversight</b></br>
<li>Lead the design, development, and qualification of fit-for-purpose biomarker assays (fluid, tissue, imaging, molecular, and cellular).</li>
<li>Oversee biomarker implementation in preclinical models and clinical studies, ensuring robust data generation and interpretation.</li>
<li>Manage CROs and external collaborators/vendors to deliver high-quality biomarker data.</li>
<li>Collaborate with discovery teams to translate preclinical biomarker hypotheses into clinically actionable endpoints.</li>
<li>Provide expertise on novel technologies (e.g., immunoassays, LC-MS, SIMOA, RNA-seq, digital pathology, imaging biomarkers, multiparameter flow cytometry).</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/head-of-biomarker-development-scholar-rock/69d3be1ec8e81216cd0b9200</link><guid isPermaLink="true">http://biotechroles.com/head-of-biomarker-development-scholar-rock/69d3be1ec8e81216cd0b9200</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Field Medical Advisor, South]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Field Medical Advisor will represent the real time voice of KOL/HCP input related to product development opportunities and scientific exchange on pipeline and commercial products, including conducting clinical presentations to payers.&nbsp; The ideal candidate will be a strong leader with a proven ability to leverage their high scientific acumen to engage and educate on scientifically complex concepts and products. The preferred candidate will also have a proven strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.</div></br><b>Position Responsibilities</b></br><li>Become an SMA and apitegromab medical/clinical/scientific expert</li><li>Build and foster relationships with local, regional, and national KOLs and possibly payers</li><li>Effectively deliver medical/clinical/scientific presentations to a diverse external audience</li><li>Support clinical development activities including investigator recruitment and education</li><li>Develop and execute the Territory Management Plan (TMP) that is aligned with the overall Medical Goals and plan</li><li>Contribute to developing metrics, qualitative and quantitative MSL reports, SOPs/Business Practices for the MSL function</li><li>Respond to unsolicited medical information requests submitted by Scholar Rock field teams (eg. Sales and Market Access) </li><li>Compliantly partner with Sales and Market Access on high-level regional engagement</li><li>Provide internal teams with insights from interactions and discussions with HCPs</li><li>Co-create and deliver training materials</li><li>Provide content development support for FMA materials, alongside the Director of Medical Communications</li><li>Contribute to the development of the Global, Regional, and Country Medical Plans for apitegromab in SMA</li><li>&nbsp;Participate in Advisory Board meeting, Advisory Group meetings, speaker trainings, etc. as needed</li><li>Coordinate local and regional investigator-initiated research (IIR)</li><li>Compliantly manage IIR milestones and objectives</li><li>Report on scientific sessions and conduct scientific exchange to unsolicited questions at SRRK medical booths at congresses</li><li>May respond to and document unsolicited requests for scientific information</li><li>Conduct all activities and responsibilities in accordance with all relevant legal, regulatory and corporate regulations and guidelines, including the Scholar Rock Business Conduct &amp; Ethics, policies and procedures</li></br><b>Candidate Requirements</b></br><li>MD, PharmD, or PhD preferred.&nbsp;&nbsp;</li><li>Minimum of 7 years of experience as an MSL or equivalent medical affairs role in the biotechnology or pharmaceutical industry</li><li>Must be Native or Business Fluent German Speaker; Fluency in English is preferred</li><li>Neurology and/or rare disease experience with prior launch experience preferred</li><li>Demonstrated knowledge of regulatory, commercial and clinical issues affecting the pharmaceutical industry is critical</li><li>Excellent verbal and written communication, presentation, and interpersonal skills&nbsp;</li><li>Demonstrated strategic planning, organizational and project management abilities are required</li><li>Ability to collaborate in a team environment and partner effectively across geographic areas and cross-functional groups&nbsp;</li><li>Experience in at least one “start-up” biopharma company is desirable</li><li>Must be passionate about making a difference with the highest integrity; committed to compliance, ethics and scientific standards</li><li>Demonstrate a “Will Do” attitude</li><li>Be a true collaborative Team Player</li><li>Demonstrated ability to work independently yet engage in collaborative decision making to complete tasks in a timely fashion and function in a rapidly paced environment</li><li>Experience with customer relationship management programs a plus</li><li>This will be a remote position that will require extensive overnight travel (&gt;50%)</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/field-medical-advisor-south-scholar-rock/69d3be1ec8e81216cd0b9202</link><guid isPermaLink="true">http://biotechroles.com/field-medical-advisor-south-scholar-rock/69d3be1ec8e81216cd0b9202</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Frankfurt</location><salary>$120000-160000</salary><type>Full-Time</type></item><item><title><![CDATA[Director, Upstream MSAT & Process Development]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 11pt;">We are seeking an experienced and strategic </span><b style="font-size: 11pt;">Director of Upstream MSAT and Process Development</b><span style="font-size: 11pt;"> within Technical Operations (CMC) to lead our biologics upstream MSAT and process development function across early-stage, late-stage, and commercial programs. This role will support externally partnered GMP production of Scholar Rock’s clinical and commercial assets with deep manufacturing science and technology expertise.&nbsp; The candidate will also drive the design, scale-up, and technology transfer of drug substance processes—both internally and through a global network of CDMOs. The ideal candidate combines </span><b style="font-size: 11pt;">deep upstream technical knowledge</b><span style="font-size: 11pt;">, strong organizational leadership, and proven experience managing external collaborations and in-house teams. This role is critical to ensuring robust, scalable, processes that support clinical and commercial success.</span></div></br><b>Position Responsibilities:</b></br><li>Strategic &amp; Functional Leadership:</li><li>Lead the CMC upstream MSAT and process development team for biologics (mAbs, fusion proteins, or similar).</li><li>Serve as the upstream processes thought leader for biologics manufacturing platforms, innovation, and process robustness.</li><li>Partner with stakeholders across R&amp;D, Regulatory, Manufacturing, and Quality to ensure alignment from development to commercial readiness.</li><li>Technical Program Oversight:</li><li>Design and oversee upstream process development across all stages (early/IND-enabling through BLA/commercial lifecycle).</li><li>Guide scale-up, technology transfer, and validation activities across external manufacturing sites.</li><li>Enable robust process ownership and technical oversight for clinical and commercial manufacturing.&nbsp;</li><li>Author upstream technical reports to enable program stage progression and robust regulatory filing input.</li><li>External CDMO Management:</li><li>Manage relationships with CDMOs for upstream process development, ensuring scientific rigor, quality, and timelines.</li><li>Serve as the technical upstream lead for external development and manufacturing partnerships, including CDMO selection and oversight of SOWs, budgets, and technical deliverables.</li><li>Enable successful delivery of clinical and commercial product through deviation and batch record review, change control oversight, and person-in-plan support.</li><li>Organizational Development:</li><li>Build and lead a high-performing CMC upstream MSAT and process development team</li><li>Foster a culture of scientific excellence, cross-functional collaboration, and accountability.</li><li>Regulatory Support:</li><li>Author and/or review relevant CMC sections of regulatory submissions (IND, IMPD, BLA/MAA), including process descriptions, validation strategies, and control strategies.</li><li>Support regulatory agency interactions, inspections, and responses to information requests.</li></br><b>Candidate Requirements</b></br><li>Required:</li><li>Ph.D. or M.S. in Chemical Engineering, Biochemistry, or related field.</li><li>8+ years of relevant biopharmaceutical experience encompassing both MSAT and process development functions; at least 4 years in a leadership role(s).</li><li>Proven experience developing biologics processes from early-stage through commercial launch, including PPQ and lifecycle management.</li><li>Demonstrated expertise in drug substance process development of high-concentration biologics to mitigate drug product development challenges.</li><li>Strong background in tech transfer, scale-up, and working with external CDMOs.</li><li>Experience with process ownership and technical oversight for clinical and commercial manufacturing.</li><li>Experience supporting global regulatory submissions (e.g., FDA, EMA).</li><li>Preferred:</li><li>Experience in a lean, entrepreneurial biotech environment.</li><li>Familiarity with integrated CMC program leadership or technical operations governance frameworks.</li><li>Competencies:</li><li>Strategic and enterprise mindset</li><li>Deep technical expertise with strong decision-making capability</li><li>Effective communicator with cross-functional and external partners</li><li>Proactive, solution-oriented leadership style</li><li>High standards of scientific rigor and compliance</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/director-upstream-msat-and-process-development-scholar-rock/69d3be1ec8e81216cd0b91fd</link><guid isPermaLink="true">http://biotechroles.com/director-upstream-msat-and-process-development-scholar-rock/69d3be1ec8e81216cd0b91fd</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Director/Sr. Director, Regulatory Strategy]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Director or Senior Director, Regulatory Strategy, reporting to the SVP, Global Head of Regulatory Affairs, is responsible for the development and implementation of the Global Strategy for assigned clinical and/or pipeline programs globally depending on the program. As a subject matter expert, this individual will represent regulatory affairs at the appropriate program team, highlighting risks and opportunities to inform program strategy and plan. The successful candidate will lead interactions with the regulatory authorities, directing the preparation and submission of regulatory submissions and correspondence.</div></br><b>Position Responsibilities</b></br>
<li>Serve as a thought leader on regulatory affairs, defining global regulatory strategy and plan to maximize regulatory success.</li>
<li>Serve as the global regulatory lead, providing strategic and operational input on assigned clinical and/or pipeline programs, such as the subcutaneous (IV to SC) and OPAL (&lt;2 years old) program teams to achieve program objectives while ensuring compliance with applicable regulatory requirements in the region.</li>
<li>Be responsible for leading the global supplemental/type 2 variation filing lead for OPAL (&lt;2 years old)</li>
<li>Develop regulatory roadmap to inform and guide agency engagement strategy; partner with key stakeholders to develop and implement a comprehensive regulatory engagement plan</li>
<li>Lead and managing regulatory interactions on assigned programs, building trusted relationships with regulatory authorities</li>
<li>Lead cross-functional effort to ensure timely submission of key regulatory documents (e.g., Module 1, briefing documents)</li>
<li>Ensure program team members and cross-functional stakeholders are informed of internal and external events that may impact regulatory success</li>
<li>Identify regulatory risks and opportunities and work with key stakeholders to develop solutions</li>
<li>Partner with global market access and medical affairs colleagues to support interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable</li>
<li>Partner with Global and local Marketing/ Commercial as needed to align Regulatory Plan and Marketing/Commercial plan</li>
<li>Ensure strong representation of regulatory voice at key governance bodies and teams (e.g., DRC, program teams, clinical development teams, study teams)</li>
<li>Maintain currency of regulatory requirements and approvals to inform regulatory strategies and drive proactive plans to ensure compliance</li>
<li>Monitor and analyze global and country specific regulatory landscape to assess potential impact on the program; collaborate with teams to ensure compliance</li>
<li>Provide support to local regulatory experts</li>
<li>Provide regulatory support for cross-functional activities (e.g., SOPs, business development, clinical labeling, disclosure) as needed</li>
</br><b>Candidate Requirements</b></br>
<li>Education in life sciences required</li>
<li>Greater Boston-based with ability to be regularly present in the Cambridge, MA office</li>
<li>7+ years of experience Regulatory Affairs in biopharmaceutical industry with deep understanding of EU regulatory requirements</li>
<li>Demonstrated experience of leading successful engagement with EMA</li>
<li>Expertise and experience with biologics (particularly monoclonal antibody therapeutics) and rare diseases strongly preferred but not required</li>
<li>Demonstrated reputation as a well-respected, dynamic team leader with strong leadership and people management skills</li>
<li>Strong written, verbal communication skills, and interpersonal skills</li>
<li>Capable of managing shifting priorities in a rapidly changing and environment</li>
<li>Ability to travel domestically and internationally (~10%)</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/directorsr.-director-regulatory-strategy-scholar-rock/69d3be1ec8e81216cd0b91fe</link><guid isPermaLink="true">http://biotechroles.com/directorsr.-director-regulatory-strategy-scholar-rock/69d3be1ec8e81216cd0b91fe</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Director of Accounting Operations]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>Reporting to the SVP, Finance, the Director of Accounting Operations will have responsibility for the Accounting operations function at Scholar Rock. The successful candidate will have a proven track record in managing accounting processes in a public company with a commercial asset. To lead the accounting function, the candidate will be required to have in-depth knowledge of accounting processes and systems including the general ledger, payroll, equity, and T&amp;E systems. &nbsp;The successful candidate will have a working knowledge of consolidations, accounting for clinical trials, cost accounting, transparency reporting, intercompany reconciliations, payroll, and equity, as well as having a strategic focus to ensure the systems and processes are scalable to meet the growing needs of the Company, while still maintaining compliance with internal control requirements.</div>
<div>&nbsp;</div>
<div>This position will require a hands-on approach, strong organization, clear communication, attention to detail and a great sense of teamwork. This position represents a great opportunity to help build a critical function at a growing and evolving, multi-product candidate biotechnology company.</div></br><b>Position Responsibilities</b></br>
<li>Oversee and lead all accounting operations activities including consolidations involving multiple subsidiaries, monthly close processes, intercompany, payroll and equity.</li>
<li>Help to build and scale accounting operations team, including creating processes to enable timely closing procedures that are scalable for growth</li>
<li>Ensure strong internal control environment is maintained</li>
<li>Assist in setting up policies related to travel and transparency reporting;</li>
<li>Position will also require partnership with various members of cross functional teams</li>
<li>Ability to capitalize on team member strengths and raise the team as a whole</li>
<li>Assist in ad-hoc projects as needed</li>
</br><b>Candidate Requirements</b></br>
<li>Bachelor’s degree in business, Accounting, or Finance</li>
<li>CPA and/or MBA preferred</li>
<li>Hands-on knowledge of accounting operations and processes</li>
<li>Prior management of an accounting team</li>
<li>Excellent communication and relationship building skills</li>
<li>Familiarity with internal controls requirements in a public company</li>
<li>Strong organizational and problem-solving skills with the ability to manage multiple projects at one time</li>
<li>Thrives in a dynamic environment</li>
<li>Ability to work effectively with cross-functional teams</li>
<li>At least 10 years of applicable experience in a pharmaceutical or biotechnology environment with prior experience in a public company</li>
<li>Experience with Netsuite and/or SAP a plus</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/director-of-accounting-operations-scholar-rock/69d3be1ec8e81216cd0b91fa</link><guid isPermaLink="true">http://biotechroles.com/director-of-accounting-operations-scholar-rock/69d3be1ec8e81216cd0b91fa</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Director, National Accounts (Northeast)]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>
<p style="line-height: 15pt; margin: 0in; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">The Director, National Accounts role is an opportunity for an experienced payer account executive to help launch apitegromab, Scholar Rock’s investigational drug for the treatment of Spinal Muscular Atrophy (SMA). This team will have a direct impact on our ability to deliver value to patients and the trajectory of the company’s first launch. This role will be accountable for establishing Scholar Rock’s presence with key payers, achieving rapid, appropriate coverage for apitegromab in assigned accounts and regions, and supporting ongoing patient access efforts through launch.</span></p>
</div></br><b>Position Responsibilities:</b></br><div>
<ul style="margin-bottom: 0in; margin-top: 0px;">
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Lead account planning, management, and engagement activities at assigned payers to achieve rapid and clinically appropriate access for patients.&nbsp; This includes establishing and further developing relationships with decision makers at key customers</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Support development of apitegromab’s value proposition and other supporting materials, including any account-specific needs </span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Maintain a strong understanding of apitegromab Commercial objectives and how to help achieve these goals through assigned accounts</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Work across teams to ensure patient access objectives are met, including pull-through </span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Ensure all programs are aligned to Scholar Rock values and remain compliant with regulations </span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Lead presence with target accounts at access-related meetings, events and congresses (e.g., AMCP, PCMA, Asembia, Medicaid meetings, etc)</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Collaborate with Insights and Analytics and Commercial Operations to derive account-level insights and actions; communicate access and coverage performance regularly to internal stakeholders </span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Proactively identify and execute against opportunities to improve patient access to care, within and outside of Value &amp; Access</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Be a content expert on relevant industry trends, market dynamics, policy and legislation and define implications and actions for Scholar Rock</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Be a collaborative, strategic market access presence throughout the Scholar Rock organization</span></li>

</ul></div></br><b>Candidate Requirements:</b></br><div>
<ul style="margin-bottom: 0in; margin-top: 0px;">
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Bachelors degree</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">At least 6 years’ experience in US Market Access with a deep understanding of evolving access, coverage, and reimbursement landscape</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Experience and relationships with national and key regional Commercial, Medicaid, and other Government payers.&nbsp; Experience with VA/DoD/Tricare and Humana are strongly encouraged</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Proven track record of achieving rapid, broad, and clinically appropriate coverage for medical benefit and/or rare disease products at launch</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Comprehensive understanding of payer decision making bodies and cycles, processes/procedures, and data and reporting</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Experience negotiating agreements with large healthcare systems preferred</span></li>
<li style="margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Cambria, serif;"><span style="font-size: 11.0pt; font-family: Arial, sans-serif;">Pre-launch experience at a small, start-up biotechnology company preferred</span></li>

</ul></div></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/director-national-accounts-(northeast)-scholar-rock/69d3be1ec8e81216cd0b91fc</link><guid isPermaLink="true">http://biotechroles.com/director-national-accounts-(northeast)-scholar-rock/69d3be1ec8e81216cd0b91fc</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Remote</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Country Medical Director, Germany]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 11pt;">As Country Medical Director, this person will be a strategic thought partner providing expert medical leadership and contributing to the development and execution of the Country launch strategy.&nbsp; This person will lead content development, KOL education programs, and support our cross-functional teams in Germany. As a key member of the European Medical team, reporting to EU Head of Medical Affairs, this person will be accountable for advancing Scholar Rock’s scientific leadership in Rare Neuromuscular Diseases including SMA and other pipeline indications. This person will thrive in this role if he/she is a self-starter and a highly collaborative individual who cares to have impact on patients in the rare disease space.</span></div><div><br></div><div>Scholar Rock is in the process of building its team in Germany, and the location of the future German headquarter is currently under evaluation, with Munich and Frankfurt being the leading options.</div></br><b>Position Responsibilities</b></br><li>Provide scientific and medical leadership, including development of strategic country medical affairs (pre) launch plans, identifying specific unmet medical needs, and data gaps</li><li>Lead the country medical team including field Medical Advisors</li><li>Interface, educate, and gain insights from external stakeholders, including government agencies, professional medical societies, guidance committees, key opinion leaders and key decision makers, on issues related to Scholar Rock’s assets</li><li>Oversee gathering and reporting field medical insights through existing CRM system and in line with company rules and requirements</li><li>Organize external expert advisory boards, support scientific symposia, and CME programs</li><li>Pull through medical insights across different areas to inform cross-functional strategies and tactics</li><li>Ensure cross-functional collaboration and input from key stakeholders to optimally manage relationships and ensure alignment and effective execution of the country’s medical strategy</li><li>Lead medical content development and other high impact strategic activities such as advisory boards and medical education with help of external vendor management to ensure timely delivery of medical materials and initiatives</li><li>Provide medical expertise and editorial support in the data dissemination at conferences and in medical journals</li><li>Oversee Medical activities related to review of promotional and scientific materials</li><li>Collaborate with functional groups as subject matter expert including Patient Advocacy, Commercial Operations, New Products, and many other internal stakeholders in support of pipeline products</li><li>Provide medical leadership to guide internal and external decision-making &nbsp;</li><li>Establish and maintain strong knowledge in SMA to optimize clinical study protocols development and execution</li><li>Assists in publication activities, including review and approval of abstracts and manuscripts, local publication strategy development and collaboration with authors as needed</li><li>Support the medical part of the market access dossiers and give strong input in the benefit assessment strategy during the process</li><li>Establish and maintain strong relationships with experts in the field, academics and professionals </li><li>Ensure a patient-centric approach to development of clinical studies under your supervision &nbsp;</li><li>Collaborate cross functionally to execute the clinical studies under your responsibility in alignment with the Brand plan and Global Medical Plan</li><li>Develops and maintains, together with Field Medical Advisors, close professional relationships with Key Opinion Leaders and emerging scientific leaders in the community</li><li>Foster strong relationships with internal and external stakeholders to identify unique opportunities to improve and evolve educational and training content</li><li>Manage budget for assigned projects</li><li>Accountable for understanding HCP needs and developing a strategic and tactical medical affairs plan designed to improve patient care and generate evidence of relevance for SMA in country</li><li>Support in country Clinical Trials (CT) enrollment </li><li>Travel required, comprising approximately 20-40%</li><li>Other duties as assigned</li></br><b>Basic Qualifications and Requirements</b></br><li>MD, PharmD, PhD or equivalent scientific degree. MBA desirable</li><li>Minimum 7 years’ experience in industry R&amp;D or Medical</li><li>Line Management experience</li><li>Excellent written and communication skills, highly organized and able to manage supporting multiple initiatives</li><li>Solid track record of achievement in Medical Affairs in the biotech/pharma industry</li><li>Native or Business Fluent German Speaker</li><li>Fluent in English</li></br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/country-medical-director-germany-scholar-rock/69d3be1ec8e81216cd0b91fb</link><guid isPermaLink="true">http://biotechroles.com/country-medical-director-germany-scholar-rock/69d3be1ec8e81216cd0b91fb</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Frankfurt</location><salary>$220000-350000</salary><type>Full-Time</type></item><item><title><![CDATA[Contracts Director]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>We are seeking a Contracts Director to lead our contracts processes and negotiations and provide general contracting advice across functional teams, including Development, Research, CMC/Technical Operations, Commercial and IT. &nbsp;This is an outstanding opportunity to join the legal team of a well-funded, growing biotechnology company preparing for its first product commercial launch, after recently receiving positive Phase III data and completing a successful financing. &nbsp;The primary responsibilities of the Contracts Director will be overseeing the contracts process as well as drafting, revising, and negotiating a high volume of time-sensitive agreements. &nbsp;You will be responsible for leading the contracts management function, implementing special projects such as the contracts management system, managing external law firms, and creating, and implementing new processes, trainings, reports, and systems related to managing the company’s agreements. &nbsp;You will be an integral member of a growing legal team where you will have the opportunity to be part of a collaborative team and work with experienced corporate and IP attorneys and compliance experts. &nbsp;This position reports to the Vice President, Corporate Legal and is located in the Cambridge office. &nbsp;The Company has flexibility with hybrid work arrangements.</div></br><b>Position Responsibilities</b></br>
<li>
<p>Lead the drafting and negotiations of contracts customary to a biotech company in the process of launching its first product, with a primary focus on Development, Research, CMC/Technical Operations, and IT contracts. Responsible for drafting and negotiating biotechnology-related agreements, including master service agreements, material transfer agreements, consulting agreements, confidentiality agreements, research agreements and clinical trial site agreements and related statements of work.</p>
</li>
<li>
<p>Manage and maintain contracts management system and associated contracting processes, including providing company-wide trainings.</p>
</li>
<li>
<p>Provide legal support across the organization, including quickly and effectively identifying complex legal and compliance issues and providing advice in a manner that integrates legal risk management with the company’s business objectives.</p>
</li>
<li>
<p>Ability to work in a fast-paced environment, prioritize tasks, and successfully manage multiple projects.</p>
</li>
<li>
<p>Develop and maintain strong business relationships across the company and contribute to cross-functional or departmental projects and teams.</p>
</li>
<li>
<p>Maintain a positive team culture.</p>
</li>
<li>
<p>Manage and complete any additional projects or legal matters as needed, including general corporate matters.</p>
<p><strong>&nbsp;</strong></p>
<p>&nbsp;</p>
</li>
</br><b>Candidate Requirements</b></br>
<li>License to practice Law in Massachusetts or equivalent preferred, but candidates without a J.D. will be considered who have deep industry experience</li>
<li>Ten or more years’ experience drafting and negotiating biotechnology-related agreements, including master service agreements, SOWs, research agreements, clinical trial related agreements, manufacturing or supply chain agreements, and commercial contracts in the life sciences industry</li>
<li>Previous experience working on an in-house legal team at a biotechnology company required</li>
<li>Ability to work independently with strong attention to detail, sound judgment, organization and time management required</li>
<li>Strong interpersonal skills and desire to engage collaboratively required</li>
<li>Strong oral and written communication skills required, including the ability to provide concise and timely advice to business partners</li>
<li>Familiarity with contracts management systems such as Ironclad and DocuSign eSignature preferred</li>
<li>Bachelor’s degree from accredited university required</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/contracts-director-scholar-rock/69d3be1ec8e81216cd0b91f9</link><guid isPermaLink="true">http://biotechroles.com/contracts-director-scholar-rock/69d3be1ec8e81216cd0b91f9</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-260000</salary><type>Full-Time</type></item><item><title><![CDATA[Chief Information Officer, VP of Information Technology]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div>The Chief Information Officer (CIO)/VP of IT will lead Scholar Rock’s global IT function through a period of rapid growth, modernization, and strategic transformation. This executive will ensure workplace enablement and IT service reliability today, while defining and executing a forward-looking technology vision that enables global commercialization, compliant operations, and digital innovation.</div>
<div>&nbsp;</div>
<div>A proven builder and scaler of IT organizations and systems, the CIO/VP IT will establish the people, processes, and platforms needed to support Scholar Rock’s growth from a development-stage biotech to a fully integrated global commercial company. The CIO/VP IT will also be a visible leader with regular engagement at the Executive Team and Board level, providing updates on IT performance, cybersecurity, compliance, and digital strategy.</div></br><b>Position Responsibilities: </b></br>
<li><strong>Workplace Enablement &amp; Operational Excellence:</strong></li>
<li>Ensure reliable IT operations and service delivery for employees, labs, and field teams.</li>
<li>Build a customer-focused IT culture with clear governance, metrics, and accountability.</li>
<li>Modernize collaboration and productivity platforms to improve hybrid work and global connectivity.</li>
<li><strong>Strategic IT &amp; Technology Enablement:</strong></li>
<li>Define and execute a visionary IT strategy aligned with Scholar Rock’s scientific, operational, and commercial goals.</li>
<li>Enable data-driven decision-making through modern data platforms, analytics, and integration across R&amp;D, clinical, supply chain, G&amp;A, and commercial functions.</li>
<li>Explore and implement emerging technologies (cloud, AI/ML, digital engagement) to create competitive advantage.</li>
<li>Serve as a thought partner to the Executive Team and the business on technology investments and digital transformation.</li>
<li>Provide frequent updates to the Executive Team and Board on IT performance, risk management, and progress toward strategic objectives.</li>
<li><strong>GxP, Commercial &amp; G&amp;A Systems:</strong></li>
<li>Oversee implementation and compliance of GxP systems across manufacturing, quality, supply chain, and pharmacovigilance.</li>
<li>Deliver validated enterprise applications (ERP, QMS, LIMS, serialization, data platforms) that are scalable for commercial operations.</li>
<li>Lead deployment of commercial IT systems:&nbsp;</li>
<li>CRM platforms for field force effectiveness (e.g., Veeva, Salesforce).</li>
<li>Commercial data hub / data warehouse to integrate patient services, market access, sales, and medical data.</li>
<li>Field force enablement tools to support omnichannel engagement, analytics, and reporting.</li>
<li>Build and optimize G&amp;A systems including:</li>
<li>Finance/ERP systems to support SOX compliance, reporting, and global operations.</li>
<li>HRIS/HCM platforms to support workforce growth, talent management, and global mobility.</li>
<li>Procurement, contracts, and compliance tools for a public company environment.</li>
<li><strong>Cybersecurity &amp; Global Infrastructure:</strong></li>
<li>Build a robust cybersecurity program to protect sensitive clinical, commercial, employee, and patient data.</li>
<li>Ensure compliance with GDPR, HIPAA, SOX, and other global data regulations.</li>
<li>Develop scalable IT infrastructure and networks to support Scholar Rock’s international expansion.</li>
<li><strong>IT Organization Build &amp; Resourcing:</strong></li>
<li>Establish and scale a global IT organization with the right mix of internal talent and external partners.</li>
<li>Define the operating model, including in-house IT leadership, managed service providers, and strategic vendors.</li>
<li>Build an IT team capable of supporting 24/7 operations across regions, with clear roles in workplace support, GxP/commercial systems, cybersecurity, and enterprise applications.</li>
<li>Develop succession planning, talent pipelines, and governance structures for long-term scalability.</li>
</br><b>Candidate Qualifications: </b></br>
<li>15+ years of IT leadership, including senior executive experience in biotech, pharma, or life sciences.</li>
<li>Required: Demonstrated success building and scaling IT organizations and enterprise systems to support global business growth.</li>
<li>Proven track record in stabilizing IT operations while delivering long-term digital strategy.</li>
<li>Deep knowledge of GxP IT systems, validation, and global regulatory requirements.</li>
<li>Experience implementing and managing commercial IT platforms (CRM, data hub, analytics, field force tools).</li>
<li>Experience leading Finance (ERP) and HRIS/HCM systems implementation and optimization in a public company context.</li>
<li>Strong background in data strategy, digital innovation, and technology enablement.</li>
<li>Excellent leadership, vendor management, and change management skills.</li>
<li>Strong boardroom presence, with experience preparing and delivering executive and board-level updates.</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/chief-information-officer-vp-of-information-technology-scholar-rock/69d3be1ec8e81216cd0b91f7</link><guid isPermaLink="true">http://biotechroles.com/chief-information-officer-vp-of-information-technology-scholar-rock/69d3be1ec8e81216cd0b91f7</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$280000-450000</salary><type>Full-Time</type></item><item><title><![CDATA[Associate Director/Director of Toxicology]]></title><description><![CDATA[<div><i>Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. </i></div><div><i>&nbsp;</i></div><div><i>Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at </i><a rel="noopener noreferrer" class="postings-link" href="http://www.scholarrock.com/"><i>ScholarRock.com</i></a><i> and follow </i><a rel="noopener noreferrer" class="postings-link" href="http://www.twitter.com/scholarrock"><i>@ScholarRock</i></a><i> and on </i><a rel="noopener noreferrer" class="postings-link" href="https://www.linkedin.com/company/scholar-rock"><i>LinkedIn</i></a><i>.</i></div><div><br></div><div><b style="font-size: 18px;">Summary of Position:</b></div><div><br></div><div><span style="font-size: 12pt;">Scholar Rock is seeking a Associate Director/Director of Toxicology that will be responsible for the creation and execution of the nonclinical safety strategy.&nbsp;&nbsp;The successful candidate will be responsible for operational oversight as well as the interpretation and communication of toxicology data to support the advancement of Scholar Rock’s discovery and development portfolio.&nbsp;&nbsp;&nbsp;Reporting to the Vice President, Head of Preclinical Sciences, this individual will design and implement fit-for-purpose toxicology approaches (including the incorporation of NAMs), oversee studies conducted at CROs, interpret and communicate safety data, and serve as a key contributor to program strategy and regulatory submissions. This individual will be a member of the Research Leadership Team.&nbsp;</span></div></br><b>Strategic Leadership & Vision </b></br>
<li>Define and drive the&nbsp;toxicology testing&nbsp;strategy across preclinical and clinical programs, ensuring alignment with overall portfolio goals.&nbsp;</li>
<li>Serve as a&nbsp;PreClinical&nbsp;Science thought leader, integrating&nbsp;existing and emerging&nbsp;toxicological&nbsp;approaches into program strategy&nbsp;and&nbsp;clinical development plans&nbsp;in support of program advancement and&nbsp;key regulatory milestones.&nbsp;&nbsp;</li>
<li>Represent&nbsp;toxicology&nbsp;in cross-functional governance and portfolio planning forums.&nbsp;</li>
<li>Partner with other functions (Translational Biomarkers, Research, and clinical teams) to guide evaluation of targets and programs to&nbsp;contextualize&nbsp;nonclinical&nbsp;safety findings.&nbsp;</li>
</br><b>Functional & Scientific Oversight</b></br>
<li>Operational excellence of Toxicology Function: Includes the fostering of&nbsp;collaborative&nbsp;CRO&nbsp;interactions&nbsp;to&nbsp;deliver&nbsp;timely&nbsp;and&nbsp;high-quality&nbsp;toxicology&nbsp;data, maintenance of timelines, costs, and risk assessment/management.&nbsp;</li>
<li>Leverage existing and emerging NAMs&nbsp;to support&nbsp;the advancement of monoclonal antibodies across the research and development portfolio.&nbsp;&nbsp;&nbsp;</li>
<li>Lead the design&nbsp;and execution of toxicology studies, working cross-functionally&nbsp;to&nbsp;incorporate bioanalytical and translational biomarkers&nbsp;to address nonclinical safety questions.&nbsp;</li>
<li>Author and review&nbsp;toxicology&nbsp;sections of INDs, CTAs, IBs, CSRs, and other regulatory filings.&nbsp;</li>
<li>Collaborate with Clinical Development&nbsp;to&nbsp;understand the potential relevance of nonclinical safety signals.&nbsp;</li>
<li>Distill large&nbsp;nonclinical&nbsp;safety datasets&nbsp;for&nbsp;key messaging; interpret and communicate findings to key stakeholders within Research and Development.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</li>
<li>Contribute to the&nbsp;evaluation&nbsp;of novel modalities and combination strategies to support advancement of Scholar Rock’s portfolio.&nbsp;&nbsp;&nbsp;</li>
</br><div><i>Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees</i>.&nbsp;</div>]]></description><link>http://biotechroles.com/associate-directordirector-of-toxicology-scholar-rock/69d3be1ec8e81216cd0b91f8</link><guid isPermaLink="true">http://biotechroles.com/associate-directordirector-of-toxicology-scholar-rock/69d3be1ec8e81216cd0b91f8</guid><pubDate>Mon, 06 Apr 2026 14:07:26 GMT</pubDate><company>Scholar Rock</company><location>Cambridge, MA</location><salary>$180000-250000</salary><type>Full-Time</type></item><item><title><![CDATA[Vice President, Clinical Development and Trial Innovation]]></title><description><![CDATA[<div><b><span style="font-size: 12pt;">About Us</span></b></div><div><br></div><div><span style="font-size: 12pt;">Our mission is to cure cancer through high performance, accessible early cancer detection. That means saving lives.</span></div><div><br></div><div><span style="font-size: 12pt;">Delfi Diagnostics is a Johns Hopkins spinoff focused on the non-invasive detection of cancer at earlier stages, when it is most curable. DELFI uses artificial intelligence and whole-genome sequencing to detect unique patterns of DNA fragmentation in the blood of patients with cancer. These analyses are performed through simultaneous examination of millions of DNA sequences using machine learning to identify tumor-specific abnormalities.</span></div><div><br></div><div><span style="font-size: 12pt;">In our passionate pursuit to radically improve health outcomes, we serve humanity when we:</span></div><div><b><span style="font-size: 12pt;">Lead with Science, Anchor in Pragmatism</span></b><span style="font-size: 12pt;">: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times.</span></div><div><br></div><div><b><span style="font-size: 12pt;">Build With &amp; For All</span></b><span style="font-size: 12pt;">: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product—we aim to disrupt the path of cancer for all, no matter geography or socioeconomic class.</span></div><div><br></div><div><b><span style="font-size: 12pt;">Put We over I</span></b><span style="font-size: 12pt;">: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us win. We show up with empathy, humility, and integrity at every step of the journey.</span></div><div><br></div><div><b style="font-size: 12pt;">About the Role</b></div><div><br></div><div><span style="font-size: 12pt;">The VP, Clinical Development and Trial Innovation provides strategic leadership across DELFI’s clinical study portfolio, working closely with executive leadership and cross-functional teams including R&amp;D, medical, quality, and regulatory. This leader defines and shapes the comprehensive strategy for all DELFI clinical studies while executing on our key trials supporting product development, launch, and reimbursement. We seek an adaptable, rigorous, future-thinking, and decisive leader who is solidly grounded in clinical development and will champion the use of AI to innovate on clinical trial efficiency. The role requires technical expertise in clinical study design and development, oncology, and preferably diagnostics product development.</span></div></br><b>What You'll Do</b></br><li><b>Clinical Study Design &amp; Development</b></li><li>Design, develop, and execute clinical studies that generate robust evidence for DELFI's current and future pipeline of product claims, including studies that establish clinical validity and clinical utility</li><li>Advance DELFI’s development of diagnostic products for cancer, with the detection of lung cancer in USPSTF-eligible individuals as the first indication</li><li>Establish and implement a comprehensive five-year clinical development strategy based on the latest clinical science, evidence gaps, and unmet needs in cancer diagnostics</li><li>Partner with R&amp;D Biostatistics to design case-control and prospective clinical studies, and to analyze those studies in accordance with statistical analysis plans</li><li>Manage the clinical development &amp; clinical operations groups and affiliated CROs, including vendor selection/management/monitoring, site selection, patient enrollment and follow-up, etc.</li><li>Develop and manage clinical trial timelines, budget, and risks in accordance with overall product development processes and plans</li><div><br></div><li><b>Regulatory &amp; Evidence Management</b></li><li>Interact with FDA on submissions for IVD product approval, including face-to-face/virtual meetings and written presubmissions in coordination with Regulatory Affairs</li><li>Author relevant sections of IVD documents pertaining to clinical development activities, design controls, requirements, etc.</li><li>Work closely with Medical Affairs to identify evidence gaps and generate real-world data for DELFI's product(s)</li><div><br></div><li><b>AI-Enabled Trial Innovation and Product Development</b></li><li>Liaise with the head of R&amp;D and the PIs of research &amp; clinical studies sponsored by DELFI to develop sub-studies and relevant aims that advance DELFI’s R&amp;D pipeline</li><li>Champion the use of AI to innovate on clinical trial recruitment or efficiency</li><li>Work with digital health providers in the US, EU, and Asia to streamline and accelerate trial data collection and scale the cross-referencing of longitudinal clinical and genomic data with national disease registries, health-promotion programs, and socioeconomic and environmental records</li><li>Collaborate with Data Engineering to store, curate, and cross-reference DELFI's clinical data</li><div><br></div><li><b>Communication, Thought Leadership, and Outreach</b></li><li>Participate in industry stakeholder groups and consortia such as BLOODPAC or the Global Alliance for Genomics and Health</li><li>Present to senior leadership, board of directors, company-wide, and at key national and international scientific &amp; clinical meetings</li></br><b>What You’ll Bring to DELFI</b></br><li>PhD in the physical or natural sciences, or MD.&nbsp;Disciplinary expertise in cancer biology strongly preferred</li><li>10+ years’ expertise leading the design &amp; development of clinical studies for either pharmaceutical or diagnostics development, as evidenced by strong publication record or successful product releases</li><li>3-5 years’ experience in IVD diagnostics development</li><li>Knowledge of relevant clinical &amp; regulatory standards such as ICH E6(R3) GCP, ISO 14155, ISO 13485, 21 CFR part 820</li><li>Familiarity with cutting-edge AI approaches in clinical trials (NLP or LLM for EHRs, digital twins, digital pathology) as well as international data standards such as FAIR principles, FHIR-OMOP, or Common Data Models</li><li>10+ years’ management experience including best practices in recruiting, coaching, performance management, and career development</li><li>Superb communication skills including mastery in written &amp; oral presentations, large- and small-group forums</li><li>Start-up mindset: passionate, innovative, accountable, able to rapidly prioritize and triage, biased to action</li><li>Proactive, decisive, and composed with a balance of high IQ &amp; EQ</li></br>]]></description><link>http://biotechroles.com/vice-president-clinical-development-and-trial-innovation-delfi-diagnostics/69d3be0dc8e81216cd0b91d0</link><guid isPermaLink="true">http://biotechroles.com/vice-president-clinical-development-and-trial-innovation-delfi-diagnostics/69d3be0dc8e81216cd0b91d0</guid><pubDate>Mon, 06 Apr 2026 14:07:09 GMT</pubDate><company>Delfi Diagnostics</company><location>Palo Alto, CA</location><salary>$280000-450000</salary><type>Full-Time</type></item><item><title><![CDATA[Senior Staff Scientist, IVD Assay Verification and Validation (Contract)]]></title><description><![CDATA[<div><b style="font-size: 18px">About Us</b></div><div><br></div><div><span style="font-size: 16px;">DELFI Diagnostics, Inc. (DELFI Diagnostics) is developing next-generation, blood-based tests that are reliable, accessible and deliver a new way to help detect cancer. Employing advanced machine-learning methods to whole-genome sequencing data, the DELFI ("DNA EvaLuation of Fragments for early Interception") platform is built to address the highest-burden health challenges. DELFI Diagnostics prioritizes solutions that have the potential to save lives on a global scale, including for historically underserved populations. DELFI Diagnostics’ platform relies on fragmentomics – the discovery that cancer cells are more chaotic than normal cells and, when they die, leave behind tell-tale patterns and characteristics of cell-free DNA (cfDNA) fragments. FirstLook Lung, for individuals eligible for lung cancer screening, is DELFI Diagnostics’ first laboratory-developed screening test and can be part of routine blood work. FirstLook Lung uses millions of data points to reliably identify individuals who may have cancer detected through low-dose CT, including early stage disease with a negative predictive value of 99.8 percent. This test has not been cleared or approved by the FDA.</span></div><div><br></div><div><span style="font-size: 16px;">In our passionate pursuit to radically improve health outcomes, we serve humanity when we:</span></div><div><br></div><div><b><span style="font-size: 16px;">Lead with Science, Anchor in Pragmatism</span></b><span style="font-size: 16px;">: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times. We explore thoughtfully, experiment smartly, and deliver impact with conviction. </span></div><div><br></div><div><b><span style="font-size: 16px;">Build With &amp; For All</span></b><span style="font-size: 16px;">: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product - we aim to disrupt the path of cancer for all - no matter geography or socioeconomic class&nbsp;</span></div><div><br></div><div><b><span style="font-size: 16px;">Put We over I</span></b><span style="font-size: 16px;">: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us--win. We show up with empathy, humility, and integrity at every step of the journey.</span></div><div><br></div><div><b style="font-size: 16px">DELFI has 1-2 designated in-office working days each week for employees who live within within 50 miles of Palo Alto CA or Baltimore MD offices</b></div><div><br></div><div><b><span style="font-size: 18px;">About the Role</span></b></div><div><br></div><div><span style="font-size: 16px;">In this role, you will drive efforts to verify and validate the performance of an automated IVD Next-Generation Sequencing-based assay under development for early cancer detection. You will have the opportunity to design, plan and execute design verification studies that will serve as the basis for the assay’s analytical performance claims. Additionally, you will collaborate closely with the quality and regulatory functions to ensure that product design, development, and transfer comply with design control and risk management requirements.</span></div></br><b>What you’ll do</b></br><li>Help establish Delfi’s culture of compliance through scalable tools, structures, and processes for compliant product development</li><li>Drive the verification and validation of products that are compliant with CLIA, FDA, and international regulatory standards</li><li>Implement and improve Delfi’s design control process throughout all stages of the product life cycle</li><li>Design, plan, and coordinate the execution of analytical validation (AV),other design verification studies or design transfer activities</li><li>Collaborate with R&amp;D and Lab Operations, Biostatisticians and Quality, Regulatory teams to create and execute study plans</li><li>Prepare design verification and validation study documentation, such as study protocols and reportsContribute directly to FDA PMA submissions</li><li>Create and present Formal Design Review presentations at key milestones</li><li>Collaborate with Systems Engineering to document product requirements while ensuring the requirements are met during design verification</li></br><b>What you'll bring to DELFI (Required) </b></br><li>Degree in relevant field (biomedical engineering, molecular biology, genetics, or genomics)</li><li>Minimum of 10 years of experience developing IVD products in regulated environments</li><li>Expertise in IVD regulatory requirements (FDA 21 CFR Part 820, ISO14971, ISO13485, IVDR)</li><li>Demonstrated IVD and AV experience gained from development and ideally FDA approval of multi marker genomic or other ’omic assays</li><li>High level of analytical ability to solve complex technical problems</li><li>Proven ability to collaborate cross-functionally</li><li>Skill in technical and non-technical communication</li></br><div>We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div><div><br></div><div><b>This position is not eligible for agency partnership. Resumes and outreach from staffing representatives will be declined.</b></div><div><br></div>]]></description><link>http://biotechroles.com/senior-staff-scientist-ivd-assay-verification-and-validation-(contract)-delfi-diagnostics/69d3be0dc8e81216cd0b91cf</link><guid isPermaLink="true">http://biotechroles.com/senior-staff-scientist-ivd-assay-verification-and-validation-(contract)-delfi-diagnostics/69d3be0dc8e81216cd0b91cf</guid><pubDate>Mon, 06 Apr 2026 14:07:09 GMT</pubDate><company>Delfi Diagnostics</company><location>Palo Alto, CA</location><salary>$180000-250000</salary><type>Contract</type></item><item><title><![CDATA[Senior Staff Clinical Data Manager]]></title><description><![CDATA[<div><b style="font-size: 18px">About Us</b></div><div><br></div><div><span style="font-size: 16px;">DELFI Diagnostics, Inc. (DELFI Diagnostics) is developing next-generation, blood-based tests that are reliable, accessible and deliver a new way to help detect cancer. Employing advanced machine-learning methods to whole-genome sequencing data, the DELFI ("DNA EvaLuation of Fragments for early Interception") platform is built to address the highest-burden health challenges. DELFI Diagnostics prioritizes solutions that have the potential to save lives on a global scale, including for historically underserved populations. DELFI Diagnostics’ platform relies on fragmentomics – the discovery that cancer cells are more chaotic than normal cells and, when they die, leave behind tell-tale patterns and characteristics of cell-free DNA (cfDNA) fragments. FirstLook Lung, for individuals eligible for lung cancer screening, is DELFI Diagnostics’ first laboratory-developed screening test and can be part of routine blood work. FirstLook Lung uses millions of data points to reliably identify individuals who may have cancer detected through low-dose CT, including early stage disease with a negative predictive value of 99.8 percent. This test has not been cleared or approved by the FDA.</span></div><div><br></div><div><span style="font-size: 16px;">In our passionate pursuit to radically improve health outcomes, we serve humanity when we:</span></div><div><br></div><div><b><span style="font-size: 16px;">Lead with Science, Anchor in Pragmatism</span></b><span style="font-size: 16px;">: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times. We explore thoughtfully, experiment smartly, and deliver impact with conviction. </span></div><div><br></div><div><b><span style="font-size: 16px;">Build With &amp; For All</span></b><span style="font-size: 16px;">: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product - we aim to disrupt the path of cancer for all - no matter geography or socioeconomic class&nbsp;</span></div><div><br></div><div><b><span style="font-size: 16px;">Put We over I</span></b><span style="font-size: 16px;">: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us--win. We show up with empathy, humility, and integrity at every step of the journey.</span></div><div><br></div><div><b style="font-size: 16px">DELFI has 1-2 designated in-office working days each week for employees who live within within 50 miles of Palo Alto CA or Baltimore MD offices</b></div><div><br></div><div><span style="font-size: 16px;">We are entering a pivotal year at DELFI. With multiple key clinical study milestones on the horizon supporting our IVD submission, we need a Clinical Data Management (CDM) leader who can drive execution with precision and speed.</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">You will play a central leadership role in our key clinical validation studies. Whether leading a study end-to-end or driving critical data milestones for our regulatory submissions, you will hold high accountability for the integrity and timely delivery of our clinical data and key mentorship and oversight of junior team members. You’re a nimble problem solver who is willing to jump into any responsibility, from high-level strategy to query resolution. You are a highly skilled communicator with a deep understanding of how to navigate cross-functional relationships, driving progress towards shared goals. </span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">This role sits within the Data Engineering function, a strategic choice that places Clinical Data Management directly adjacent to the technical tools that power our business. We are not looking for a software developer, but rather a Clinical Data Management expert who is eager to leverage a modern data stack (Databricks, SQL, R/Python). Alongside the Clinical Operations team, you will drive our clinical data operations, ensure audit-ready data quality for our regulatory submissions, and partner with our incoming Digital Health leadership to modernize how we capture, interpret and analyze patient data.</span></div></br><b>What You'll Do (80% Clinical Execution)</b></br>
<li>Lead Clinical Data Operations: Own the end-to-end data lifecycle for our clinical studies. Establish timelines and drive team adherence towards interim analysis data cuts, database locks and final validation readouts</li>
<li>Sample &amp; Data Reconciliation: Manage the complex reconciliation between clinical data (EDC) and biological sample data (LIMS). Ensure the life-cycle of the sample matches the clinical data</li>
<li>Data Quality &amp; Regulatory Readiness: Own, execute, and oversee compliance with the Clinical Data Management Plan (CDMP). Author and oversee the generation of Data Quality Review listings (DQR) to support IVD clinical validation. Ensure all clinical data activities are inspection-ready. Proactively organize and perform ongoing data review throughout study conduct to ensure timely and appropriate identification of errors, trends, discrepancies, completeness, and quality issues</li>
<li>Ensure proper closeout and archiving of data management study related materials, e.g., CDMPs, database change documentation, validation documents, and final participant casebooks</li>
<li>Vendor Oversight: Manage CROs and EDC vendors to ensure they meet DELFI’s standards, study-specific plans, and contractual obligations. Review eCRF designs, edit checks, and UAT specifications to minimize downstream data issues</li>
<li>Cross-Functional Leadership: Serve as a primary data management representative in clinical study team meetings. Develop and maintain departmental procedures in accordance with regulatory requirements Proactively assess project and CDM issues and risks working with the Clinical Operations team</li>
<li>Mentorship: While this role is an individual contributor, a critical function will be to provide oversight to deliverables of junior team members</li>
</br><b>What You’ll Do (20% Tech Modernization)</b></br>
<li>Leverage Modern Tools: Work directly within Databricks to review data. Instead of waiting for static PDF listings, you will query data (SQL) or run existing QC scripts (R/Python) to identify discrepancies in real-time</li>
<li>Bridge the Gap: Act as the translator between Clinical Development and Data Engineering. When the data engineers build pipelines, you define the clinical logic. When the clinical team needs data, you help them access it self-service</li>
<li>Digital Health Adaptation: As we integrate new digital health endpoints, you will adapt our data management processes to handle EMR and real world data alongside traditional EDC data</li>
</br><div>We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div><div><br></div><div><b>This position is not eligible for agency partnership. Resumes and outreach from staffing representatives will be declined.</b></div><div><br></div>]]></description><link>http://biotechroles.com/senior-staff-clinical-data-manager-delfi-diagnostics/69d3be0dc8e81216cd0b91ce</link><guid isPermaLink="true">http://biotechroles.com/senior-staff-clinical-data-manager-delfi-diagnostics/69d3be0dc8e81216cd0b91ce</guid><pubDate>Mon, 06 Apr 2026 14:07:09 GMT</pubDate><company>Delfi Diagnostics</company><location>Palo Alto, CA</location><salary>$140000-190000</salary><type>Full-Time</type></item><item><title><![CDATA[Clinical Laboratory Scientist (Contract)]]></title><description><![CDATA[<div><b style="font-size: 18px">About Us</b></div><div><br></div><div><span style="font-size: 16px;">DELFI Diagnostics, Inc. (DELFI Diagnostics) is developing next-generation, blood-based tests that are reliable, accessible and deliver a new way to help detect cancer. Employing advanced machine-learning methods to whole-genome sequencing data, the DELFI ("DNA EvaLuation of Fragments for early Interception") platform is built to address the highest-burden health challenges. DELFI Diagnostics prioritizes solutions that have the potential to save lives on a global scale, including for historically underserved populations. DELFI Diagnostics’ platform relies on fragmentomics – the discovery that cancer cells are more chaotic than normal cells and, when they die, leave behind tell-tale patterns and characteristics of cell-free DNA (cfDNA) fragments. FirstLook Lung, for individuals eligible for lung cancer screening, is DELFI Diagnostics’ first laboratory-developed screening test and can be part of routine blood work. FirstLook Lung uses millions of data points to reliably identify individuals who may have cancer detected through low-dose CT, including early stage disease with a negative predictive value of 99.8 percent. This test has not been cleared or approved by the FDA.</span></div><div><br></div><div><span style="font-size: 16px;">In our passionate pursuit to radically improve health outcomes, we serve humanity when we:</span></div><div><br></div><div><b><span style="font-size: 16px;">Lead with Science, Anchor in Pragmatism</span></b><span style="font-size: 16px;">: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times. We explore thoughtfully, experiment smartly, and deliver impact with conviction. </span></div><div><br></div><div><b><span style="font-size: 16px;">Build With &amp; For All</span></b><span style="font-size: 16px;">: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product - we aim to disrupt the path of cancer for all - no matter geography or socioeconomic class&nbsp;</span></div><div><br></div><div><b><span style="font-size: 16px;">Put We over I</span></b><span style="font-size: 16px;">: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us--win. We show up with empathy, humility, and integrity at every step of the journey.</span></div><div><br></div><div><b style="font-size: 16px">DELFI has 1-2 designated in-office working days each week for employees who live within within 50 miles of Palo Alto CA or Baltimore MD offices</b></div><div><br></div><div><span style="font-size: 16px;">In this contract role, you will be responsible for performing high complexity laboratory testing for cancer detection via next generation sequencing. You will work closely with automation, assay development and technology transfer scientists to build scalable infrastructure within the Clinical Laboratory. You will be part of a cross-functional team working to launch products for clinical use.</span></div></br><b>What You'll Do</b></br>
<li>Perform laboratory tests, procedures, analyses, and reporting of patient results per approved procedures</li>
<li>Identify and troubleshoot high complexity problems that may adversely affect the test performance</li>
<li>Perform and document reagent manufacturing and qualification per approved procedures</li>
<li>Verify instrument performance through inspection, calibration, and maintenance per approved procedures</li>
<li>Organize and conduct the training of new and existing laboratory personnel on current and new procedures</li>
</br><b>What You’ll Bring to DELFI</b></br>
<li>Must possess an active and valid Clinical Laboratory Scientist (CLS) or Clinical Genetic Molecular Biologist Scientist (CGMBS) license issued by the state of California pursuant to Division 2, Chapter 3 of the California Business and Professions Code or to practice medicine, osteopathy, or podiatry pursuant to Division 2, Chapter 5 of the California Business and Professions Code appropriate to the specialty being performed</li>
<li>Must fulfill requirements stated in 42 CFR 493.1489 or <a rel="noopener noreferrer" href="http://493.1491" class="postings-link">493.1491</a></li>
<li>Must fulfill requirements stated in the College of American Pathologists Molecular Pathology Checklist</li>
<li>BS in Biomedical Laboratory Sciences, Clinical Science, or equivalent</li>
<li>Ability to communicate complex technical results to a cross-functional audience</li>
<li>Desire to learn about cancer genetics and contribute to a diverse, collaborative and mutually respectful working environment</li>
<li>2+ years of Clinical Laboratory experience or equivalent high complexity and volume laboratory experience</li>
<li>Laboratory experience within the last year</li>
<li>Experience with next generation sequencing, molecular biology techniques and automated liquid handlers</li>
<li>Working knowledge of local, state, and federal laboratory regulations</li>
</br><div>We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div><div><br></div><div><b>This position is not eligible for agency partnership. Resumes and outreach from staffing representatives will be declined.</b></div><div><br></div>]]></description><link>http://biotechroles.com/clinical-laboratory-scientist-(contract)-delfi-diagnostics/69d3be0dc8e81216cd0b91cd</link><guid isPermaLink="true">http://biotechroles.com/clinical-laboratory-scientist-(contract)-delfi-diagnostics/69d3be0dc8e81216cd0b91cd</guid><pubDate>Mon, 06 Apr 2026 14:07:09 GMT</pubDate><company>Delfi Diagnostics</company><location>Palo Alto, CA</location><salary>$75000-110000</salary><type>Contract</type></item><item><title><![CDATA[Director, Pharmacovigilance Scientist]]></title><description><![CDATA[<div>Cullinan Therapeutics is a biopharmaceutical company developing potential first- or best-in-class, high-impact therapies for autoimmune diseases and cancer. Cullinan pursues promising therapeutic targets while leveraging core expertise in T cell engagers, which are established in oncology and are now advancing into autoimmune diseases. With a clinical-stage pipeline built on a rigorous scientific approach and purposeful innovation, Cullinan is advancing its mission to deliver new standards of care for patients.</div>
<div>&nbsp;</div>
<div>The Pharmacovigilance Scientist (PVS) participates in the development and planning of safety strategies for assigned products in early clinical development (Phase I and II clinical studies). This will include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment. PVS will play essential role in developing PV/Safety documents in collaboration with other PV team members and cross-functional teams e.g., medical, clinical operations, biostatistics, and regulatory affairs.&nbsp;</div></br><b>Position Responsibilities</b></br>
<li>Provide complete Cullinan product life-cycle support for assigned product(s) and participate in clinical study team meetings as appropriate for assigned products</li>
<li>Represent PV for assigned compounds as a PV lead in cross-functional teams, including Cullinan Safety Management Team (SMT), Safety Review committee (SRC) and other teams with members external to Cullinan.</li>
<li>Perform ongoing quality review of ICSR representing company review in accordance with study Safety Management Plans, Safety exchange agreements, and SOPs.</li>
<li>Perform signal detection activities for assigned products in line with approved safety surveillance plan. Perform signal evaluation for any identified signals and author the safety evaluation report. Ensure timely, quality reports/safety analyses related to core deliverables with oversight as appropriate.</li>
<li>Analyze the safety data, prepare and deliver presentations at SMT meetings.</li>
<li>Responsible for authoring, preparation and review of safety documents including DSUR, response to health authority or other stakeholder safety queries etc.</li>
<li>Collaborate with clinical/Medical team to foster communication of potential safety concerns.</li>
<li>Alert the Head of PV and Medical Safety Physicians to potential safety issues recognized through single case medical review or aggregated data sets.</li>
<li>Participate and collaborate with the Clinical/Medical team in other risk management/mitigation activities in the clinical studies as appropriate for assigned compounds.</li>
<li>Responsible for authoring the RSI section of the IB with an ability to provide expectedness of events for regulatory reporting purposes.</li>
<li>Responsible for authoring the safety section in collaboration with team members on regulatory responses, IBs, review Informed Consent Forms (ICF), CRFs, and providing the necessary quality control for safety assessment.</li>
<li>Participate and collaborate with Clinical/Medical function in the development of protocols, and ensure safety oversight in cooperation/leadership of the clinical trial medical team</li>
<li>Ensure timely, quality reports/safety analyses related to core deliverables with oversight as appropriate.</li>
<li>Serve as a Pharmacovigilance resource to the cross-functional teams.</li>
<li>Collaborate with clinical/Medical team to foster communication of the potential safety concerns.</li>
<li>Able to work with and collaborate with Pharmacovigilance Operations (PVO) to manage PV related activities by CRO. &nbsp;</li>
<li>Participate and collaborate with PVO for SAE reconciliation activities between the clinical and safety databases in accordance with SOPs.</li>
<li>Participating in and collaborating with PVO in the process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents.</li>
<li>Review and provide input and support with other departments (e.g., clinical/medical, clinical operations, medical information, regulatory affairs, and data management) groups on PV-related topics for study protocols, statistical analysis plans, and other clinical-related documents.</li>
</br><b>Candidate Requirements</b></br>
<li>MS, PhD, or PharmD</li>
<li>Previous experience as PV/drug safety or clinical research safety (preferably in early clinical development) typically with at least 5 years of experience.</li>
<li>Experience primarily in immunology and oncology therapeutic areas and any relevant experience or understanding of CART-cell therapy or T Cell engagers would be preferred.</li>
<li>Ability to utilize safety system database (Argus) for purposes of medical case review and simple queries.</li>
<li>Knowledge of current and emerging regulatory requirements and expectations including ICH guidelines, EMA GVP Modules, FDA IND and NDA reporting requirements, CIOMS.</li>
<li>Have led the authoring/preparation of aggregate safety reports (DSURs) for products to meet regulatory requirements.</li>
<li>Passion, dedication, and a can-do attitude to the career of PVS, able to multi-task.</li>
<li>Effective written and oral communication skills.</li>
<li>Demonstrated presentation and collaboration skills.</li>
</br><div><strong style="font-size: 12pt;">Location</strong></div>
<div>This position may be remote with occasional travel to the office, or hybrid/based at our corporate offices in Cambridge, MA.</div>
<div>&nbsp;</div>
<div><strong>Compensation</strong></div>
<div>The salary range for this role is $210,000 - $270,000. The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Actual base salary pay for the role may vary within the range based on several factors including, but not limited to, geographic location, candidate experience, skills, relevant education/qualifications, competencies, external market, internal equity, business needs and/or other job-related factors permitted by law.</div>
<div>Additional compensation/benefits include annual bonus opportunity (25% of salary), annual equity awards, medical, dental, vision, life and disability insurance, 401(K) plan with employer match, stock options, employee stock purchase plan, flexible non-accrual paid time off, paid holidays, end-of-year shut down, cell phone reimbursement, tuition reimbursement, paid parental leave.</div>
<div>&nbsp;</div>
<div><em style="font-size: 16px;">Cullinan Therapeutics is proud to be an Equal Opportunity Employer. We are committed to creating an inclusive and diverse environment for all employees and applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.</em>&nbsp;</div>]]></description><link>http://biotechroles.com/director-pharmacovigilance-scientist-cullinan-oncology/69d3be06c8e81216cd0b91ca</link><guid isPermaLink="true">http://biotechroles.com/director-pharmacovigilance-scientist-cullinan-oncology/69d3be06c8e81216cd0b91ca</guid><pubDate>Mon, 06 Apr 2026 14:06:53 GMT</pubDate><company>Cullinan Oncology</company><location>United States</location><salary>$160000-220000</salary><type></type></item><item><title><![CDATA[Associate Director, Biologics CMC Drug Product]]></title><description><![CDATA[<div>Cullinan Therapeutics (NASDAQ: CGEM) is a clinical-stage biotech company developing potential first- or best-in-class, high-impact molecules in autoimmune diseases and cancer, where exceptional scientific expertise, strategic risk-taking, and rigorous decision-making unite to improve peoples’ lives.</div><div><br></div><div>We believe in a future where those living with autoimmune diseases and cancer spend less time managing their conditions and more time on what matters most. With deep expertise in immune modulation, Cullinan is where speed meets strategy to move profound innovations forward.</div><div><br></div><div>But movement isn’t just about speed — it’s about meaning. Our work is fueled by curiosity, determination, and compassion. We work side by side with our partners across the life science ecosystem to channel our collective potential into improving the lives of people living with autoimmune diseases and cancer.</div><div><br></div><div>The Associate Director, Biologics CMC Drug Product Development position is a key role responsible for conducting drug product development and manufacturing from preclinical through early and late (pivotal) clinical development to commercialization for a pipeline of novel biologics products.&nbsp; The Associate Director, Biologics CMC Drug Product will be a member of the CMC team (within Technical Operations), reporting to the Executive Director, Biologics CMC Drug Product.&nbsp; This role provides the opportunity to contribute to Cullinan’s biologics drug product capabilities and involves close collaboration with various teams including process development, analytical sciences, supply chain, quality, regulatory, research, clinical, finance, and legal.&nbsp; The execution of all development, manufacturing, and testing for Cullinan Therapeutics is entirely via a network of external providers.&nbsp;</div></br><b>Position Responsibilities</b></br><li>Develop biologics drug product formulations, processes, and administration/delivery methods throughout program’s lifecycle (preclinical through commercialization).</li><li>Contribute to and manage biologics drug product process technical transfer to CMOs and provide oversight during manufacturing.</li><li>Develop and manage external drug product development and manufacturing capabilities and network.</li><li>Ensure compliance with FDA, cGMPs, and ICH guidelines.</li><li>Author and review technical documents and regulatory filings; support associated agency interactions and product-related inspections.</li><li>Support development and implementation of new process technologies to meet business and portfolio needs. </li><li>Remain current on trends and new technology advancements across the biopharmaceutical industry.</li></br><b>Candidate Requirements</b></br><li>Ph.D. or Master’s degree in Pharmaceutical Sciences, Chemical Engineering or relevant field. </li><li>Minimum 8+ years of relevant experience in biotech/pharma industry, with a focus on drug product development and manufacturing for therapeutic protein products.</li><li>Extensive hands‐on experience and in-depth knowledge and understanding of protein formulation development, fill-finish process engineering, and administration/delivery, with working knowledge of non-monoclonal antibody formats.</li><li>Proven ability to manage global, external vendors for development, manufacturing, and testing is essential.</li><li>Proven experience in the generation of CMC regulatory sections of IND, IMPD, BLA, and MAA filings.&nbsp; Extensive familiarity with phase-appropriate cGMP requirements and FDA, EU, and ICH guidelines. </li><li>Previous success working effectively in a multidisciplinary, highly matrixed environment with ability to collaborate and drive for results.&nbsp;</li><li>Excellent decision-making, written and verbal communication skills. </li><li>Motivated self-starter with excellent interpersonal and organizational skills. Strong self-awareness of the impact communication and working style has on others. </li><li>Qualities of the successful candidate include the following: collaboration, accountability, cross-functional engagement, and program management.&nbsp;</li></br><div><b style="font-size: 12pt">Location</b></div><div><span style="font-size: 11pt">&nbsp;</span></div><div><span style="font-size: 16px">This position may be remote with occasional travel to the office or hybrid/based at our corporate offices in Cambridge, MA. </span></div><div><b>&nbsp;</b></div><div><b>Compensation</b></div><div>The salary range for this role is $160,000 - $200,000. The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Actual base salary pay for the role may vary within the range based on several factors including, but not limited to, geographic location, candidate experience, skills, relevant education/qualifications, competencies, external market, internal equity, business needs and/or other job-related factors permitted by law. </div><div>Additional compensation/benefits include annual bonus opportunity (20% of salary), annual equity awards, medical, dental, vision, life and disability insurance, 401(K) plan with employer match, stock options, employee stock purchase plan, flexible non-accrual paid time off, paid holidays, end-of-year shut down, cell phone reimbursement, tuition reimbursement, paid parental leave.&nbsp;</div><div><br></div><div><i>Cullinan Therapeutics is proud to be an Equal Opportunity Employer. We are committed to creating an inclusive and diverse environment for all employees and applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.</i></div>]]></description><link>http://biotechroles.com/associate-director-biologics-cmc-drug-product-cullinan-oncology/69d3be06c8e81216cd0b91c9</link><guid isPermaLink="true">http://biotechroles.com/associate-director-biologics-cmc-drug-product-cullinan-oncology/69d3be06c8e81216cd0b91c9</guid><pubDate>Mon, 06 Apr 2026 14:06:53 GMT</pubDate><company>Cullinan Oncology</company><location>United States</location><salary>$150000-220000</salary><type>Remote</type></item><item><title><![CDATA[Senior Director, CMC Technical Operations, siRNA Therapeutics]]></title><description><![CDATA[<div>Our mission is to develop therapies that empower the immune system to combat neurodegeneration and our team is focused on developing treatments for some of the most challenging diseases facing our society. By harnessing advancements in genetics, immunology and neuroscience, we are pioneering the development of potential therapies to counteract the devastating progression of neurodegeneration. We are supported in this mission by experienced and accomplished scientists and clinicians, a novel portfolio of programs, leading healthcare investors, and pharma company partners, who share in our commitment to bettering the lives of patients and realizing a world where we make brain disorders history.</div><div><br></div><div>As the Senior Director, CMC Technical Operations, siRNA Therapeutics, you are a senior technical leader advancing siRNA programs from late discovery through clinical development and toward commercialization. You will serve as the CMC technical lead across internal teams and external partners, ensuring robust, scalable, and phase-appropriate manufacturing processes for siRNA drug substance and drug product.</div>
<div>This is an individual contributor role with broad cross-functional influence. You will report to the Vice President of Technical Operations and partner closely with Research, Process Development, Analytical Development, Regulatory, Quality, and CDMOs to deliver high-quality siRNA therapeutics in a dynamic biotech environment.</div></br><b>Key Goals and Accountabilities:</b></br>
<li>Lead CMC strategy for one or more siRNA programs, aligning manufacturing plans with development timelines and corporate objectives to enable seamless clinical progression and long-term commercialization readiness</li>
<li>Drive development, optimization, scale-up, and tech transfer of oligonucleotide drug substance processes—including solid-phase synthesis, deprotection, purification (e.g., HPLC, TFF), and GMP manufacturing—to ensure robust and reliable supply</li>
<li>Advance drug product development, including formulation and lipid nanoparticle (LNP) encapsulation, delivering phase-appropriate control strategies, comparability plans, and risk assessments that support regulatory success</li>
<li>Provide strong technical oversight of CDMOs, leading manufacturing campaigns, managing deviations and investigations, and ensuring quality and regulatory alignment across global partners</li>
<li>Integrate innovative technologies—including AI-enabled data analysis and digital process tools—into CMC operations to accelerate development timelines, enhance decision-making, and conserve valuable resources</li>
</br><b>Required Qualifications:</b></br>
<li>BS, MS, or PhD in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline</li>
<li>12+ years experience in CMC development within biotechnology, with direct experience in siRNA, oligonucleotide, or other RNA-based therapeutics</li>
<li>Demonstrated expertise in oligonucleotide drug substance manufacturing, including scale-up and GMP tech transfer</li>
<li>Experience overseeing CDMO partnerships and external manufacturing activities in a clinical-stage setting</li>
<li>Strong knowledge of global regulatory expectations for CMC documentation and phase-appropriate development strategies, with experience supporting IND and early clinical programs</li>
<li>Excellent technical writing and communication skills, with the ability to influence cross-functional stakeholders</li>
<li>Active user of large language models (LLMs) with a strong interest in evolving AI technologies and their application to CMC and technical operations</li>
</br><div>#LI-DM1</div><div><br></div><div>At Alector, our vision is bold, people are our priority, and our values are at the core of everything we do. Our dynamic and flexible environment encourages our teams to experiment, take ownership of decisions, and question convention to solve complex problems. We value shared wins, perseverance, and a growth mindset, which drives us forward, together.&nbsp;&nbsp;</div><div><br></div><div>Among the things you'll discover at Alector from your very first day are our committed and driven colleagues, a bold company vision, and new, modern offices designed to inspire innovation and collaboration in South San Francisco, right at the heart of Biotech Bay. Our benefits are thoughtfully designed around Alectorians and their loved ones and include flexible hybrid work options, competitive compensation, and comprehensive and unique benefits that enhance your health and well-being. Come join us!&nbsp;</div><div>&nbsp;</div><div>We believe that hard-working teams include people from a wide variety of backgrounds and experiences who can challenge each other’s assumptions with fresh perspectives and bring creative ideas to the table. We are committed to building an open, diverse, and inclusive environment for all employees. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, sexual orientation, age, marital status, veteran status, or disability status, or any other characteristics protected under applicable federal, state, or local laws.&nbsp;&nbsp;</div><div><br></div><div>We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.&nbsp;</div><div><br></div><div>Review our <a class="postings-link" href="https://alector.com/privacy-policy/">Privacy Policy</a></div>]]></description><link>http://biotechroles.com/senior-director-cmc-technical-operations-sirna-therapeutics-alector/69d3bdf6c8e81216cd0b91b8</link><guid isPermaLink="true">http://biotechroles.com/senior-director-cmc-technical-operations-sirna-therapeutics-alector/69d3bdf6c8e81216cd0b91b8</guid><pubDate>Mon, 06 Apr 2026 14:06:46 GMT</pubDate><company>Alector</company><location>South San Francisco, CA</location><salary>$220000-320000</salary><type>Full-time Exempt</type></item><item><title><![CDATA[People Operations Specialist (Part Time/Temporary)]]></title><description><![CDATA[<div>
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<h3 data-section-id="10tum4p" data-start="68" data-end="91"><span role="text"><strong data-start="72" data-end="89">About Alector</strong></span></h3>
<p data-start="92" data-end="505">Alector is a late-stage clinical biotechnology company focused on developing therapies that counteract the devastating progression of neurodegeneration. We are committed to advancing science that empowers the immune system to restore brain health. We believe that bold thinking, deep collaboration, and continuous innovation—especially through emerging technologies like AI—are essential to achieving our mission.</p>
<h3 data-section-id="9y1lge" data-start="512" data-end="534"><span role="text"><strong data-start="516" data-end="532">Role Summary</strong></span></h3>
<p data-start="535" data-end="897">As a People Operations Systems Specialist (Temporary), you will strengthen and scale our People Operations infrastructure with a focus on workflow design, automation, and employee experience. You will be a key driver in transforming how work gets done—using AI, large language models (LLMs), and automation tools to improve efficiency, accuracy, and scalability.</p>
<p data-start="899" data-end="1183">You will serve as a trusted front-line resource for employees while partnering cross-functionally with IT, Payroll, Finance, Facilities, and Talent Acquisition. We are looking for someone who is energized by solving operational challenges and reimagining processes through technology.</p>
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</div></br><b>Key Goals & Accountabilities</b></br><div>
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<li data-section-id="1gw7mw0" data-start="1229" data-end="1406">Deliver exceptional employee support! Serve as a front-line resource for benefits and People Operations inquiries, resolving issues end-to-end with speed, clarity, and care.</li>
<li data-section-id="9ry3b1" data-start="1407" data-end="1575">Reimagine how we work! Evaluate, redesign, and automate workflows using AI, LLMs, and integration tools to significantly reduce manual effort and increase accuracy.</li>
<li data-section-id="l0s2ns" data-start="1576" data-end="1759">Elevate operational excellence! Ensure data integrity, compliance, and seamless execution across the employee lifecycle while proactively identifying and correcting discrepancies.</li>
<li data-section-id="nngx53" data-start="1760" data-end="1919">Strengthen cross-functional systems! Partner with IT, Payroll, Finance, Facilities, and Talent Acquisition to optimize integrations and improve data flows.</li>
<li data-section-id="14iw4ci" data-start="1920" data-end="2204">Drive high-impact improvements! Identify and implement system enhancements, workflow automations, and key initiatives (e.g., open enrollment), from concept through continuous optimization—including integrating innovative AI solutions to accelerate outcomes and conserve resources!</li>

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</div></br><b>Required Qualifications</b></br><div>
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<li data-section-id="1clzb87" data-start="2245" data-end="2342">You are a proactive self-starter who asks thoughtful questions and seeks effective solutions.</li>
<li data-section-id="6e34yf" data-start="2343" data-end="2541">You are an active user of large language models (LLMs) with a strong interest in advancing AI-driven workflows; you have hands-on experience applying automation tools to real business processes.</li>
<li data-section-id="3psdft" data-start="2542" data-end="2645">You have experience serving as a front-line resource for employees and resolving issues end-to-end.</li>
<li data-section-id="4mce2e" data-start="2646" data-end="2774">You bring an analytical mindset, with experience in data-driven or operational roles and an interest in People/HR functions.</li>
<li data-section-id="asdlbk" data-start="2775" data-end="2890">You have demonstrated success managing cross-functional projects independently with strong attention to detail.</li>

</ul></div></br><div>#LI-DM1</div>]]></description><link>http://biotechroles.com/people-operations-specialist-(part-timetemporary)-alector/69d3bdf6c8e81216cd0b91b7</link><guid isPermaLink="true">http://biotechroles.com/people-operations-specialist-(part-timetemporary)-alector/69d3bdf6c8e81216cd0b91b7</guid><pubDate>Mon, 06 Apr 2026 14:06:46 GMT</pubDate><company>Alector</company><location>South San Francisco, CA</location><salary>$3000-5000</salary><type>Part-time</type></item><item><title><![CDATA[Senior AI Data Engineer/AI Data Engineer]]></title><description><![CDATA[<div>Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.</div>
<div>&nbsp;</div>
<div>At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a&nbsp;<a href="https://medium.com/@peter.gassner/public-benefit-corporation-pbc-486e1e9508a6">public benefit corporation</a>&nbsp;(PBC), legally bound to balancing the interests of customers, employees, society, and investors.</div>
<div>&nbsp;</div>
<div>As a&nbsp;<a href="https://careers.veeva.com/work-anywhere/">Work Anywhere</a>&nbsp;company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.</div>
<div>&nbsp;</div>
<div>Join us in&nbsp;<a href="https://www.youtube.com/watch?v=TaPSP8cCSKY&amp;ab_channel=Forbes">transforming the life sciences industry</a>, committed to making a positive impact on its customers, employees, and communities.</div><div><br></div><div><strong style="font-size: 18px;">The Role</strong></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">This role is responsible for ensuring the reliability, accuracy, and safety of our Veeva AI Agents through rigorous evaluation and systematic validation methodologies. We're looking for experienced candidates with:</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">1. A meticulous, critical, and curious mindset with a dedication to product quality in a rapidly evolving technological domain</span></div>
<div><span style="font-size: 16px;">2. Exceptional analytical and systematic problem-solving capabilities</span></div>
<div><span style="font-size: 16px;">3. Excellent ability to communicate technical findings to both engineering and product management audiences</span></div>
<div><span style="font-size: 16px;">4. Ability to learn application areas quickly</span></div>
<div>&nbsp;</div>
<div><span style="font-size: 16px;">Thrive in our Work Anywhere environment: We support your flexibility to work remotely or in the office within Canada or the US, ensuring seamless collaboration within your product team's time zone.</span></div>
<div><span style="font-size: 16px;">&nbsp;</span></div>
<div><span style="font-size: 16px;">Join us and be part of a mission-driven organization transforming the life sciences industry.</span></div></br><b>What You'll Do</b></br>
<li><strong>Evaluation&nbsp;Strategy &amp; Planning:</strong> Define and establish comprehensive evaluation strategies for new AI Agents. Prioritize the integrity and coverage of test data sets to reflect real-world usage and potential failure modes</li>
<li><strong>LLM Output Integrity Assessment:</strong> Programmatically and manually evaluate the quality of LLM-generated content against predefined metrics (e.g., factual accuracy, contextual relevance, coherence, and safety standards)</li>
<li><strong>Creating High-Fidelity Datasets:</strong> Design, curate, and generate diverse, high-quality test data sets, including challenging prompts and scenarios. Evaluate LLM outputs to proactively identify system biases, unsafe content, hallucinations, and critical edge cases</li>
<li><strong>Automation of Evaluation Pipelines:</strong> Develop, implement, and maintain scalable automated evaluations to ensure efficient, continuous validation of agent behavior and prevent regressions with new features and model updates</li>
<li><strong>Root Cause Analysis:</strong> Understand model behaviors and assist in the trace and root-cause analysis of identified defects or performance degradations</li>
<li><strong>Reporting &amp; Performance Metrics:</strong> Clearly document, track, and communicate performance metrics, validation results, and bug status to the broader development and product teams</li>
</br><b>Requirements</b></br>
<li><strong>Data Integrity &amp; Validation:</strong> A strong, specialized understanding of data quality principles, including methods for validating datasets against bias, integrity concerns, and quality standards. Ability to craft diverse and adversarial test data to uncover AI edge cases</li>
<li><strong>Prompt Engineering &amp; Model Expertise:</strong> Demonstrated skill in advanced prompt engineering techniques to create evaluation scenarios that test the AI's reasoning, action planning, and adherence to system instructions. Deep knowledge of LLM common failure modes (hallucination, incoherence, jailbreaking)</li>
<li><strong>Automated Evaluation Implementation:</strong> 5+ years of experience designing and deploying automated evaluation pipelines to assess complex, agentic AI behaviors. Familiarity with quality metrics such as task success rate, semantic similarity, and sentiment analysis for output measurement</li>
<li><strong>Debugging Agentic Systems:</strong> Must be comfortable with the specific challenges of debugging agentic systems, including tracing and interpreting an agent's internal reasoning, tool use, and action sequence to pinpoint failure points</li>
<li><strong>Programming &amp; Frameworks:</strong> 5+ years of experience using Python to develop custom evaluation frameworks, writing scripts, and integrating pipelines with CI/CD systems. Familiarity with standard test automation tools (e.g., Pytest, modern web automation tools)</li>
<li>Bachelor's degree in Data Science, Machine Learning, Computer Science, or a related field, with experience in Gen AI / LLMs</li>
<li>High work ethic. Veeva is a hard-working company</li>
<li>High integrity and honesty. Veeva is a PBC and a “do the right thing” company. We expect that from all employees</li>
<li>Applicants must have the unrestricted right to work in the United States or Canada. Veeva will not provide sponsorship at this time</li>
</br><div><span style="font-size: 10px;">#LI-Remote</span></div>
<div><span style="font-size: 10px;">#LI-MidSenior</span></div><div><br></div><div>Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.</div>
<div>&nbsp;</div>
<div>Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at&nbsp;<a href="mailto:talent_accommodations@veeva.com">talent_accommodations@veeva.com</a>.</div>]]></description><link>http://biotechroles.com/senior-ai-data-engineerai-data-engineer-veeva/69d3bde3c8e81216cd0b91a8</link><guid isPermaLink="true">http://biotechroles.com/senior-ai-data-engineerai-data-engineer-veeva/69d3bde3c8e81216cd0b91a8</guid><pubDate>Mon, 06 Apr 2026 14:06:18 GMT</pubDate><company>Veeva</company><location>Canada - Toronto</location><salary>$120000-180000</salary><type>Full-Time</type></item><item><title><![CDATA[Vice President, Analytical Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Vice President of Analytical Development will provide technical, operational, and strategic leadership for Umoja’s analytical development organization, with responsibility for release, characterization, and lifecycle management of analytical methods supporting clinical and commercial cell and gene therapy products. Reporting to the Chief Technical Officer (CTO), this role will define and execute the company’s end-to-end analytical strategy in close partnership with Quality, Manufacturing, Regulatory, and Research.&lt;/p&gt;
&lt;p&gt;This individual will be a critical leader at the interface of Research and Discovery, GMP Manufacturing, Quality, and CMC Regulatory, with accountability for analytical method development, qualification, validation, transfer, and specification setting for GMP products. The ideal candidate brings deep regulatory experience—particularly IND and BLA submissions—strong people leadership, and a proven ability to scale analytical organizations in fast-paced biotech environments.&lt;/p&gt;
&lt;p&gt;This position is based in Louisville, CO (preferred) or Seattle, WA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific requirements include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Strategic Leadership &amp;amp; Execution&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide strategic leadership and operational oversight for the Analytical Development and Process Analytics teams, including routine testing to support process and product development.&lt;/li&gt;
&lt;li&gt;Define and own Umoja’s overarching analytical strategy across development stages, from early clinical programs through BLA and commercialization.&lt;/li&gt;
&lt;li&gt;Lead the design, implementation, and continuous improvement of laboratory systems and workflows, including development of high-throughput and automated testing strategies.&lt;/li&gt;
&lt;li&gt;Drive organizational change initiatives to continuously improve efficiency, quality, and business outcomes.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Analytical Development &amp;amp; CMC&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead analytical method development, process analytics, and lifecycle management for intermediates, drug substance, and drug product testing.&lt;/li&gt;
&lt;li&gt;Establish analytical strategies for specification setting, comparability, and assay robustness consistent with regulatory expectations.&lt;/li&gt;
&lt;li&gt;Provide subject matter expertise to support CMC strategy, regulatory interactions, and responses to agency questions.&lt;/li&gt;
&lt;li&gt;Author and be accountable for analytical sections of regulatory submissions, including INDs and BLAs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Cross-Functional Leadership&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build and maintain strong cross-functional partnerships to ensure effective handoffs of technologies, methods, and data across Research, Manufacturing, Quality, and Regulatory.&lt;/li&gt;
&lt;li&gt;Review CMC project plans and timelines; ensure appropriate prioritization and on-time delivery of analytical milestones.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;People, Budget &amp;amp; External Partnerships&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic planning, annual goal setting, talent development, succession planning, and organizational design for the function.&lt;/li&gt;
&lt;li&gt;Own OPEX and CAPEX planning and execution in collaboration with Finance and HR.&lt;/li&gt;
&lt;li&gt;Ensure the organization meets budgeted financial goals and operates within approved timelines.&lt;/li&gt;
&lt;li&gt;Select, manage, and oversee external contract laboratories and vendors.&lt;/li&gt;
&lt;li&gt;Champion Umoja’s cultural values and foster a high-performance, inclusive, and collaborative team environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Leadership Competencies&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Setting Strategy&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Articulates a clear, compelling vision for the Analytical Development organization aligned with Umoja’s mission and long-term goals.&lt;/li&gt;
&lt;li&gt;Demonstrates creativity and entrepreneurial thinking to push scientific and operational boundaries.&lt;/li&gt;
&lt;li&gt;Translates strategy into realistic, executable plans with measurable outcomes.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Executing for Results&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Sets ambitious goals and holds self and others accountable for delivery.&lt;/li&gt;
&lt;li&gt;Thrives in ambiguous, rapidly evolving environments and leads effectively through change.&lt;/li&gt;
&lt;li&gt;Acts with integrity, transparency, and sound judgment in decision-making.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Leading Teams&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Builds trust, inspires collaboration, and develops talent across functions and geographies.&lt;/li&gt;
&lt;li&gt;Models resilience, perseverance, and a commitment to excellence.&lt;/li&gt;
&lt;li&gt;Embraces feedback, self-reflection, and continuous improvement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Relationships &amp;amp; Influence&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Builds strong, authentic relationships through emotional intelligence and clear communication.&lt;/li&gt;
&lt;li&gt;Influences through credibility, passion, and purpose rather than authority alone.&lt;/li&gt;
&lt;li&gt;Celebrates team success and creates a shared sense of meaning and ownership.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Advanced degree in Biology, Biochemistry, Chemistry, or a related life sciences discipline (MS or PhD preferred).&lt;/li&gt;
&lt;li&gt;Minimum of 15 years of experience in biopharmaceutical development, with significant leadership experience in analytical development.&lt;/li&gt;
&lt;li&gt;Minimum of 5 years’ experience building, leading, and developing high-performing teams.&lt;/li&gt;
&lt;li&gt;Deep expertise in analytical techniques relevant to cell and gene therapies, including flow cytometry, ELISA, qPCR, ddPCR, and cell-based assays.&lt;/li&gt;
&lt;li&gt;Extensive experience authoring and supporting IND and BLA submissions and engaging with regulatory agencies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong working knowledge of analytical development, CMC regulatory strategy, and Quality systems in the cell and gene therapy space.&lt;/li&gt;
&lt;li&gt;Demonstrated success scaling organizations and infrastructure in growth-stage biotech companies.&lt;/li&gt;
&lt;li&gt;Strong understanding of ICH guidelines, pharmacopeial standards, and global regulations governing GMP release testing.&lt;/li&gt;
&lt;li&gt;Excellent strategic, operational, financial, and business acumen.&lt;/li&gt;
&lt;li&gt;Ability to manage complexity, prioritize across multiple programs, and influence across a diverse stakeholder landscape.&lt;/li&gt;
&lt;li&gt;A clear vision for building a sustainable, equitable, and values-driven culture across technical functions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to travel up to 20%&lt;/li&gt;
&lt;li&gt;Ability to work onsite at our Louisville, CO (preferred) or Seattle, WA location&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $310,000 - $350,000&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vice-president-analytical-development-umoja-biopharma/69d3bd0bc8e81216cd0b9143</link><guid isPermaLink="true">http://biotechroles.com/vice-president-analytical-development-umoja-biopharma/69d3bd0bc8e81216cd0b9143</guid><pubDate>Mon, 06 Apr 2026 14:02:51 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Specialist, Quality Assurance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY &lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Umoja Biopharma is seeking a Quality Assurance Specialist to support GMP operations at Umoja’s state-of-the-art lentiviral vector development and GMP manufacturing and testing facility, The CLIMB, in Louisville, CO. This position will provide quality oversight of incoming materials, manufacturing, and general QA support of GMP operations at The CLIMB.&lt;/p&gt;
&lt;p&gt;This role is fully onsite based out of our Louisville, CO location.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;br&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Exemplify and role model Umoja’s quality culture&lt;/li&gt;
&lt;li&gt;Build strong, effective, and productive cross-functional working relationships&lt;/li&gt;
&lt;li&gt;Interfaces with other departments (e.g., Manufacturing, Supply Chain, Quality Control, Facilities, Engineering) to ensure compliance with all applicable procedures, policies, regulations, and standards.&lt;/li&gt;
&lt;li&gt;Provides QA “on the floor” support to Manufacturing during routine GMP operations at the site and Warehouse for material support and disposition.&lt;/li&gt;
&lt;li&gt;Reviews and approves work instructions, Standard Operating Procedures (SOPs), Material specifications, and other controlled documents related to GMP operations and other cGMP activities as needed&lt;/li&gt;
&lt;li&gt;Performs disposition of incoming GMP materials &amp;nbsp;&lt;/li&gt;
&lt;li&gt;Initiates Quality Holds as required&lt;/li&gt;
&lt;li&gt;Provides oversite on new material introductions including review and approval of new GMP material onboarding requests&lt;/li&gt;
&lt;li&gt;Partners with Manufacturing to review and post-approve GMP executed batch records and protocols&lt;/li&gt;
&lt;li&gt;Reviews and approves Master Batch Records, process SOPs, and supporting forms for products&lt;/li&gt;
&lt;li&gt;Supports line clearance/product changeover activities including the review and approval of associated documentation&lt;/li&gt;
&lt;li&gt;Approves work orders within Blue Mountain Regulatory Asset Manager (BMRAM), as needed&lt;/li&gt;
&lt;li&gt;Review and approves QC documentation (e.g., stability protocols)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Provides Quality support to approve, review and close quality records (e.g., Change Controls, Deviations, and CAPAs, etc.) as necessary&lt;/li&gt;
&lt;li&gt;&amp;nbsp;Identify, propose, and actively participate in opportunities for continuous improvement&lt;/li&gt;
&lt;li&gt;Provides additional support within the Quality organization, as needed&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Engineering, Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with minimum of 5 years of work experience in an FDA regulated industry&lt;/li&gt;
&lt;li&gt;Previous experience in a Quality organization supporting cGMP biopharmaceutical internal manufacturing facility operations&lt;/li&gt;
&lt;li&gt;Knowledge and understanding of regulatory governing bodies, requirements, and guidance documents, and how to practically apply these in a cGMP biopharmaceutical environment&lt;/li&gt;
&lt;li&gt;An understanding of foundational Quality systems (e.g., Good Documentation Practices, data integrity, audits/inspections, Change Control, Deviation/CAPA, etc.)&lt;/li&gt;
&lt;li&gt;Risk-based and practical decision-making capability, with an understanding on when decision making escalation is required&lt;/li&gt;
&lt;li&gt;Ability to work effectively and efficiently in a collaborative manner across multiple functional areas&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in cGMP cell and gene therapy manufacturing facility&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to work onsite 5 days/week at our Louisville, CO location&lt;/li&gt;
&lt;li&gt;Ability to lift up to 20 lbs. on occasion&lt;/li&gt;
&lt;li&gt;Ability to stand for extended periods of time&lt;/li&gt;
&lt;li&gt;Adherence to proper personal protective equipment (PPE) when necessary, such as but not limited to high-visibility safety vest, cold gloves, lab coat, safety glasses, gowning for manufacturing (scrubs, coveralls, hair net, beard net, etc), etc.&lt;/li&gt;
&lt;li&gt;Ability to support off-hours work on evenings, holidays, and/or weekends when necessary&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $85,300 - $105,300&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/specialist-quality-assurance-umoja-biopharma/69d3bd07c8e81216cd0b913f</link><guid isPermaLink="true">http://biotechroles.com/specialist-quality-assurance-umoja-biopharma/69d3bd07c8e81216cd0b913f</guid><pubDate>Mon, 06 Apr 2026 14:02:47 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$75000-105000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Finance]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Who We Are&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a biotechnology company that invents and builds platform companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble capital to allow them to take courageous leaps. Those big leaps in human health and sustainability exponentially accelerate scientific progress in areas ranging from cancer detection and treatment to nature-positive agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance biotechnology by uniting life science innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;br&gt;&lt;/strong&gt;The VP of Finance at Flagship Labs will serve as a strategic finance partner to a portfolio of early-stage platform companies (pre-Series A through Series B). This individual will advise company leadership on financial strategy while overseeing the day-to-day financial operations of each portfolio company, including month-end closing, cash management, budgeting and forecasting, administrative functions, and technology oversight.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate with platform company leadership teams to develop long-term strategic plans, define key milestones, and build detailed financial models and projections&lt;/li&gt;
&lt;li&gt;Partner with Pioneering Business Unit (PBU) Leadership, Flagship Labs Leadership, Business Analytics and Pipeline &amp;amp; Product Innovation (P&amp;amp;PI) team to create value maps with potential unlocks for portfolio companies&lt;/li&gt;
&lt;li&gt;Oversee cash flow planning in alignment with financing requirements and scientific milestones&lt;/li&gt;
&lt;li&gt;Oversee annual budgets, rolling monthly forecasts and long-range plans for responsible portfolio companies in partnership with FP&amp;amp;A.&lt;/li&gt;
&lt;li&gt;Prepare financial materials for Board of Directors meetings and other governance meetings. Support corporate governance activities.&lt;/li&gt;
&lt;li&gt;Oversee the Venture Debt strategy, execution, and governance across Flagship Lab, ensuring disciplined paydowns, amortization schedules, vehicle drawdowns &amp;amp; extensions and financials reporting.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Partner with the Flagship Facilities team to strategically optimize space allocation across portfolio companies, proactively planning for headcount growth and evolving capital requirements.&lt;/li&gt;
&lt;li&gt;Drive high-impact projects typical of rapidly scaling biotechnology startups, including efficient system implementations, standardized processes, and operational process improvements across portfolio companies&lt;/li&gt;
&lt;li&gt;Provide ad hoc financial reporting and strategic analysis as needed&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Minimum Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of financial and accounting experience in the life sciences / biotechnology industry. Experience in a company that completed a successful IPO is a plus&lt;/li&gt;
&lt;li&gt;BS/BA in accounting or finance; MBA and/or CPA preferred&lt;/li&gt;
&lt;li&gt;Strong business acumen: proven ability to effectively scrutinize and challenge assumptions and interpret the strategy and priorities of the organization in financial terms&lt;/li&gt;
&lt;li&gt;Excellent project management / consultative skills with demonstrated track record and ability to manage competing priorities and stakeholders&lt;/li&gt;
&lt;li&gt;Strong presentation skills to deliver succinctly and effectively deliver recommendations to senior leaders and frame complex concepts&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;Flagship Pioneering and our ecosystem companies are committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/strong&gt;&lt;/em&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $265,000 - $330,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/vice-president-finance-flagship-pioneering/69d3bd06c8e81216cd0b913e</link><guid isPermaLink="true">http://biotechroles.com/vice-president-finance-flagship-pioneering/69d3bd06c8e81216cd0b913e</guid><pubDate>Mon, 06 Apr 2026 14:02:46 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$280000-450000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Specialist, Quality Assurance, External Supplier]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated individual to join our growing Quality Assurance team. This individual will play a key role in Umoja’s state-of-the-art lentiviral vector development and manufacturing facility, The CLIMB, in Louisville, CO.&lt;/p&gt;
&lt;p&gt;In collaboration with Quality management and multiple functions, this individual will execute, mature, and drive continuous improvement of key aspects of the vendor management program.&amp;nbsp; Additionally, this role will collaborate with cross-functional teams to ensure quality requirements are defined, clearly communicated and understood, and met as part of routine and advancing GxP operations.&amp;nbsp; &lt;br&gt;&lt;strong&gt;&lt;u&gt;&lt;br&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Works effectively and leads cross-functionally across Umoja to fulfill Vendor QA oversight and performance monitoring responsibilities.&lt;/li&gt;
&lt;li&gt;Manages the GMP supplier notification and change process with limited Management oversight and direction, working with cross-functional subject matter experts (SMEs) to assess and document impact.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Manages the Supplier Corrective Action Record (SCAR) process and material defect management process with limited Management oversight and direction.&lt;/li&gt;
&lt;li&gt;Performs vendor recertification events for identified vendors with limited Management oversight and direction in collaboration with cross-functional SME.&lt;/li&gt;
&lt;li&gt;Provide support for the Vendor Management program, as needed.&lt;/li&gt;
&lt;li&gt;Executes controlled document archival process, when required.&lt;/li&gt;
&lt;li&gt;Authors, reviews, and/or approves Standard Operating Procedures (SOPs) and other controlled documents as Quality Assurance representative.&lt;/li&gt;
&lt;li&gt;Provide additional support within the Quality Assurance organization to provide Quality oversight and support to GxP tasks and programs, when needed.&lt;/li&gt;
&lt;li&gt;Support organizations outside of Quality, if needed, to accomplish facility objectives and routine operations.&lt;/li&gt;
&lt;li&gt;Other duties, as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with a minimum of 8+ years of experience in an FDA regulated industry, or similar combination of education and experience.&lt;/li&gt;
&lt;li&gt;Extensive experience with quality management systems and vendor management.&lt;/li&gt;
&lt;li&gt;Experience participating in external (vendor) audits.&lt;/li&gt;
&lt;li&gt;Knowledge of relevant pharmaceutical regulations and regulatory guidance.&lt;/li&gt;
&lt;li&gt;Understanding of, and ability to apply, risk management principles and philosophy within the quality system in support of Phase 1/first-in-human products/programs.&lt;/li&gt;
&lt;li&gt;Strong communication and organizational skills and a passion for teamwork.&lt;/li&gt;
&lt;li&gt;Ability to work effectively and efficiently in a collaborative manner across multiple functional areas and vendors with minimal supervision.&lt;/li&gt;
&lt;li&gt;Previous experience in a Quality organization supporting a cGMP biopharmaceutical manufacturing facility startup and/or operations environment.&lt;/li&gt;
&lt;li&gt;Experience leading and implementing operational excellence initiatives and process simplification.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Previous experience with a vendor management program in a current Good Manufacturing Practice (cGMP) environment.&lt;/li&gt;
&lt;li&gt;Experience in cGMP cell and gene therapy manufacturing and/or testing facility.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to gown aseptically and work in a Clean Room environment, if required&lt;/li&gt;
&lt;li&gt;Ability to work while gowned for extended periods of time, including standing for extended periods of time.&lt;/li&gt;
&lt;li&gt;Ability to sit in office setting for extended periods of time.&lt;/li&gt;
&lt;li&gt;Ability to work occasional nights and weekends as needed.&lt;/li&gt;
&lt;li&gt;Ability to work onsite 5 days/week&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $105,100 - $130,000&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-specialist-quality-assurance-external-supplier-umoja-biopharma/69d3bd03c8e81216cd0b913d</link><guid isPermaLink="true">http://biotechroles.com/senior-specialist-quality-assurance-external-supplier-umoja-biopharma/69d3bd03c8e81216cd0b913d</guid><pubDate>Mon, 06 Apr 2026 14:02:42 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Data Platform]]></title><description><![CDATA[&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Position Summary&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship&#39;s Pioneering Intelligence seeks a VP AI Data Platform to lead the strategy and development of our AI-native data technologies. This platform leverages our unique breadth of portfolio company data in partnership with our AI scientists to return differentiated AI models and tools to the benefit of our portfolio companies. This leader partners with our scientific, technical, business, and legal colleagues to enable new AI capabilities while maintaining strong controls, trust, and compliance.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Own strategy and continued development of an AI-native data platform for benefits dozens of portfolio companies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Deliver a product-minded and user-centered roadmap for the data platform&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Lead a high-performing technical team to implement the roadmap&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Build strategic co-development partnerships with external collaborators&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work with leaders across the portfolio to ensure enthusiastic adoption of data platform tools&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Drives adoption across all&amp;nbsp;wholly-owned&amp;nbsp;portfolio companies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work with colleagues in Pioneering Intelligence to enable differentiated and innovative molecular models and agentic systems that&amp;nbsp;leverage&amp;nbsp;the data platform&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensures secure, compliant cross-company data governance&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience designing and delivering scalable data platforms used in machine learning contexts with sensitive proprietary data&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience balancing performance and cost of hardware and software vendor solutions with internal development efforts&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong knowledge of user-centered software product development &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience working with machine learning teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated ability to understand concerns, align value, and enable shared outcomes across many stakeholders&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;History of leading a high-functioning technical team of software and infrastructure engineers&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with technical and legal data governance frameworks&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Communicates clearly with executive and nontechnical stakeholders&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Objectives&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Adoption of the Flagship Data Exchange by all&amp;nbsp;wholly-owned&amp;nbsp;portfolio companies by June 2026&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Improve leverage of data for individual companies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Enable sharing of new AI models trained on pan-portfolio data&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Enable well-governed cross-company data access&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;#LI-NM1&lt;/span&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $275,000 - $365,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/vice-president-data-platform-flagship-pioneering/69d3bd01c8e81216cd0b913a</link><guid isPermaLink="true">http://biotechroles.com/vice-president-data-platform-flagship-pioneering/69d3bd01c8e81216cd0b913a</guid><pubDate>Mon, 06 Apr 2026 14:02:40 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Quality Control Analytical]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Model Umoja values by setting clear expectations, coaching performance, and building an inclusive, high-accountability culture within QC Analytical.&lt;/li&gt;
&lt;li&gt;Own day-to-day QC Analytical lab operations (planning, staffing, scheduling, and execution) across analytical testing, stability programs, and sample management to ensure compliant, on-time delivery of testing results in support of corporate goals and program milestones.&lt;/li&gt;
&lt;li&gt;Lead a matrixed team of full time employees and contractors, including recruiting, performance management, and talent development&lt;/li&gt;
&lt;li&gt;Oversee use and continuous improvement of QC Analytical programs, processes, and systems to ensure consistent cGMP execution and scalability.&lt;/li&gt;
&lt;li&gt;Drive implementation and adoption of lab digital and automation tools (e.g., LIMS, reagent management, electronic lab notebook) to improve throughput, right-first-time performance, and compliance.&lt;/li&gt;
&lt;li&gt;As QC Analytical management, collaborate with Analytical Development to ensure method readiness for QC (transfer, qualification/validation, training, and routine execution) in support of analytical method lifecycle activities.&lt;/li&gt;
&lt;li&gt;Forecast demand and build capacity plans (headcount, training, equipment, and coverage) aligned to manufacturing timelines and program needs.&lt;/li&gt;
&lt;li&gt;Champion Operational Excellence/Lean by establishing metrics, standard work, and continuous improvement initiatives that measurably improve quality, cycle time, and efficiency.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science, plus 8+ years of experience in cGMP Quality Control. Equivalent combinations of advanced education and experience will be considered. Extensive knowledge of analytical method qualification, validation, and transfer.&lt;/li&gt;
&lt;li&gt;4+ years of demonstrated people leadership experience in a cGMP environment—hiring, coaching, developing, and retaining talent while setting clear priorities and driving accountability.&lt;/li&gt;
&lt;li&gt;Deep hands-on and applied knowledge of molecular biology analytical techniques (e.g., PCR, ELISA, flow cytometry, cell-based assays)&lt;/li&gt;
&lt;li&gt;Working knowledge of applicable regulations and compendial/industry guidance (e.g., ICH, USP) with the ability to translate requirements into practical, inspection-ready QC practices.&lt;/li&gt;
&lt;li&gt;Experience leading teams with direct reports, including performance management, talent development, and building a culture of quality, collaboration, and continuous improvement.&lt;/li&gt;
&lt;li&gt;Proven Operational Excellence/Continuous Improvement capability, applying Lean principles and data-driven problem solving to improve quality, throughput, and right-first-time performance.&lt;/li&gt;
&lt;li&gt;Strong judgment and risk-based decision-making—able to propose solutions, communicate risks, and anticipate downstream impact in a fast-paced, evolving environment.&lt;/li&gt;
&lt;li&gt;Track record of raising team performance through clear expectations, effective communication, strong follow-through, and consistent accountability.&lt;/li&gt;
&lt;li&gt;Proven ability to lead cross-functionally and deliver results by aligning stakeholders, removing roadblocks, and communicating progress, risks, and decisions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience building and scaling an early phase QC laboratory, including quality systems and analytical method lifecycle ownership (transfer, qualification, validation, and method performance).&lt;/li&gt;
&lt;li&gt;Cell and gene therapy experience in a cGMP setting, specifically QC testing in support of lot release/stability and successful cross-functional partnerships with Technical Operations, Analytical Development and Quality.&lt;/li&gt;
&lt;li&gt;Experience leading through audits/inspections (internal, client, or regulatory) and driving inspection readiness.&lt;/li&gt;
&lt;li&gt;Experience implementing and optimizing LIMS/data integrity controls and digital transformation at scale.&lt;/li&gt;
&lt;li&gt;Experience owning or partnering on deviations/investigations, CAPA, and change control for QC labs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to work onsite 5 days/week at our Louisville, CO location&lt;/li&gt;
&lt;li&gt;Ability to work evenings and/or weekends as needed&lt;/li&gt;
&lt;li&gt;Ability to gown aseptically and work in a Clean Room environment&lt;/li&gt;
&lt;li&gt;Ability to wear personal protective equipment including gloves, protective clothing, and eye safety glasses.&lt;/li&gt;
&lt;li&gt;Ability to work while gowned for extended periods of time&lt;/li&gt;
&lt;li&gt;Must have the ability to work around laboratories, manufacturing areas and equipment, and regularly lift 10-20 lbs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: &amp;nbsp;$152,700 - $188,700&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-quality-control-analytical-umoja-biopharma/69d3bcfec8e81216cd0b9137</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-quality-control-analytical-umoja-biopharma/69d3bcfec8e81216cd0b9137</guid><pubDate>Mon, 06 Apr 2026 14:02:38 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Business Development & Partnerships – Japan]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;About Flagship Pioneering Japan:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at &lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;Our Japanese subsidiary is focused on bridging Flagship’s innovative ecosystem with the Japanese biotech, pharmaceutical and biomedical ecosystem to fostering strategic partnerships in one of the world’s critical healthcare markets.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Chair of Flagship APAC, we are seeking an accomplished and dynamic individual to join our team as the Vice President of Alliances and Partnerships for Flagship Pioneering Japan. The successful candidate will be responsible for spearheading strategic initiatives, fostering and managing partnerships, and driving business growth in the Japanese market. This role requires a visionary leader with a deep understanding of the life&lt;/p&gt;
&lt;p&gt;sciences industry, exceptional strategic thinking skills, and the ability to build and maintain high-level relationships.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strategic Planning:
&lt;ul&gt;
&lt;li&gt;Working closely with Flagships Corporate and Business Development teams. Define and execute the partnership strategy in alignment with Flagship Pioneering’s global objectives&lt;/li&gt;
&lt;li&gt;Identify and evaluate new business opportunities, potential partners, and market trends in Japan.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Partnership Development:
&lt;ul&gt;
&lt;li&gt;Lead efforts to establish and nurture strategic alliances with pharmaceutical companies, biotech firms, research institutions, and other relevant stakeholders in Japan.&lt;/li&gt;
&lt;li&gt;Negotiate and finalize partnership agreements to drive mutual growth and innovation.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Market Expansion:
&lt;ul&gt;
&lt;li&gt;Develop and implement strategies to expand Flagship Pioneering’s presence and influence in the Japanese market.&lt;/li&gt;
&lt;li&gt;Engage with key opinion leaders, industry experts, and regulatory bodies to enhance market access and visibility.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Collaborative Initiatives:
&lt;ul&gt;
&lt;li&gt;Work collaboratively with Flagship Pioneering’s global leadership and global engagement team in Cambridge, MA to align efforts and share best practices.&lt;/li&gt;
&lt;li&gt;Facilitate cross-functional collaboration to support portfolio company growth and development.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Financial Accountability:
&lt;ul&gt;
&lt;li&gt;Develop and manage budgets, forecasts, and financial models to support business development activities.&lt;/li&gt;
&lt;li&gt;Track and report on key performance indicators (KPIs) and milestones.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A minimum of 10-15 years of experience in business development, partnerships, or related roles within the life sciences sector.&lt;/li&gt;
&lt;li&gt;Proven track record of successfully developing and managing strategic partnerships in Japan.&lt;/li&gt;
&lt;li&gt;Strong understanding of the Japanese healthcare and regulatory environment.&lt;/li&gt;
&lt;li&gt;Exceptional negotiation, communication, and interpersonal skills.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to think strategically and drive long-term business growth.&lt;/li&gt;
&lt;li&gt;Fluency in Japanese and English, both written and spoken.&lt;/li&gt;
&lt;li&gt;Advanced degree (MBA, Ph.D., or equivalent) preferred with an emphasis on business or life sciences.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-JR3&lt;/p&gt;]]></description><link>http://biotechroles.com/vice-president-business-development-and-partnerships-japan-flagship-pioneering/69d3bcfdc8e81216cd0b9130</link><guid isPermaLink="true">http://biotechroles.com/vice-president-business-development-and-partnerships-japan-flagship-pioneering/69d3bcfdc8e81216cd0b9130</guid><pubDate>Mon, 06 Apr 2026 14:02:36 GMT</pubDate><company>Flagship Pioneering</company><location>Tokyo, Japan</location><salary>$180000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Enterprise Systems Analyst]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Umoja is seeking a skilled Senior Enterprise Systems Analyst to support and enhance our portfolio of enterprise applications. This role serves as a subject‑matter expert across systems supporting Supply Chain, Finance, Accounting, Procurement, HR, and Quality. You will manage day‑to‑day system operations, troubleshoot issues, and lead the delivery of new capabilities. In partnership with cross‑functional teams, you will translate business needs into technical solutions, drive process improvements, support projects from design through implementation, and ensure regulatory compliance in a fast‑paced biotech environment. While NetSuite is the primary system of ownership, this role will also administer and support additional enterprise applications across the organization&lt;em&gt;.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;This role is based in our Louisville, CO site and is expected to work onsite at least 3 days/week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop, test, implement, and support enterprise systems to ensure reliable business operations.&lt;/li&gt;
&lt;li&gt;Administer and optimize the NetSuite ERP platform, including configuration, master data, reporting, integrations, and issue resolution.&lt;/li&gt;
&lt;li&gt;Provide hands‑on application support to troubleshoot and quickly resolve system issues.&lt;/li&gt;
&lt;li&gt;Collaborate with internal teams and external vendor partners to maintain and enhance enterprise applications.&lt;/li&gt;
&lt;li&gt;Support planning, design, and rollout of new capabilities, ensuring strong adoption and change readiness.&lt;/li&gt;
&lt;li&gt;Partner with IT to monitor, troubleshoot, and enhance integrations across enterprise systems.&lt;/li&gt;
&lt;li&gt;Ensure systems comply with SOX, SEC, and FDA 21 CFR Part 11 requirements and support audit activities.&lt;/li&gt;
&lt;li&gt;Support validated system lifecycle activities including release management, change control, testing, user access reviews, and periodic audit readiness.&lt;/li&gt;
&lt;li&gt;Gather business requirements and contribute to IT roadmaps, translating needs into actionable initiatives.&lt;/li&gt;
&lt;li&gt;Develop documentation, deliver user training, and support organizational change management.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree or higher in Information Systems, Business Administration, or related field and 5-8 years of professional experience.&lt;/li&gt;
&lt;li&gt;5+ years of hands‑on NetSuite administration experience, with a strong focus on Supply Chain, Inventory, WMS, and Procurement.&lt;/li&gt;
&lt;li&gt;Proficiency with NetSuite workflows, saved searches, and SuiteScript.&lt;/li&gt;
&lt;li&gt;Experience supporting core SCM functions: item management, demand planning, purchasing, inventory, and WMS.&lt;/li&gt;
&lt;li&gt;Hands on experience with SOX, FDA 21 CFR Part 11, ISPE GAMP 5, compliance frameworks.&lt;/li&gt;
&lt;li&gt;Experience administering or supporting other enterprise SaaS applications (HRIS, Quality, Budget, P2P, etc.)&lt;/li&gt;
&lt;li&gt;Ability to troubleshoot system issues, manage integrations, and support end‑users across operational teams.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong understanding of NetSuite SCM, Inventory, WMS, Finance, Procurement, and Manufacturing modules.&lt;/li&gt;
&lt;li&gt;Experience in manufacturing environments and familiarity with production workflows, BOMs, routings, quality, and MRP.&lt;/li&gt;
&lt;li&gt;Experience with cloud-based enterprise applications: Coupa (Procure‑to‑Pay or Invoice‑to‑Pay); FloQast; Veeva; UKG or similar solutions.&lt;/li&gt;
&lt;li&gt;Strong business process analysis and system design skills.&lt;/li&gt;
&lt;li&gt;Excellent relationship‑building skills and a collaborative, positive mindset.&lt;/li&gt;
&lt;li&gt;Experience in biotech, life sciences, manufacturing, or other regulated industries.&lt;/li&gt;
&lt;li&gt;Familiarity with integration platforms such as Celigo or Boomi.&lt;/li&gt;
&lt;li&gt;Strong understanding of procurement best practices, supplier management, and supply chain operations.&lt;/li&gt;
&lt;li&gt;A positive, proactive, and service-oriented approach, with a commitment to continuous learning and improvement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to sit for prolonged periods of time&lt;/li&gt;
&lt;li&gt;Ability to work onsite in Louisville, CO at least 3 days/week&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $116,800 - $144,300&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-enterprise-systems-analyst-umoja-biopharma/69d3bcfac8e81216cd0b912b</link><guid isPermaLink="true">http://biotechroles.com/senior-enterprise-systems-analyst-umoja-biopharma/69d3bcfac8e81216cd0b912b</guid><pubDate>Mon, 06 Apr 2026 14:02:34 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Vice President, AI & Digital Platform]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;THE ROLE&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Pioneering Intelligence team at Flagship Pioneering builds the digital and AI foundation that accelerates the creation and growth our companies. We are seeking a&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Senior Vice President (SVP) – AI &amp;amp; Digital Platform&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt; to enable AI tooling across our enterprise, shepherd our AI-native data platform, maintain and evolve the digital backbone of our early stage companies, and lead a world-class technology team though support, empowerment, and accountability. This is a senior leadership role within the Pioneering Intelligence Initiative, offering the opportunity to shape the strategy, execution, and impact of AI across Flagship’s ecosystem.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;As the &lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;SVP – AI &amp;amp; Digital Platform&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;, you will be responsible for defining and executing the vision for how AI and digital technologies enable Flagship and its portfolio companies. You will shepherd and deliver the platforms, tools, and infrastructure that power AI-native operations and empower scientific and business teams. This role combines strategic leadership with deep technical expertise, requiring you to operate in highly ambiguous environments, shape long-term direction, and build organizational capabilities that endure.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Enable AI tooling and capabilities across scientific and operational workflows.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Architect and implement an AI-native data platform that empowers Agentic AI and AI Modeling teams.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Maintain and evolve the PI Digital Backbone—Flagship’s shared infrastructure “starter kit” for new company launches, including compute, shared code, and AI tools.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Support and develop a high-performing, product-minded technology organization.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Partner with portfolio company founders, venture teams, scientific leaders, and functional teams to align and drive adoption of our shared digital strategy.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop and communicate strategy for Flagship’s AI initiatives internally and externally.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;15+ years of progressive leadership experience in AI, data platforms, or digital technology, ideally spanning both technology and life sciences.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated success in building and scaling platforms that deliver measurable scientific or business outcomes.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Deep expertise in AI, ML, and data architectures, paired with strong product and business acumen.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven ability to thrive in highly ambiguous, rapidly evolving environments.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Track record of building and leading diverse, high-performing teams.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication and collaboration skills, with the ability to influence at all levels of an organization.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:281,&amp;quot;335559739&amp;quot;:281}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience creating or scaling digital platforms in complex or scientific domains.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Familiarity with life sciences R&amp;amp;D workflows and the opportunities for AI-driven acceleration.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with early-stage B2B software product development.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong network within the AI and digital innovation ecosystem.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;WHY PIONEERING INTELLIGENCE?&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Lead a bold initiative at the intersection of AI, digital platforms, and pioneering science.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Help define the future of Flagship’s digital and AI strategy, impacting multiple portfolio companies.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with visionary founders, scientists, and innovators across Flagship’s ecosystem.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Build in a supportive, mission-driven culture with access to world-class technical and operational resources.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Competitive compensation and benefits, including equity, commensurate with experience.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;#LI-NM1&lt;/span&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $325,000 - $450,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-vice-president-ai-and-digital-platform-flagship-pioneering/69d3bcf8c8e81216cd0b9124</link><guid isPermaLink="true">http://biotechroles.com/senior-vice-president-ai-and-digital-platform-flagship-pioneering/69d3bcf8c8e81216cd0b9124</guid><pubDate>Mon, 06 Apr 2026 14:02:32 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$350000-600000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, GMP Quality Assurance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY &lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Sr. Director, GMP Quality Assurance (GMP QA) is responsible for overseeing all quality assurance operations for Umoja related to Good Manufacturing Practices (GMPs) for Umoja’s product portfolio across all phases of the product lifecycle. This senior leadership role will lead a GMP QA organization comprised of quality professionals supporting internal and external GMP manufacturing operations, quality systems, and oversight of GMP vendors. As a senior leader within the company and Quality organization, this role will provide strategic leadership and direction, collaborating across all relevant internal and external stakeholders (e.g., Manufacturing, Supply Chain, Facilities &amp;amp; Engineering, CMC, Regulatory, etc.) to develop high performing &amp;amp; collaborative teams and mature and execute a comprehensive functional vision in alignment with company and organizational goals. This role will oversee and direct the maturation and continual improvement of GMP quality systems and processes that assure product quality &amp;amp; patient safety in accordance with Umoja quality principles and compliance with applicable laws, regulations, industry Standards, and Health Authority requirements &amp;amp; expectations appropriate for applicable phases of the product lifecycle.&lt;/p&gt;
&lt;p&gt;This role shall also serve as a member of the senior Quality Leadership Team to set and execute strategic initiatives, maintain and encourage a strong continual improvement mindset, and serve as a critical leader in establishing, maturing, and championing Umoja’s quality culture.&lt;/p&gt;
&lt;p&gt;This position is an on-site role based at Umoja’s GMP manufacturing facility, The CLIMB, in Louisville, Colorado, and will report directly to the Head of Quality.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Leading the GMP Quality Assurance (GMP QA) function at Umoja in support of Umoja’s multi-product, multi-jurisdiction, multi-partner portfolio through all phases of development (e.g., Phase 1, Pivotal, PPQ, commercial launch, etc.)&lt;/li&gt;
&lt;li&gt;Building, mentoring, and leading a high-performing GMP QA team,&amp;nbsp;fostering a culture of quality, accountability, collaboration, and organizational flexibility &amp;amp; adaptability within the team and across the organization in alignment with Umoja’s values &amp;amp; principles and Umoja’s quality culture&lt;/li&gt;
&lt;li&gt;Developing, implementing, and executing a comprehensive organizational vision and strategy in alignment with Quality organization, site, and corporate goals &amp;amp; objectives&lt;/li&gt;
&lt;li&gt;Active engagement in Umoja’s Quality Leadership Team (QLT) to set strategic organizational initiatives and champion Umoja’s quality culture&lt;/li&gt;
&lt;li&gt;Establishing and monitoring quality and compliance goals and operational performance metrics to identify and drive continuous improvement initiatives and operational excellence&lt;/li&gt;
&lt;li&gt;Establishing and maturing consistent ways of working within the GMP QA organization and all relevant stakeholders (e.g., Manufacturing, Supply Chain, Facilities &amp;amp; Engineering, CMC, Regulatory, etc.) in alignment with a defined risk profile appropriate for applicable phases of development&lt;/li&gt;
&lt;li&gt;Establishing a functional budget and monitoring adherence to accomplish organizational objectives in alignment with company financial guidelines&lt;/li&gt;
&lt;li&gt;Monitoring, maturing, and continually improving components of Umoja’s Quality Management System relevant to GMP operations through compliance with, and practical application of, phase-appropriate global GMPs (e.g., FDA, EMA, MHRA, PMDA, ICH, etc.), data integrity standards, Health Authority expectations &amp;amp; requirements, applicable laws, and company policies&lt;/li&gt;
&lt;li&gt;Overseeing the development, implementation, and maintenance of GMP QA policies, quality agreements, SOPs, and quality systems processes and workflows to disposition material &amp;amp; product and effectively manage quality records and events (e.g., deviations, CAPA, change control, product complaints, etc.)&lt;/li&gt;
&lt;li&gt;Overseeing the selection, qualification, and ongoing monitoring of all GMP vendors, including contract manufacturers, suppliers, and testing laboratories, ensuring vendor compliance with contractual obligations, quality agreements, and regulatory requirements&lt;/li&gt;
&lt;li&gt;Overseeing a phase-appropriate approach to Quality Management Review, ensuring applicable and meaningful metrics are evaluated to assess control and identify areas for continual improvement&lt;/li&gt;
&lt;li&gt;Ensuring effective quality risk management practices are in place, including identification, communication, assessment, and resolution of quality-related risks&lt;/li&gt;
&lt;li&gt;Providing strategic support and leadership review of CMC-related sections within regulatory submissions in support of US and ex-US jurisdictional filings in close collaboration with cross-functional teams&lt;/li&gt;
&lt;li&gt;Leading and supporting preparation for, and execution of, partner audits and health authority inspections, overseeing closure of appropriate responses and other actions per established timelines&lt;/li&gt;
&lt;li&gt;Representing GMP QA in regulatory inspections, partner audits, due diligence activities, and health authority communications&lt;/li&gt;
&lt;li&gt;Ensuring all product complaints are received, evaluated, and investigated, and closed in accordance with internal procedures and health authority expectations&lt;/li&gt;
&lt;li&gt;Ensuring appropriate data integrity controls, systems, and processes are in place and function as required in support of GMP processes&lt;/li&gt;
&lt;li&gt;Reviewing and approving audit reports, CAPA plans, and follow-up actions to ensure effective resolution of related quality events&lt;/li&gt;
&lt;li&gt;Providing expert guidance on GMP compliance and escalating critical quality events, nonconformances, and compliance issues to cross-functional teams and senior management&lt;/li&gt;
&lt;li&gt;Providing QA leadership, direction, and effective cross-functional communication in support of product recall events&lt;/li&gt;
&lt;li&gt;Representing the QA and/or Quality function on various Umoja senior leadership governance committees and leadership forums, where appropriate&lt;/li&gt;
&lt;li&gt;Monitoring industry trends and emerging best practices to innovate and proactively enhance quality processes&lt;/li&gt;
&lt;li&gt;Other duties as required&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS/BA degree (or equivalent) in life sciences with a minimum of 15 years of progressive and extensive quality and compliance background in pharma/biotech across all phases of development (e.g., Phase 1, Pivotal, PPQ, commercial launch, etc.)&lt;/li&gt;
&lt;li&gt;Minimum of 8 years management (direct or matrix) experience with proven track record of building &amp;amp; developing highly collaborative, effective, and successful individuals, teams, &amp;amp; organizations&lt;/li&gt;
&lt;li&gt;Strong patient-focused and quality culture mindset rooted in collaboration and continual improvement&lt;/li&gt;
&lt;li&gt;Proven track record of effective and collaborative organizational leadership, setting and executing a strategic organizational vision, and developing leaders and organizations in alignment with company and individual goals and objectives&lt;/li&gt;
&lt;li&gt;Extensive experience with comprehensive GMP quality assurance organizations, processes, and systems supporting internal manufacturing operations within a multi-product GMP manufacturing facility&lt;/li&gt;
&lt;li&gt;Extensive experience with designing, implementing, and maturing effective, efficient, and appropriately risk-based quality systems suitable for intended use across all phases of development&lt;/li&gt;
&lt;li&gt;Strong understanding of health authority submission dossier composition and effective CMC section strategy &amp;amp; content from INDs through BLAs (or equivalent) across multiple jurisdictions&lt;/li&gt;
&lt;li&gt;Experience with health authority interactions, site inspections, and regulatory submissions&lt;/li&gt;
&lt;li&gt;Experience defining, implementing, and maturing six sigma quality systems throughout the product lifecycle&lt;/li&gt;
&lt;li&gt;Strong understanding of tech transfer processes and standards&lt;/li&gt;
&lt;li&gt;Proficiency in making practical, risk-based decisions in alignment with quality &amp;amp; compliance requirements and expectations in a dynamic environment&lt;/li&gt;
&lt;li&gt;Extensive experience in providing QA support and oversight of GMP electronic systems implementation and execution (e.g., SAP, Veeva, BMRAM, etc.)&lt;/li&gt;
&lt;li&gt;Extensive experience with novel therapies progressing from early phase to late phase to commercial&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Extensive Quality organization experience within cell and/or gene therapy across all phases of development&lt;/li&gt;
&lt;li&gt;Experience with various GMP electronic systems (e.g., BMRAM, Veeva, LIMS, etc.)&lt;/li&gt;
&lt;li&gt;Experience designing, implementing, and/or maturing six sigma quality systems and Lean methodologies&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to travel occasionally&lt;/li&gt;
&lt;li&gt;Ability to sit for prolonged periods of time&lt;/li&gt;
&lt;li&gt;Ability to gown-in to support and/or observe on-the-floor work (e.g., Manufacturing, Supply Chain, Facilities &amp;amp; Engineering, etc.)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $234,260 - $289,380&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-gmp-quality-assurance-umoja-biopharma/69d3bcf6c8e81216cd0b9116</link><guid isPermaLink="true">http://biotechroles.com/senior-director-gmp-quality-assurance-umoja-biopharma/69d3bcf6c8e81216cd0b9116</guid><pubDate>Mon, 06 Apr 2026 14:02:30 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior UX Designer, Agentic AI]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;ABOUT PIONEERING INTELLIGENCE&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding&amp;nbsp;cutting-edge&amp;nbsp;science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;THE ROLE&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;Pioneering Intelligence is seeking a Senior UXD&amp;nbsp;&lt;/span&gt;&lt;span data-contrast=&quot;none&quot;&gt;to partner across&amp;nbsp;Product,&amp;nbsp;AI research, engineering, legal, communications and marketing, multi-disciplinary scientific&amp;nbsp;groups&amp;nbsp;and venture creation teams&amp;nbsp;to solve the most impactful challenges in AI for the life sciences.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;We are building a next-generation digital foundation that integrates computational science, AI/ML, knowledge engineering, data platforms, and workflow automation. These capabilities support Flagship’s unique model of exploring the unknown and translating scientific insight into world-changing companies.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;5608de39-acc8-52c5-8723-06e2503f1031|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[201342446,&amp;quot;1&amp;quot;,201342447,&amp;quot;5&amp;quot;,201342448,&amp;quot;1&amp;quot;,201342449,&amp;quot;1&amp;quot;,469777841,&amp;quot;Times New Roman&amp;quot;,469777842,&amp;quot;Times New Roman&amp;quot;,469777843,&amp;quot;Times New Roman&amp;quot;,469777844,&amp;quot;Times New Roman&amp;quot;,201341986,&amp;quot;1&amp;quot;,469769226,&amp;quot;Times New Roman&amp;quot;,268442635,&amp;quot;24&amp;quot;,469775450,&amp;quot;p1&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;p1&amp;quot;,335572020,&amp;quot;1&amp;quot;,335559740,&amp;quot;240&amp;quot;,201341983,&amp;quot;0&amp;quot;,134233118,&amp;quot;true&amp;quot;,134233117,&amp;quot;true&amp;quot;,469778324,&amp;quot;Normal&amp;quot;]}&quot;&gt;The&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;UX Designer, Agentic AI&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;will&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;design intuitive,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;high-impact&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;trustworthy user experiences for agentic AI&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;products thereby accelerating&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;product&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;adoption,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;Delighting&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;users and driving&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;business&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;impact.&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;This is an individual contributor role with ownership of UX across key AI-integrated products and a mandate to shape&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;scalable UX patterns and systems&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;for the Agentic AI organization.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;As part of a multidisciplinary (product, software engineers, AI scientists) team, you&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;will work closely with scientists&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;business&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;stakeholders&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;shape how&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;they&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;apply&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;agentic systems&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;to reimagine workflows&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;,&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;translating complex capabilities into trusted, valuable experiences while helping establish strong UX practices in a fast-moving startup environment&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;KEY&amp;nbsp;RESPONSIBILITIES&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Own UX for defined product areas with&amp;nbsp;product guidance&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;5608de39-acc8-52c5-8723-06e2503f1031|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[201342446,&amp;quot;1&amp;quot;,201342447,&amp;quot;5&amp;quot;,201342448,&amp;quot;1&amp;quot;,201342449,&amp;quot;1&amp;quot;,469777841,&amp;quot;Times New Roman&amp;quot;,469777842,&amp;quot;Times New Roman&amp;quot;,469777843,&amp;quot;Times New Roman&amp;quot;,469777844,&amp;quot;Times New Roman&amp;quot;,201341986,&amp;quot;1&amp;quot;,469769226,&amp;quot;Times New Roman&amp;quot;,268442635,&amp;quot;24&amp;quot;,469775450,&amp;quot;p1&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;p1&amp;quot;,335572020,&amp;quot;1&amp;quot;,335559740,&amp;quot;240&amp;quot;,201341983,&amp;quot;0&amp;quot;,134233118,&amp;quot;true&amp;quot;,134233117,&amp;quot;true&amp;quot;,469778324,&amp;quot;Normal&amp;quot;]}&quot;&gt;Translate AI behavior into intuitive&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;, trustworthy&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;experiences&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;that drive outcomes&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;Partner with product and engineering&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;to iterate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;designs&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;based on&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;user research and&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;&amp;nbsp;user and product data&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;p1&quot;&gt;Prototype, test, and iterate rapidly with users&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Contribute to&amp;nbsp;scalable UX patterns and systems&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;QUALIFICATIONS&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Minimum&amp;nbsp;5-6&amp;nbsp;years of experience designing products for scientific users&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Background in biotech or life sciences&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Demonstrated&amp;nbsp;evidence-based, user-centered design&amp;nbsp;practice&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience with continuous discovery methods&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ownership mindset with bias toward action&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Comfort working through ambiguity&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240,&amp;quot;335559991&amp;quot;:360}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;PREFERRED QUALIFICATIONS&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Demonstrated experience designing AI-powered&amp;nbsp;experiences, including human-in-the-loop&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Familiarity with agentic workflows, automated&amp;nbsp;systems&amp;nbsp;and/or&amp;nbsp;decision&amp;nbsp;support&amp;nbsp;systems&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Background in human-computer interaction&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience prototyping adaptive interfaces, including AI&amp;nbsp;assisted&amp;nbsp;eg.&amp;nbsp;vibe coding&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Comfort working in fast-changing environments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Contribute to&amp;nbsp;Design&amp;nbsp;Systems,&amp;nbsp;improving speed and consistency&amp;nbsp;of development&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;OBJECTIVES&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Reduce friction in human–AI collaboration, including increase user trust in AI powered products&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Accelerate&amp;nbsp;product adoption&amp;nbsp;and&amp;nbsp;improve&amp;nbsp;engagement&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Increase user delight and perceived value&amp;nbsp;of products&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $108,000 - $170,700. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-ux-designer-agentic-ai-flagship-pioneering/69d3bcf4c8e81216cd0b910e</link><guid isPermaLink="true">http://biotechroles.com/senior-ux-designer-agentic-ai-flagship-pioneering/69d3bcf4c8e81216cd0b910e</guid><pubDate>Mon, 06 Apr 2026 14:02:27 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Clinical Regulatory Affairs]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Senior Director, Regulatory Affairs reports to the Head of Regulatory Affairs and is responsible for content development, compilation, maintenance, and review of the Nonclinical and Clinical Modules for regulatory submissions to support Umoja’s drug products including, DMF, IND and NDA/BLA applications, Health Authority (HA) responses, and briefing packages (including participating in/leading HA meetings). In this role, the Senior Director will be the Regulatory Affairs leader on program teams and will provide expertise to support the development of our in vivo CAR-T therapy programs. This individual will play a critical role in regulatory strategy, study design, execution, and in leading regulatory interactions.&lt;/p&gt;
&lt;p&gt;The ideal candidate will bring deep experience in cell &amp;amp; gene therapy and a strong track record in oncology or rheumatology drug development.&lt;/p&gt;
&lt;p&gt;This role will develop and implement regulatory strategies leading to successful registration and life-cycle management of unique and technologically complex products serving patients with cancer and other unmet medical needs. It builds and relies on critical partnerships with key stakeholders to execute the strategies in alignment with business priorities.&lt;/p&gt;
&lt;p&gt;We will consider candidates at either the Senior Director or Executive Director level based on candidate&#39;s qualifications and experience.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Independently provide regulatory leadership and oversight for ongoing and planned in vivo CAR-T therapy programs.&lt;/li&gt;
&lt;li&gt;Develop and execute global regulatory strategies to support indication selection, trial design, and endpoints, to support program advancement.&lt;/li&gt;
&lt;li&gt;Develop registration strategies and plans (e.g., TPP development and assessment) to achieve regulatory approvals and desired product labeling.&lt;/li&gt;
&lt;li&gt;Lead global regulatory filings (IND/CTA/BLA/MAA submissions), setting strategy for submissions of product registration documents for health authorities worldwide.&lt;/li&gt;
&lt;li&gt;Primary point of contact with global regulatory agencies to support program advancement.&lt;/li&gt;
&lt;li&gt;Effectively communicate the regulatory strategy, risks, mitigations and overall plans to Regulatory Affairs, program teams, senior management, and external stakeholders (as relevant).&lt;/li&gt;
&lt;li&gt;Identify, communicate, and propose resolutions to both routine and complex issues.&lt;/li&gt;
&lt;li&gt;Provide regulatory advice and guidance in the context of available and expected scientific data, regulatory guidance, and precedent to project teams to support decision making and program advancement.&lt;/li&gt;
&lt;li&gt;Collaborate closely with translational medicine, preclinical, clinical, CMC Regulatory, and technical teams to align overall strategy with scientific discoveries. Demonstrate ability to engage and effectively influence team members across multidisciplinary teams.&lt;/li&gt;
&lt;li&gt;Stay current on emerging trends, competitors, and regulatory guidance in cell &amp;amp; gene therapy and oncology and/or autoimmune therapeutic areas. Conduct regulatory research to assess the impact of relevant global regulations, guidance, and current regulatory environment. Provide interpretation of regulatory authority feedback, policies, guidelines, and directives.&lt;/li&gt;
&lt;li&gt;Work with external program partners collaboratively and effectively to deliver on contractual obligations while moving toward corporate goals and priorities.&lt;/li&gt;
&lt;li&gt;Provide organizational support and mentoring as company grows its product development pipeline.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Senior Director Level:&amp;nbsp;&lt;/strong&gt;PhD/MS/BS in a relevant scientific field required with a minimum of 12/15/15+ years, respectively, of relevant experience in regulatory affairs. Experience in Oncology, Hematology, or related specialty strongly preferred. Successful track record of regulatory submissions and approvals.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Executive Director Level: PhD&lt;/strong&gt;/MS/BS in a relevant scientific field required with a minimum of 15/18/18+ years, respectively, of relevant experience in regulatory affairs. Experience in Oncology, Hematology, or related specialty strongly preferred. Successful track record of regulatory submissions and approvals.&lt;/li&gt;
&lt;li&gt;Demonstrated expertise in cell &amp;amp; gene therapy, ideally with CAR-T or T-cell engaging modalities preferred; experience in in vivo gene delivery a plus.&lt;/li&gt;
&lt;li&gt;Strong knowledge of global regulatory requirements for early- and late-stage development of gene and cell therapies.&lt;/li&gt;
&lt;li&gt;Proven ability to interact with regulatory authorities.&lt;/li&gt;
&lt;li&gt;Excellent communication, leadership, and cross-functional collaboration skills.&lt;/li&gt;
&lt;li&gt;Passion for innovation and commitment to advancing transformative therapies for patients.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;em&gt;Ability to travel (~20%) for team meetings and/or regulatory interactions as required. Some international travel possible.&lt;/em&gt;&lt;/li&gt;
&lt;li&gt;&lt;em&gt;Ability to sit for prolonged periods of time&lt;/em&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Senior Director Salary Range: $253,000 - $312,500&lt;br&gt;Executive Director Salary Range: $272,900 - $337,000&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-clinical-regulatory-affairs-umoja-biopharma/69d3bcf2c8e81216cd0b910b</link><guid isPermaLink="true">http://biotechroles.com/senior-director-clinical-regulatory-affairs-umoja-biopharma/69d3bcf2c8e81216cd0b910b</guid><pubDate>Mon, 06 Apr 2026 14:02:26 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States; Remote; Seattle, Washington, United States</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Software Engineer, Front End]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Position Summary&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:160,&amp;quot;335559739&amp;quot;:80}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;We are seeking a Senior Front End Engineer. As a key contributor&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;in&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; this early-stage initiative, you will &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;architect and implement the user experience&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; for a new platform that &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;leverages&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; large language models (LLMs) and AI agents to enhance complex, high-stakes workflows.&lt;/span&gt;&lt;/span&gt; &lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;This is a &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;user-first, AI-augmented product&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; — your work will transform abstract reasoning tasks into intuitive, high-performance tools that empower experts across diverse research domains.&lt;/span&gt;&lt;/span&gt; &lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;You will lead front-end development and collaborate closely with engineers, AI scientists, product designers, and end users. This is a rare opportunity to &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;shape a greenfield product&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; at the intersection of usability, flexibility, and advanced reasoning.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:160,&amp;quot;335559739&amp;quot;:80}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Architect, develop, and &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;maintain&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; high-quality, testable front-end code and workflows aligned with complex scientific and analytical use cases.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Translate user stories, wireframes, and prototypes into production-ready &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;features&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; emphasizing clarity, maintainability, and reusability.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Implement responsive, accessible, and performant UIs &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;optimized&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; for data-rich, interactive workflows.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Ensure security, scalability, and observability of front-end services in cloud environments (AWS).&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Design and implement user interfaces from scratch, combining strong visual design with robust engineering.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Create and &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;maintain&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; scalable, consistent, and visually appealing UI components using a modern &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;React.js&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; stack.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Maintain front-end quality through comprehensive testing and validation of user flows and &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;interface&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; behavior.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Develop and &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;maintain&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; test suites (unit, integration, and end-to-end) for UI reliability.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Apply &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;DevOps/&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;GitOps&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; practices for automated testing, deployment, and monitoring.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Mentor engineers and scientists, driving technical quality and ensuring extensibility and performance across evolving use cases.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:160,&amp;quot;335559739&amp;quot;:80}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;B.S. in Computer Science, Engineering, or related field, with &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;6+ years&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; of professional software development experience.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; with modern front-end frameworks and tools, including &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;React.js, TypeScript, Tailwind CSS, Redux Toolkit, Playwright, and &lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Shadcn&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Strong experience with &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Node.js&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Skilled in writing and &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;maintaining&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; comprehensive test suites (&lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Jest, React Testing Library, Cypress&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;).&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Experience with system design, performance optimization, observability, and operational excellence for parallel LLM workloads.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Strong intuition for UX design and a passion for building intuitive, workflow-first products.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Excellent communication skills and a collaborative mindset in fast-moving, cross-functional environments.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:160,&amp;quot;335559739&amp;quot;:80}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Background in scientific domains such as biology, chemistry, or complex systems (a plus, not &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;required&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;).&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Why Join Us&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:160,&amp;quot;335559739&amp;quot;:80}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;By joining this initiative within Flagship’s Pioneering Intelligence group, you will:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Help define a &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;new category of intelligent software tools&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; for real-time human–AI collaboration.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Build a &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;greenfield product&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; at the intersection of usability, reasoning, and scientific innovation.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Collaborate with &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;visionary thinkers and top-tier researchers&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; across Flagship’s ecosystem.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Thrive in a &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;supportive, mission-driven culture&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; with access to world-class technical and operational resources.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Shape the &lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;future of AI-powered discovery&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; in a role that combines engineering excellence with health impact.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $108,000 - $176,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-software-engineer-front-end-flagship-pioneering/69d3bcefc8e81216cd0b9108</link><guid isPermaLink="true">http://biotechroles.com/senior-software-engineer-front-end-flagship-pioneering/69d3bcefc8e81216cd0b9108</guid><pubDate>Mon, 06 Apr 2026 14:02:23 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Bioprocessing Associate, Downstream]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a passionate and capable Sr. Bioprocessing Associate to support downstream Manufacturing Operations at our early-stage cell/gene therapy GMP manufacturing facility located in Louisville, CO. This role will support routine Manufacturing Operations and primarily focus on the downstream purification of our process, however, could be expected to support other manufacturing functions as well.&lt;/p&gt;
&lt;p&gt;Primary job responsibilities include, but are not limited to, executing buffer prep, chromatography, and TFF batch records, material management, personnel gowning, adhering to personnel/material flow, facility cleaning, onboarding new manufacturing processes/products, and assisting in the implementation of facility quality systems. Success is measured by full qualification on downstream manufacturing unit operations and successful execution to create lentiviral drug products.&lt;/p&gt;
&lt;p&gt;This role will interact on a regular basis with internal process engineers, Process Sciences, facilities, warehouse/supply chain, EHS, Quality Assurance, and Quality Control. Strong communication skills are essential to effectively work in our matrix team environment. This is an opportunity to be part of an excellent team working in an exciting environment, focused on realizing the challenge of targeting solid tumors successfully with novel cell/gene therapies.   &amp;nbsp;&lt;/p&gt;
&lt;p&gt;This is a fully onsite role at our Louisville, CO site. This role will start as 5 days/week and convert to a 4x10 schedule after completing onboarding/training.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Adhere to Standard Operating Procedures, good manufacturing practices, and good documentation practices. Revise processing SOPs, equipment SOPs, and batch records as necessary&lt;/li&gt;
&lt;li&gt;Perform weigh/dispense and buffer prep operations in a clean-room environment (ISO9)&lt;/li&gt;
&lt;li&gt;Observe, participate, and perform in downstream unit operation execution, and initial internal technology transfer runs from Process Sciences to Manufacturing&lt;/li&gt;
&lt;li&gt;Assist in the implementation of compliant and technically sound programs and systems in support of GMP manufacturing&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Actively participate in the receipt of internal technology transfer of novel cell/gene therapy manufacturing processes at various scales. &lt;/li&gt;
&lt;li&gt;Perform activities related to the introduction of new raw materials specifications from draft through approval&lt;/li&gt;
&lt;li&gt;Perform equipment cleanings, as required, per routine maintenance events, and pre/post process requirements.&lt;/li&gt;
&lt;li&gt;Perform aseptic manufacture of lentiviral products in an aseptic clean-room environment (ISO5, ISO7, ISO8, ISO9)&lt;/li&gt;
&lt;li&gt;Maintain inventory and perform stocking activities for gowning, cleaning, and consumable materials to ensure sufficient inventory is available to support manufacturing operations&lt;/li&gt;
&lt;li&gt;Perform material management activities related to kitting of Bill of Materials items&lt;/li&gt;
&lt;li&gt;Other duties as needed &amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Associate’s degree/Bachelor’s degree in a related biotechnology or life-sciences field with 5/3+ years of cGMP manufacturing experience (respectively) in the pharmaceutical and/or biologics field is desired or equivalent in work experience or education &lt;/li&gt;
&lt;li&gt;Prior Commercial GMP manufacturing experience is required &lt;/li&gt;
&lt;li&gt;Downstream purification knowledge or experience is required (e.g., depth-filtration, tangential flow filtration, and/or chromatography), specifically Cytiva’s AKTA Ready and Repligen’s KMPi systems.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior Commercial launch GMP manufacturing experience preferred&lt;/li&gt;
&lt;li&gt;Prior experience receiving a technology transfer is a bonus &lt;/li&gt;
&lt;li&gt;Demonstrated experience working on results-oriented teams where contribution and collaboration were critical to project success&lt;/li&gt;
&lt;li&gt;Proficient in computer applications such as word processing, spreadsheets, and web-based applications&lt;/li&gt;
&lt;li&gt;Self-motivated with strong organization and communication skills and can work independently or as part of a multi-disciplinary matrixed team. &amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to gown aseptically and work in a Clean Room environment &lt;/li&gt;
&lt;li&gt;Ability to work while gowned for extended periods of time &lt;/li&gt;
&lt;li&gt;Extensive use of laboratory equipment includes handling chemicals and biological materials&lt;/li&gt;
&lt;li&gt;Must have the ability to work around laboratories, manufacturing areas and equipment, and regularly lift 10-20 lbs. and periodically lift up to 50 lbs.&lt;/li&gt;
&lt;li&gt;Ability to work nights and weekends as needed &amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to work holidays and on-call as needed&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range for Senior Bioprocessing Associate:&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;$36.06 – $44.57/hour This is a non-exempt role.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Salary Range for Bioprocessing Associate II: $30.05-$37.11/hr This is a non-exempt role.&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-bioprocessing-associate-downstream-umoja-biopharma/69d3bceec8e81216cd0b9107</link><guid isPermaLink="true">http://biotechroles.com/senior-bioprocessing-associate-downstream-umoja-biopharma/69d3bceec8e81216cd0b9107</guid><pubDate>Mon, 06 Apr 2026 14:02:21 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Scientist, Nanopore]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;The Company&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 110 Inc. (FL110) is a privately held, early-stage technology company developing a fully integrated, end-to-end platform to enable next generation proteomics. Our platform integrates groundbreaking innovations in bioengineering, machine learning, and custom microelectronics to offer a level of precision and insight never before achieved.&lt;/p&gt;
&lt;p&gt;FL110 is backed by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. We are uniquely cross-functional and collaborative. Our teams thrive in unstructured and creative environments. Therefore, we seek individuals with an inclusive mindset and a diversity of thought.&lt;/p&gt;
&lt;p&gt;If this sounds like an environment you’d love to work in, even if you only have some of the experience listed below, please apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL110 is seeking a creative and talented (&lt;strong&gt;Senior) Scientist, Nanopore &lt;/strong&gt;to join our team. Leveling is flexible based on experience. This role will focus on developing nanopore sensing technologies and will join a team creating a nanopore based protein reading system.&lt;/p&gt;
&lt;p&gt;You will be part of a dynamic, cross-functional team, working closely with chemists, bioinformaticians, software developers, and hardware engineers. The ideal candidate has a strong background in nanopore technology, specifically with protein translocation, as well as either experience in biotech industry or a record of scientific achievement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Conduct advanced research in nanopore technology to drive technological advancements and deliver impactful results&lt;/li&gt;
&lt;li&gt;Develop and implement innovative research strategies and methodologies&lt;/li&gt;
&lt;li&gt;Collaborate with cross-functional teams to align research activities with company objectives&lt;/li&gt;
&lt;li&gt;Manage resources and timelines effectively&lt;/li&gt;
&lt;li&gt;Foster a culture of innovation and scientific excellence within the team&lt;/li&gt;
&lt;li&gt;Collaborate with internal and external stakeholders, including academic institutions, industry partners, and regulatory bodies&lt;/li&gt;
&lt;li&gt;Present research findings at scientific conferences and contribute to patent applications&lt;/li&gt;
&lt;li&gt;Communicate complex scientific concepts and project updates to diverse audiences, including non-scientific stakeholders&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Basic Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Physics, Molecular Biology, or related field&lt;/li&gt;
&lt;li&gt;Demonstrated experience in nanopore experimentation and protein translocation&lt;/li&gt;
&lt;li&gt;Experience with python-based data analysis and R&lt;/li&gt;
&lt;li&gt;Proven track record of scientific achievements demonstrated through publications, patents, and successful project completions&lt;/li&gt;
&lt;li&gt;Strong leadership and project management skills&lt;/li&gt;
&lt;li&gt;Excellent problem-solving abilities, analytical skills, and attention to detail&lt;/li&gt;
&lt;li&gt;Strong communication skills, both written and verbal, with the ability to convey complex scientific information to diverse audiences&lt;/li&gt;
&lt;li&gt;Ability to work independently and collaboratively in a fast-paced, dynamic environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice-to-Haves&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrated expertise in protein biochemistry including protein expression and purification&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Who Will Love This Job&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A&amp;nbsp;rigorous individual with a curious mind and a love of learning who enjoys working in a fast-paced environment with a driven and collaborative team&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp; Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL110 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL110&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-scientist-nanopore-flagship-pioneering/69d3bcebc8e81216cd0b9104</link><guid isPermaLink="true">http://biotechroles.com/(senior)-scientist-nanopore-flagship-pioneering/69d3bcebc8e81216cd0b9104</guid><pubDate>Mon, 06 Apr 2026 14:02:19 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Analyst, Quality Control Microbiology]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Umoja Biopharma is looking for a Senior Analyst, Quality Control Microbiology to perform testing and monitoring activities in support of the QC Microbiology laboratory and manufacturing areas at Umoja’s lentiviral vector manufacturing facility.&lt;/p&gt;
&lt;p&gt;This role reports to the Senior Manager, Quality Control Microbiology and will be based fully onsite in Louisville, CO.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;REQUIREMENTS&lt;/u&gt;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Performs and reviews routine Quality Control laboratory work, including environmental monitoring, clean utility sampling and testing, microbiological material qualification and maintenance, microbial identification, raw material sampling and inspection, bioburden testing, endotoxin testing, compendial testing, and container closure integrity testing&lt;/li&gt;
&lt;li&gt;Generates and revises Quality Control documents according to established document management processes&lt;/li&gt;
&lt;li&gt;Assists in the development of training materials and independently delivers training to staff for QC programs, systems, and processes&lt;/li&gt;
&lt;li&gt;With management oversight, executes qualification/validation activities for QC laboratory equipment, instruments, and systems&lt;/li&gt;
&lt;li&gt;With management oversight, executes internal and external method establishment (e.g., qualify, validate, verify, transfer) protocols to ensure QC readiness for production activities&lt;/li&gt;
&lt;li&gt;Initiates and supports microbial excursion investigations related to facility and personnel monitoring programs (e.g., environmental monitoring, aseptic gowning, utility monitoring, etc.) through collaboration with other functions (Engineering, Manufacturing, MSAT, etc.)&lt;/li&gt;
&lt;li&gt;Applies and advances Operational Excellence/LEAN philosophy within the QC laboratories to ensure continuous improvement across all programs, processes, and systems&lt;/li&gt;
&lt;li&gt;Prepares, ships, and tracks samples to outside testing laboratories&lt;/li&gt;
&lt;li&gt;Demonstrates the Umoja values as part of a high-performing, people-focused, inclusive, and collaborative organization&lt;/li&gt;
&lt;li&gt;Performs additional duties within the Quality organization, as required&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with 3-5 years of experience working in a cGMP regulated QC environment. Equivalent combinations of education and experience will be considered.&lt;/li&gt;
&lt;li&gt;A passion for teamwork and unwavering commitment to purpose, team success, and contribution to an outstanding workplace culture&lt;/li&gt;
&lt;li&gt;An understanding of Operational Excellence/Continuous Improvement philosophies and experience with practical application in a regulated laboratory environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Quality Control experience in an FDA-regulated industry supporting cGMP manufacturing areas&lt;/li&gt;
&lt;li&gt;Previous experience working in a clean room environment&lt;/li&gt;
&lt;li&gt;Previous experience working in cGMP cell and gene therapy manufacturing and/or testing facility&lt;/li&gt;
&lt;li&gt;Previous experience implementing a Laboratory Information Management System along with associated processes and documents&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to work on-site 5 days/week at Umoja’s manufacturing facility in Louisville, CO&lt;/li&gt;
&lt;li&gt;Ability to aseptically gown and work while standing for extended periods of time&lt;/li&gt;
&lt;li&gt;Ability to regularly lift 20 lbs. and periodically lift up to 50 lbs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Salary Range: $71,000 - $87,800&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-analyst-quality-control-microbiology-umoja-biopharma/69d3bceac8e81216cd0b90fe</link><guid isPermaLink="true">http://biotechroles.com/senior-analyst-quality-control-microbiology-umoja-biopharma/69d3bceac8e81216cd0b90fe</guid><pubDate>Mon, 06 Apr 2026 14:02:18 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Molecular Biology]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are building a new venture, FL122, pioneering genomic technologies at the intersection of human health and assisted reproduction. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Tessera Therapeutics, and Quotient Therapeutics. We are an equal opportunity employer.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a first Molecular Biology hire, who will define and build the experimental foundation of the company’s scientific platform. As an early stage hire, you will operate with significant ownership, designing core protocols, establishing technical standards, and shaping the direction of experimental strategy from first principles, reporting the results to senior leadership. We are looking for someone who is resourceful, is open to a rapidly changing, agile environment and has bias to action. The ideal candidate combines deep technical rigor with a growth mindset, pays attention to detail, and has a deep-rooted desire to achieve excellence. Being collaborative is key – the environment is an early stage startup, where all members of the team need to work closely together to break new ground in science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Deliver molecular biology research projects with a high degree of autonomy, including project design, implementation, troubleshooting, interpretation and reporting results to senior leadership&lt;/li&gt;
&lt;li&gt;Help implement appropriate instrumentation, reagents, and consistent workflows to support scalable and reliable experimental operations&lt;/li&gt;
&lt;li&gt;Handle and process human biospecimen, specifically human gametes, in a BSL2 setting with rigorous adherence to quality and reproducibility standards&lt;/li&gt;
&lt;li&gt;Develop, optimize, and benchmark workflows for extracting and quantifying minute amounts of nucleic acids from single cells and other low-input samples&lt;/li&gt;
&lt;li&gt;Test, compare and implement multiple single cell RNA sequencing methods, including library quantification and QC required for Illumina sequencing&lt;/li&gt;
&lt;li&gt;Interact with external advisors, leveraging their inputs and building high-quality relationships&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in biology, molecular biology, genetics or a related discipline with 5+ years of relevant post-academic or industry experience with an excellent research track record&lt;/li&gt;
&lt;li&gt;Deep expertise in the handling of minute amounts of nucleic acids, including rigorous QC and troubleshooting of low-input workflows&lt;/li&gt;
&lt;li&gt;Experience testing and optimizing single cell RNA sequencing methods end-to-end, including library quantification and QC (e.g., yield, size distribution, complexity)&lt;/li&gt;
&lt;li&gt;Demonstrated ability to independently design, troubleshoot, and iterate on technically demanding experimental systems&lt;/li&gt;
&lt;li&gt;Comfort operating in fast-moving, ambiguous startup environments with high ownership and accountability&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background &lt;strong&gt;and interest in Flagship&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL122 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL122&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-molecular-biology-flagship-pioneering/69d3bce7c8e81216cd0b90f7</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-molecular-biology-flagship-pioneering/69d3bce7c8e81216cd0b90f7</guid><pubDate>Mon, 06 Apr 2026 14:02:15 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Materials Handler]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a passionate and capable Materials Handler to join our Supply Chain team. As a member of the Supply Chain group, you will be working with many departments, such as Manufacturing, Quality, and Laboratory Materials groups to ensure that all the material needs of the business are met.&lt;/p&gt;
&lt;p&gt;The Materials Handler will be primarily tasked with receipt, stocking, inventory management, and data entry for materials to support pre-clinical/tox/engineering and GMP manufacturing activities. Certain activities will be managed by Standard Operating Procedures (SOPs), and the Materials Handler must ensure that they are able to follow all SOPs and work instructions.&lt;/p&gt;
&lt;p&gt;The successful candidate will partner closely with stakeholders to anticipate needs, resolve issues quickly, and deliver a consistent, high-quality service-based experience. We are looking for someone who takes ownership, communicates clearly, and works collaboratively to ensure our partners receive timely and effective support.&lt;/p&gt;
&lt;p&gt;Additional activities may include communication with Umoja teams and feedback on warehouse processes. Ideal candidate will have good communication skills, be highly organized, and detail oriented.&lt;/p&gt;
&lt;p&gt;Prior experience with a GMP environment and experience driving a forklift highly preferred.&lt;/p&gt;
&lt;p&gt;This role will support supply chain activities, reporting to the Warehouse Manager onsite 5 days/week in Louisville, CO.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Correct and timely receipt and processing of GMP and non-GMP materials at The CLIMB warehouse in Louisville, CO.&lt;/li&gt;
&lt;li&gt;Maintaining a safe, clean, and orderly warehouse in support of manufacturing activity&lt;/li&gt;
&lt;li&gt;Overseeing Raw Material kitting and transfer&lt;/li&gt;
&lt;li&gt;Cycle counting warehouse inventory and maintaining high accuracy with data entry&lt;/li&gt;
&lt;li&gt;Operating the warehouse according to and in compliance with Umoja SOPs and Quality Systems&lt;/li&gt;
&lt;li&gt;Safely operating machinery such as forklifts and order pickers&lt;/li&gt;
&lt;li&gt;Collaborating with other departments like Manufacturing, Quality, and Laboratory Materials to ensure all material needs are met&lt;/li&gt;
&lt;li&gt;Demonstrate proactive, service-oriented mindset and the ability to work effectively with cross functional partners.&lt;/li&gt;
&lt;li&gt;Demonstrating the Umoja Values of Unified in Purpose, Meaningful Impact, Obsessed with Solutions, Joyful, and Accountable.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A GED or equivalent degree with at least 2 years of experience in a Supply Chain/Warehouse/Inventory Role&lt;/li&gt;
&lt;li&gt;High attention to detail and excellent organizational skills&lt;/li&gt;
&lt;li&gt;Excellent communication skills&lt;/li&gt;
&lt;li&gt;Proficiency with Microsoft Office suite&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Forklift operating license&lt;/li&gt;
&lt;li&gt;Experience with NetSuite or other Inventory management software&lt;/li&gt;
&lt;li&gt;Experience operating in a cGMP environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to lift, push, pull, and carry to 50 lbs&lt;/li&gt;
&lt;li&gt;Comfortable being on your feet for extended periods of time.&lt;/li&gt;
&lt;li&gt;Exposure to warehousing and manufacturing areas at +5°C including storage freezer at –20°C&lt;/li&gt;
&lt;li&gt;Adherence to wearing proper personal protective equipment (PPE) such as but not limited to safety vest, eye protection (when required), cold/cut proof gloves (when required), steel-toed shoes, manufacturing gowning, line harness, and fall protection.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Hourly Range: $25.79 - $31.85 &lt;/strong&gt;(This role is non-exempt and is overtime eligible.)&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/materials-handler-umoja-biopharma/69d3bce5c8e81216cd0b90ef</link><guid isPermaLink="true">http://biotechroles.com/materials-handler-umoja-biopharma/69d3bce5c8e81216cd0b90ef</guid><pubDate>Mon, 06 Apr 2026 14:02:13 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$40000-55000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Scientist, ML/AI Antibody Design]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL106 Inc., is a privately held, early-stage biotechnology company focused on developing novel drug delivery modalities. FL106 is backed by Flagship Pioneering, bringing the vision and resources to guide FL106 from platform validation to real-world solutions that meaningfully improve patient care.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a passionate, creative, and self-driven (senior) scientist with expertise in computational protein design and state of the art AI/ML tooling for antibody and protein design to join our team. This candidate will pioneer the design of novel protein-based delivery modalities and collaborate with the experimental teams to test and iterate on computational designs. S/he will thrive in an entrepreneurial, fast-paced, and highly collaborative start-up environment, with the opportunity to work closely with Flagship Pioneering founders and become a leader in advancing FL106’s scientific platform and patient-focused mission.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive the AI/ML computational protein design&lt;/li&gt;
&lt;li&gt;Engage with Pioneering Intelligence at Flagship to explore and implement novel ML models that benefit FL106 design principles&lt;/li&gt;
&lt;li&gt;Advance both antibody engineering and &lt;em&gt;de novo&lt;/em&gt; antibody design pipelines&lt;/li&gt;
&lt;li&gt;Collaborate closely with the FL106 experimental scientists to test and iterate on constructs&lt;/li&gt;
&lt;li&gt;Engineer novel functionalities into protein scaffolds, leveraging structural modeling, rational design, and/or directed evolution&lt;/li&gt;
&lt;li&gt;Be abreast of the computational protein design field to advise design and strategic directions for protein engineering, implementing the latest technologies where necessary&lt;/li&gt;
&lt;li&gt;Contribute to strategic direction of the computational team at FL106, helping shape our design platform at the forefront of scientific innovation&lt;/li&gt;
&lt;li&gt;Identify and lead external research relationships with academic and commercial partners&lt;/li&gt;
&lt;li&gt;Report results to scientific team and Flagship Pioneering management&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Key Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. &lt;em&gt;(with 2+ yrs of industry research experience&lt;/em&gt;) in computational protein design, protein biochemistry, computational biophysics, computational biology, physics, or related field&lt;/li&gt;
&lt;li&gt;Expertise in computational protein modeling and design, structural biology, and biophysics is required&lt;/li&gt;
&lt;li&gt;Deep expertise with ML tools for computational protein design such as AlphaFold, RosettaFold, ESMFold, ProteinMPNN, RFDiffusion, Chroma, IgFold, DeepAb, Parapredis is required&lt;/li&gt;
&lt;li&gt;Experience with antibody and/or nanobody modeling and design is strongly preferred.&lt;/li&gt;
&lt;li&gt;Knowledge of critical wet-lab techniques used in protein engineering such as phage display, SPR, ITC, CD-spectroscopy is preferred&lt;/li&gt;
&lt;li&gt;Strategic thinker, able to shift seamlessly between rigorous scientific details and high-level context and implications&lt;/li&gt;
&lt;li&gt;Instinctive team player with excellent communication skills and great attention to detail&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company&amp;nbsp;that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in generation of over 500 patents, initiation of over 50 clinical trials for novel therapeutic agents and an aggregate value of more than $90 billion. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $115,000 - $258,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL108 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL108&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-scientist-mlai-antibody-design-flagship-pioneering/69d3bce2c8e81216cd0b90ea</link><guid isPermaLink="true">http://biotechroles.com/(senior)-scientist-mlai-antibody-design-flagship-pioneering/69d3bce2c8e81216cd0b90ea</guid><pubDate>Mon, 06 Apr 2026 14:02:10 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$160000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Lab Materials Associate]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals.&amp;nbsp; We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.&lt;/p&gt;
&lt;p&gt;Umoja Biopharma – Your Body. Your Hope. Your Cure.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;POSITION SUMMARY&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Umoja is seeking a highly motivated, organized, and detail-oriented Laboratory Materials Associate to support our Research and Development (R&amp;amp;D) and Quality Control (QC) laboratories at Umoja’s Colorado Laboratory, Innovation and Manufacturing Building (CLIMB) facility. The ideal candidate will have a good understanding of and experience supporting the day-to-day operations of a Biology/Cell Culture lab. This position will be responsible for restocking routinely used supplies, shipping and receiving, inventory counts, reordering inventory, and processing incoming inventory. This position will also include opportunities to take an active role in continuous improvement projects and support additional Supply Chain duties as needed.&lt;/p&gt;
&lt;p&gt;This role is based onsite 5 days/week at our Louisville, CO location.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;CORE ACCOUNTABILITIES&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific responsibilities include:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Perform routine onsite supply chain responsibilities daily, following applicable Standard Operating Procedures (SOPs)&lt;/li&gt;
&lt;li&gt;Order and restock routinely used supplies&lt;/li&gt;
&lt;li&gt;Lab shipping and receiving&lt;/li&gt;
&lt;li&gt;Repack and store incoming inventory&lt;/li&gt;
&lt;li&gt;Maintain accurate inventory counts in Benchling&lt;/li&gt;
&lt;li&gt;Regular lab presence to assess material needs&lt;/li&gt;
&lt;li&gt;Collaborate with various stakeholders such as lab area owners and EHS to ensure lab safety needs are met&lt;/li&gt;
&lt;li&gt;Requesting quotes for lab materials and sourcing alternate items from vendors&lt;/li&gt;
&lt;li&gt;Interact with LIMS (Laboratory Information Management Systems) with tracking materials for Quality Control Microbiology and Analytical&lt;/li&gt;
&lt;li&gt;Collaborate with cross-functional teams to drive continuous process improvement&lt;/li&gt;
&lt;li&gt;Invoice reconciliation as needed&lt;/li&gt;
&lt;li&gt;Other duties as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The successful candidate will have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Associate Degree or experience in laboratory science or supply chain with a minimum of 2 years of inventory/supply chain/laboratory experience&lt;/li&gt;
&lt;li&gt;Experience working within a lab and managing its operations&lt;/li&gt;
&lt;li&gt;Experience working with a team in a fast-paced environment&lt;/li&gt;
&lt;li&gt;Strong Microsoft office application skills, specifically Microsoft Excel&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Biotech start-up/life science industry and/or gene therapy experience is a plus&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Working knowledge of a KANBAN system&lt;/li&gt;
&lt;li&gt;Experience with Benchling/LIMS is a plus&lt;/li&gt;
&lt;li&gt;Experience with ERP systems, especially NetSuite, is a plus&lt;/li&gt;
&lt;li&gt;Ability to prioritize multiple concurrent competing tasks&lt;/li&gt;
&lt;li&gt;Experience working across multiple locations&lt;/li&gt;
&lt;li&gt;Team player, respectful of others, and open to new ideas&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Strong&amp;nbsp;communication skills&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to work independently&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Self-motivated and&amp;nbsp;passionate about&amp;nbsp;operational excellence&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Great attention to detail, resourceful, and well organized&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Able to thrive in a&amp;nbsp;fast-paced environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Physical Requirements:&amp;nbsp;&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to lift and maneuver 50lbs&lt;/li&gt;
&lt;li&gt;Ability to stand, bend, kneel for extended periods&lt;/li&gt;
&lt;li&gt;Ability to work on-call, after hours, and/or weekends on occasion or in emergencies&lt;/li&gt;
&lt;li&gt;This position is required to be onsite 5 days/week&lt;/li&gt;
&lt;li&gt;Adherence to wearing proper personal protective equipment (PPE) when necessary, such as lab coats, eye protection, cold gloves, safety vest, etc.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Hourly Range: $23.91 – $29.53 &lt;/strong&gt;(This role is non-exempt and is overtime eligible.)&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h4&gt;Benefits Offerings&lt;/h4&gt;
&lt;p&gt;&lt;span class=&quot;ui-provider ed bxe bds bxf bxg bxh bxi bxj bxk bxl bxm bxn bxo bxp bxq bxr bxs bxt bxu bxv bxw bxx bxy bxz bya byb byc byd bye byf byg byh byi byj byk&quot;&gt;&lt;em&gt;Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the &lt;strong&gt;&lt;u&gt;Benefits&lt;/u&gt;&lt;/strong&gt; section of our website.&lt;/em&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/lab-materials-associate-umoja-biopharma/69d3bce1c8e81216cd0b90e9</link><guid isPermaLink="true">http://biotechroles.com/lab-materials-associate-umoja-biopharma/69d3bce1c8e81216cd0b90e9</guid><pubDate>Mon, 06 Apr 2026 14:02:09 GMT</pubDate><company>Umoja Biopharma</company><location>Louisville, Colorado, United States</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Scientist, Machine Learning]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Build Models Where None Exist Yet.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;At Flagship Pioneering, we create companies from first principles. Within Flagship Labs, small founding teams define new technical theses, test them rapidly, and build ventures around breakthrough ideas.&lt;/p&gt;
&lt;p&gt;We are forming a machine learning team inside a newly launched venture, Flagship Labs 120. Our work focuses on extracting latent structure from information-rich measurements of complex physical systems—often requiring mechanism-informed modeling, thoughtful inductive bias design, and principled approaches to inverse problems.&lt;/p&gt;
&lt;p&gt;This is a zero-to-one role focused on modeling innovation rather than routine optimization. You’ll design, prototype, test, and refine new approaches that help define the technical foundation of a platform from day one.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What You’ll Do&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and iterate on ML models for complex measurement data, from representation design through validation&lt;/li&gt;
&lt;li&gt;Design objectives and architectures that respect known constraints, symmetries, or latent structure in the data&lt;/li&gt;
&lt;li&gt;Explore and compare modeling strategies, balancing strong baselines with more experimental approaches when appropriate&lt;/li&gt;
&lt;li&gt;Investigate model behavior and failure modes to improve robustness and interpretability&lt;/li&gt;
&lt;li&gt;Collaborate closely with experimental and technical teammates to align modeling with data generation&lt;/li&gt;
&lt;li&gt;Contribute to shaping the long-term ML strategy and technical direction of a new venture&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Who You Are&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;You may come from physics, applied mathematics, engineering, computer science, or another quantitative field.&amp;nbsp; You have hands-on experience developing machine learning models—ideally in deep learning, representation learning, probabilistic modeling, or related areas. You are comfortable implementing and modifying models, training them end-to-end, and working directly with real data.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;You likely:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Think algorithmically and reason from underlying structure&lt;/li&gt;
&lt;li&gt;Are comfortable adapting or extending model architectures when needed&lt;/li&gt;
&lt;li&gt;Have built and debugged meaningful ML systems or research prototypes&lt;/li&gt;
&lt;li&gt;Enjoy operating in dynamic, early-stage environments&lt;/li&gt;
&lt;li&gt;Read papers, build prototypes to test ideas, and translate concepts into working systems&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;What matters most is your ability to reason across data, models, and the systems they represent.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Technical Background&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;Required&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong hands-on experience building and training modern ML models&lt;/li&gt;
&lt;li&gt;Fluency in Python and at least one major ML framework (e.g., PyTorch or equivalent)&lt;/li&gt;
&lt;li&gt;Experience working with real-world or experimentally generated data&lt;/li&gt;
&lt;li&gt;Ability to design, run, and interpret ML experiments&lt;/li&gt;
&lt;li&gt;Comfort working in practical development environments (e.g., cloud infrastructure, experiment tracking, reproducible workflows)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;Helpful&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with inverse problems, latent-variable inference, or structured generative modeling (e.g., diffusion or flow-based methods)&lt;/li&gt;
&lt;li&gt;Familiarity with geometric or symmetry-aware architectures&lt;/li&gt;
&lt;li&gt;Experience incorporating physical or structural constraints into learning systems&lt;/li&gt;
&lt;li&gt;Experience working with time-series or high-dimensional signal data&lt;/li&gt;
&lt;li&gt;Exposure to biology, chemistry, physics, or related sciences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $130,000 - $230,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL120 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL120&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-scientist-machine-learning-flagship-pioneering/69d3bcddc8e81216cd0b90e6</link><guid isPermaLink="true">http://biotechroles.com/(senior)-scientist-machine-learning-flagship-pioneering/69d3bcddc8e81216cd0b90e6</guid><pubDate>Mon, 06 Apr 2026 14:02:05 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Supply Chain & External Manufacturing]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;We are seeking a Director of Supply Chain and External Manufacturing to join our CMC group at Tessera Therapeutics. This position will offer an exciting opportunity to build and manage the overall supply chain and external manufacturing function. We are searching for a driven, enthusiastic, and self-motivated individual who is comfortable multitasking and working independently on various aspects of the platform. This individual will join a dynamic, rapidly growing, and highly collaborative team.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;You are interested in:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Designing, building, and implementing phase appropriate supply chain and external manufacturing network strategies that ensure timely growth of capabilities and continuous supply of critical materials&lt;/li&gt;
&lt;li&gt;Driving the identification, contracting, relationship management, and performance of critical GMP supply chain and CMO partners&lt;/li&gt;
&lt;li&gt;Engaging in portfolio and program planning to ensure processes and capabilities are established to meet company needs and that critical materials are delivered on time&lt;/li&gt;
&lt;li&gt;Working collaboratively with Process Development, Manufacturing, Quality, Regulatory, Legal, Procurement, Finance, and other key stakeholders&lt;/li&gt;
&lt;li&gt;Establishing and leading cross-functional teams responsible for ensuring successful project execution with CMO partners&lt;/li&gt;
&lt;li&gt;Providing financial oversight and leading/supporting overall business improvement opportunities with External Parties&lt;/li&gt;
&lt;li&gt;Being responsible for supply chain and external manufacturing budgeting and providing strategic input into long-range planning processes&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Your Experience Includes:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS in Engineering or Life Science Discipline with 15 years related experience or Masters with 13 years related experience or PhD with 10 years of related experience&lt;/li&gt;
&lt;li&gt;Proven leadership in all areas of Supply Chain and CMO relationship management&lt;/li&gt;
&lt;li&gt;Broad experience in supply chain processes, methodologies, and technologies&lt;/li&gt;
&lt;li&gt;Experience and ability to draft, revise, review, and negotiate complex CMO contract terms&lt;/li&gt;
&lt;li&gt;Strong financial acumen with experience managing budget and P&amp;amp;L&lt;/li&gt;
&lt;li&gt;Exceptional written and verbal communication skills&lt;/li&gt;
&lt;li&gt;Proven ability for strategic thinking in a complex business environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Certifications in clinical supply chain management, project management&lt;/li&gt;
&lt;li&gt;Knowledge of gene therapy regulatory guidance&lt;/li&gt;
&lt;li&gt;Experience working in a gene therapy supply chain role or with gene therapy modalities&lt;/li&gt;
&lt;li&gt;Experience building clinical supply chain capabilities in US and EU&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Meet your Manager:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;All inquiries regarding the posted position should be directed to the Talent Partner (see below). Interested individuals must apply directly to be considered for the opening.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;a href=&quot;https://www.linkedin.com/in/jacob-claridge-35117726/&quot;&gt;&lt;strong&gt;Jacob Claridge – Senior Director, Technical Operations&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Jacob Claridge currently serves as the Senior Director of Technical Operations at Tessera Therapeutics where he leads a multidisciplinary team responsible for building, implementing, and supporting GMP manufacturing operations to enable material supply for Tessera’s pipeline programs.&lt;/p&gt;
&lt;p&gt;Prior to joining Tessera, Jacob previously held technical leadership roles at Astellas, Moderna, Momenta, and Regeneron where he had the opportunity to work with several drug modalities.&amp;nbsp; He has a passion for translating complex scientific processes into scalable, reproducible operations and building out teams that enable this capability.&amp;nbsp; Jacob holds an MBA from UC Berkeley and a BS in Bioengineering from Lehigh University.&lt;/p&gt;
&lt;p&gt;&lt;a href=&quot;https://www.tesseratherapeutics.com/leadership&quot;&gt;&lt;strong&gt;Meet our Leadership Team and Board of Directors&lt;/strong&gt;&lt;/a&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Meet your Talent Partner:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;a href=&quot;https://www.linkedin.com/in/labcoat2sportcoat/&quot;&gt;&lt;strong&gt;Ben Hoogheem – Senior Director, Head of Talent Management&lt;/strong&gt;&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;As Head of Talent Management at Tessera Therapeutics, Ben leads Tessera’s talent strategy across talent acquisition, performance management, and talent mobility.&lt;/p&gt;
&lt;p&gt;Ben began his career as an in vivo Pharmacologist, which gave him a lasting appreciation for the rigor, creativity, and collaboration that drive scientific discovery. That foundation continues to shape how he helps build organizations designed to enable science thrive.&lt;/p&gt;
&lt;p&gt;Ben is focused on aligning exceptional people with bold science – creating the structure, clarity, and culture that empower teams to scale effectively and achieve meaningful impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Compensation:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The stated base salary range represents Tessera’s good-faith estimate for this role. Actual compensation will be determined based on a number of factors, including but not limited to individual qualifications, years of relevant experience, internal compensation alignment, and external market data.&lt;/p&gt;
&lt;p&gt;Tessera offers a competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness, and financial security of our employees and their families. Benefits currently include group medical, vision, and dental coverage; group life and disability insurance; a 401(k) plan with company contribution; tuition reimbursement; and more.&lt;/p&gt;
&lt;p&gt;This position is also eligible for an annual incentive bonus and equity grants as part of Tessera’s total rewards program.&lt;/p&gt;
&lt;p&gt;Per Year Salary Range: $186,000 - $239,000 USD&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Tessera Therapeutics is pioneering Gene Writing™— a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Gene Writing holds the potential to become a new category in genetic medicine, building upon recent breakthroughs in gene therapy and gene editing while eliminating important limitations in their reach, utilization, and efficacy.&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot; style=&quot;margin-bottom: 0in; line-height: normal; text-align: justify;&quot;&gt;&lt;strong&gt;More about Tessera Therapeutics:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tessera is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, marital status, genetics, protected veteran status, citizenship status, sexual orientation, gender identity or expression, or any other characteristic identified by federal, state, or local laws where we operate. Tessera provides reasonable accommodations to qualified applicants and employees with disabilities. To begin an interactive dialogue with Tessera regarding a reasonable accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied, please contact the recruiter or &lt;a href=&quot;mailto:Accommodations@tesseratx.com&quot;&gt;Accommodations@tesseratx.com&lt;/a&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Tessera Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Tessera Therapeutics or its employees is strictly prohibited unless contacted directly by Tessera Therapeutics’ internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Tessera Therapeutics, and Tessera Therapeutics will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-supply-chain-and-external-manufacturing-tessera-therapeutics/69d3bcdcc8e81216cd0b90e4</link><guid isPermaLink="true">http://biotechroles.com/director-supply-chain-and-external-manufacturing-tessera-therapeutics/69d3bcdcc8e81216cd0b90e4</guid><pubDate>Mon, 06 Apr 2026 14:02:04 GMT</pubDate><company>Tessera Therapeutics</company><location>Somerville, Massachusetts, United States</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, LNP Formulations]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases. It was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly experienced Lipid Nanoparticle (LNP) Formulation Senior Scientist to lead the design, execution, and interpretation of advanced Design of Experiments (DOE) strategies to drive innovation in next-generation LNP formulations. This role will play a central role in shaping formulation and delivery strategies for nucleic acid therapeutics within a dynamic and collaborative research environment.&lt;/p&gt;
&lt;p&gt;The successful candidate will not only develop, optimize, and characterize LNP systems, but also lead the design and establishment of a high-throughput LNP screening platform spanning in vitro systems and small and large animal models. This includes defining experimental frameworks, selecting and implementing appropriate assays, and building scalable workflows to accelerate candidate evaluation and selection.&lt;/p&gt;
&lt;p&gt;As a senior scientific contributor, this individual will be expected to operate with a high degree of independence, influence cross-functional program direction, and identify innovative solutions to advance platform capabilities. The role also includes mentoring junior scientists and contributing to the broader scientific strategy through internal leadership and external scientific engagement.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive the development, optimization, and implementation of a high-throughput LNP screening platform across small and large animal models, including experimental design, assay selection, and data analysis pipelines.&lt;/li&gt;
&lt;li&gt;Independently define scientific strategies and experimental roadmaps aligned with program goals.&lt;/li&gt;
&lt;li&gt;Serve as a scientific lead for one or more programs, influencing cross-functional decisions across biology, formulation, and translational teams.&lt;/li&gt;
&lt;li&gt;Identify technical gaps and proactively propose innovative solutions to improve platform capabilities and throughput.&lt;/li&gt;
&lt;li&gt;Mentor junior scientists and contribute to building a strong, collaborative scientific culture.&lt;/li&gt;
&lt;li&gt;Communicate findings clearly to internal stakeholders and external partners; contribute to publications, patents, and regulatory documentation.&lt;/li&gt;
&lt;li&gt;Stay at the forefront of LNP delivery technologies and emerging screening methodologies, integrating new approaches where appropriate.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Professional experience and qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD or MS in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Science, or a related field and 5+ years of industry experience&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Proven track record of independently leading research projects and delivering impactful results.&lt;/li&gt;
&lt;li&gt;Demonstrated experience in nanoparticle/LNP design, screening, and &lt;em&gt;in vivo&lt;/em&gt; evaluation, preferably including large animal models.&lt;/li&gt;
&lt;li&gt;Experience in developing or scaling high-throughput screening platforms is strongly preferred.&lt;/li&gt;
&lt;li&gt;Strong understanding of experimental design, statistics, and data interpretation.&lt;/li&gt;
&lt;li&gt;Evidence of scientific leadership (e.g., mentoring, leading collaborations, publications, patents).&lt;/li&gt;
&lt;li&gt;Excellent communication and cross-functional collaboration skills.&lt;/li&gt;
&lt;li&gt;Strong hands-on experience with LNP formulations, including formulation development and optimization&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What We Offer&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Opportunity to work at the forefront of LNP formulation innovation&lt;/li&gt;
&lt;li&gt;Collaborative, science-driven culture with high impact research&lt;/li&gt;
&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship https://url.us.m.mimecastprotect.com/s/xLXBCqxk3LTk9pwcZf3CEkjif?domain=flagshippioneering.com.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $143,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-lnp-formulations-flagship-pioneering/69d3bcd9c8e81216cd0b90e2</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-lnp-formulations-flagship-pioneering/69d3bcd9c8e81216cd0b90e2</guid><pubDate>Mon, 06 Apr 2026 14:02:00 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Careers@Tessera]]></title><description><![CDATA[&lt;p&gt;&lt;strong style=&quot;color: rgb(0, 0, 0); font-family: &#39;Helvetica Neue&#39;, Helvetica, Arial, sans-serif; font-size: 13px; font-style: normal;   letter-spacing: normal;  text-align: start;   white-space: normal;  word-spacing: 0px;    &quot;&gt;Don&#39;t see anything listed that fits your background?&amp;nbsp; Please use this link to share your profile with us and we will keep you in mind for future roles.&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Tessera Therapeutics is pioneering Gene Writing™— a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Gene Writing holds the potential to become a new category in genetic medicine, building upon recent breakthroughs in gene therapy and gene editing while eliminating important limitations in their reach, utilization, and efficacy.&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot; style=&quot;margin-bottom: 0in; line-height: normal; text-align: justify;&quot;&gt;&lt;strong&gt;More about Tessera Therapeutics:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Tessera is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, marital status, genetics, protected veteran status, citizenship status, sexual orientation, gender identity or expression, or any other characteristic identified by federal, state, or local laws where we operate. Tessera provides reasonable accommodations to qualified applicants and employees with disabilities. To begin an interactive dialogue with Tessera regarding a reasonable accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied, please contact the recruiter or &lt;a href=&quot;mailto:Accommodations@tesseratx.com&quot;&gt;Accommodations@tesseratx.com&lt;/a&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Tessera Therapeutics does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Tessera Therapeutics or its employees is strictly prohibited unless contacted directly by Tessera Therapeutics’ internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Tessera Therapeutics, and Tessera Therapeutics will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/careers@tessera-tessera-therapeutics/69d3bcd8c8e81216cd0b90e0</link><guid isPermaLink="true">http://biotechroles.com/careers@tessera-tessera-therapeutics/69d3bcd8c8e81216cd0b90e0</guid><pubDate>Mon, 06 Apr 2026 14:01:57 GMT</pubDate><company>Tessera Therapeutics</company><location>Somerville, Massachusetts, United States</location><salary>$75000-150000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Scientist, Lipid and Polymer Science]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Company Description&amp;nbsp;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 110 Inc. (FL110) is a privately held, early-stage technology company developing a fully integrated, end-to-end platform to enable next generation proteomics.&lt;/p&gt;
&lt;p&gt;Our platform integrates groundbreaking innovations in bioengineering, machine learning, and custom microelectronics to offer a level of precision and insight never before achieved. By empowering researchers to explore proteins in unprecedented detail, we are transforming the way biology is understood and applied.&lt;/p&gt;
&lt;p&gt;FL110 is backed by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. At FL110, we are uniquely cross-functional and collaborative. We are actively reimagining the way teams work together and communicate. Therefore, we seek individuals with an inclusive mindset and a diversity of thought. Our teams thrive in unstructured and creative environments. All voices are heard because we know that experience comes in many forms, skills are transferable, and passion goes a long way.&lt;/p&gt;
&lt;p&gt;If this sounds like an environment you’d love to work in, even if you only have some of the experience listed below, please apply.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated Scientist specializing in the design, synthesis, and characterization of lipids, polymers, and functional materials to support the development of next-generation protein sequencing platforms and products. The successful candidate will apply strong chemical intuition, experimental rigor, and materials science expertise to create and optimize novel molecular and macromolecular systems with defined structure–function relationships.&lt;/p&gt;
&lt;p&gt;This role involves close collaboration with a multidisciplinary team spanning chemistry, biology, engineering, and nanopore sciences.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Key Responsibilities:&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, synthesize, and optimize novel lipids, polymers, and functional materials for research and product development applications&lt;/li&gt;
&lt;li&gt;Develop and execute synthetic routes for small molecules, oligomers, and polymers, including scale-up considerations&lt;/li&gt;
&lt;li&gt;Evaluate lipid membrane and material functionality in nanopore-based assays and devices&lt;/li&gt;
&lt;li&gt;Perform materials characterization, including:
&lt;ul&gt;
&lt;li&gt;NMR, LC-MS, GPC/SEC&lt;/li&gt;
&lt;li&gt;DSC, TGA, DLS, rheology, and surface analysis (as applicable)&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Establish structure–property relationships to guide iterative material design&lt;/li&gt;
&lt;li&gt;Troubleshoot synthetic challenges and optimize reaction conditions for yield, purity, and reproducibility&lt;/li&gt;
&lt;li&gt;Work with and/or manage projects with CROs&lt;/li&gt;
&lt;li&gt;Maintain detailed experimental documentation and data integrity&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Required Qualifications&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Education &amp;amp; Training
&lt;ul&gt;
&lt;li&gt;PhD in Chemistry, Polymer Science, Materials Science, Chemical Engineering, or a related field with 0-5 years of industry experience&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Technical Expertise
&lt;ul&gt;
&lt;li&gt;Demonstrated experience with organic synthesis and polymer synthesis&lt;/li&gt;
&lt;li&gt;Strong understanding of lipid chemistry and analysis&lt;/li&gt;
&lt;li&gt;Proficiency in analytical and characterization techniques (e.g., NMR, MS, GPC/SEC, DSC, TGA, DLS, rheology)&lt;/li&gt;
&lt;li&gt;Experience designing experiments independently and interpreting complex datasets&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Professional Skills
&lt;ul&gt;
&lt;li&gt;Strong problem-solving and critical-thinking abilities&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills&lt;/li&gt;
&lt;li&gt;Ability to manage multiple projects in a fast-paced research environment&lt;/li&gt;
&lt;li&gt;Collaborative mindset with a strong sense of scientific ownership&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;Preferred Expertise&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong understanding of polymer architectures and material structure–function relationships&lt;/li&gt;
&lt;li&gt;Experience with multiple types of polymerization initiation such as photo-initiated polymerization&lt;/li&gt;
&lt;li&gt;Experience working with biomolecules and protein chemistry&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $160,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL110 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL110&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-scientist-lipid-and-polymer-science-flagship-pioneering/69d3bcd3c8e81216cd0b90dc</link><guid isPermaLink="true">http://biotechroles.com/(senior)-scientist-lipid-and-polymer-science-flagship-pioneering/69d3bcd3c8e81216cd0b90dc</guid><pubDate>Mon, 06 Apr 2026 14:01:55 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Clinical Trial Associate]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Clinical Trial Associate/ Senior Clinical Trial Associate&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Responsibilities&lt;/u&gt;&lt;/strong&gt;&lt;strong&gt;:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Organize, participate in, and maintain agendas and meeting minutes for all internal and cross-functional team meetings. Review external meeting minutes as required.&lt;/li&gt;
&lt;li&gt;Work closely with our clinical consultants to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews).&lt;/li&gt;
&lt;li&gt;Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required.&lt;/li&gt;
&lt;li&gt;Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly.&lt;/li&gt;
&lt;li&gt;Create and maintain study personnel contact lists for all studies and KOLs by disease indication.&lt;/li&gt;
&lt;li&gt;Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs).&lt;/li&gt;
&lt;li&gt;Assist with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes.&lt;/li&gt;
&lt;li&gt;Assist with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines).&lt;/li&gt;
&lt;li&gt;Assist with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts).&lt;/li&gt;
&lt;li&gt;Assist with monitoring trip report across the program.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Education/Skills/Experience Requirements: &lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Relevant education and training required; Bachelor’s degree in administrative, science or medical areas of study is a plus.&lt;/li&gt;
&lt;li&gt;At least 3-5 years of successful administrative experience in biotech/life sciences, health care or clinical study management (title commensurate with experience)&lt;/li&gt;
&lt;li&gt;Prefers to contribute as both independent, self-starter, and a collaborative team member.&lt;/li&gt;
&lt;li&gt;Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.&lt;/li&gt;
&lt;li&gt;Excellent verbal and written communication skills.&lt;/li&gt;
&lt;li&gt;Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential. SharePoint and SmartSheet preferred.&lt;/li&gt;
&lt;li&gt;Veeva TMF working knowledge.&lt;/li&gt;
&lt;li&gt;Demonstrated multi-tasking and project management skills.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $100,000-150,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;&lt;u&gt;About Skyhawk&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Skyhawk is committed to discovering, developing and commercializing small molecule therapeutics that modify RNA expression. We use our novel SkySTAR® platform (Skyhawk Small molecule Therapeutics for Alternative splicing of RNA) to develop drug candidates directed toward targets for some of the world’s most intractable diseases including neurological conditions, cancer, and traditionally “undruggable” targets.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr.-clinical-trial-associate-skyhawk-therapeutics/69d3bccfc8e81216cd0b90da</link><guid isPermaLink="true">http://biotechroles.com/sr.-clinical-trial-associate-skyhawk-therapeutics/69d3bccfc8e81216cd0b90da</guid><pubDate>Mon, 06 Apr 2026 14:01:51 GMT</pubDate><company>Skyhawk Therapeutics</company><location>Waltham, MA</location><salary>$85000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist II/Principal Scientist, Microbial Protein Sciences]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company that invents and builds companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health, sustainability and beyond exponentially accelerate scientific progress in areas ranging from disease detection and treatment and nature-positive agriculture to novel applications of AI that are driving the creation of new technologies. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance science and technology by uniting innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This role will be the first hire on the Protein Sciences team of a startup that is focused on environmental and planetary health. This role will serve as both a technical leader and foundational builder of the function. The individual will own the strategy, design, and execution of protein construct development and production across multiple expression systems and scales, working in close partnership with discovery research. They will determine the feasibility and application of advanced protein science approaches, translating scientific objectives into robust, scalable workflows aligned with company priorities. In addition to hands-on technical leadership, this role will guide external CRO partnerships, contribute to strategic planning, and help establish processes, standards, and capabilities that support long-term growth. Depending on experience, this role may expand to include team leadership and broader organizational influence.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead the design, development, and implementation of protein expression and production strategies, determining the feasibility and optimal application of scientific approaches across targets;&lt;/li&gt;
&lt;li&gt;Own protein production workflows across multiple hosts and scales (e.g., &lt;em&gt; coli&lt;/em&gt;, &lt;em&gt;B. subtilis&lt;/em&gt;, &lt;em&gt;Pichia pastoris&lt;/em&gt;, cell-free systems; deep-well plates and shake flasks), ensuring rigor, reproducibility, and alignment with scientific and company objectives;&lt;/li&gt;
&lt;li&gt;Provide high-level technical expertise in protein quantification and validation, establishing fit-for-purpose analytical strategies (e.g., HiBit, Western analysis, related methods) to support decision-making;&lt;/li&gt;
&lt;li&gt;Manage and direct external CRO relationships, including protocol development, tech transfer, timelines, and budget considerations, while ensuring quality and strategic alignment;&lt;/li&gt;
&lt;li&gt;Contribute to the development of the Protein Sciences team by establishing best practices, documentation standards, and collaboration; support strategic planning and, with team growth, mentor or manage additional scientists.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD (or equivalent industry experience) in protein science, biochemistry, molecular biology, bioengineering, or a related discipline, with 8-12 years (at least 3 in industry with 5+ strongly preferred) of deep hands-on experience in protein expression and production&lt;/li&gt;
&lt;li&gt;Demonstrated ownership of protein construct design and production across multiple expression systems and scales, including microbial and/or cell-free platforms, with a track record of delivering reproducible, decision-enabling data&lt;/li&gt;
&lt;li&gt;Experience determining the feasibility and application of advanced protein science approaches to support scientific programs, including selecting hosts, formats, and analytical strategies aligned with program objectives&lt;/li&gt;
&lt;li&gt;Proven ability to lead complex technical work with minimal oversight, including managing external CRO relationships, protocol development or transfer, timelines, and resource considerations (e.g., budgets, trade-offs)&lt;/li&gt;
&lt;li&gt;Experience operating as a technical leader-either through mentoring scientists, guiding cross-functional collaborators, establishing best practices, or contributing to strategic scientific planning in an industry setting (startup experience strongly preferred)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TL1&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $143,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Protocos currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Protocos&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-iiprincipal-scientist-microbial-protein-sciences-flagship-pioneering/69d3bccfc8e81216cd0b90d8</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-iiprincipal-scientist-microbial-protein-sciences-flagship-pioneering/69d3bccfc8e81216cd0b90d8</guid><pubDate>Mon, 06 Apr 2026 14:01:50 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist II/Principal Scientist, Bioprocess Development]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Principal Scientist or Senior Scientist II to build and lead bioprocess development and microbial production for a high impact, novel biological platform. This role will focus primarily on fermentation process development, scale-up strategy, and production robustness, translating early-stage biological systems into scalable and manufacturable processes. The successful candidate will work at the interface of microbial engineering and bioprocess optimization, guiding both process development and targeted strain improvements that enable industrial production. This individual will serve as a technical leader within a multidisciplinary team and help establish foundational capabilities in microbial manufacturing as the company grows.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead development and optimization of microbial fermentation processes from laboratory scale through pilot-scale production&lt;/li&gt;
&lt;li&gt;Design scalable fermentation strategies including media development, feeding regimes, oxygen transfer optimization, and process control&lt;/li&gt;
&lt;li&gt;Translate biological discoveries into robust production systems by improving yield, productivity, and process reproducibility&lt;/li&gt;
&lt;li&gt;Establish experimental frameworks for systematic process improvement, including DOE-based optimization and fermentation analytics&lt;/li&gt;
&lt;li&gt;Develop and execute scale-up strategies and support technology transfer to external CROs, CMOs, or manufacturing partners&lt;/li&gt;
&lt;li&gt;Contribute to long-term manufacturing strategy and help build the company’s microbial production platform&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in biochemical engineering, microbiology, chemical engineering, or a related discipline
&lt;ul&gt;
&lt;li&gt;Scientist II: At least 8 years of professional experience, including 3+ years developing microbial fermentation processes in an industrial or translational setting&lt;/li&gt;
&lt;li&gt;Principal Scientist: At least 12 years of professional experience, including 5+ years developing microbial fermentation processes in an industrial or translational setting&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Demonstrated expertise in fermentation scale-up, optimizing parameters such as oxygen transfer, feeding regimes, media composition, etc.&lt;/li&gt;
&lt;li&gt;Hands-on experience developing and optimizing microbial fermentation across scales (e.g., 250 mL bench reactors through 50 L pilot-scale systems)&lt;/li&gt;
&lt;li&gt;Experience designing and executing fermentation experiments using systematic optimization approaches, such as DOE or structured process screening&lt;/li&gt;
&lt;li&gt;Experience working with external partners (CROs, CMOs, or manufacturing facilities) to develop or transfer fermentation processes, including preparation of process documentation and technical oversight&lt;/li&gt;
&lt;li&gt;Experience operating as a technical leader, either through mentoring scientists, guiding cross-functional collaborators, establishing technical best practices, or contributing to strategic scientific planning in an industry environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PREFERRED EXPERIENCE&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience developing fed-batch fermentation processes across a range of industrial microbial hosts, including bacteria, yeast, and filamentous fungi&lt;/li&gt;
&lt;li&gt;Experience optimizing high-cell-density microbial fermentations&lt;/li&gt;
&lt;li&gt;Experience building fermentation or bioprocess development capabilities and facilities within a start-up environment&lt;/li&gt;
&lt;li&gt;Experience improving production performance through close collaboration or co-ownership of targeted strain engineering activities&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TL1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $143,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Protocos currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Protocos&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-iiprincipal-scientist-bioprocess-development-flagship-pioneering/69d3bccac8e81216cd0b90d7</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-iiprincipal-scientist-bioprocess-development-flagship-pioneering/69d3bccac8e81216cd0b90d7</guid><pubDate>Mon, 06 Apr 2026 14:01:46 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Program and Portfolio Management]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.&lt;/p&gt;
&lt;p&gt;We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.&lt;/p&gt;
&lt;p&gt;We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;For more information see: &lt;a href=&quot;http://www.septerna.com&quot;&gt;www.septerna.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;
&lt;p&gt;&lt;strong&gt;About The Role&lt;/strong&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Septerna is seeking an experienced Vice President, Program and Portfolio Management to lead our program and portfolio management across the organization. This executive role will drive strategic alignment, operational excellence, and cross-functional execution across Septerna’s pipeline from discovery through clinical development.&lt;/p&gt;
&lt;p&gt;The VP will serve as a key strategic partner to executive leadership and the core program teams to ensure that the development programs progress efficiently and that portfolio decisions align with corporate priorities and resource allocation. This leader will establish and scale best-in-class program management capabilities, enabling integrated planning, governance, and decision-making across the portfolio and work closely with the research, preclinical, regulatory, manufacturing, and clinical development functions.&amp;nbsp; The role will be responsible for leading and scaling the project management function as the company grows.&lt;/p&gt;
&lt;p&gt;This role reports to the President &amp;amp; COO and works closely with executive leadership and the functional heads across Research, Development, Regulatory, Manufacturing, and Commercial Strategy.&amp;nbsp; This is an in-person role at Septerna’s South San Francisco headquarters.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Portfolio &amp;amp; Program Leadership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead program and portfolio management function across Septerna’s therapeutic pipeline from discovery through clinical development.&lt;/li&gt;
&lt;li&gt;Develop and drive integrated program strategies and ensure programs progress through key development milestones.&lt;/li&gt;
&lt;li&gt;Drive the prioritization of programs and resource allocation discussions with executive leadership.&lt;/li&gt;
&lt;li&gt;Facilitate data-driven decision making, identify critical issues and opportunities, and lead scenario planning across the portfolio.&lt;/li&gt;
&lt;li&gt;Ensure alignment between corporate strategy and goals, program objectives, and operational execution.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Cross-Functional Leadership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional program teams spanning research, preclinical development, regulatory, clinical development and operations, manufacturing, and commercial strategy.&lt;/li&gt;
&lt;li&gt;Serve as a strategic thought partner to scientific and development leaders to translate strategy into executable plans.&lt;/li&gt;
&lt;li&gt;Foster collaboration and alignment among diverse stakeholders in a highly matrixed environment.&lt;/li&gt;
&lt;li&gt;Provide clear and consistent communication within and between project teams and executive leadership on decisions and status.&lt;/li&gt;
&lt;li&gt;Provide alliance management support, as needed, for existing and future corporate collaborations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Executive Governance &amp;amp; Decision Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead governance committees to ensure program and portfolio oversight.&lt;/li&gt;
&lt;li&gt;Provide executive leadership with clear visibility into program status, key risks, and milestone progress.&lt;/li&gt;
&lt;li&gt;Identify critical path issues, lead cross-functional decision-making processes and ensure timely escalation of critical issues.&lt;/li&gt;
&lt;li&gt;Prepare and deliver strategic program updates for executive leadership and board of directors.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Strategic Planning &amp;amp; Operational Excellence&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and oversee integrated program plans, timelines, resource planning, and budgets across programs.&lt;/li&gt;
&lt;li&gt;Identify portfolio-level risks and opportunities and develop mitigation strategies.&lt;/li&gt;
&lt;li&gt;Implement best-in-class program management processes, tools, analytics, and governance frameworks.&lt;/li&gt;
&lt;li&gt;Build scalable infrastructure for program planning, forecasting, and reporting as the company grows.&lt;/li&gt;
&lt;li&gt;Partner closely with key functions, including Finance on budget and long-range planning processes&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Organizational Leadership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build, lead, and mentor a high-performing Program Management team that scales with the organization&lt;/li&gt;
&lt;li&gt;Establish standards, processes, and best practices across the organization.&lt;/li&gt;
&lt;li&gt;Promote a culture of accountability, transparency, and execution excellence.&lt;/li&gt;
&lt;li&gt;Contribute to broader organizational strategy and leadership initiatives.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;ABOUT YOU&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Advanced degree in a relevant scientific or medical field (PhD, PharmD, MD) or MBA preferred.&lt;/li&gt;
&lt;li&gt;15+ years of experience in biotechnology or pharmaceutical development.&lt;/li&gt;
&lt;li&gt;Significant leadership experience managing programs across discovery through clinical development.&lt;/li&gt;
&lt;li&gt;Demonstrated experience in portfolio strategy and governance within a biotech or pharmaceutical organization.&lt;/li&gt;
&lt;li&gt;Track record of successfully advancing programs through key development milestones including IND/CTA submissions and early clinical development.&lt;/li&gt;
&lt;li&gt;Deep understanding of the drug development process across discovery, preclinical, regulatory, and clinical stages.&lt;/li&gt;
&lt;li&gt;Strong strategic thinking and decision-making capabilities.&lt;/li&gt;
&lt;li&gt;Experience managing complex cross-functional programs in a matrixed organization and aligning parties on key topics.&lt;/li&gt;
&lt;li&gt;Proven ability to influence senior stakeholders and drive alignment across functions.&lt;/li&gt;
&lt;li&gt;Strong communication and executive presentation skills.&lt;/li&gt;
&lt;li&gt;Ability to navigate ambiguity and lead in a fast-paced biotech environment.&lt;/li&gt;
&lt;li&gt;Highly organized with strong problem-solving and risk-management capabilities.&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;
&lt;p&gt;The anticipated salary range for candidates who will work in South San Francisco, CA is $310,000 - $350,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna&#39;s compensation package also includes benefits, stock options, and annual target bonus for full-time positions.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&lt;/em&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;div style=&quot;line-height: 1;&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div style=&quot;line-height: 1;&quot;&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Septerna participates in the E-Verify program.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;California Consumer Privacy Act Privacy Notice For Job Applicants.&amp;nbsp; If you are a California resident, click &lt;a href=&quot;https://septerna.com/california-consumer-privacy-act-privacy-notice-for-job-applicants/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; for our CCPA Notice.&lt;/span&gt;&lt;/em&gt;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vice-president-program-and-portfolio-management-septerna/69d3bccac8e81216cd0b90d5</link><guid isPermaLink="true">http://biotechroles.com/vice-president-program-and-portfolio-management-septerna/69d3bccac8e81216cd0b90d5</guid><pubDate>Mon, 06 Apr 2026 14:01:45 GMT</pubDate><company>Septerna</company><location>South San Francisco, California, United States</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist I/II, Microbial Strain Engineering]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company that invents and builds companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health, sustainability and beyond exponentially accelerate scientific progress in areas ranging from disease detection and treatment and nature-positive agriculture to novel applications of AI that are driving the creation of new technologies. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance science and technology by uniting innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Senior Scientist I or II to lead microbial strain engineering efforts to support a novel biological platform within one of Flagship Pioneering&#39;s stealth mode startups. This role will focus on designing, constructing, and optimizing engineered microbial strains to enable scalable production systems. The successful candidate will drive strain development cycles from genetic design through experimental validation, working closely with our discovery and bioprocess development teams to translate early biological insight into strains that perform robustly in fermentation environments. This individual will contribute technical leadership within the technical operations function and help establish best practices for microbial engineering within a collaborative and fast-moving R&amp;amp;D environment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and implement microbial strain engineering strategies to improve production performance, stability, and robustness&lt;/li&gt;
&lt;li&gt;Construct and evaluate engineered strains using modern molecular biology and microbial engineering techniques (e.g., genome editing, pathway optimization, promoter engineering)&lt;/li&gt;
&lt;li&gt;Develop and execute iterative design-build-test-learn cycles to improve strain performance&lt;/li&gt;
&lt;li&gt;Characterize engineered strains using appropriate analytical assays and collaborate with bioprocess teams to evaluate strain performance under fermentation conditions&lt;/li&gt;
&lt;li&gt;Interpret experimental data and guide subsequent strain design decisions to advance production performance&lt;/li&gt;
&lt;li&gt;Contribute to the development of strain engineering workflows, best practices, and experimental infrastructure within the organization&lt;/li&gt;
&lt;li&gt;Mentor junior scientists or research associates and contribute to collaborative scientific planning&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in microbiology, molecular biology, synthetic biology, microbial engineering, or related discipline
&lt;ul&gt;
&lt;li&gt;Scientist I: at least 5+ years of relevant experience in molecular or synthetic biology, with at least 2 years’ experience developing engineered microbial production strains&lt;/li&gt;
&lt;li&gt;Scientist II: at least 8+ years of relevant experience in molecular or synthetic biology, with at least 4 years’ experience developing engineered microbial production strains&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Demonstrated experience designing and executing microbial genetic engineering programs, including cloning, genome editing, or pathway engineering&lt;/li&gt;
&lt;li&gt;Experience working with one or more microbial hosts such as bacteria, yeast, or filamentous fungi&lt;/li&gt;
&lt;li&gt;Ability to independently design experiments, analyze results, and guide strain optimization strategies&lt;/li&gt;
&lt;li&gt;Strong documentation and data management practices to ensure reproducibility and knowledge transfer&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PREFERRED EXPERIENCE&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience engineering industrial microbial hosts such as E. coli, Bacillus, yeast, or filamentous fungal systems for protein secretion and display&lt;/li&gt;
&lt;li&gt;Experience with modern DNA assembly and genome engineering techniques (e.g., Gibson assembly, Golden Gate, CRISPR-based editing)&lt;/li&gt;
&lt;li&gt;Experience evaluating strain performance in microbial fermentation systems&lt;/li&gt;
&lt;li&gt;Experience collaborating closely with bioprocess development teams to optimize strain performance in production environments&lt;/li&gt;
&lt;li&gt;Experience working in startup or fast-paced R&amp;amp;D environments&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TL1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Protocos currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Protocos&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-iii-microbial-strain-engineering-flagship-pioneering/69d3bcc6c8e81216cd0b90d4</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-iii-microbial-strain-engineering-flagship-pioneering/69d3bcc6c8e81216cd0b90d4</guid><pubDate>Mon, 06 Apr 2026 14:01:42 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Senior DevOps Engineer – Research Cloud & Scientific Computing (AWS)(Biotech industry experience required)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.&lt;/p&gt;
&lt;p&gt;We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.&lt;/p&gt;
&lt;p&gt;We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;For more information see: &lt;a href=&quot;http://www.septerna.com&quot;&gt;www.septerna.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Senior DevOps Engineer to join the Technology Department to serve as a key technical partner enabling cloud-based scientific computing and drug discovery efforts focused on G-protein-coupled receptors (GPCRs). This role is embedded within Research and works day-to-day with computational biologists and chemists, and the data science team to design, build, and operate scalable AWS infrastructure for data- and compute-intensive scientific applications.&lt;/p&gt;
&lt;p&gt;This role requires close collaboration with IT to ensure alignment with enterprise standards for security, compliance, identity management, and cost governance. The successful candidate will be comfortable operating at the intersection of research agility and enterprise rigor, translating scientific needs into robust cloud solutions while partnering effectively across organizational boundaries.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities &amp;amp; Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS in Computer Science, Engineering, or a related discipline with minimum 5 years industry experience within a biotech environment&lt;/li&gt;
&lt;li&gt;Proven experience designing, deploying, and operating AWS-based cloud infrastructure (EC2, S3, EKS/ECS, RDS, IAM, VPC, CloudWatch, Lambda) in a research or engineering environment&lt;/li&gt;
&lt;li&gt;Experience with AWS SageMaker (Studio, Processing Jobs, Training, Endpoints) or comparable managed ML platforms, supporting data science and machine learning workflows&lt;/li&gt;
&lt;li&gt;Experience with data lake architectures and analytics infrastructure (S3, Athena, Glue, or similar query/cataloging services)&lt;/li&gt;
&lt;li&gt;Experience with infrastructure as code and automation (Terraform, CloudFormation, or CDK) and CI/CD pipeline development&lt;/li&gt;
&lt;li&gt;Hands-on experience with containerized scientific applications and orchestration platforms (Docker, Kubernetes)&lt;/li&gt;
&lt;li&gt;Experience supporting high-performance, distributed, or large-scale data processing workloads in the cloud&lt;/li&gt;
&lt;li&gt;Experience with cloud cost management, including Reserved Instances, Savings Plans, or spot instance strategies for compute-intensive workloads&lt;/li&gt;
&lt;li&gt;Proficiency in scripting and programming languages such as Python, Bash, or Go&lt;/li&gt;
&lt;li&gt;Strong track record of embedding DevOps capabilities directly within R&amp;amp;D or scientific teams, supporting rapid iteration and experimental workflows, with demonstrated deep analytical skills applied to troubleshooting code and resolving infrastructure issues&lt;/li&gt;
&lt;li&gt;Ability to interface effectively with IT, aligning research infrastructure with enterprise policies for security, networking, identity, and compliance&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience troubleshooting and optimizing cloud networking (VPCs, subnets, NAT gateways, VPN/Direct Connect, security groups) and diagnosing connectivity issues in hybrid on-prem/cloud environments&lt;/li&gt;
&lt;li&gt;Experience supporting GPU-based workloads for machine learning training and inference&lt;/li&gt;
&lt;li&gt;Experience deploying and managing computational chemistry platforms (Schrödinger, OpenEye, MOE, ChemAxon, or similar) including license server management and job scheduling&lt;/li&gt;
&lt;li&gt;Familiarity with HPC job schedulers (Slurm, PBS, LSF) or cloud-based equivalents (AWS Batch, ParallelCluster)&lt;/li&gt;
&lt;li&gt;Understanding of cloud security, access controls, and auditability, particularly in regulated or research-driven organizations&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The anticipated salary range for candidates who will work in South San Francisco, CA is $160,000 - $185,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna&#39;s compensation package also includes benefits, stock options, and annual target bonus for full-time positions.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;div style=&quot;line-height: 1;&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div style=&quot;line-height: 1;&quot;&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Septerna participates in the E-Verify program.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;California Consumer Privacy Act Privacy Notice For Job Applicants.&amp;nbsp; If you are a California resident, click &lt;a href=&quot;https://septerna.com/california-consumer-privacy-act-privacy-notice-for-job-applicants/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; for our CCPA Notice.&lt;/span&gt;&lt;/em&gt;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-devops-engineer-research-cloud-and-scientific-computing-(aws)(biotech-industry-experience-required)-septerna/69d3bcc5c8e81216cd0b90d2</link><guid isPermaLink="true">http://biotechroles.com/senior-devops-engineer-research-cloud-and-scientific-computing-(aws)(biotech-industry-experience-required)-septerna/69d3bcc5c8e81216cd0b90d2</guid><pubDate>Mon, 06 Apr 2026 14:01:41 GMT</pubDate><company>Septerna</company><location>South San Francisco, California, United States</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Conjugation Biochemistry]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Description:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;In today’s healthcare system, disease diagnosis often relies on invasive procedures, such as biopsies, which enable direct interrogation of cellular and tissue health at the suspected source of disease. Due to their invasiveness, cost, and general inconvenience to the patient, biopsies are often conducted after onset of symptomatic disease presenting one of the largest barriers to delivering interventions early in disease progression when they are likely to be most impactful. Flagship Labs 103, Inc. is a privately held early-stage company that is building advanced technological and computational platforms to pioneer the detection of cellular dynamics from minimally invasive biospecimens that can be leveraged to connect individuals to the most effective interventions to prevent onset and progression of disease&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Job Description:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking an experienced and motivated Senior Scientist to join and lead our conjugation efforts to drive FL103’s programs forward. Ideal candidates will be self-motivated, independent, and committed to the generation of high-quality data within a fast-paced and innovative research team. The Conjugation Biochemist will support ongoing bioconjugation projects in several research and development areas.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, synthesis, purification and analysis of oligonucleotide-conjugates on antibodies and other modalities. Develop and optimize conjugation protocols using established and novel chemistries and technologies as part of an assay development platform.&lt;/li&gt;
&lt;li&gt;Collaborate closely with the assay development team to guide and optimize conjugates to support FL103’s programs.&lt;/li&gt;
&lt;li&gt;Work as part of a cross-functional team to manage and maintain progress against multiple project timelines, deliver routine updates, and communicate progress to the team.&lt;/li&gt;
&lt;li&gt;Establish and maintain excellent working relationships with critical collaborative partners throughout the company to advance discovery research activities to pre-clinical development.&lt;/li&gt;
&lt;li&gt;Contribute to the preparation of research reports and presentations for internal project teams, leadership team, and external audiences.&lt;/li&gt;
&lt;li&gt;Maintain updated and well-organized lab notebooks and batch records.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Qualifications&lt;/strong&gt;:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Biochemistry, Chemistry, or related scientific discipline&lt;/li&gt;
&lt;li&gt;5+ years of bioconjugation-related industrial experience, preferably in designing, preparing, and validating oligonucleotide conjugates.&lt;/li&gt;
&lt;li&gt;Understanding project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders.&lt;/li&gt;
&lt;li&gt;Strong problem-solving skills and a proactive attitude towards exploring new approaches.&lt;/li&gt;
&lt;li&gt;Demonstrates strong written and verbal communication skills, with the ability to clearly present complex scientific data to cross‑functional and senior leadership teams.&lt;/li&gt;
&lt;li&gt;Hands-on expertise with current and cutting-edge bioconjugation techniques for antibodies, proteins, peptides, and other biomolecules.&lt;/li&gt;
&lt;li&gt;Demonstrated hands‑on experience in analytical characterization of conjugates with a strong analytical mindset.&amp;nbsp; Proficiency in purification techniques such as RP-HPLC, FPLC, SEC, and IEX.&lt;/li&gt;
&lt;li&gt;Able to work independently or in cross-functional team settings with minimal supervision.&lt;/li&gt;
&lt;li&gt;Adaptable and flexible, able to navigate shifting priorities and handle day‑to‑day challenges with professionalism and confidence in fast‑moving environments.&lt;/li&gt;
&lt;li&gt;Self‑motivated with strong interpersonal, organizational, and communication skills, and able to take a hands‑on approach in a dynamic, fast‑paced, and collaborative environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp; Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL103 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL103&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-conjugation-biochemistry-flagship-pioneering/69d3bcc1c8e81216cd0b90d0</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-conjugation-biochemistry-flagship-pioneering/69d3bcc1c8e81216cd0b90d0</guid><pubDate>Mon, 06 Apr 2026 14:01:37 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Assistant (biotech experience required - Contract)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.&lt;/p&gt;
&lt;p&gt;We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.&lt;/p&gt;
&lt;p&gt;We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;For more information see: &lt;a href=&quot;http://www.septerna.com&quot;&gt;www.septerna.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;
&lt;p&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly proactive and detail-oriented Executive Assistant to support four senior leaders across Development Sciences, Drug Discovery, Biological Sciences, and People &amp;amp; Culture. This role serves as a critical partner to executives, managing complex calendars, coordinating high-impact meetings and travel, and acting as a key liaison to scientific advisors, KOLs, and external partners. The ideal candidate thrives in a fast-paced environment, anticipates needs before they arise, and ensures leaders are fully prepared for all engagements. This individual will also play an important role in driving operational excellence, supporting cross-functional initiatives, and contributing to a strong, collaborative company culture.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Proactively coordinate and schedule CEO direct reports executive meetings. Manage and prioritize dynamic executives’ schedules for - 4 SVPs in Development Sciences, Drug Discovery, Biological Sciences, and the Chief People Officer.&lt;/li&gt;
&lt;li&gt;Proactively manage executives’ team engagement activities, such as their and their respective teams&#39; group meetings, such as leadership team meetings, advisory meetings, research updates, team offsites, as well as teams’ participation at external medical, scientific, and research conferences and presentations on behalf of Septerna.&lt;/li&gt;
&lt;li&gt;Serve as a front-line point of contact to liaise with key stakeholders, including Septerna’s Scientific Advisors, Key Opinion Leaders (KOLs), and current and potential Contract Research Organizations (CROs).&lt;/li&gt;
&lt;li&gt;Schedule and coordinate Scientific and Medical Advisory meetings and panels and ensure meeting logistics run smoothly.&lt;/li&gt;
&lt;li&gt;Process intellectual property documents – coordinate with the IP attorney to complete them with signatures and notarization for various patents. Manage internal IP document filing .&lt;/li&gt;
&lt;li&gt;Help keep executives well-prepared and informed about upcoming commitments by proactively mentioning key activities for the day or week. Ensure executives have all the necessary information in advance (e.g., printed copies of resumes before interviews, etc.).&lt;/li&gt;
&lt;li&gt;Proactively organize and coordinate all domestic and international travel arrangements. Prepare travel itineraries and other information needed to make the executive’s experience run smoothly. Be available to address any issues or needs that may come up related to their travel. Timely prepare expense reports post-travel.&lt;/li&gt;
&lt;li&gt;Draft clear, professional emails and memos with meticulous attention to detail, especially with key external stakeholders, KOLs, scientific advisors, etc.&lt;/li&gt;
&lt;li&gt;Streamline and improve operational processes and tasks to effectively schedule meetings, track, and file documents, etc. Work with Project Management to ensure meetings are timely and with the appropriate attendees and agendas.&lt;/li&gt;
&lt;li&gt;Work with executives and the People &amp;amp; Culture team to ensure all new hire onboarding preparation is completed, including ensuring orientation schedules are prepared, computer access is provided, workspace is set up, etc.&lt;/li&gt;
&lt;li&gt;Participate in the company social committee to help coordinate important cultural company events, including monthly happy hours and other events throughout the year, such as holiday parties, volunteer events, etc.&lt;/li&gt;
&lt;li&gt;Collaborate with People &amp;amp; Culture, Facilities, and the Technology team to ensure company All-Hands meetings are effectively set up and run smoothly behind the scenes.&lt;/li&gt;
&lt;li&gt;Collaborate with People &amp;amp; Culture to ensure interviewing candidates have printed schedules and a point of contact to help them with their needs, including lunch coordination with Forkable if required.&lt;/li&gt;
&lt;li&gt;Back up CEO COO, CFO and CLO Sr. Executive Assistant by working closely to provide top-notch administrative support to Septerna’s leadership team, including additional projects, coverage when EA is out of the office, and backup support for Board of Directors meetings and dinner events.&lt;/li&gt;
&lt;li&gt;Support other administrative projects and needs as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education/Experience&lt;br&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of administrative or operational experience, ideally in a startup or growing company environment.&lt;/li&gt;
&lt;li&gt;Advanced Microsoft Office suite skills and familiarity with other technologies for automating or organizing workflows.&lt;/li&gt;
&lt;li&gt;Ability to manage various administrative responsibilities with a keen eye for detail.&lt;/li&gt;
&lt;li&gt;Demonstrates professional and effective communication both internally and with external stakeholders.&lt;/li&gt;
&lt;li&gt;Flexibility and ability to learn and adapt to a fast-paced and evolving work environment.&lt;/li&gt;
&lt;li&gt;Ability to take on new responsibilities, including supporting executives with key strategic initiatives.&lt;/li&gt;
&lt;li&gt;Ability to work both independently and in a team environment.&lt;/li&gt;
&lt;li&gt;Initiative-taking mindset and approach to anticipate executive needs and help prepare them for success.&lt;/li&gt;
&lt;li&gt;Experience in a biotech or pharma company a plus.&lt;/li&gt;
&lt;li&gt;Experience supporting sr. executives who report to the CEO required.&lt;/li&gt;
&lt;li&gt;Notary Public certification a plus&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;
&lt;div&gt;The anticipated salary range for candidates who will work in South San Francisco, CA is $60/hr - 72/hr. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training.&amp;nbsp;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;div style=&quot;line-height: 1;&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div style=&quot;line-height: 1;&quot;&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Septerna participates in the E-Verify program.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;California Consumer Privacy Act Privacy Notice For Job Applicants.&amp;nbsp; If you are a California resident, click &lt;a href=&quot;https://septerna.com/california-consumer-privacy-act-privacy-notice-for-job-applicants/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; for our CCPA Notice.&lt;/span&gt;&lt;/em&gt;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/executive-assistant-(biotech-experience-required-contract)-septerna/69d3bcc1c8e81216cd0b90cf</link><guid isPermaLink="true">http://biotechroles.com/executive-assistant-(biotech-experience-required-contract)-septerna/69d3bcc1c8e81216cd0b90cf</guid><pubDate>Mon, 06 Apr 2026 14:01:37 GMT</pubDate><company>Septerna</company><location>South San Francisco, California, United States</location><salary>$75000-110000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Computational Protein Design]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;About&amp;nbsp;Abiologics&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Abiologics&amp;nbsp;is a Flagship Pioneering company developing&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Synteins™&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;— a transformative class of fully synthetic proteins composed entirely of artificial building blocks such as D-amino acids and non-canonical&amp;nbsp;residues.&amp;nbsp;Synteins&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-fontsize=&quot;12&quot;&gt;TM&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;are designed to transcend the limitations of traditional biologics, with improved oral stability, immune evasion, and metabolic durability — all while being fully programmable by design.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Powered by a proprietary AI-enabled discovery platform,&amp;nbsp;Abiologics&amp;nbsp;integrates&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;generative design&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;automated synthesis&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;, and&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;rapid experimental screening&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;to enable iterative optimization at scale.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Position Summary&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Protein Design Scientist&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;to&amp;nbsp;join the Computational Protein Design team and help&amp;nbsp;drive&amp;nbsp;structure-based design and optimization of synthetic proteins. This is a highly interdisciplinary role at the interface of computational design, structural biology, and protein engineering.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ideal candidates have deep experience in&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;de novo protein design&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;miniproteins&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;, and&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;binders&amp;nbsp;engineering&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;and are eager to push the boundaries of non-natural protein design in a fast-moving, data-rich environment.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Design and execute&amp;nbsp;Synteins&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-fontsize=&quot;12&quot;&gt;TM&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;engineering campaigns to generate drug candidates.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Create computational design strategies to deliver drug candidates drawing from array of ML tools and Rosetta scripts.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with computation, chemistry, and experimental biology teams to optimize designs for function, solubility, and stability.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Integrate structural and biophysical data (e.g., binding, CD, HDX-MS,&amp;nbsp;CryoEM) into iterative optimization cycles&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Required&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;PhD in structural biology, biophysics, protein design, or related field&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;2+ years of hands-on experience in&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;structure-guided protein design&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated&amp;nbsp;proficiency&amp;nbsp;with modern structure prediction and design tools such as&amp;nbsp;RFdiffusion,&amp;nbsp;proteinMPNN, AF2, Boltz2,&amp;nbsp;BoltzGen, Rosetta or equivalent SOTA tools for in-silico protein engineering.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong understanding of the biophysics of protein folding and interface energetics&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated ability to progress designs from concept to experimental testing&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication skills&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience designing&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;minibinders&amp;nbsp;or proteins &amp;lt;100 AAs&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Familiarity with non-canonical&amp;nbsp;amino acid design&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Familiarity with molecular&amp;nbsp;dynamics tools.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Exposure to high-throughput or automated protein engineering environments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Prior work on platform-based or early-stage biotech teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Why Join&amp;nbsp;Abiologics&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Help invent a&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;new class of programmable synthetic proteins&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Be part of a&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;high-velocity discovery platform&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;with real-time synthesis and screening&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with a deeply interdisciplinary, mission-driven team&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Redefine the limits of what proteins can do&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
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&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;#LI-MB1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $146,000 - $209,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Abiologics, Inc currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Abiologics, Inc&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-computational-protein-design-flagship-pioneering/69d3bcbdc8e81216cd0b90cd</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-computational-protein-design-flagship-pioneering/69d3bcbdc8e81216cd0b90cd</guid><pubDate>Mon, 06 Apr 2026 14:01:33 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, GCP Quality Assurance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.&lt;/p&gt;
&lt;p&gt;We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.&lt;/p&gt;
&lt;p&gt;We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;For more information see: &lt;a href=&quot;http://www.septerna.com&quot;&gt;www.septerna.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking an experienced, dynamic, and results-driven&amp;nbsp;Associate Director / Director of GCP Quality Assurance our on-site team in South San Francisco. This role is critical in providing both strategic and operational quality oversight of clinical studies and vendor programs, ensuring compliance with ICH GCP and global regulatory requirements, and upholding our high standards for data integrity. The ideal candidate will collaborate closely with clinical study teams and cross-functional partners, fostering a culture of quality and maintaining a state of continual GCP compliance across all programs.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide quality oversight and GCP guidance to clinical study teams and CROs/vendors to ensure compliance with ICH GCP, applicable regulatory requirements, and Septerna standards.&lt;/li&gt;
&lt;li&gt;Ensure clinical trials are conducted in accordance with GCP principles, producing high-quality and reliable data.&lt;/li&gt;
&lt;li&gt;Evaluate clinical trial documentation, study processes, and operational plans to confirm alignment with Septerna expectations and applicable regulations.&lt;/li&gt;
&lt;li&gt;Interpret and apply clinical and regulatory compliance requirements to support Septerna’s objectives and ensure effective implementation across programs.&lt;/li&gt;
&lt;li&gt;Collaborate with clinical study teams to provide vendor quality oversight, identify and assess risks, and recommend appropriate remediation actions.&lt;/li&gt;
&lt;li&gt;Develop and execute GCP audit plans for assigned clinical studies as part of ongoing quality oversight.&lt;/li&gt;
&lt;li&gt;Partner with clinical functions to provide quality guidance and drive the implementation of fit-for-purpose procedures that ensure data and documentation are generated and managed in compliance with GCP.&lt;/li&gt;
&lt;li&gt;Work with cross-functional teams to assess and manage risks associated with vendors, supporting study compliance, data integrity, and participant safety.&lt;/li&gt;
&lt;li&gt;Assist in periodic reporting of key quality metrics to leadership to support continuous improvement in GCP compliance across Septerna.&lt;/li&gt;
&lt;li&gt;Promote a culture of quality through effective communication, training, and proactive engagement with internal and external stakeholders.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in life sciences or a related field; an advanced degree is preferred.&lt;/li&gt;
&lt;li&gt;8–10 years of professional experience in Quality Assurance within the biopharmaceutical industry, with progressive responsibilities in Clinical QA.&lt;/li&gt;
&lt;li&gt;Minimum of 6 years of direct GCP audit experience, including investigator sites, CROs, and other clinical vendors.&lt;/li&gt;
&lt;li&gt;Proven ability to evaluate the effectiveness of CAPAs and follow up on audit findings to ensure timely and complete resolution.&lt;/li&gt;
&lt;li&gt;Strong knowledge of ICH GCP and applicable global regulatory requirements governing clinical research.&lt;/li&gt;
&lt;li&gt;Demonstrated experience providing GCP oversight of clinical studies and vendor programs.&lt;/li&gt;
&lt;li&gt;Skilled in authoring and revising SOPs, implementing process improvements, and ensuring quality systems remain phase-appropriate and fit-for-purpose.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to assess compliance risks, interpret regulations, and implement practical, risk-based quality solutions.&lt;/li&gt;
&lt;li&gt;Excellent collaboration and communication skills with the ability to work effectively across functional areas and external partners.&lt;/li&gt;
&lt;li&gt;Highly organized and detail-oriented, with the ability to manage multiple priorities in a fast-paced, evolving environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The anticipated salary range for candidates who will work in South San Francisco, CA is $220,000 - $240,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna&#39;s compensation package also includes benefits, stock options, and annual target bonus for full-time positions.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;div style=&quot;line-height: 1;&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div style=&quot;line-height: 1;&quot;&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Septerna participates in the E-Verify program.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;California Consumer Privacy Act Privacy Notice For Job Applicants.&amp;nbsp; If you are a California resident, click &lt;a href=&quot;https://septerna.com/california-consumer-privacy-act-privacy-notice-for-job-applicants/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; for our CCPA Notice.&lt;/span&gt;&lt;/em&gt;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-gcp-quality-assurance-septerna/69d3bcbbc8e81216cd0b90cc</link><guid isPermaLink="true">http://biotechroles.com/director-gcp-quality-assurance-septerna/69d3bcbbc8e81216cd0b90cc</guid><pubDate>Mon, 06 Apr 2026 14:01:31 GMT</pubDate><company>Septerna</company><location>South San Francisco, California, United States</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Computational Genomics]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are building a new venture, FL122, pioneering genomic technologies at the intersection of human health and assisted reproduction. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Tessera Therapeutics, and Quotient Therapeutics. We are an equal opportunity employer.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a first Computational Genomics hire, who will conduct crucial research that will form the basis of the company’s scientific platform. As an early stage hire, you will operate with significant ownership, shaping analytical strategy from first principals, intersecting the fields of genomics, statistical genetics and statistical modeling. The role includes responsibility of the end-to-end delivery of computational research projects, including project design, implementation, interpretation and reporting results to senior leadership. We are looking for someone who is resourceful, is open to a rapidly changing, agile environment and has bias to action. The ideal candidate combines deep technical rigor with a growth mindset, pays attention to detail, and has a deep-rooted desire to achieve excellence. Being collaborative is key – the environment is an early stage startup, where all members of the team need to work closely together to break new ground in science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Deliver computational research projects with a high degree of autonomy, including project design, implementation, interpretation and reporting results to senior leadership&lt;/li&gt;
&lt;li&gt;Collaborate with cloud engineers to set up the required infrastructure to process and store genomics datasets&lt;/li&gt;
&lt;li&gt;Integrate multiple NGS data types into coherent analyses, going from raw input files to variant calls and higher level analyses&lt;/li&gt;
&lt;li&gt;Develop probabilistic and Bayesian models that rigorously incorporate priors, uncertainty, and missing data to inform decision-making&lt;/li&gt;
&lt;li&gt;Interact with external advisors, leveraging their inputs and building high-quality relationships&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in biology, statistics, genetics, computational biology or a related quantitative discipline with 5+ years of relevant post-academic or industry experience with an excellent research track record&lt;/li&gt;
&lt;li&gt;Deep expertise in the analysis of genomics data derived from Illumina sequencing platforms (expertise with additional sequencing technologies is a plus)&lt;/li&gt;
&lt;li&gt;Experience processing&amp;nbsp;&lt;strong&gt;next-generation sequencing data end-to-end&lt;/strong&gt;, from raw reads through alignment, QC, and variant calling&lt;/li&gt;
&lt;li&gt;Experience integrating and jointly analyzing&amp;nbsp;&lt;strong&gt;multi-modal sequencing datasets&lt;/strong&gt;, including DNA and RNA&lt;/li&gt;
&lt;li&gt;Expertise in statistical genetics, computing polygenic risk scores using published methods and adapting or extending these methods for novel applications&lt;/li&gt;
&lt;li&gt;Expertise in building&amp;nbsp;&lt;strong&gt;probabilistic statistical models&lt;/strong&gt; that explicitly account for uncertainty, prior information, and incomplete observations&lt;/li&gt;
&lt;li&gt;Comfort operating in fast-moving, ambiguous startup environments with high ownership and accountability&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background &lt;strong&gt;and interest in Flagship&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $146,000 - $209,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL122 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL122&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-computational-genomics-flagship-pioneering/69d3bcb8c8e81216cd0b90c9</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-computational-genomics-flagship-pioneering/69d3bcb8c8e81216cd0b90c9</guid><pubDate>Mon, 06 Apr 2026 14:01:28 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Clinical Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.&lt;/p&gt;
&lt;p&gt;We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.&lt;/p&gt;
&lt;p&gt;We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;For more information see: &lt;a href=&quot;http://www.septerna.com&quot;&gt;www.septerna.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;
&lt;p&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Septerna is seeking an experienced and highly motivated Director of Clinical Development to provide scientific and operational leadership across our early clinical development programs. This individual will play a critical role in the design, execution, and interpretation of clinical studies, working cross-functionally to ensure high-quality, decision-ready data that advances our pipeline.&lt;/p&gt;
&lt;p&gt;The ideal candidate will bring deep expertise in clinical development, a strong scientific foundation, and the ability to operate effectively in a fast-paced biotech environment. This position will work closely with Clinical Development, Clinical Operations, Regulatory, Early Development, Biometrics, and Program Management functions and will report to the Senior Medical Director, Clinical Development.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead the design, planning, and execution of early-phase clinical trials (Phase 1 and Phase 2), including protocol development and study-related documents.&lt;/li&gt;
&lt;li&gt;Drive development of key study documents including protocols, investigator brochures, clinical study reports (CSRs), and informed consent forms.&lt;/li&gt;
&lt;li&gt;Collaborate with Clinical Operations to ensure effective study execution, including site selection, enrollment strategies, and timeline management.&lt;/li&gt;
&lt;li&gt;Partner with multi-disciplinary team to define endpoints, biomarkers, and data analysis plans that enable clear interpretation of study results.&lt;/li&gt;
&lt;li&gt;Contribute to clinical development plans, including indication strategy, study design, and dose selection.&lt;/li&gt;
&lt;li&gt;Analyze and interpret clinical data; present findings to internal stakeholders and support decision-making at governance forums.&lt;/li&gt;
&lt;li&gt;Support regulatory submissions (e.g., INDs/CTAs, briefing documents) and participate in health authority interactions as needed.&lt;/li&gt;
&lt;li&gt;Identify clinical and operational risks and work proactively with cross-functional teams to develop mitigation strategies.&lt;/li&gt;
&lt;li&gt;Ensure clinical studies are conducted in compliance with GCP and applicable regulatory requirements.&lt;/li&gt;
&lt;li&gt;Contribute to building scalable Clinical Sciences processes and capabilities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in life sciences or related field; advanced degree (PhD, PharmD, or MD) strongly preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in Clinical Sciences, Clinical Development, or a related function within the biopharmaceutical industry.&lt;/li&gt;
&lt;li&gt;Demonstrated experience supporting or leading early-phase clinical trials (Phase 1/2), including protocol development and data interpretation.&lt;/li&gt;
&lt;li&gt;Strong understanding of clinical drug development, including study design, endpoints, and regulatory considerations.&lt;/li&gt;
&lt;li&gt;Experience working in cross-functional teams, with the ability to influence without authority.&lt;/li&gt;
&lt;li&gt;Excellent analytical, organizational, and communication skills, with the ability to translate complex data into clear insights.&lt;/li&gt;
&lt;li&gt;High attention to detail and commitment to data quality and scientific rigor.&lt;/li&gt;
&lt;li&gt;Ability to thrive in a dynamic, fast-paced environment and manage multiple priorities effectively.&lt;/li&gt;
&lt;li&gt;Collaborative, hands-on, and solution-oriented mindset with a passion for advancing innovative therapies.&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;
&lt;div&gt;The anticipated salary range for candidates who will work in South San Francisco, CA is $235,000 - $260,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna&#39;s compensation package also includes benefits, stock options, and annual target bonus for full-time positions.&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;div style=&quot;line-height: 1;&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div style=&quot;line-height: 1;&quot;&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;&lt;em&gt;Septerna participates in the E-Verify program.&amp;nbsp; &lt;/em&gt;&lt;/span&gt;&lt;em&gt;&lt;span style=&quot;font-size: 8pt;&quot;&gt;California Consumer Privacy Act Privacy Notice For Job Applicants.&amp;nbsp; If you are a California resident, click &lt;a href=&quot;https://septerna.com/california-consumer-privacy-act-privacy-notice-for-job-applicants/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt; for our CCPA Notice.&lt;/span&gt;&lt;/em&gt;&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-clinical-development-septerna/69d3bcb7c8e81216cd0b90c8</link><guid isPermaLink="true">http://biotechroles.com/director-clinical-development-septerna/69d3bcb7c8e81216cd0b90c8</guid><pubDate>Mon, 06 Apr 2026 14:01:26 GMT</pubDate><company>Septerna</company><location>South San Francisco, California, United States</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Binder Design and Development]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;What if…&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;you could pioneer&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;a new approach&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;to designing life&#39;s most essential molecules&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;?&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;FL&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;116&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;,&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;backed by Flagship Pioneering, is an early-stage biotechnology company transforming the way&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;biomolecules&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;are synthesized&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;.&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Our innovative platform has the potential to transform the way these critical research&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;, diagnostic, and therapeutic&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;tools are manufactured&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;We are&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;seeking&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;a creative, motivated, and technically exceptional&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Senior Scientist&lt;/span&gt;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;to lead the design, development, and screening of peptide and protein-based binders targeting small-molecule substrates. This individual will build and scale high-throughput workflows for binder discovery, affinity characterization, and functional validation, playing&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;a central role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;in shaping a novel molecular control platform.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;This is a rare opportunity to build foundational technology within a deeply integrated, fast-moving startup backed by Flagship’s venture creation engine.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Position Summary&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;S&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;enior Scientist&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;–&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Peptide &amp;amp; Protein Binder Design and Development&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;The Senior&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;Scientist&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;will lead efforts to design, engineer, express, and characterize genetically encoded peptide and protein binders against defined small-molecule targets. This role spans the full discovery workflow&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;from scaffold selection and library design,&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;to assay development, high-throughput expression, affinity screening, and hit-to-lead optimization.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;The ideal candidate is a hands-on protein&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;/peptide&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;engineer with deep&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;in binder discovery platforms and quantitative biophysical characterization. They are comfortable building scalable screening systems, handling large datasets, and iterating rapidly through design–build–test–learn (DBTL) cycles&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;with machine learning / computational support.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Lead the design and engineering of peptide and protein-based binders targeting small-molecule substrates,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;leveraging&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; rational design, library construction, and directed evolution strategies.&lt;/span&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Build and execute high-throughput discovery and screening workflows, including display-based selection platforms and scalable expression systems capable of evaluating large variant libraries.&lt;/span&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Develop and apply quantitative biophysical assays (e.g., BLI, SPR, FP, ITC) to generate affinity curves,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;determine&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;kinetic parameters (&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;kon&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;/&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;koff&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;), calculate KD values, and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;establish&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt; selectivity profiles.&lt;/span&gt;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Drive iterative design–build–test–learn (DBTL) campaigns, integrating affinity and functional data with computational modeling to rapidly&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;optimize&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;binder performance.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Provide scientific and strategic leadership within the binder engineering workstream, contributing to IP development, cross-functional collaboration, and the establishment of a rigorous, high-velocity experimental culture.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Qualifications&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Ph.D. in Protein Engineering, Biochemistry, Structural Biology, Molecular Biology, or related discipline.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;4+ years of relevant industry experience&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Demonstrated experience in protein or peptide binder discovery and optimization.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Hands-on&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;in quantitative affinity screening (BLI, SPR, FP, ITC, or related technologies).&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Experience designing and executing high-throughput screening workflows.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Strong understanding of protein-ligand interaction principles and binding thermodynamics.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;3&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Proven ability to run iterative design–build–test cycles in a fast-paced environment.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Who You Are&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;7&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Innovative Pioneer:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;You thrive in breaking new ground scientifically and are passionate about&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;leveraging&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;protein biochemistry to create transformative technologies.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;7&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Collaborative Contributor:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;You excel in cross-functional teams, readily share&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;, and value the input of colleagues.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;7&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Inventive Problem Solver:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;You proactively identify challenges and rapidly&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;ideate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;creative solutions.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;7&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;Mission-Driven Individual:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;You are driven by an ambition to fundamentally change how&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;biomolecules&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;are synthesized and to meaningfully&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;impact&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;human health and biotechnology.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;More About Flagship Pioneering&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category life sciences companies to transform human health and sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, generating billions in value. Flagship companies are known for addressing humanity’s most pressing challenges and advancing innovative solutions with global impact.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;We are an equal opportunity employer and are dedicated to building diverse and inclusive teams. If you have some of the qualifications listed&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;above&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;but not all, we still encourage you to apply. We value passion, experience in many forms, and unique backgrounds.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Come pioneer the future with us.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Recruitment &amp;amp; Staffing Agencies&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is&amp;nbsp;strictly prohibited&amp;nbsp;unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL116 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL116&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-scientist-binder-design-and-development-flagship-pioneering/69d3bcb2c8e81216cd0b90c2</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-binder-design-and-development-flagship-pioneering/69d3bcb2c8e81216cd0b90c2</guid><pubDate>Mon, 06 Apr 2026 14:01:22 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Market Insights & Corporate Development]]></title><description><![CDATA[&lt;p&gt;Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM&amp;nbsp;technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit&amp;nbsp;&lt;a href=&quot;https://www.seaporttx.com/&quot;&gt;www.seaporttx.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is seeking a &lt;strong&gt;Senior Manager, Market Insights &amp;amp; Corporate Development &lt;/strong&gt;to join our team. The ideal candidate will have a “roll up your sleeves” mentality, strong analytical skills, and expertise in competitive intelligence, market research, and corporate strategy&lt;em&gt;.&lt;/em&gt; This individual will act as the commercial voice on cross-functional development teams, collaborating with stakeholders across the organization to optimize product value and future success. This individual will also support business development activities, including evaluation of strategic partnership opportunities. The role will report to the Senior Director, Corporate Development and work cross-functionally, including exposure to the Executive Leadership Team.&lt;/p&gt;
&lt;p&gt;This position is based in Boston’s Seaport area, with a strong preference for being onsite 4 days per week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;It is expected that this individual will participate in three main areas:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Market Insights&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Conduct strategic landscape analyses for Seaport’s pipeline assets and understand market needs and opportunities in applicable indications; specific tasks include:&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Conduct primary market research (e.g., qualitative interviews, quantitative surveys) with various stakeholders&lt;/li&gt;
&lt;li&gt;Perform extensive secondary/literature research to understand and characterize the landscape for Seaport’s assets&lt;/li&gt;
&lt;li&gt;Share research findings with Program Teams and Executive Leadership Team&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Lead competitive intelligence efforts across Seaport’s pipeline, keeping internal stakeholders apprised of important market and competitive developments&lt;/li&gt;
&lt;li&gt;Collaborate with Program Teams to develop target product profiles and value propositions aligned with market expectations and business goals&lt;/li&gt;
&lt;li&gt;Maintain revenue forecasts for Seaport programs and ensure that models are updated regularly with latest assumptions&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Business Development&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide support in identifying, evaluating, and securing partnerships that drive growth and support for Seaport’s strategic goals&lt;/li&gt;
&lt;li&gt;Manage operational aspects of business development activities, including but not limited to CDAs, secure data rooms, and meeting documentation&lt;/li&gt;
&lt;li&gt;Conduct deal comparator analyses and support business case development for potential strategic partnerships&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Corporate Strategy &amp;amp; Special Projects&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support corporate strategy efforts that require a combination of commercial perspectives, business development insights, and/or rigorous financial analytics&lt;/li&gt;
&lt;li&gt;Create content for Board of Director meetings that adheres to and drives meeting agendas&lt;/li&gt;
&lt;li&gt;Provide bandwidth for other cross-functional initiatives on an ad hoc basis&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&amp;nbsp; &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree&lt;/li&gt;
&lt;li&gt;Advanced degree is a plus (e.g., MBA, PhD) but not required&lt;/li&gt;
&lt;li&gt;5+ years of experience in biotech/pharma corporate strategy, management consulting, venture capital, and/or investment banking&lt;/li&gt;
&lt;li&gt;Ability to identify, analyze, and distill large amounts of complex information into clear and actionable business insights&lt;/li&gt;
&lt;li&gt;Comfort with ambiguity and a track record of creating analytical frameworks&lt;/li&gt;
&lt;li&gt;Outstanding oral and written communication skills&lt;/li&gt;
&lt;li&gt;Highly motivated and results-driven with a strong desire to work in a fast-paced organization&lt;/li&gt;
&lt;li&gt;Passionate about Seaport’s mission to help patients living with neuropsychiatric disorders&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;At Seaport, we believe transparency and fairness are key to building a culture of trust, respect, and collaboration. We care deeply about the happiness of our team and strive to ensure our total rewards (monetary and non-monetary) program reflects the value each person brings. The expected salary range for this role is $160,000-$170,000 with the final offer based on experience, market data, and internal equity. We encourage open conversations with our talent acquisition team about compensation early in the process to ensure alignment from the start.&lt;/em&gt;&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-manager-market-insights-and-corporate-development-seaport-therapeutics/69d3bcb2c8e81216cd0b90c1</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-market-insights-and-corporate-development-seaport-therapeutics/69d3bcb2c8e81216cd0b90c1</guid><pubDate>Mon, 06 Apr 2026 14:01:22 GMT</pubDate><company>Seaport Therapeutics</company><location>Boston, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Research Associate, Protein Science]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;u&gt;Company Description&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 110 Inc. (FL110) is a privately held, early-stage technology company developing a fully integrated, end-to-end platform to enable next generation proteomics. Our platform integrates groundbreaking innovations in bioengineering, machine learning, and custom microelectronics to offer a level of precision and insight never before achieved.&lt;/p&gt;
&lt;p&gt;FL110 is backed by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. We are uniquely cross-functional and collaborative. Our teams thrive in unstructured and creative environments. Therefore, we seek individuals with an inclusive mindset and a diversity of thought.&lt;/p&gt;
&lt;p&gt;If this sounds like an environment you’d love to work in, even if you only have some of the experience listed below, please apply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;About the Role&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated Senior Research Associate with experience in recombinant protein expression, purification, and characterization to support the development of FL110’s next-generation protein sequencing platforms and products.&lt;/p&gt;
&lt;p&gt;In this role, you will design, execute, and optimize protein production workflows from construct design through biochemical and biophysical characterization. You will work in a collaborative, interdisciplinary environment where teams rapidly interpret and respond to experimental results to guide platform development. The ideal candidate is an organized and creative experimentalist who enjoys troubleshooting challenging protein targets and contributing to new technologies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Basic Requirements&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS or MS degree in Biochemistry, Molecular Biology, or a related field, with 4+ years of research experience in an academic or industry laboratory.&lt;/li&gt;
&lt;li&gt;Extensive hands-on experience in bacterial recombinant protein expression and purification, spanning the full workflow from DNA construct design and transformation through chromatographic purification using affinity, ion-exchange, and size-exclusion techniques.&lt;/li&gt;
&lt;li&gt;Proficiency with ÄKTA purification systems, including designing and executing protein purification methods.&lt;/li&gt;
&lt;li&gt;Familiarity with analytical techniques used to assess recombinant protein quality.&lt;/li&gt;
&lt;li&gt;Strong organizational skills and the ability to document experimental work in an ELN and maintain records in an electronic LIMS.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Strong Candidates Will Have&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to independently design, execute, troubleshoot, and interpret experiments related to protein expression, purification, and stability.&lt;/li&gt;
&lt;li&gt;Hands-on work with nanopore-forming proteins or related membrane protein systems.&lt;/li&gt;
&lt;li&gt;Familiarity with automation in a biochemistry setting.&lt;/li&gt;
&lt;li&gt;Experience developing functional assays to evaluate protein activity or performance.&lt;/li&gt;
&lt;li&gt;A track record of improving protein yield through construct and protocol optimization.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Key Responsibilities&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, express, purify, and characterize soluble and membrane proteins.&lt;/li&gt;
&lt;li&gt;Develop and optimize expression and purification strategies for challenging protein targets.&lt;/li&gt;
&lt;li&gt;Design and evaluate new protein constructs and variants informed by experimental results.&lt;/li&gt;
&lt;li&gt;Characterize proteins using biochemical and biophysical methods to assess purity, stability, and function.&lt;/li&gt;
&lt;li&gt;Collaborate with experimental and computational teams to interpret results and guide future protein and nanopore designs.&lt;/li&gt;
&lt;li&gt;Document experimental workflows and contribute to shared lab knowledge and technical documentation.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;About Flagship Pioneering&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies&lt;/strong&gt;&lt;/em&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $81,000 - $107,250. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL110 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL110&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-research-associate-protein-science-flagship-pioneering/69d3bcacc8e81216cd0b90be</link><guid isPermaLink="true">http://biotechroles.com/senior-research-associate-protein-science-flagship-pioneering/69d3bcacc8e81216cd0b90be</guid><pubDate>Mon, 06 Apr 2026 14:01:16 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Director/Vice President, Clinical Development]]></title><description><![CDATA[&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit www.seaporttx.com.&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is seeking a hands-on clinical development leader to drive the strategic and operational execution of our global clinical programs across current and future pipeline assets. This role will report to the Chief Medical Officer and oversee clinical trial design and execution, partner with regulatory strategy, biostatistics, program management and other cross-functional stakeholders and external partners including regulatory agencies, KOLs, and investigators. The ideal candidate will bring deep expertise in neuroscience or neurology, a proven track record of successful IND/NDA submissions, experience with Ph III clinical development, and a passion for partnering with high-performing teams and advancing innovative therapies in neurological and neuropsychiatric diseases.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The ideal candidate will embrace a collaborative, innovative culture that embodies our values of service to patients impacted by mental health conditions, with a “we own it” mentality, demonstrating entrepreneurial spirit and technical excellence while fostering teamwork and continuous improvement. This position is based in Boston’s Seaport area, with a strong preference for being onsite 4 days per week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;· Establish and drive the clinical development strategy and hands-on tactical execution plans on programs against the current and future development portfolio.&lt;/p&gt;
&lt;p&gt;· Manage effective internal and external relationships, internally with members of the executive leadership team, regulatory affairs, clinical operations and medical affairs, and externally including regulatory agencies, partners, KOLs, and investigators.&lt;/p&gt;
&lt;p&gt;· Medical oversight of ongoing clinical trials in the neuropsychiatric therapeutic area.&lt;/p&gt;
&lt;p&gt;· Lead clinical sections of regulatory documents (IND, BLA/NDA).&lt;/p&gt;
&lt;p&gt;· Work with Regulatory Affairs to prepare for meetings with FDA and healthcare authorities.&lt;/p&gt;
&lt;p&gt;· Work with Scientific Communications/ Medical Affairs team members to organize and prepare for advisory board meetings.&lt;/p&gt;
&lt;p&gt;· Work with other members of the Program team through all phases of development through commercialization.&lt;/p&gt;
&lt;p&gt;· Prioritize and develop the company’s current drug candidates as well as future pipeline compounds and contribute to go / no-go decisions.&lt;/p&gt;
&lt;p&gt;· Literature review, KOL interactions, attending scientific meetings, and presenting the clinical development plan to the relevant internal stakeholders to help shape the new indication selection process.&lt;/p&gt;
&lt;p&gt;· Ensure that standard operating procedures (SOP) for Clinical Development facilitate the development of effective clinical research protocols and are compliant with clinical/medical and industry standards.&lt;/p&gt;
&lt;p&gt;· Actively participate in strategic planning for the clinical development organization and provide support to business development / licensing activities.&lt;/p&gt;
&lt;p&gt;· Maintain an understanding of competitors and clinical developments in relevant therapeutic areas.&lt;/p&gt;
&lt;p&gt;· Build and maintain medical advisory boards based on solid working relationships with KOLs and lead clinical investigators.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;· MD training in psychiatry and/or neuroscience required.&lt;/p&gt;
&lt;p&gt;· 8+ (ED) 10+(VP) years of clinical development experience within a biotech/pharmaceutical setting with a strong track record of successful clinical program execution in the field of neuropsychiatric drug development. Prior clinical/academic experience required as well.&lt;/p&gt;
&lt;p&gt;· Experience with mood/anxiety disorders preferred.&lt;/p&gt;
&lt;p&gt;· Experience with GCP/ICH/FDA requirements, clinical trial design and strategies, interpretation of clinical data and generation of supporting regulatory submissions of clinical study documents.&lt;/p&gt;
&lt;p&gt;· Demonstrated track record and experience working cross-functionally in a collaborative and productive manner across R&amp;amp;D functions and beyond.&lt;/p&gt;
&lt;p&gt;· Exceptional interpersonal, influencing, presentation, and written and verbal communication skills.&lt;/p&gt;
&lt;p&gt;· Experience with successful NDA submissions and approvals and interactions with regulatory agencies are highly desired.&lt;/p&gt;
&lt;p&gt;· Experience with Phases I-III clinical development required.&lt;/p&gt;
&lt;p&gt;· Understanding of the general healthcare environment in the US and elsewhere-including laws, regulations, and evolving market access trends and issues.&lt;/p&gt;
&lt;p&gt;· Knowledge and experience of building clinical development infrastructure aligned with the needs of a growing organization.&lt;/p&gt;
&lt;p&gt;· Occasional work travel as required.&lt;/p&gt;
&lt;p&gt;At Seaport, we believe transparency and fairness are key to building a culture of trust, respect, and collaboration. We care deeply about the happiness of our team and strive to ensure our total rewards (monetary and non-monetary) program reflects the value each person brings. The expected salary range for this role at the Executive Director Level is $297,000-$340,000 $the expected salary range for the role at the Vice President Level is $324,000-370,000 with the final title and offer based on experience, market data, and internal equity.&lt;/p&gt;
&lt;p&gt;We encourage open conversations with our talent acquisition team about compensation early in the process to ensure alignment from the start.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/executive-directorvice-president-clinical-development-seaport-therapeutics/69d3bcacc8e81216cd0b90bd</link><guid isPermaLink="true">http://biotechroles.com/executive-directorvice-president-clinical-development-seaport-therapeutics/69d3bcacc8e81216cd0b90bd</guid><pubDate>Mon, 06 Apr 2026 14:01:16 GMT</pubDate><company>Seaport Therapeutics</company><location>Boston, MA</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Research Associate, Formulations]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a platform innovation company that invents and builds companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health, sustainability and beyond exponentially accelerate scientific progress in areas ranging from disease detection and treatment and nature-positive agriculture to novel applications of AI that are driving the creation of new technologies. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance science and technology by uniting innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This role will be a foundational hire supporting our formulation and product development efforts, with a primary focus on the development, screening, and optimization of dried powder formulations. The individual will play a critical hands-on role in executing formulation strategies using techniques such as lyophilization and spray drying, while contributing experimental rigor, physical insight, and data-driven decision-making to early-stage platform development.&lt;/p&gt;
&lt;p&gt;The Senior Research Associate will work closely with process development partners to produce robust, stable, and scalable powders. In addition to executing experiments, this role will contribute to experimental design, data interpretation, and the establishment of best practices for formulation screening, characterization, and documentation in a fast-moving, early-stage environment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, execute, and optimize dried powder formulations using lyophilization and spray drying, with a focus on stability, reproducibility, and performance across multiple formulation variables;&lt;/li&gt;
&lt;li&gt;Execute formulation screening efforts using statistically grounded experimental designs (e.g., DoEs), including selection of factors, responses, and experimental conditions, and translate results into actionable next steps;&lt;/li&gt;
&lt;li&gt;Evaluate the impact of excipients, processing conditions, and storage environments on material stability, integrity, and functionality, including under accelerated or stress conditions;&lt;/li&gt;
&lt;li&gt;Characterize dried powder products using appropriate analytical and physical methods (e.g., particle size and morphology, thermal analysis, moisture content, bulk properties) to inform formulation and process decisions;&lt;/li&gt;
&lt;li&gt;Support process development and scale-awareness by documenting critical parameters, identifying sources of variability, and generating data relevant to future scale-up, tech transfer, or external partnerships;&lt;/li&gt;
&lt;li&gt;Maintain clear, rigorous experimental documentation and generate high-quality summaries, figures, and datasets suitable for internal decision-making, patent disclosures, and external communication;&lt;/li&gt;
&lt;li&gt;Contribute to the establishment of long-term formulation workflows, best practices, and standards that support platform development in a small, highly collaborative team.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree (with 5-7 years of relevant research experience) or Master’s degree (with 3-5 years of relevant research experience) in chemistry, chemical engineering, pharmaceutical sciences, materials science, biotechnology, or a related discipline.&lt;/li&gt;
&lt;li&gt;Demonstrated experience with drying-based formulation techniques, including lyophilization and/or spray drying, and an understanding of how process parameters influence solid-state properties;&lt;/li&gt;
&lt;li&gt;Strong grounding in physical chemistry or materials science principles relevant to dried systems, including glass transition behavior, crystallinity, moisture interactions, and excipient effects;&lt;/li&gt;
&lt;li&gt;Experience designing and executing statistically informed experiments (e.g., DoEs), with the ability to interpret interaction effects and use data to guide experimental iteration;&lt;/li&gt;
&lt;li&gt;Familiarity with analytical and characterization techniques for powders and solid-state materials (e.g., DSC, TGA, particle sizing, microscopy, bulk property measurements), and the ability to select fit-for-purpose methods;&lt;/li&gt;
&lt;li&gt;Familiarity with downstream processing operations (e.g., tangential flow filtration and other purification workflows);&lt;/li&gt;
&lt;li&gt;Proven ability to work independently in a dynamic, early-stage research environment, balancing hands-on execution with thoughtful experimental planning and cross-functional communication;&lt;/li&gt;
&lt;li&gt;Strong scientific documentation and communication skills, with experience generating reproducible records and decision-enabling datasets;&lt;/li&gt;
&lt;li&gt;Embodies resilience and scientific rigor in pursuing complex technical questions by iteratively testing hypotheses and refining parameters through uncertainty to converge on robust, optimized solutions.&lt;/li&gt;
&lt;li&gt;Demonstrated curiosity, adaptability, and comfort working across disciplines, with an interest in translating early scientific concepts into robust, scalable technologies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;#LI-TL1&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $81,000 - $107,250. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Protocos currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Protocos&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-research-associate-formulations-flagship-pioneering/69d3bca8c8e81216cd0b90b9</link><guid isPermaLink="true">http://biotechroles.com/senior-research-associate-formulations-flagship-pioneering/69d3bca8c8e81216cd0b90b9</guid><pubDate>Mon, 06 Apr 2026 14:01:12 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Director, Program Leader]]></title><description><![CDATA[&lt;p&gt;Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit www.seaporttx.com.&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is seeking a talented and experienced Program Leader (PL) to be an integrative cross-functional leader who is responsible for driving the GlyphAllo Program in order to maximize its future clinical and commercial success in the treatment of depression. This is a highly visible leadership role that bridges scientific, clinical, operational, and commercial disciplines. The GlyphAllo program is currently enrolling a Phase 2b study and the PL will lead the program to execute the current plans within timelines/budget and to plan for future pivotal clinical studies, initial global regulatory filings and pre-commercial activities. He/she will provide leadership across the spectrum of drug development and pre-commercialization activities, ensuring achievement of program and corporate goals. The ideal candidate will be a strategic and entrepreneurial leader well-versed in drug development and commercialization, and a strong influencer who can integrate multiple perspectives effectively and align stakeholders across different functions and levels of the organization.&lt;/p&gt;
&lt;p&gt;This position requires a presence in the Seaport area of Boston, with a strong preference for being onsite 4 days per week to foster collaboration and effective leadership as the GlyphAllo program grows in complexity and importance.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Summary of Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;· Serve as the overall program lead, accountable for end-to-end planning, execution, and delivery of key milestones of clinical studies through NDA submission.&lt;/p&gt;
&lt;p&gt;· Work collaboratively and cross-functionally with Research, Nonclinical Development, Clinical Operations, Clinical Research, Regulatory Affairs, Medical Affairs, Manufacturing, Quality Assurance, Drug Safety &amp;amp; Pharmacovigilance, Program Management, Distribution &amp;amp; Supply, Commercial and Finance to deliver on program goals within established timelines and budget.&lt;/p&gt;
&lt;p&gt;· Partner closely with Program Management to drive alignment and execution across the cross-functional program team, including development and maintenance of integrated, cross-functional strategic plans, timelines, and budgets; proactive identification of risks; and implementation of mitigation strategies.&lt;/p&gt;
&lt;p&gt;· Oversee the development of market research plans to gather deep insights from patients, providers, payers, and other stakeholders. Integrate the insights and other market competitive intelligence into program strategies.&lt;/p&gt;
&lt;p&gt;· Integrate cross-functional perspectives, ensuring that program strategy is informed by scientific evidence, clinical data, and the evolving competitive landscape. On an ongoing basis, proactively anticipate issues and ensure contingency plans are put in place; identify barriers and identify solutions to mitigate them; identify opportunities and strategies to capitalize on them.&lt;/p&gt;
&lt;p&gt;· Working with functional leaders, ensure that appropriate prioritization and adequate resource allocation (financial and personnel) are present to meet the program timelines and deliverables.&lt;/p&gt;
&lt;p&gt;· Maintain a high performing cross-functional program team, monitoring program resourcing, managing conflict, and building team culture; create a positive atmosphere to get the most out of the team.&lt;/p&gt;
&lt;p&gt;· Serve as an internal and external ambassador for the program, fostering broad engagement to cultivate strategic KOL relationships and enabling overall integration of external insights to inform program strategies.&lt;/p&gt;
&lt;p&gt;· Summarize and represent the program to Seaport leadership, Board of Directors, collaborators, and other external parties, as requested.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;· BA/BS degree required; advanced medical, scientific or business degree strongly preferred.&lt;/p&gt;
&lt;p&gt;· 10+ years biopharmaceutical development and commercialization experience, with previous demonstrated program leadership responsibilities; demonstrated experience leading cross-functional teams in drug development and pre-commercialization.&lt;/p&gt;
&lt;p&gt;· Deep understanding of drug development and global product registration is required, ideally in neuropsychiatry (with preference for experience in depression or anxiety). Commercialization and /or Medical Affairs experience considered a strong plus. Leadership of a recent successful program (positive pivotal data, regulatory approval, etc.) would be ideal.&lt;/p&gt;
&lt;p&gt;· Proactive “hands-on” individual with collaborative orientation, who manages teams effectively, is very self-motivated and can smoothly establish strong working relationships within both internal and external organizations. Entrepreneurial problem solver. Achieves goals within timelines and budgets while anticipating and navigating obstacles effectively.&lt;/p&gt;
&lt;p&gt;· Initiative and independence to identify short and long-term program needs, creatively formulate plans with team input, efficiently achieve timely decisions/alignment, and organize and deploy resources.&lt;/p&gt;
&lt;p&gt;· Exceptional written and verbal communication skills; able to articulate program vision and motivate the team; communicates in an open, direct and timely manner; ensures broader organization is aligned with and aware of the program strategy, status and risks.&lt;/p&gt;
&lt;p&gt;· Motivated by patient focus and personal commitment to high performance and results.&lt;/p&gt;
&lt;p&gt;· Possesses high integrity and exceptional work ethic.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;At Seaport, we believe transparency and fairness are key to building a culture of trust, respect, and collaboration. We care deeply about the happiness of our team and strive to ensure our total rewards (monetary and non-monetary) program reflects the value each person brings. The expected salary range for this role is $275,000-$310,000 with the final offer based on experience, market data, and internal equity.&lt;/p&gt;
&lt;p&gt;We encourage open conversations with our talent acquisition team about compensation early in the process to ensure alignment from the start.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/executive-director-program-leader-seaport-therapeutics/69d3bca7c8e81216cd0b90b8</link><guid isPermaLink="true">http://biotechroles.com/executive-director-program-leader-seaport-therapeutics/69d3bca7c8e81216cd0b90b8</guid><pubDate>Mon, 06 Apr 2026 14:01:11 GMT</pubDate><company>Seaport Therapeutics</company><location>Boston, MA</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Research Associate, Cardiometabolic Discovery]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics Ltd is a privately held, early-stage company developing a novel genomics platform and therapeutics for diseases with a large unmet need.&lt;/p&gt;
&lt;p&gt;The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS). We are an equal opportunity employer.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a motivated and creative Senior Research Associate to join our team focused on performing in vitro studies to characterize novel somatic variants in the context of Cardiometabolic disease. This role requires a strong background in life sciences to execute experiments that investigate somatic variant function to validate potential drug targets. The position involves a combination of hands-on lab work, data analysis, and scientific communication to ensure a target&#39;s potential benefit for a disease. The successful candidate will be a self-starter, able to thrive in a fast-paced, action-oriented team environment.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Perform a variety of laboratory experiments, including cell-based assays, molecular biology techniques, and sometimes in vivo studies, to validate new targets and test drug candidates&lt;/li&gt;
&lt;li&gt;Utilize techniques such as RNA purification, qPCR, ELISA and Western blotting to analyze cellular and molecular responses&lt;/li&gt;
&lt;li&gt;Assist in the design and optimization of research protocols to validate therapeutic targets&lt;/li&gt;
&lt;li&gt;Collect, analyze, and interpret scientific data, with a strong ability to use tools like Excel and GraphPad Prism&lt;/li&gt;
&lt;li&gt;Maintain a detailed and up-to-date electronic lab notebook and write high quality experimental protocols&lt;/li&gt;
&lt;li&gt;Work in a team-oriented environment, sharing findings and collaborating with other scientists&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Professional Experience and Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Master’s degree in life sciences, biotechnology, biology, or related field with 0-2 years of relevant experience in industry&lt;/li&gt;
&lt;li&gt;Bachelor’s degree in life sciences, biotechnology, biology, or related field with 2-4 years of relevant experience in industry&lt;/li&gt;
&lt;li&gt;Hands-on experience with cell culture, molecular biology and protein techniques (academic or industry settings)&lt;/li&gt;
&lt;li&gt;Preferred experience in organoid/spheroid primary cell culture systems with steatosis and fibrosis readouts&lt;/li&gt;
&lt;li&gt;Ability to manage multiple tasks, work independently, and thrive in a collaborative team environment&lt;/li&gt;
&lt;li&gt;Familiarity with electronic lab notebooks (ELNs) or related data-management tools&lt;/li&gt;
&lt;li&gt;Must possess a high degree of flexibility and adaptability to evolving job requirements and priorities&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and Behaviors:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship is an experiment in institutional, entrepreneurial, and innovation practiced in the context of a small company with an insurgent mindset. We are seeking individuals with an entrepreneurial spirit, strong communication skills, and comfort in working in and contributing to a dynamic and cross-functional team environment.&lt;/p&gt;
&lt;p&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, we encourage you to apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background. The level of the role will be commensurate with the education and years of experience of the identified candidates.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering and our ecosystem companies are&amp;nbsp;&lt;strong&gt;committed to equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $81,000 - $107,250. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Quotient Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Quotient Therapeutics, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-research-associate-cardiometabolic-discovery-flagship-pioneering/69d3bca4c8e81216cd0b90b6</link><guid isPermaLink="true">http://biotechroles.com/senior-research-associate-cardiometabolic-discovery-flagship-pioneering/69d3bca4c8e81216cd0b90b6</guid><pubDate>Mon, 06 Apr 2026 14:01:08 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Analytical Research and Development CMC]]></title><description><![CDATA[&lt;p&gt;Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary Glyph&lt;sup&gt;TM&amp;nbsp;&lt;/sup&gt;technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit&amp;nbsp;&lt;a href=&quot;https://www.seaporttx.com/&quot;&gt;www.seaporttx.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is hiring a &lt;strong&gt;Director, Analytical Research and Development, CMC &lt;/strong&gt;to oversee the analytical method development and phase-appropriate validation of analytical methods for drug substance and drug product in pre-clinical and clinical development. This role reports to the Senior Director, Analytical Research and Development, CMC. In the near term, the role will focus on method development and validation of Phase 1 Phase 2 and early Phase 3 drug substance and drug product candidates.&amp;nbsp; The role will assist with preparation and review of CMC Regulatory filings. This person will coordinate activities at various CDMO’s to achieve company objectives related to the analytical contribution of process and product development.&lt;/p&gt;
&lt;p&gt;The ideal candidate will embrace a collaborative, innovative culture that embodies our values of &lt;em&gt;service &lt;/em&gt;to patients impacted by mental health conditions, with a &lt;em&gt;“we own it”&lt;/em&gt; mentality, demonstrating entrepreneurial spirit and technical excellence while fostering teamwork and continuous improvement. This position is based in Boston’s Seaport area, with a strong preference for being onsite 4 days per week.&amp;nbsp; Up to 25% travel to CDMO sites will be required.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee CDMO activites for drug substance and drug product analytical method development, validation and transfer for Seaport Therapeutics as assigned by the Senior Director of Analytical Research and Development&lt;/li&gt;
&lt;li&gt;Represent the analytical CMC function at team meetings with CDMO’s and internal staff.&lt;/li&gt;
&lt;li&gt;Provide strategic oversight and day-to-day governance of assigned CDMO’s including project scope, adherence to timelines, quality, and integrity of data.&lt;/li&gt;
&lt;li&gt;Perform hands-on data review to ensure high-quality data reporting.&lt;/li&gt;
&lt;li&gt;Ensure compliance with regulatory standards, industry guidelines, internal SOPs applicable to the role.&lt;/li&gt;
&lt;li&gt;Support progress at CDMO’s via periodic onsite visits.&lt;/li&gt;
&lt;li&gt;Create and maintain release and stability databases gathered from CDMO stability reports.&lt;/li&gt;
&lt;li&gt;Work with ICH-compliant statistical stability software for stability data trending and shelf life predictions&lt;/li&gt;
&lt;li&gt;Partner cross-functionally with Discovery, Program Teams, Regulatory Affairs, Quality Assurance to support data-driven decision-making and operational excellence at our partner CDMO’s.&lt;/li&gt;
&lt;li&gt;Advise CDMO’s on the analytical tools required to successfully complete method development and validation to industry standards.&lt;/li&gt;
&lt;li&gt;Plan and manage budgets, solicit quotes from vendors, create purchase orders and track spending.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;MS/Ph.D. in Analytical Chemistry or Physical Chemistry and 7+ years in early stage method development, method transfer, method validation for lipophilic drug substances and drug product.&lt;/li&gt;
&lt;li&gt;Demonstrated expertise in analytical development with complex drug substances and drug product formulations&lt;/li&gt;
&lt;li&gt;Experience with drug product formulations utilizing SEDDS in soft-gelatin dosage forms.&lt;/li&gt;
&lt;li&gt;Demonstrated expertise in chromatographic techniques (for example: GC, LC, IC, GC, chiral separations,) employing the following (but not limited to) detectors: UV/vis, CAD, MS (SIM, MRM) fluorescence, FID, ECD.&lt;/li&gt;
&lt;li&gt;Experience with management of CDMO’s for drug substance and drug product for multiple product lines.&lt;/li&gt;
&lt;li&gt;Knowledge of global regulatory requirements, ICH and other relevant guidelines&lt;/li&gt;
&lt;li&gt;Proficiency in the use of Microsoft Office Suite products.&lt;/li&gt;
&lt;li&gt;Excellent communication, collaboration, and leadership skills.&lt;/li&gt;
&lt;li&gt;Comfortable with oversees travel approximately 25% of the time.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Seaport, we believe transparency and fairness are key to building a culture of trust, respect, and collaboration. We care deeply about the happiness of our team and strive to ensure our total rewards (monetary and non-monetary) program reflects the value each person brings. The expected salary range for this role is &lt;strong&gt;$198,000-233,000&lt;/strong&gt;&lt;strong&gt;,&lt;/strong&gt; with the final offer based on experience, market data, and internal equity. We encourage open conversations with our talent acquisition team about compensation early in the process to ensure alignment from the start.&lt;/p&gt;
&lt;h1&gt;&amp;nbsp;&lt;/h1&gt;]]></description><link>http://biotechroles.com/director-analytical-research-and-development-cmc-seaport-therapeutics/69d3bca3c8e81216cd0b90b5</link><guid isPermaLink="true">http://biotechroles.com/director-analytical-research-and-development-cmc-seaport-therapeutics/69d3bca3c8e81216cd0b90b5</guid><pubDate>Mon, 06 Apr 2026 14:01:07 GMT</pubDate><company>Seaport Therapeutics</company><location>Boston, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Research Associate/Associate Scientist, Biochemistry]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Our start-up is building a novel chemical discovery platform to reshape how we develop formulations at the molecular level. By combining artificial intelligence with a cutting-edge laboratory discovery pipeline, our interdisciplinary team will chart an unexplored chemical landscape, enabling breakthroughs in drug delivery, agrichemical formulation, and safe, high-performance industrial chemicals.&lt;/p&gt;
&lt;p&gt;Our company is backed by Flagship Pioneering, a biotechnology origination company that has founded and developed over 115 scientific ventures over the past 25 years. Flagship Pioneering is dedicated to the development of an ecosystem of first-in-category life sciences companies, resulting in $20+ billion in aggregate value, 500+ issued patents, and more than 50 clinical trials for novel therapeutic agents.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated Senior Research Associate or Associate Scientist to support the characterization of biomolecules within a rapidly evolving formulation discovery platform. This role will apply a variety of biophysical and biochemical techniques to evaluate how formulations influence biomolecular integrity, aggregation, and functional stability. They can expect to work closely with chemistry and machine-learning scientists to generate high-quality experimental data that inform formulation design and predictive modeling efforts. An ideal candidate will have a strong foundation in biochemistry, structural biology, or biopolymer engineering, along with hands-on experience operating analytical instrumentation used for biomolecular characterization.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Biomolecular characterization&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Conduct experiments to assess biomolecular stability and solubility in diverse formulation conditions.&lt;/li&gt;
&lt;li&gt;Evaluate structural integrity and folding of cargo using circular dichroism (CD) spectroscopy and complementary biophysical methods.&lt;/li&gt;
&lt;li&gt;Measure biomolecular interactions and stability using spectroscopy, dynamic light scattering, and electrophoretic techniques.&lt;/li&gt;
&lt;li&gt;Prepare samples for varied external workflows to assess molecular integrity and degradation.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Experimental pipeline support&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate closely with formulation chemists to screen cargo-formulation interactions across diverse experimental conditions.&lt;/li&gt;
&lt;li&gt;Generate high-quality experimental datasets to support internal modeling and data analysis pipelines.&lt;/li&gt;
&lt;li&gt;Assist in maintaining and troubleshooting laboratory instrumentation&lt;/li&gt;
&lt;li&gt;Maintain organized laboratory records, analyze results, and communicate findings clearly to cross-functional teams.&lt;/li&gt;
&lt;li&gt;Develop reproducible workflows and assist in development of standard operating procedures (SOPs).&lt;/li&gt;
&lt;li&gt;Support the scale-up and automation of experimental workflows as the platform evolves.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Required&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s or Master’s degree in Biochemistry, Structural Biology, Molecular Biology, Biophysics, Chemical Biology, or a related field&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree and 5-8+ years of biotechnology industry experience&lt;/li&gt;
&lt;li&gt;Master’s degree and 3-6+ years of biotechnology industry experience&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Experience working with proteins or other biomolecules in vitro.&lt;/li&gt;
&lt;li&gt;Strong experience operating circular dichroism (CD) spectroscopy instruments, dynamic light scattering (DLS) instrumentation, and UV-Vis spectroscopy.&lt;/li&gt;
&lt;li&gt;Familiarity with SDS-PAGE and electrophoresis techniques.&lt;/li&gt;
&lt;li&gt;Strong organizational skills, attention to detail, and ability to maintain rigorous experimental documentation.&lt;/li&gt;
&lt;li&gt;Ability to work collaboratively in a fast-paced, interdisciplinary startup environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Preferred&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Background in computational structural biology or protein biophysics.&lt;/li&gt;
&lt;li&gt;Experience working with cell culture or tissue culture&lt;/li&gt;
&lt;li&gt;Experience with IR or FTIR spectroscopy&lt;/li&gt;
&lt;li&gt;Experience with chromatography and mass spectrometry sample preparation&lt;/li&gt;
&lt;li&gt;Familiarity with calorimetry and other physical chemistry techniques&lt;/li&gt;
&lt;li&gt;Experience analyzing biomolecular stability, aggregation, or degradation in complex chemical environments&lt;/li&gt;
&lt;li&gt;Exposure to formulation development in agriculture, nutrition, or industrial applications.&lt;/li&gt;
&lt;li&gt;Exposure to high-throughput or screening workflows.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp; &lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at &lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TL1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $81,000 - $126,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL118 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL118&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-research-associateassociate-scientist-biochemistry-flagship-pioneering/69d3bca0c8e81216cd0b90b3</link><guid isPermaLink="true">http://biotechroles.com/senior-research-associateassociate-scientist-biochemistry-flagship-pioneering/69d3bca0c8e81216cd0b90b3</guid><pubDate>Mon, 06 Apr 2026 14:01:04 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Bioanalytical Co-Op -Northeastern University Students]]></title><description><![CDATA[&lt;p&gt;Seaport Therapeutics is a clinical-stage therapeutics company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient needs. The Company has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM&amp;nbsp;technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects. Seaport is led by an experienced team that invented and advanced important neuropsychiatric medicines and are guided by an extensive network of renowned scientists, clinicians and key opinion leaders. For more information, please visit&amp;nbsp;&lt;a href=&quot;https://www.seaporttx.com/&quot;&gt;www.seaporttx.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Job Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Seaport Therapeutics is seeking a co-op student for a lab-based bioanalysis position to be part of our Discovery team. This role will begin in June 2026. This co-op will have a focus on LC-MS to assist in the screening of novel drugs. We are looking for a highly motivated individual who is looking to be a part of a multidisciplinary team and to gain experience in a startup environment. This position will contribute to advancing the pipeline of impactful candidates generated from our novel Glyph™ prodrug platform.&lt;/p&gt;
&lt;p&gt;Some of the responsibilities will include:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Executing &lt;em&gt;in vitro &lt;/em&gt;experiments, using LC-MS, for the screening of lipid prodrugs to support preclinical discovery&lt;/li&gt;
&lt;li&gt;Processing and analyzing &lt;em&gt;in vivo&lt;/em&gt; samples (plasma, lymph fluid, etc.) to generate DMPK data for various prodrugs&lt;/li&gt;
&lt;li&gt;Contributing to the development and optimization of LC-MS methods for both quantitative and qualitative analysis&lt;/li&gt;
&lt;li&gt;Routine use and troubleshooting of LC-MS instrumentation&lt;/li&gt;
&lt;li&gt;Documenting all experiments using an electronic notebook and analyzing data for reports and regular internal presentations&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Experience and Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Enrolled in a Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or related program at the Undergraduate or&amp;nbsp; Master’s Level&lt;/li&gt;
&lt;li&gt;Previous Co-op or lab experience is strongly preferred&lt;/li&gt;
&lt;li&gt;Knowledge of or experience with: HPLC, reverse phase chromatography, mass spectrometry instrumentation, enzyme kinetics, protein precipitation, liquid-liquid extraction&lt;/li&gt;
&lt;li&gt;Strong organizational skills, attention to detail, and eagerness to learn.&lt;/li&gt;
&lt;/ul&gt;]]></description><link>http://biotechroles.com/bioanalytical-co-op-northeastern-university-students-seaport-therapeutics/69d3bc9fc8e81216cd0b90b2</link><guid isPermaLink="true">http://biotechroles.com/bioanalytical-co-op-northeastern-university-students-seaport-therapeutics/69d3bc9fc8e81216cd0b90b2</guid><pubDate>Mon, 06 Apr 2026 14:01:03 GMT</pubDate><company>Seaport Therapeutics</company><location>Boston, MA</location><salary>$3000-4000</salary><type>Full-time</type></item><item><title><![CDATA[Senior / Principal Scientist, Structural Biology]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;What if…&amp;nbsp;&lt;/strong&gt;you could join an organization that creates, resources, and builds life sciences companies that invent breakthrough technologies in order to transform health care and sustainability?&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Company Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Expedition Medicines is a privately held, early-stage biotechnology company pioneering the emerging field of Protein Editing. At Expedition Medicines we create small molecules that edit protein structure and function to unlock presently undruggable targets and a broad array of therapeutic modalities. Our platform integrates novel small molecule chemistry and chemoproteomic discovery technologies with Machine Learning (ML) to enable generative design. Expedition Medicines is backed by Flagship Pioneering, bringing their courage, vision, and resources to guide Expedition Medicines from platform validation to patient impact. We are seeking collaborative, relentless problem solvers that share our passion for impact to join us! &lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The role of Senior/Principal Scientist, Structural Biologist will focus upon determination of protein-ligand complex structures by X-ray crystallography and cryo-EM.&amp;nbsp; The scientist in this position will be responsible for delivering structures and collaborating with project teams to enable structure-based drug design and elucidate the mechanism-of-action of small molecules.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Candidate responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and execute structural biology strategy for one or more projects&lt;/li&gt;
&lt;li&gt;Oversee construct design, expression and purification of proteins for structure determination&lt;/li&gt;
&lt;li&gt;Develop and execute protocols to obtain high quality crystals for X-ray structures&lt;/li&gt;
&lt;li&gt;Develop and execute protocols for grid optimization, data collection, and data analysis for structure determination using cryo-EM&lt;/li&gt;
&lt;li&gt;Obtain and refine structures of protein-ligand complexes, communicate the results and collaborate with project teams to drive hit-to-lead and lead optimization&lt;/li&gt;
&lt;li&gt;Manage CROs for effective delivery of protein expression and structural biology services&lt;/li&gt;
&lt;li&gt;Expand our capabilities and serve as a trusted expert in structural biology&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD/MS degree in structural biology, biochemistry, molecular biology, or a related field with at least 3 years of drug discovery experience in an industry setting&lt;/li&gt;
&lt;li&gt;In-depth knowledge and hands-on experience in X-ray crystallography and cryo-EM, including crystal optimization, grid preparation, data collection, data processing, structure refinement, and interpretation of protein structures&lt;/li&gt;
&lt;li&gt;Experience managing CROs for protein production and structural biology&lt;/li&gt;
&lt;li&gt;Excellent collaboration, communication, and organizational skills&lt;/li&gt;
&lt;li&gt;Strong desire to learn and implement new methods in protein biochemistry, biophysics, and structural biology&lt;/li&gt;
&lt;li&gt;Experience with biophysical methods (SPR, DSF, MST) or mass spectrometry (intact MS, peptide mapping, proteomics) is a plus&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&amp;nbsp;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s&lt;/em&gt;&lt;em&gt; internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Expedition Medicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Expedition Medicines&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-principal-scientist-structural-biology-flagship-pioneering/69d3bc9cc8e81216cd0b90af</link><guid isPermaLink="true">http://biotechroles.com/senior-principal-scientist-structural-biology-flagship-pioneering/69d3bc9cc8e81216cd0b90af</guid><pubDate>Mon, 06 Apr 2026 14:01:00 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager or Associate Director, Biostatistics]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we’re driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we’re doing this with extraordinary science and awesome people (affectionately called Rapptors).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies.&amp;nbsp;We are excited about the potential of our lead program, RAP-219. &amp;nbsp;Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder.&lt;/p&gt;
&lt;p&gt;The strength of Rapport comes from our Rapptors – who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you’re as excited about this opportunity as we are!&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 12pt;&quot;&gt;Your Impact:&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Rapport is seeking a Senior Manager / Associate Director of Biostatistics who will have a hands-on role in shaping the design, analysis, and interpretation of clinical trial data for our precision neuromedicine programs. Reporting to the Senior Director of Biostatistics, you will collaborate closely with multidisciplinary teams to advance groundbreaking therapies, ensuring statistical rigor and the highest standards of data integrity throughout the drug development process.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;color: rgb(22, 145, 121);&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 12pt;&quot;&gt;Your Day-to-Day:&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee the production of protocol development (study design, endpoint selection, sample size calculation and statistical methods) and Statistical Analysis Plan (SAP) that lead to comprehensive clinical study reports suitable for regulatory submissions.&lt;/li&gt;
&lt;li&gt;Support statistical programming to plan, execute and deliver SDTM and ADaM datasets, tables, listings, and figures (TLFs). Ensure compliance with CDISC standards (SDTM, ADaM) and regulatory guidelines (ICH, FDA, EMA).&lt;/li&gt;
&lt;li&gt;Provide statistical input and the interpretation of results to clinical study reports, regulatory submissions documents, and publications, in collaboration with the clinical, regulatory, and medical affairs teams.&lt;/li&gt;
&lt;li&gt;Perform and validate statistical analyses of clinical trial data using SAS and/or R in accordance with regulatory and internal standards.&lt;/li&gt;
&lt;li&gt;Participate in the development and review of case report forms (CRFs) and data management plans to ensure accurate data collection aligned with study objectives.&lt;/li&gt;
&lt;li&gt;Oversee and manager external CROs and vendors to ensure high-quality and timely deliverables.&lt;/li&gt;
&lt;li&gt;Participate in cross-functional team meetings, providing statistical support and insights to influence decision-making.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121);&quot;&gt;&lt;strong&gt;Must-Haves:&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Senior manager: PhD with 3+ or MS with 6+ years of biostatistics experience&lt;/li&gt;
&lt;li&gt;Associate director: &amp;nbsp;PhD with 6+ years or MS with 9+ years of biostatistics experience&lt;/li&gt;
&lt;li&gt;CNS therapeutic area experience is a plus&lt;/li&gt;
&lt;li&gt;Skilled in scientific programming including SAS or R, or Python for data analysis, graphing, and simulation&lt;/li&gt;
&lt;li&gt;Comprehensive knowledge of clinical trial design, advanced statistical analysis methods, and familiarity with regulatory guidelines (FDA, EMA, ICH)&lt;/li&gt;
&lt;li&gt;Extensive knowledge with CDISC standards (SDTM, ADaM) and industry best practices for data collection, analysis, and reporting&lt;/li&gt;
&lt;li&gt;Ability to communicate complex statistical concepts clearly to non-statistical audiences.&lt;/li&gt;
&lt;li&gt;Ability to manage multiple projects in a fast-paced environment, flexibility to adapt to changing priorities and timelines&lt;/li&gt;
&lt;li&gt;Ability to effectively collaborate with internal stakeholders and manage the statistical work of external stakeholders/vendors&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;What makes Rapport special:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Your perspective matters. Stick your neck out, share your ideas – we work as a team.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We have FUN. We hire smart, dedicated, down-to-earth people that you’ll enjoy spending time with.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Leadership that CARES – about you, your growth + development.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We&#39;re bicoastal. Whether you&#39;re in the lab full-time in San Diego or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;You get to be YOU! Show up as you are and make every day count.&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;Your Compensation:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this?&amp;nbsp; We tell you about our hiring range now - we expect the hiring range for this role to be $190,000-$220,000 for the Associate Director level. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here - if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;Hybrid Work Environment:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We prioritize in person connection with our fellow Rapptors! Our team members come together onsite at our Boston office on Monday, Tuesday and Wednesday to create more opportunities for innovation, collaboration, and connection.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p class=&quot;MsoNormal&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Note to Employment Agencies:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt; Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;CCPA disclosure notice can be found &lt;a href=&quot;https://www.rapportrx.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt;.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-or-associate-director-biostatistics-rapport-therapeutics/69d3bc9ac8e81216cd0b90ad</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-or-associate-director-biostatistics-rapport-therapeutics/69d3bc9ac8e81216cd0b90ad</guid><pubDate>Mon, 06 Apr 2026 14:00:57 GMT</pubDate><company>Rapport Therapeutics</company><location>99 High Street, Suite 2100 , Boston, MA 02110; Remote</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior / Principal Scientist, Medicinal Chemistry]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;What if… &lt;/strong&gt;you could join an organization that creates, resources, and builds life sciences companies that invent breakthrough technologies in order to transform health care and sustainability?&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Company Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Expedition Medicines is a privately held, early-stage biotechnology company pioneering the emerging field of Protein Editing. At Expedition Medicines we create small molecules that edit protein structure and function to unlock presently undruggable targets and a broad array of therapeutic modalities. Our platform integrates novel small molecule chemistry and chemoproteomic discovery technologies with Machine Learning (ML) to enable generative design. Expedition Medicines is backed by Flagship Pioneering, bringing their courage, vision, and resources to guide Expedition Medicines from platform validation to patient impact. We are seeking collaborative, relentless problem solvers that share our passion for impact to join us! &lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About the role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Senior / Principal Scientist level medicinal chemist to join our chemistry team at Expedition Medicines. This position will be responsible for the medicinal chemistry strategy and delivery on one or more projects. &amp;nbsp;A candidate with experience collaborating with a machine learning team to deliver against project goals is a plus.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Candidate responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and deliver medicinal chemistry strategy on project(s).&lt;/li&gt;
&lt;li&gt;Optimize small molecules through analysis of biochemical, biological, and ADME assay data.&lt;/li&gt;
&lt;li&gt;Manage chemistry CROs for timely delivery of synthetic efforts.&lt;/li&gt;
&lt;li&gt;Collaborate with cross-functional teams for project needs in high-paced data-driven environment.&lt;/li&gt;
&lt;li&gt;Collaborate with machine learning team for delivery against medicinal chemistry strategy.&lt;/li&gt;
&lt;li&gt;Contribute to patent applications and scientific publications.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in synthetic organic or medicinal chemistry with at least 5 years’ drug discovery experience in pharmaceutical industry or BS/BA in chemistry with at least 10 years’ experience in pharmaceutical industry.&lt;/li&gt;
&lt;li&gt;Strong modern synthetic background preferred with knowledge of state-of-the-art organic chemistry methodologies.&lt;/li&gt;
&lt;li&gt;Experience managing external chemistry CROs.&lt;/li&gt;
&lt;li&gt;Experience collaborating with machine learning teams preferred.&lt;/li&gt;
&lt;li&gt;Experience with both traditional small molecules and beyond-rule-of-5 therapeutic modalities is a plus.&lt;/li&gt;
&lt;li&gt;Strong communication and interpersonal skills.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION: &lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Expedition Medicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Expedition Medicines&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-principal-scientist-medicinal-chemistry-flagship-pioneering/69d3bc98c8e81216cd0b90ac</link><guid isPermaLink="true">http://biotechroles.com/senior-principal-scientist-medicinal-chemistry-flagship-pioneering/69d3bc98c8e81216cd0b90ac</guid><pubDate>Mon, 06 Apr 2026 14:00:56 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Regulatory Strategy]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we’re driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we’re doing this with extraordinary science and awesome people (affectionately called Rapptors).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies.&amp;nbsp;We are excited about the potential of our lead program, RAP-219. &amp;nbsp;Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder.&lt;/p&gt;
&lt;p&gt;The strength of Rapport comes from our Rapptors – who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you’re as excited about this opportunity as we are!&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 12pt;&quot;&gt;Your Impact:&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Director of Regulatory Strategy will play a pivotal role in leading strategic regulatory initiatives for assigned drug development programs.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;color: rgb(22, 145, 121);&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 12pt;&quot;&gt;Your Day-to-Day:&lt;/span&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Create and implement innovative and effective regulatory strategies to support the development of Rapport global drug development programs&lt;/li&gt;
&lt;li&gt;Provide regulatory expertise and advise to cross-functional team members including clinical, CMC, clinical pharmacology, and nonclinical&lt;/li&gt;
&lt;li&gt;Accountable for the maintenance of regulatory applications such as INDs, CTAs, NDAs, etc.&lt;/li&gt;
&lt;li&gt;Identify regulatory risks and mitigation plans&lt;/li&gt;
&lt;li&gt;Serve as the regulatory lead on project teams&lt;/li&gt;
&lt;li&gt;Ensure compliance with local and international submission requirements, manage CROs as applicable.&lt;/li&gt;
&lt;li&gt;Represents Rapport as the point of contact for regulatory health authorities, as assigned ensuring exemplary ethics and transparency within the company and with health authorities&lt;/li&gt;
&lt;li&gt;Keeps current with global regulatory landscape and advises project teams on potential impact to programs&lt;/li&gt;
&lt;li&gt;Provide mentorship and support to junior team members to foster their professional growth and development&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121);&quot;&gt;&lt;strong&gt;Must-Haves:&lt;/strong&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelors degree in a life science or related discipline&lt;/li&gt;
&lt;li&gt;12+ years of experience in the pharmaceutical or biotech industry&lt;/li&gt;
&lt;li&gt;Experience in neurology and small molecules preferred&lt;/li&gt;
&lt;li&gt;Global drug development experience&lt;/li&gt;
&lt;li&gt;Experience working with DAAP or Neurology FDA Divisions&lt;/li&gt;
&lt;li&gt;Ability to manage competing priorities, influence and integrate within a team, manage timelines and deliver on corporate and program goals.&lt;/li&gt;
&lt;li&gt;Strong interpersonal skills and alignment with Rapport’s values and company culture&lt;/li&gt;
&lt;li&gt;Must demonstrate strong leadership and team building skills, including experience with conflict resolution and real time problem solving.&lt;/li&gt;
&lt;li&gt;Thorough understanding of the development phases within a fast-moving biopharmaceutical organization.&lt;/li&gt;
&lt;li&gt;Exceptional written and verbal communication skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;What makes Rapport special:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Your perspective matters. Stick your neck out, share your ideas – we work as a team.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We have FUN. We hire smart, dedicated, down-to-earth people that you’ll enjoy spending time with.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Leadership that CARES – about you, your growth + development.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We&#39;re bicoastal. Whether you&#39;re in the lab full-time in San Diego or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;You get to be YOU! Show up as you are and make every day count.&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;Your Compensation:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this?&amp;nbsp; We tell you about our hiring range now - we expect the hiring range for this role to be $220,000 to $240,000. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here - if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(22, 145, 121); font-family: helvetica, arial, sans-serif;&quot;&gt;&lt;strong&gt;Hybrid Work Environment:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-family: helvetica, arial, sans-serif;&quot;&gt;We prioritize in person connection with our fellow Rapptors! Our team members come together onsite at our Boston office on Monday, Tuesday and Wednesday to create more opportunities for innovation, collaboration, and connection.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p class=&quot;MsoNormal&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Note to Employment Agencies:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt; Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;CCPA disclosure notice can be found &lt;a href=&quot;https://www.rapportrx.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt;.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-regulatory-strategy-rapport-therapeutics/69d3bc95c8e81216cd0b90a9</link><guid isPermaLink="true">http://biotechroles.com/director-regulatory-strategy-rapport-therapeutics/69d3bc95c8e81216cd0b90a9</guid><pubDate>Mon, 06 Apr 2026 14:00:53 GMT</pubDate><company>Rapport Therapeutics</company><location>99 High Street, Suite 2100 , Boston, MA 02110</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior/Principal Scientist, Biostatistics & Computational Biology]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;dhkj5-0-0&quot;&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound Therapeutics is seeking a pioneering &lt;strong&gt;Senior&lt;/strong&gt; &lt;strong&gt;Scientist/Principal Scientist, Biostatistics &amp;amp; Computational Biology&lt;/strong&gt; to advance the ProFoundry™ Platform through rigorous statistical modeling, inference, and translational analytics. This role is ideal for a candidate with deep expertise in &lt;strong&gt;biostatistics, theoretical statistics&lt;/strong&gt;, and quantitative data analysis, who is passionate about applying statistical principles to complex biological data relevant to &lt;strong&gt;cardiometabolic or neurodegenerative disorders&lt;/strong&gt; to drive therapeutic discovery. The ProFoundry Atlas—a proprietary resource of genetic, transcriptomic, proteomic, and imaging data—offers a unique opportunity to uncover novel biological insights and prioritize targets for drug development. The successful candidate will play a central role in developing statistical frameworks and analytical pipelines that support preclinical research, target validation, and portfolio decision-making.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Company Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound Therapeutics is a privately held, early-stage biotechnology company founded by &lt;strong&gt;Flagship Pioneering&lt;/strong&gt;, the creators of over 75 transformative companies including Moderna Therapeutics (NASDAQ: MRNA), Seres Therapeutics (MCRB), and Indigo Agriculture. ProFound is built on a foundation of scientific innovation and entrepreneurial spirit, with a mission to redefine the boundaries of human therapeutics.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and implement statistical models for analyzing high-dimensional biological data, including genomics, transcriptomics, proteomics, and imaging relevant to &lt;strong&gt;cardiometabolic or neurodegenerative disorders&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;Apply principles of &lt;strong&gt;theoretical and applied statistics&lt;/strong&gt; to develop novel inference methods tailored to biological questions&lt;/li&gt;
&lt;li&gt;Lead the development of robust, reproducible pipelines for hypothesis testing, causal inference, and predictive modeling across multi-omics datasets&lt;/li&gt;
&lt;li&gt;Collaborate with interdisciplinary teams to translate statistical findings into biological insights and therapeutic hypotheses&lt;/li&gt;
&lt;li&gt;Develop simulation frameworks and statistical benchmarking tools to evaluate model performance and data quality&lt;/li&gt;
&lt;li&gt;Apply advanced statistical modeling to support &lt;strong&gt;target discovery, prioritization, and validation&lt;/strong&gt;, integrating multi-omics and functional data&lt;/li&gt;
&lt;li&gt;Design and analyze &lt;strong&gt;preclinical experiments&lt;/strong&gt;, including dose-response studies, biomarker discovery, and mechanistic investigations&lt;/li&gt;
&lt;li&gt;Use &lt;strong&gt;Bayesian and frequentist frameworks&lt;/strong&gt; to quantify uncertainty and support decision-making in early-stage drug development&lt;/li&gt;
&lt;li&gt;Build &lt;strong&gt;simulation models&lt;/strong&gt; to assess study designs, optimize resource allocation, and forecast outcomes in preclinical pipelines&lt;/li&gt;
&lt;li&gt;Contribute to &lt;strong&gt;portfolio-level analytics&lt;/strong&gt;, helping prioritize targets based on statistical evidence, biological plausibility, and translational potential&lt;/li&gt;
&lt;li&gt;Support &lt;strong&gt;statistical planning&lt;/strong&gt; for in vitro and in vivo studies, including power calculations, randomization schemes, and reproducibility assessments&lt;/li&gt;
&lt;li&gt;Develop &lt;strong&gt;scoring systems and prioritization frameworks&lt;/strong&gt; for ranking therapeutic targets using multi-dimensional data inputs&lt;/li&gt;
&lt;li&gt;Ensure statistical rigor in the interpretation of experimental results, guiding go/no-go decisions and milestone reviews&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Minimum Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in &lt;strong&gt;Biostatistics, Statistics, Applied Mathematics&lt;/strong&gt;, or a related quantitative field with 3+ years of postdoctoral or industry experience; or MS with 7+ years of relevant experience&lt;/li&gt;
&lt;li&gt;Strong foundation in statistical theory, including probability, inference, regression, and multivariate analysis&lt;/li&gt;
&lt;li&gt;Experience applying statistical methods to biological or biomedical datasets, including genomics, transcriptomics, or clinical data relevant to &lt;strong&gt;cardiometabolic/neurodegenerative disorders&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;Proficiency in statistical programming languages (e.g., R, Python) and familiarity with statistical computing environments&lt;/li&gt;
&lt;li&gt;Demonstrated ability to develop and validate statistical models and algorithms for complex, high-dimensional data&lt;/li&gt;
&lt;li&gt;Commitment to reproducible research and collaborative problem-solving&lt;/li&gt;
&lt;li&gt;Excellent communication skills, with the ability to explain statistical concepts to non-statistical audiences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Expertise in &lt;strong&gt;Bayesian statistics&lt;/strong&gt;, hierarchical modeling, and probabilistic graphical models&lt;/li&gt;
&lt;li&gt;Experience with &lt;strong&gt;longitudinal data analysis&lt;/strong&gt;, survival analysis, and time-to-event modeling in clinical or biomedical contexts relevant to &lt;strong&gt;cardiometabolic/neurodegenerative disorders&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;Familiarity with &lt;strong&gt;causal inference frameworks&lt;/strong&gt;, such as propensity score methods, instrumental variables, or structural equation modeling&lt;/li&gt;
&lt;li&gt;Knowledge of &lt;strong&gt;experimental design&lt;/strong&gt;, including randomized trials, adaptive designs, and observational study methodologies&lt;/li&gt;
&lt;li&gt;Experience with &lt;strong&gt;dimension reduction techniques&lt;/strong&gt; (e.g., factor analysis, t-SNE, UMAP) and &lt;strong&gt;high-dimensional inference&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;Exposure to &lt;strong&gt;functional data analysis&lt;/strong&gt;, spatial statistics, or statistical methods for imaging data&lt;/li&gt;
&lt;li&gt;Familiarity with &lt;strong&gt;meta-analysis&lt;/strong&gt;, statistical harmonization, and federated data analysis across cohorts&lt;/li&gt;
&lt;li&gt;Experience with &lt;strong&gt;statistical consulting or collaboration&lt;/strong&gt; in multidisciplinary teams, especially in biomedical or pharmaceutical settings&lt;/li&gt;
&lt;li&gt;Knowledge of &lt;strong&gt;regulatory standards&lt;/strong&gt; and statistical considerations in drug development (e.g., FDA guidelines, ICH E9/E10)&lt;/li&gt;
&lt;li&gt;Experience with &lt;strong&gt;statistical software development&lt;/strong&gt;, package creation in R/Python, or contributions to open-source statistical tools&lt;/li&gt;
&lt;li&gt;Familiarity with &lt;strong&gt;cloud-based statistical workflows&lt;/strong&gt; and scalable computing (e.g., parallel processing, distributed computing frameworks)&lt;/li&gt;
&lt;li&gt;Experience in &lt;strong&gt;preclinical biostatistics&lt;/strong&gt;, including statistical design and analysis of in vitro and in vivo studies&lt;/li&gt;
&lt;li&gt;Familiarity with &lt;strong&gt;dose-response modeling&lt;/strong&gt;, pharmacokinetic/pharmacodynamic (PK/PD) modeling, and biomarker evaluation&lt;/li&gt;
&lt;li&gt;Knowledge of &lt;strong&gt;target validation pipelines&lt;/strong&gt;, including CRISPR screens, RNAi, and functional genomics&lt;/li&gt;
&lt;li&gt;Exposure to &lt;strong&gt;portfolio analytics&lt;/strong&gt; and decision-support tools used in early drug discovery&lt;/li&gt;
&lt;li&gt;Understanding of &lt;strong&gt;statistical considerations in translational research&lt;/strong&gt;, including bridging preclinical and clinical data&lt;/li&gt;
&lt;li&gt;Experience with &lt;strong&gt;model-based prioritization frameworks&lt;/strong&gt;, such as multi-criteria decision analysis (MCDA) or machine learning-based scoring systems&lt;/li&gt;
&lt;li&gt;Ability to communicate statistical findings in the context of &lt;strong&gt;biological relevance and therapeutic strategy&lt;/strong&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $146,000 - $236,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. ProFound Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on ProFound Therapeutics, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/seniorprincipal-scientist-biostatistics-and-computational-biology-flagship-pioneering/69d3bc94c8e81216cd0b90a8</link><guid isPermaLink="true">http://biotechroles.com/seniorprincipal-scientist-biostatistics-and-computational-biology-flagship-pioneering/69d3bc94c8e81216cd0b90a8</guid><pubDate>Mon, 06 Apr 2026 14:00:52 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director or Senior Manager, IT Infrastructure and Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we’re driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we’re doing this with extraordinary science and awesome people (affectionately called Rapptors).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies.&amp;nbsp;We are excited about the potential of our lead program, RAP-219. &amp;nbsp;Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder.&lt;/p&gt;
&lt;p&gt;The strength of Rapport comes from our Rapptors – who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you’re as excited about this opportunity as we are!&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;span style=&quot;color: rgb(0, 0, 0);&quot;&gt;This role is onsite and can be based in either Boston, MA or San Diego, CA&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Your impact:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Rapport Therapeutics with locations in San Diego and Boston is seeking an IT professional to lead the delivery of all IT infrastructure and related operations utilized to enable business capabilities and services across our two sites. Those include network, cloud, servers, user devices, collaboration tools, conference room AV support, telecommunication and site support. This will be a highly visible and valued role as the company builds its capabilities to advance our products through R&amp;amp;D and clinical trials. This individual will manage infrastructure and resources to meet organizational needs and will be responsible for working cross-functionally to identify long-term, scalable, and practical solutions for research, development and clinical as well as business operations.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;Your day-to-day&lt;/span&gt;:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support the IT infrastructure needs and manage the desktop support function&lt;/li&gt;
&lt;li&gt;Partner with IT Director to develop IT Infrastructure and Operations strategy and execute roadmap to optimize IT support model for growth at San Diego and Boston sites&lt;/li&gt;
&lt;li&gt;Partner with IT Director to develop and implement a company-wide cybersecurity program to support the needs of expected company growth&lt;/li&gt;
&lt;li&gt;Create and maintain IT infrastructure architecture, policies and standards&lt;/li&gt;
&lt;li&gt;Implement company-wide technology updates and hold sessions to teach employees on new features to ensure effective and consistent use and compliance with security and regulatory requirements&lt;/li&gt;
&lt;li&gt;Partner with R&amp;amp;D team to design and implement effective lab data management strategy and lab instrument support&lt;/li&gt;
&lt;li&gt;Partner with cross-functional teams to implement and operationalize controls necessary for Cyber Security, GxP, SOX other regulatory requirements and industry standards as the company matures&lt;/li&gt;
&lt;li&gt;Grow and effectively maintain cloud first infrastructure and service environment to enable agility while ensuring secure operations and efficient utilization of resources&lt;/li&gt;
&lt;li&gt;Develop and maintain budgets according to business and IT priorities and optimizing resource allocation&lt;/li&gt;
&lt;li&gt;Develop and maintain outsourcing strategies and provide oversight for IT vendors and partners to effectively deliver IT projects&lt;/li&gt;
&lt;li&gt;Maintain ongoing knowledge of industry trends and ability to utilize that knowledge to determine the most efficient ways to meet the Company’s evolving business needs&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Must-Haves:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Degree in computer science or related technical discipline plus 8+ years of relevant experience managing IT department, infrastructure and services with at least 2 years in a biotech environment, public company experience preferred&lt;/li&gt;
&lt;li&gt;Excellent working knowledge of Cisco Meraki network, Microsoft O365 administration, and OKTA, basic knowledge of AWS&lt;/li&gt;
&lt;li&gt;Experience in developing and executing RFPs and SOWs for IT services and negotiating service agreements with IT vendors&lt;/li&gt;
&lt;li&gt;Strong project management capabilities working with cross-functional and partner-based project teams&lt;/li&gt;
&lt;li&gt;Prior experience in successfully implementing, utilizing and leveraging outsourcing strategies with managed service providers and other specialty partners&lt;/li&gt;
&lt;li&gt;Ability to identify impediments to complex business and research issues and provide timely and cost-effective solutions&lt;/li&gt;
&lt;li&gt;Ability to adapt to increasing scope and complexity of work brought on by growth and help others manage through change&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;What makes Rapport special:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.&lt;/li&gt;
&lt;li&gt;We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.&lt;/li&gt;
&lt;li&gt;Your perspective matters. Stick your neck out, share your ideas – we work as a team.&lt;/li&gt;
&lt;li&gt;We have FUN. We hire smart, dedicated, down-to-earth people that you’ll enjoy spending time with.&lt;/li&gt;
&lt;li&gt;Leadership that CARES – about you, your growth + development.&lt;/li&gt;
&lt;li&gt;We&#39;re bicoastal. Whether you&#39;re in the lab full-time in San Diego or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.&lt;/li&gt;
&lt;li&gt;Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!&lt;/li&gt;
&lt;li&gt;You get to be YOU! Show up as you are and make every day count.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Your Compensation:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this?&amp;nbsp; We tell you about our hiring range now - we expect the hiring range for this role to be $180,000-$200,000 at the Associate Director level. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here - if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Hybrid Work Environment:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We prioritize in person connection with our fellow Rapptors! Our team members come together onsite at our Boston office on Monday, Tuesday and Wednesday to create more opportunities for innovation, collaboration, and connection. In San Diego, our Rapptors are onsite 4-5 days a week.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p class=&quot;MsoNormal&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Note to Employment Agencies:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt; Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;CCPA disclosure notice can be found &lt;a href=&quot;https://www.rapportrx.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt;.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-or-senior-manager-it-infrastructure-and-operations-rapport-therapeutics/69d3bc88c8e81216cd0b90a2</link><guid isPermaLink="true">http://biotechroles.com/associate-director-or-senior-manager-it-infrastructure-and-operations-rapport-therapeutics/69d3bc88c8e81216cd0b90a2</guid><pubDate>Mon, 06 Apr 2026 14:00:40 GMT</pubDate><company>Rapport Therapeutics</company><location>9880 Campus Point Drive, Suite 510, San Diego, CA; 99 High Street, Suite 2100 , Boston, MA 02110</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Manager, QC]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;Prime Medicine was founded to bring the promise of gene editing to patients. We use Prime Editing, a next-generation technology that can “search and replace” to restore normal genetic function almost anywhere in the genome. Prime Editing searches to find the precise place in the genome to edit and replaces the segment of faulty DNA with a correct copy of DNA.&amp;nbsp; A single Prime Editor can correct the individual mutations found across patients, meaning Prime Editing can potentially address more than 90 percent of known disease-causing genetic mutations.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We envision a world where this technology can cure, halt, and ultimately prevent genetic diseases, providing lifelong benefit to patients.&amp;nbsp; Prime Medicine offers the opportunity to shape the future of gene editing and transform how medicines are used to treat disease. Realizing the promise of Prime Editing requires a talented team with diversity of viewpoints and expertise. We’re building a group of dedicated, scientifically curious individuals who are passionate about helping patients live longer, healthier lives.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a talented and motivated Sr. Manager to join the Analytical Development &amp;amp; QC team within Technology, Development &amp;amp; Operations. This role will focus on Quality Control (QC) related activities for all programs, including management and technical oversight of tech transfer, qualification/validation and release and stability testing carried out at both CDMOs, CTLs and internally at Prime for our prime editing ex vivo cell therapy and in vivo LNP-based drug products.&lt;/p&gt;
&lt;p&gt;The successful candidate will have deep understanding of method lifecycle management, including method optimization, qualification, validation/verification, transfer, and implementation in a cGMP environment, as well as previous hands-on experience in at least some aspects of the above. This is a role requiring strong cross-functional collaboration with Analytical Development, Quality, Process Development, Formulation, Informatics, and external partners (CTLs/CDMOs).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The ideal candidate thrives in a matrixed, fast-paced environment, works effectively with limited supervision, and demonstrates strong technical ownership and execution.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design or review analytical procedures and protocols supporting method lifecycle activities, including optimization, qualification, validation, transfer, verification, performance monitoring, bridging, and comparability studies&lt;/li&gt;
&lt;li&gt;Manage and conduct select release, stability, and in-process testing for drug substances, drug products, and gene-editing components, and carry out data analysis and trending&lt;/li&gt;
&lt;li&gt;Support and/or manage analytical method transfer to CTLs/CDMOs, providing oversight, troubleshooting, and ensuring technical and timeline objectives are met&lt;/li&gt;
&lt;li&gt;Manage GMP sample inventory and chain-of-custody documentation&lt;/li&gt;
&lt;li&gt;Lead, manage and maintain well-designed stability programs and reference standard programs&lt;/li&gt;
&lt;li&gt;Author and review protocols, reports, SOPs, and analytical sections of regulatory submissions&lt;/li&gt;
&lt;li&gt;Familiarity with and ability to learn and use new tools for productivity, project management, documentation, tracking scheduling, and data management.&lt;/li&gt;
&lt;li&gt;Support IQ/OQ/PQ of QC equipment and ensure compliance with 21 CFR Part 11&lt;/li&gt;
&lt;li&gt;Maintain GxP-compliant electronic documentation and thorough laboratory records&lt;/li&gt;
&lt;li&gt;Collaborate with Quality to ensure data integrity, regulatory compliance, and audit readiness&lt;/li&gt;
&lt;li&gt;Lead or support investigations, deviations, and root-cause analyses&lt;/li&gt;
&lt;li&gt;Present data and findings to cross-functional teams&lt;/li&gt;
&lt;li&gt;Prepare technical reports and documents for global regulatory submissions&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Education &amp;amp; Experience&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS/MS/PhD in Biochemistry, Molecular biology, Chemistry, Bioengineering, or a related discipline&lt;/li&gt;
&lt;li&gt;Industry experience:&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;BS: 10+ years&lt;/li&gt;
&lt;li&gt;MS: 8+ years&lt;/li&gt;
&lt;li&gt;PhD: 3+ years&lt;/li&gt;
&lt;/ul&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Technical Expertise&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with analytical method optimization, tech-transfer, qualification, validation, and verification used for critical components, drug substance and drug product release and stability testing&lt;/li&gt;
&lt;li&gt;Hands-on experience with analytical methodologies such as:&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Chromatography-based assays&lt;/li&gt;
&lt;li&gt;Absorbance-based assays&lt;/li&gt;
&lt;li&gt;Cell-based assays&lt;/li&gt;
&lt;li&gt;Compendial assays&lt;/li&gt;
&lt;li&gt;Molecular-based assays&lt;/li&gt;
&lt;li&gt;Flow cytometry assays&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;Familiarity with ICH and FDA guidelines for CMC development during clinical stage is required&lt;/li&gt;
&lt;li&gt;Experience in advanced cell and gene-editing therapeutics development is not mandatory, but highly desirable&lt;/li&gt;
&lt;li&gt;Experience working with CMOs/CDMOs is required&lt;/li&gt;
&lt;li&gt;Experience with stability and/or reference standard programs is a plus&lt;/li&gt;
&lt;li&gt;Knowledge of assays, instrumentation, and facility qualification/validation requirements is desirable&lt;/li&gt;
&lt;li&gt;Familiarity with regulatory writing&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Personal Attributes&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Highly self-motivated with strong project ownership&lt;/li&gt;
&lt;li&gt;Strong collaborator with internal cross-functional and external partners&lt;/li&gt;
&lt;li&gt;Adaptable in a dynamic, fast-paced environment&lt;/li&gt;
&lt;li&gt;Detail-oriented with strong troubleshooting and problem-solving skills&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills&lt;/li&gt;
&lt;li&gt;Strong abilities to lead and facilitate technical meetings with CDMO and CTL SMEs&lt;/li&gt;
&lt;li&gt;Work with purpose and drive meaningful results&lt;/li&gt;
&lt;li&gt;Ability to innovate and challenge industry status quo&lt;/li&gt;
&lt;li&gt;Ability to travel for up to 5 - 10% of the time&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$144,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$176,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr.-manager-qc-prime-medicine/69d3bc75c8e81216cd0b909a</link><guid isPermaLink="true">http://biotechroles.com/sr.-manager-qc-prime-medicine/69d3bc75c8e81216cd0b909a</guid><pubDate>Mon, 06 Apr 2026 14:00:21 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior / Principal Neuromorphic Systems Architect]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;The Company&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 119 Inc. (FL119) is an early-stage technology company pioneering a new frontier at the intersection of neuroscience and computation. We are developing next-generation technologies to transform how intelligent systems are built. We believe that the future of artificial intelligence demands a fundamental rethinking of today’s paradigms. Our mission is bold and urgent: to build a future where naturalistic, robust intelligence can emerge and operate sustainably at scale.&lt;/p&gt;
&lt;p&gt;FL119 is backed by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. At FL119, we are uniquely cross-functional and collaborative. Our teams thrive in unstructured and creative environments. All voices are heard because we know that experience comes in many forms, skills are transferable, and passion goes a long way.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL119 is seeking a creative and deeply technical Neuromorphic Systems Architect to join our team. Leveling is flexible based on experience.&lt;/p&gt;
&lt;p&gt;This role will focus on translating nonlinear neural dynamics into next-generation computational architectures. You will work at the interface of neuroscience, dynamical systems theory, and hardware engineering to design and prototype electronic architectures that embody biologically derived principles of computation.&lt;/p&gt;
&lt;p&gt;This is not a conventional AI accelerator role. We are seeking someone who can rethink compute from first principles, designing architectures that leverage recurrence, nonlinearity, sparsity, event-driven signaling, and adaptive dynamics as foundational primitives rather than constraints.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;How You Will Contribute:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Formalize brain-derived computation using dynamical systems theory and translate these insights into hardware-relevant abstractions.&lt;/li&gt;
&lt;li&gt;Architect novel neuromorphic or neuro-inspired hardware systems (analog, mixed-signal, in-memory, or alternative substrates).&lt;/li&gt;
&lt;li&gt;Define system-level architecture, including memory models, communication schemes, and energy-efficient compute primitives.&lt;/li&gt;
&lt;li&gt;Collaborate with neuroscience, signal processing, and machine learning teams to ensure tight coupling between biological insight and architectural design.&lt;/li&gt;
&lt;li&gt;Lead feasibility studies, simulations, and early-stage prototyping efforts.&lt;/li&gt;
&lt;li&gt;Evaluate trade-offs across CMOS, emerging devices, photonic, memristive, or other unconventional compute substrates.&lt;/li&gt;
&lt;li&gt;Contribute to IP strategy, including invention disclosures and patents.&lt;/li&gt;
&lt;li&gt;Help shape the long-term compute vision of the company.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Must-have Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD (or equivalent experience) in Electrical Engineering, Applied Physics, Computational Neuroscience, Computer Engineering, or a closely related field.&lt;/li&gt;
&lt;li&gt;Deep expertise in nonlinear dynamical systems and their application to computation.&lt;/li&gt;
&lt;li&gt;Experience designing hardware architectures (ASIC, FPGA, analog/mixed-signal, or emerging device technologies such as RRAM, PCM, memristors, etc.).&lt;/li&gt;
&lt;li&gt;Strong mathematical foundation in dynamical systems, control theory, or computational modeling.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to move from theory to implementable system design.&lt;/li&gt;
&lt;li&gt;5+ years of relevant research or industry experience (level dependent)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Experience&lt;/strong&gt;:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior work in neuromorphic computing or spiking neural network hardware.&lt;/li&gt;
&lt;li&gt;Experience with event-driven or asynchronous architectures.&lt;/li&gt;
&lt;li&gt;Familiarity with reservoir computing, recurrent dynamical systems, or physical computing substrates.&lt;/li&gt;
&lt;li&gt;Experience working in early-stage, fast-paced R&amp;amp;D environments.&lt;/li&gt;
&lt;li&gt;Track record of patents or high-impact publications in neuromorphic systems or unconventional computing.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $150,000 - $250,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL119 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL119&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-principal-neuromorphic-systems-architect-flagship-pioneering/69d3bc70c8e81216cd0b9097</link><guid isPermaLink="true">http://biotechroles.com/senior-principal-neuromorphic-systems-architect-flagship-pioneering/69d3bc70c8e81216cd0b9097</guid><pubDate>Mon, 06 Apr 2026 14:00:16 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director or Director, Drug Safety Pharmacovigilance Scientist]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we’re driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we’re doing this with extraordinary science and awesome people (affectionately called Rapptors).&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies.&amp;nbsp;We are excited about the potential of our lead program, RAP-219. &amp;nbsp;Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder.&lt;/p&gt;
&lt;p&gt;The strength of Rapport comes from our Rapptors – who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you’re as excited about this opportunity as we are!&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(45, 194, 107);&quot;&gt;Your impact:&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Key supporting role for all clinical development programs to ensure ongoing safety analysis, prompt management of potential safety signals, and establishment of in-house aggregate safety reporting system for assigned programs.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt;&lt;span style=&quot;font-size: 12pt;&quot;&gt;Your day-to-day:&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;color: rgb(45, 194, 107);&quot;&gt; &lt;/span&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Product Oversight&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead aggregate reports production, DSPV Safety Science clinical study team (CST) representation and any post marketing activities, and literature review.&lt;/li&gt;
&lt;li&gt;Supports rapid responses to ad-hoc safety data and analysis requests from any source&lt;/li&gt;
&lt;li&gt;Facilitate updates to Investigator Brochure, Company Core Safety Information and other Reference Safety Information following endorsement by safety governance teams.&lt;/li&gt;
&lt;li&gt;Key analytic and safety support lead in close collaboration with the Head of DSPV, Head of Safety Science, DSPV Safety Physician, and Medical Science Lead.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Clinical Trial Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Participate in protocol design, safety CRF development, safety monitoring plan, support of DSMB/DMC activities, coding review as well as SAE reconciliation activities.&lt;/li&gt;
&lt;li&gt;Review study protocols, IB, ICF, CSR, statistical analysis plans and other clinical study-related documents.&lt;/li&gt;
&lt;li&gt;Review standard design of tables, figures, and listings for safety data from clinical studies.&lt;/li&gt;
&lt;li&gt;Participate in Integrated Safety Summary reviews, which may include narrative generation, review and approval for filing related activities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Aggregate Reports, Risk Management Plans, and REMS Activities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead development and implementation of an in-house aggregate report strategy (DSUR/PSUR/PADER), preparation and adherence to timelines with key stakeholders and vendors.&lt;/li&gt;
&lt;li&gt;Lead development and implementation of an in-house literature surveillance process.&lt;/li&gt;
&lt;li&gt;Demonstrate effective leadership skills with cross functional partners to ensure that safety data analyses/authorship for ad hoc queries and aggregate reports are of high quality and are completed and submitted according to required timelines.&lt;/li&gt;
&lt;li&gt;Support RMP updates as appropriate for the assigned product(s).&lt;/li&gt;
&lt;li&gt;Contribute to the development of Risk Evaluation and Mitigation Strategies (REMS) or REMS amendments.&lt;/li&gt;
&lt;li&gt;Supports preparation of REMS assessment reports by contributing to the safety-relevant sections.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Signal Detection and Management&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead safety signal management documentation including preparation of the Safety Topic Report and maintenance of the signal tracker, for assigned products.&lt;/li&gt;
&lt;li&gt;Review adverse event data, product complaints, literature, and other safety-relevant data for signal detection.&lt;/li&gt;
&lt;li&gt;Coordinate ad hoc safety query or health hazard evaluation response plan for analysis in conjunction with the product safety physician, biostatistics and others as needed, including performing analysis and drafting of query responses for review and finalization.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Procedures and Compliance&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure PV activities remain compliant with evolving regulations (including new US FDA requirements to track and report Anticipated SAEs and increases in SARs), that respective SOPs and work instructions regarding signaling, ad hoc and aggregate safety and risk management plans are adequate.&lt;/li&gt;
&lt;li&gt;Assisting in the successful implementation, execution and maintenance of safety processes and systems that conform to the company’s business strategy, industry standards and compliance with global regulations.&lt;/li&gt;
&lt;li&gt;Keeping updated on relevant regulations associated with the above activities. Contributes to initiatives for process improvement and cross-product process consistency.&lt;/li&gt;
&lt;li&gt;Facilitate inspection readiness activities, if applicable.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Must-Haves: &lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;RN, PharmD, NP, MD, MS, DVM&lt;/li&gt;
&lt;li&gt;Relevant life science background and a minimum of 8+ years of experience in drug safety serving in a PV Scientist or similar role
&lt;ul&gt;
&lt;li&gt;Level commensurate with experience&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Demonstrated experience in analysis and interpretation of medical and scientific data, with excellent verbal and written skills.&lt;/li&gt;
&lt;li&gt;Experience in safety surveillance systems, aggregate reports, case management and global regulatory processes, ensuring quality and compliance with regulations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to provide strategic input in the preparation of responses to Regulatory Authority(ies), authoring of safety topic reports, and aggregate report preparation.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to work effectively either independently or collaboratively in a cross-functional team environment, as well as with external colleagues.&lt;/li&gt;
&lt;li&gt;Strong organizational, project management and leadership skills: leads and conducts, independently and/or collaboratively, all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests.&lt;/li&gt;
&lt;li&gt;Oversees and mentors less experienced PV Scientist staff.&lt;/li&gt;
&lt;li&gt;Applies clinical judgment to interpret case information.&lt;/li&gt;
&lt;li&gt;Solid knowledge of pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations, including familiarity with case processing, expedited reporting rules, and safety database concepts.&lt;/li&gt;
&lt;li&gt;Experience working with all levels of management and consulting with key business stakeholders with an ability to influence for greater outcomes.&lt;/li&gt;
&lt;li&gt;Strong team player that has a customer service approach and is solution oriented.&lt;/li&gt;
&lt;li&gt;Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.&lt;/li&gt;
&lt;li&gt;Possesses strong written and verbal communication skills.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;color: rgb(45, 194, 107); font-size: 12pt;&quot;&gt;What makes Rapport special:&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Every role has meaning. We’re determined to discover a better way for patients, and you’ll feel the passion from the start.&lt;/li&gt;
&lt;li&gt;We are driven to innovate. Exciting science that pushes boundaries and opens new possibilities.&lt;/li&gt;
&lt;li&gt;Your perspective matters. Stick your neck out, share your ideas – we work as a team.&lt;/li&gt;
&lt;li&gt;We have FUN. We hire smart, dedicated, down-to-earth people that you’ll enjoy spending time with.&lt;/li&gt;
&lt;li&gt;Leadership that CARES – about you, your growth + development.&lt;/li&gt;
&lt;li&gt;We&#39;re bicoastal. Whether you&#39;re in the lab full-time in San Diego or taking advantage of a more hybrid work schedule in Boston – we make the most of our time together.&lt;/li&gt;
&lt;li&gt;Competitive benefits. Including unlimited PTO, a lifestyle spending account, commuting reimbursement, and much more!&lt;/li&gt;
&lt;li&gt;You get to be YOU! Show up as you are and make every day count.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: rgb(45, 194, 107); font-size: 12pt;&quot;&gt;&lt;strong&gt;Your Compensation:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We get it. Compensation is an important part of your offer. You shouldn’t be surprised at the end of the recruiting process, and you should know that your offer is fair and equitable. How do we do this?&amp;nbsp; We tell you about our hiring range now - we expect the hiring range for this role to be $185,000 to $205,000 for Associate Director level and $215,000-235,000 for Director level. Our actual offer will reflect a lot of factors including your relevant skills, experience, location, salary market data, and internal equity. In addition to a competitive salary, we also offer a pretty great benefits package. We don’t stop here - if you join Rapport, we go to the next level. We share our full salary ranges for every level across our company.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;font-size: 12pt; color: rgb(45, 194, 107);&quot;&gt;&lt;strong&gt;Hybrid Work Environment:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;This role is onsite in our Boston office. We prioritize in person connection with our fellow Rapptors! Our team members come together onsite at our Boston office Monday, Tuesday and Wednesday to create more opportunities for innovation, collaboration, and connection.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p class=&quot;MsoNormal&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Rapport Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;Note to Employment Agencies:&lt;/span&gt;&lt;/strong&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt; Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.&lt;/span&gt;&lt;/p&gt;
&lt;p class=&quot;MsoNormal&quot;&gt;&lt;span style=&quot;font-size: 10.0pt; line-height: 107%; font-family: &#39;Arial&#39;,sans-serif;&quot;&gt;CCPA disclosure notice can be found &lt;a href=&quot;https://www.rapportrx.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;here&lt;/a&gt;.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-or-director-drug-safety-pharmacovigilance-scientist-rapport-therapeutics/69d3bc64c8e81216cd0b9090</link><guid isPermaLink="true">http://biotechroles.com/associate-director-or-director-drug-safety-pharmacovigilance-scientist-rapport-therapeutics/69d3bc64c8e81216cd0b9090</guid><pubDate>Mon, 06 Apr 2026 14:00:04 GMT</pubDate><company>Rapport Therapeutics</company><location>99 High Street, Suite 2100 , Boston, MA 02110</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Safety Assessment]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Position Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking an enthusiastic, self-motivated Senior Scientist to join the Nonclinical Development group, supporting the nonclinical safety assessment function for IND-enabling programs across Prime Medicine’s pipeline. Reporting to the Associate Director, Safety Assessment, the successful candidate will support the design, execution, and interpretation of nonclinical safety studies conducted both in-house and at CROs, with an initial focus on liver-targeted therapeutics. This role requires hands-on involvement in assay execution and troubleshooting, as well as active participation in study oversight of work being done at CRO and data analysis.&lt;/p&gt;
&lt;p&gt;This role requires collaboration within cross-functional teams. The ideal candidate will hold a Ph.D. in toxicology or a related field with 6+ years of pharma/biotech experience in nonclinical safety assessment, or an M.S. in toxicology or a related field with 10+ years of experience in nonclinical safety assessment, the ability to work independently, provide domain expertise and leadership, as well as cross-functionally in a fast-paced, matrixed environment with a positive, flexible attitude. &amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Contribute to nonclinical safety activities as part of cross-functional Discovery and Development project teams, supporting program progression through IND-enabling stages.&lt;/li&gt;
&lt;li&gt;Design, execute, and troubleshoot nonclinical safety studies, including hands-on laboratory work (~30%) to support assay development, data generation, and issue resolution.&lt;/li&gt;
&lt;li&gt;Support the execution and oversight of nonclinical safety studies (GLP and non-GLP) at CROs, including active involvement in troubleshooting assay and study-related challenges.&lt;/li&gt;
&lt;li&gt;Analyze and interpret study data with guidance and contribute to the preparation of study reports and supporting documents for regulatory submissions.&lt;/li&gt;
&lt;li&gt;Collaborate with Pharmacology, DMPK, and other functions to support exploratory studies (e.g., exploratory toxicology, DMPK, biodistribution, and delivery platform evaluation).&lt;/li&gt;
&lt;li&gt;Contribute to evaluation of new delivery approaches, Lipid and RNA components, and emerging targets to support pipeline expansion.&lt;/li&gt;
&lt;li&gt;Assist in identifying potential safety findings and contribute to discussions on data interpretation and next steps.&lt;/li&gt;
&lt;li&gt;Ensure studies and internal activities are conducted in compliance with regulatory guidelines and internal standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in toxicology or a related discipline with 6+ years of biopharmaceutical industry experience, or M.S. in toxicology or a related field with 10+ years of relevant biopharmaceutical industry experience supporting drug development in nonclinical safety/toxicology.&lt;/li&gt;
&lt;li&gt;Experience in large molecule therapeutic development, along with a background in immunology, is desirable.&lt;/li&gt;
&lt;li&gt;Understanding of toxicology principles, nonclinical safety evaluation, and the drug development process, with some experience interpreting toxicology data and contributing to technical and scientific reports.&lt;/li&gt;
&lt;li&gt;Demonstrates strong scientific judgment and leadership with the ability to evaluate information, identify potential issues, and propose practical solutions with guidance as needed.&lt;/li&gt;
&lt;li&gt;Highly organized and detail-oriented with strong attention to accuracy and quality.&lt;/li&gt;
&lt;li&gt;Strong communication and collaboration skills, with the ability to work effectively across multidisciplinary teams and with external partners.&lt;/li&gt;
&lt;li&gt;Experience supporting nonclinical studies at CROs is preferred but not required.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$145,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$177,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-safety-assessment-prime-medicine/69d3bc62c8e81216cd0b908e</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-safety-assessment-prime-medicine/69d3bc62c8e81216cd0b908e</guid><pubDate>Mon, 06 Apr 2026 14:00:01 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$140000-200000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Fellowship and Early Origination]]></title><description><![CDATA[&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Role Description: &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is seeking an AI-native, PhD-trained scientist who is eager to think programmatically about the early stages of Flagship’s novel company creation process, which we call Origination. Under the oversight of Flagship’s Sr. Director of Fellowship and Talent Development, the Sr. Manager, Fellowship and Early Origination will manage a suite of responsibilities across the full lifecycle of the Flagship Pioneering Fellowship, from recruitment and interviewing to the planning, development and organization of materials that ensure the ongoing success of this critical pipeline of talent and ideas. The Sr. Manager will also employ rigorous evaluation and continuous quality improvement approaches to surface best practices from the Fellowship and institutionalize them across Flagship Labs. In addition to Fellowship responsibilities, the Sr. Director will become a key contributor to Flagship’s broader strategy to leverage AI and off-the-shelf productivity tools to build and maintain systems and ways of working that support scaling, collaboration and efficiency across Flagship Labs, all while maintaining our culture of innovation and entrepreneurialism.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Skills and Behaviors:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The Sr. Manager, Fellowship and Early Origination must be able to partner with the Sr. Director, work independently, and join cross-functional teams to develop, implement, and assess multiple simultaneous projects of varying scope and duration. Success will require self-motivation, independence, flexibility, effective communication, and attention to detail. We expect a strong candidate will have demonstrated these skills and behaviors through prior work managing scientific or academic programs or through experience at a startup, venture or consulting firm. A track record of successfully completing projects across various domains is a must. Experience working directly with trainees and familiarity with the best practices of program evaluation will be helpful but are not required.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Core Duties&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support the Sr. Director, Fellowship and Talent Development in strategic and operational capacities across the full lifecycle of the Flagship Pioneering Fellowship, including recruitment, explorations, data stewardship, hiring decisions, and program evaluation&lt;/li&gt;
&lt;li&gt;Serve as an independent liaison between the Sr. Director and Fellowship stakeholders across Flagship Labs&lt;/li&gt;
&lt;li&gt;Collaborate with the Sr. Director and Flagship Labs leadership to build technical and operational solutions that maximize and streamline Flagship’s company creation pipeline&lt;/li&gt;
&lt;li&gt;Ensure that timely and accurate data on Fellowship, explorations, and company starts are available to inform strategic decisions by Flagship Labs leadership&lt;/li&gt;
&lt;li&gt;Collaborate with HR to support the professional development and productivity needs of Flagship Labs Associates&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;An advanced degree (PhD or international equivalent) in any scientific or technical field&lt;/li&gt;
&lt;li&gt;Project management experience beyond a laboratory environment, preferably in corporate, academic, or other professional settings&lt;/li&gt;
&lt;li&gt;Experience using AI-based approaches to solve complex problems&lt;/li&gt;
&lt;li&gt;Fluency with collaboration and knowledge management tools (SharePoint, Notion, Slack) and comfort partnering with IT for access and data management needs&lt;/li&gt;
&lt;li&gt;Evidence of strong organization and tracking along with strong communication via email, slide decks, and direct conversation&lt;/li&gt;
&lt;li&gt;Service-oriented, collaborative approach; able to liaise with company leadership, Associates, Fellows, and internal functions&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $128,000 - $176,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-manager-fellowship-and-early-origination-flagship-pioneering/69d3bc61c8e81216cd0b908d</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-fellowship-and-early-origination-flagship-pioneering/69d3bc61c8e81216cd0b908d</guid><pubDate>Mon, 06 Apr 2026 14:00:01 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager/Associate Director FP&A]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Who We Are&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a biotechnology company that invents and builds platform companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble capital to allow them to take courageous leaps. Those big leaps in human health and sustainability exponentially accelerate scientific progress in areas ranging from cancer detection and treatment to nature-positive agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance biotechnology by uniting life science innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is seeking a&amp;nbsp;&lt;strong&gt;Senior Manager / Associate Director&lt;/strong&gt;&amp;nbsp;to join our dynamic FP&amp;amp;A Team. This position reports to the VP, FP&amp;amp;A and provides unparalleled exposure to senior leaders at Flagship, with significant opportunity for professional growth at Flagship or in the ecosystem companies.&lt;/p&gt;
&lt;p&gt;In this role, you will partner with senior leaders across Flagship’s scientific origination teams (Pioneering Business Units – PBUs), portfolio companies, and Flagship departments. You will contribute to short- and long-term financial projections for portfolio companies during critical fund-raising stages and help with strategic allocation of resources.&lt;/p&gt;
&lt;p&gt;This role is well suited for someone with a proven track record of building and deploying AI-powered dashboards and analytics solutions such as Snowflake and PowerBI. You will leverage AI and modern data platforms to automate, scale, and enhance financial planning, forecasting, and performance monitoring across a complex, multi-entity ecosystem.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support or drive, depending on companies, budgeting, forecasting, long-range planning, and variance analysis across Flagship and/or portfolio company activities&lt;/li&gt;
&lt;li&gt;Drive monthly, quarterly, and annual management reporting packages for leadership.&lt;/li&gt;
&lt;li&gt;Partner with senior finance leaders and cross-functional stakeholders to provide clear, data-driven recommendations&lt;/li&gt;
&lt;li&gt;Build, enhance and maintain AI-based dashboards and finance reporting tools to track KPIs such as cash burn, runway, headcount, capital needs&lt;/li&gt;
&lt;li&gt;Collaborate with the Principals and Associates to convert scientific assumptions into expense and headcount forecast scenarios&lt;/li&gt;
&lt;li&gt;Drive ad hoc analyses related to portfolio performance, investment planning, organizational growth, and operational efficiency.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;7–10+ years of progressive experience in FP&amp;amp;A or Finance&lt;/li&gt;
&lt;li&gt;Proven track record of designing and deploying AI-based dashboards and analytics that improved financial reporting and decision-making.&lt;/li&gt;
&lt;li&gt;Hands-on experience with Snowflake and/or Power BI is a strong plus&lt;/li&gt;
&lt;li&gt;Prior experience in Biotech, MedTech or AgTech required&lt;/li&gt;
&lt;li&gt;Data-driven mindset with exceptional attention to detail&lt;/li&gt;
&lt;li&gt;Communication and stakeholder management skills, ability to work closely with senior leadership&lt;/li&gt;
&lt;li&gt;Bachelor’s degree in Finance, Economics, or a related field; advanced degree is a plus&lt;/li&gt;
&lt;li&gt;Passion for technology and AI, ideally with exposure to high-growth or venture-backed environments&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;Flagship Pioneering and our ecosystem companies are committed to &lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/strong&gt;&lt;/em&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $128,000 - $203,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-managerassociate-director-fpanda-flagship-pioneering/69d3bc5dc8e81216cd0b908c</link><guid isPermaLink="true">http://biotechroles.com/senior-managerassociate-director-fpanda-flagship-pioneering/69d3bc5dc8e81216cd0b908c</guid><pubDate>Mon, 06 Apr 2026 13:59:57 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Drug Metabolism & Pharmacokinetics (DMPK)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;h1&gt;Position Overview&lt;/h1&gt;
&lt;p&gt;We are seeking a motivated and skilled Senior Scientist to join the Nonclinical Development group, contributing to the DMPK function in support of exploratory and IND-enabling programs across Prime Medicine’s pipeline. Reporting to the Associate Director, DMPK/Bioanalytical Sciences, this individual will independently analyze and interpret datasets from &lt;em&gt;in vivo &lt;/em&gt;studies, contribute to nonclinical regulatory documents, and work cross-functionally with pharmacology, translational biology and external CROs, to ensure high-quality DMPK data packages are delivered to support program timelines. The ideal candidate has a strong foundation in &lt;em&gt;in vivo&lt;/em&gt; pharmacokinetics for RNA therapeutics and/or LNP-based delivery systems, thrives in a fast-paced and matrixed organization, and possesses the flexibility and positive attitude needed to make meaningful contributions to the Nonclinical Development team.&lt;/p&gt;
&lt;h1&gt;Primary Responsibilities&lt;/h1&gt;
&lt;ul&gt;
&lt;li&gt;Analyze and interpret PK study data from exploratory and IND-enabling &lt;em&gt;in vivo&lt;/em&gt;&lt;/li&gt;
&lt;li&gt;Perform non-compartmental analysis (NCA) using Phoenix WinNonlin to derive key PK parameters (Cmax, AUC, T½, Vd, CL).&lt;/li&gt;
&lt;li&gt;Leverage expertise in DMPK to provide recommendations for &lt;em&gt;in vivo&lt;/em&gt; study designs in collaboration with pharmacology and key stakeholders.&lt;/li&gt;
&lt;li&gt;Perform bioanalytical assay development (30%) and collaborate with bioanalytical scientists to trouble-shoot challenges during method development to ensure quantitative methods for key analytes (LNP lipid components, mRNA, pegRNA, PD biomarkers) meet regulatory expectations and data quality standards..&lt;/li&gt;
&lt;li&gt;Contribute to nonclinical regulatory documents including pharmacokinetics summaries and nonclinical study reports under the guidance of senior stakeholders in Nonclinical Development.&lt;/li&gt;
&lt;li&gt;Maintain thorough records in the electronic laboratory notebook (ELN); prepare clear data summaries, presentations, and technical memos for program team and governance meetings.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h1&gt;Qualifications&lt;/h1&gt;
&lt;p&gt;&lt;strong&gt;Minimum Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;D. in pharmacokinetics, pharmaceutical sciences, pharmacology, biochemistry, or a related discipline.&lt;/li&gt;
&lt;li&gt;6+ years of cumulative experience. Industry experience (biotech or pharmaceutical) with direct responsibility for &lt;em&gt;in vivo&lt;/em&gt; DMPK study design, execution, and interpretation is required; postdoctoral training in a DMPK or translational pharmacology setting is strongly preferred&lt;/li&gt;
&lt;li&gt;Demonstrated experience with &lt;em&gt;in vivo&lt;/em&gt; PK studies in preclinical models and proficiency in NCA using Phoenix WinNonlin or equivalent software.&lt;/li&gt;
&lt;li&gt;Familiarity with regulatory expectations for nonclinical DMPK assessments and bioanalytical assay development.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to coordinate with external CROs, including scientific guidance, protocol development, and data review..&lt;/li&gt;
&lt;li&gt;Strong written and verbal communication skills; ability to present complex DMPK data clearly to multidisciplinary audiences.&lt;/li&gt;
&lt;li&gt;Highly self-motivated, collaborative, and organized, with the ability to manage multiple priorities independently in a fast-paced matrix environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Familiarity with PK/PD modeling concepts; experience with Phoenix WinNonlin modeling modules a plus.&lt;/li&gt;
&lt;li&gt;Experience with LNP-based delivery systems and/or RNA therapeutics (mRNA, siRNA, ASO, sgRNA or related modalities).&lt;/li&gt;
&lt;li&gt;Experience with exploratory DMPK studies, evaluating new delivery vehicles and evaluation of biodistribution using &lt;em&gt;in vivo&lt;/em&gt;&lt;/li&gt;
&lt;li&gt;Familiarity with bioanalytical platforms supporting DMPK studies, including LC-MS/MS, RT-qPCR/ddPCR, ELISA/MSD.&lt;/li&gt;
&lt;li&gt;Ability and excitement to contribute to the development and success of the Nonclinical Development team.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$145,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$177,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-drug-metabolism-and-pharmacokinetics-(dmpk)-prime-medicine/69d3bc5cc8e81216cd0b908b</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-drug-metabolism-and-pharmacokinetics-(dmpk)-prime-medicine/69d3bc5cc8e81216cd0b908b</guid><pubDate>Mon, 06 Apr 2026 13:59:56 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Machine Learning Engineer / Data Scientist]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;dhkj5-0-0&quot;&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;About ProFound Therapeutics&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound Therapeutics is pioneering the discovery of the expanded human proteome to unlock a new universe of potential therapeutics. By integrating multi-omics, advanced computation, and translational biology, we aim to reveal and characterize thousands of previously uncharted proteins and systematically explore their role in health and disease.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated Senior Machine Learning Engineer / Data Scientist to join our AI/ML team. This individual will play a central role in designing and implementing advanced AI/ML systems with a focus on Retrieval-Augmented Generation (RAG), graph-based RAG, large language models (LLMs), agentic orchestration, and conversational AI (chatbot) solutions. Working closely with the Head of AI/ML and cross-functional partners, you will build and optimize LLM-powered pipelines and multi-agent systems that integrate knowledge graphs, multi-omics data, and biological context to uncover disease-driving proteins and pathways. The insights generated will directly support therapeutic discovery and development.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Architect and implement scalable RAG and LLM-based systems that integrate multi-modal data sources, including knowledge graphs, documents, and structured biological datasets.&lt;/li&gt;
&lt;li&gt;Design and deploy RAG and graph-based RAG pipelines that leverage LLMs and knowledge graphs to retrieve, reason over, and synthesize complex biological information.&lt;/li&gt;
&lt;li&gt;Build and maintain agentic orchestration frameworks (multi-agent systems) that coordinate LLM-based agents for end-to-end scientific reasoning, data retrieval, and decision support.&lt;/li&gt;
&lt;li&gt;Collaborate with data engineering teams to design data pipelines that harmonize and prepare large-scale omics datasets for model training.&lt;/li&gt;
&lt;li&gt;Develop and optimize conversational AI (chatbot) interfaces that enable scientists and stakeholders to query, explore, and interact with internal data and model outputs using natural language.&lt;/li&gt;
&lt;li&gt;Partner with experimental scientists to ensure model outputs are biologically interpretable and experimentally testable.&lt;/li&gt;
&lt;li&gt;Stay abreast of advances in LLMs, RAG architectures, agentic AI, and conversational AI; bring innovative ideas into the team.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Computer Science, Machine Learning, Applied Mathematics, Computational Biology, or related field with 1–3 years of industry experience (preferred); or M.S. in a related field with 4–6 years of industry experience.&lt;/li&gt;
&lt;li&gt;Proven track record in building LLM-based applications, with hands-on expertise in RAG, graph-based RAG, agentic orchestration, and/or chatbot development.&lt;/li&gt;
&lt;li&gt;Proficiency in Python and LLM/ML frameworks such as LangChain, Hugging Face Transformers, PyTorch, or similar.&lt;/li&gt;
&lt;li&gt;Experience working with multi-omics or high-dimensional biological data is a plus but not required.&lt;/li&gt;
&lt;li&gt;Familiarity with probabilistic modeling, causal reasoning, or statistical inference is a plus.&lt;/li&gt;
&lt;li&gt;Strong experience with knowledge graph technologies, graph databases, and vector databases.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to work in cross-disciplinary teams, communicate complex ideas clearly, and deliver results in fast-moving environments.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Why Join Us?&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This role offers a unique opportunity to shape a next-generation AI/ML platform at the intersection of computation and drug discovery. You will work in a collaborative environment with leaders in biology, computation, and therapeutics — helping to expand the boundaries of the proteome and accelerate the development of new medicines for patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $96,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. ProFound Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on ProFound Therapeutics, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-machine-learning-engineer-data-scientist-flagship-pioneering/69d3bc59c8e81216cd0b9088</link><guid isPermaLink="true">http://biotechroles.com/(senior)-machine-learning-engineer-data-scientist-flagship-pioneering/69d3bc59c8e81216cd0b9088</guid><pubDate>Mon, 06 Apr 2026 13:59:52 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Biomarkers]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;We are seeking a Senior Scientist, Biomarkers&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Biomarker Strategy &amp;amp; Scientific Leadership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead fluid biomarker strategy for clinical programs, ensuring alignment with clinical objectives, regulatory expectations, and translational hypotheses.&lt;/li&gt;
&lt;li&gt;Design and oversee development, qualification, and validation of biomarker assays at CROs and external laboratory partners.&lt;/li&gt;
&lt;li&gt;Provide scientific oversight for assay selection, fit-for-purpose validation, and performance monitoring.&lt;/li&gt;
&lt;li&gt;Contribute to clinical protocol development, statistical analysis plans, and regulatory documents (e.g., INDs, briefing books).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Assay Development &amp;amp; Validation&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Direct development and validation/qualification of blood-based and other fluid biomarker assays (e.g., protein, enzymatic, molecular assays).&lt;/li&gt;
&lt;li&gt;Ensure assays are developed under appropriate regulatory frameworks (GLP/GCLP/CLIA as applicable).&lt;/li&gt;
&lt;li&gt;Evaluate assay performance characteristics including sensitivity, specificity, precision, robustness, and stability.&lt;/li&gt;
&lt;li&gt;Troubleshoot assay performance issues and implement corrective actions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Clinical Study Execution&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner closely with clinical operations and sample management teams to ensure seamless biomarker sample collection, handling, and analysis.&lt;/li&gt;
&lt;li&gt;Collaborate with peers responsible for immunogenicity and PK assays to ensure integrated PK/PD and biomarker analysis.&lt;/li&gt;
&lt;li&gt;Oversee data generation timelines, budgets, and vendor performance.&lt;/li&gt;
&lt;li&gt;Lead scientific review and interpretation of biomarker data to support internal decision-making.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Cross-Functional Collaboration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Work closely with Clinical Development, Regulatory, Biostatistics, CMC, and Research teams.&lt;/li&gt;
&lt;li&gt;Contribute to cross-program biomarker governance and best practices.&lt;/li&gt;
&lt;li&gt;Represent the Biomarkers group in cross-functional team meetings and external vendor discussions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Data Analysis &amp;amp; Interpretation&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Perform and/or oversee robust statistical and scientific analysis of biomarker data.&lt;/li&gt;
&lt;li&gt;Integrate biomarker findings with clinical endpoints and PK data.&lt;/li&gt;
&lt;li&gt;Prepare high-quality summaries and presentations for internal governance and external regulatory interactions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Education &amp;amp; Experience&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in Immunology, Molecular Biology, Biochemistry, Translational Medicine, or related discipline with 4+ years of industry experience; or&lt;/li&gt;
&lt;li&gt;MS with 8+ years of relevant industry experience.&lt;/li&gt;
&lt;li&gt;Demonstrated experience supporting clinical-stage programs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Technical Expertise&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong experience in assay development and fit-for-purpose validation (protein, enzymatic, or molecular assays).&lt;/li&gt;
&lt;li&gt;Hands-on experience managing assay development at CROs and external laboratories.&lt;/li&gt;
&lt;li&gt;Deep understanding of GCLP/GLP principles and regulatory expectations for clinical biomarker assays.&lt;/li&gt;
&lt;li&gt;Experience with blood-based biomarker assays required.&lt;/li&gt;
&lt;li&gt;Familiarity with PK/PD concepts and translational biomarker strategy strongly preferred.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Scientific &amp;amp; Analytical Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong data analysis skills and ability to interpret complex biomarker datasets.&lt;/li&gt;
&lt;li&gt;Experience contributing to regulatory submissions (INDs, briefing documents, clinical study reports) preferred.&lt;/li&gt;
&lt;li&gt;Ability to critically evaluate assay performance and scientific rigor.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Leadership &amp;amp; Operational Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrated ability to manage external vendors and timelines.&lt;/li&gt;
&lt;li&gt;Strong time and resource management skills.&lt;/li&gt;
&lt;li&gt;Ability to operate independently while thriving in a collaborative, cross-functional environment.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in rare disease programs.&lt;/li&gt;
&lt;li&gt;Experience with genetic medicine or gene editing platforms.&lt;/li&gt;
&lt;li&gt;Experience supporting first-in-human studies.&lt;/li&gt;
&lt;li&gt;Exposure to multiplexed, LC/MS-based, or advanced molecular biomarker platforms.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$145,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$177,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-biomarkers-prime-medicine/69d3bc57c8e81216cd0b9087</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-biomarkers-prime-medicine/69d3bc57c8e81216cd0b9087</guid><pubDate>Mon, 06 Apr 2026 13:59:51 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$140000-200000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Facilities Manager]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Senior Facilities Manager&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;What if…you could tell the story of an organization that creates, resources, and builds bioplatform companies that invent breakthrough technologies in order to transform human health and sustainability?&lt;/p&gt;
&lt;p&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category bioplatform companies to transform human health and sustainability. Since its launch in 2000, the firm has, through its Flagship Labs unit, applied its unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $130 billion in aggregate value. To date, Flagship has deployed over $2.5 billion in capital toward the founding and growth of its pioneering companies alongside more than $19 billion of follow-on investments from other institutions.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Senior Facilities Manager will oversee maintenance and upkeep of equipment, machinery, general office area and the newly created Flagship Labs Cambridge location.&amp;nbsp; This position will report to the Senior Director, Facilities and GMP Engineering Operations but will communicate with many stakeholders across the organization.&amp;nbsp; They will provide day-to-day support of manufacturing and lab operations by overseeing maintenance tasks under general guidance and will ensure continued compliance to cGXPs. This person will act as the single point of contact from a facilities infrastructure point of view to all Flagship Pioneering tenants within the building. Effective communication will be expected across all organizations and levels with “best in class” being the expectation of service.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Establishes vision for Facilities, providing hands-on leadership and development of team; oversees execution of Facility Operations.&lt;/li&gt;
&lt;li&gt;Effectively develops and leads site services with accountability for execution of site capital projects, process control automation, plant maintenance and site maintenance to enable Flagship Labs operations and other support functions to meet or exceed business expectations in cost, quality, compliance, safety, culture and capital.&lt;/li&gt;
&lt;li&gt;Maintains up to date records for all state, federal, and local licenses and inspections and maintains systems in compliance with local and state regulatory bodies associated with wastewater, sewer, emissions, waste handling/storage and disposal.&lt;/li&gt;
&lt;li&gt;Oversees overall facility and laboratory safety process&lt;/li&gt;
&lt;li&gt;Participates in facility design team meetings, provides visibility to senior management on progress and timelines. Manages general contractor and quality of build.&lt;/li&gt;
&lt;li&gt;Develops, implements, and maintains system/program for cGXP equipment maintenance and calibration; generates and revises SOPs, deviations and change controls associated with Facilities’ systems.&lt;/li&gt;
&lt;li&gt;Manages calibration, preventative and corrective maintenance of all GXP equipment, lab equipment, and building support utilities either directly or indirectly through contractor management; utility systems inclusive of but not limited to compressed gases, HVAC systems, electrical, life safety, and emergency power system (UPS).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Basic Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s Degree is preferred.&lt;/li&gt;
&lt;li&gt;7+ years of experience in a regulated environment, with 5+ years of Facility maintenance or Engineering experience.&lt;/li&gt;
&lt;li&gt;Direct experience maintaining large scale mechanical systems (HVAC/Refrigeration/Vacuum/Compressed Gases).&lt;/li&gt;
&lt;li&gt;Cleanroom Design, Operation and Maintenance is a plus.&lt;/li&gt;
&lt;li&gt;Knowledge of local and state regulatory requirements related to wastewater, emissions, sewer systems, waste handling/storage and disposal.&lt;/li&gt;
&lt;li&gt;Strong technical writing skills; Ability to work independently, with minimal supervision.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $108,000 - $148,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-facilities-manager-flagship-pioneering/69d3bc55c8e81216cd0b9085</link><guid isPermaLink="true">http://biotechroles.com/senior-facilities-manager-flagship-pioneering/69d3bc55c8e81216cd0b9085</guid><pubDate>Mon, 06 Apr 2026 13:59:49 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Laboratory Operations Associate]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;div&gt;&lt;strong&gt;&lt;u data-olk-copy-source=&quot;MailCompose&quot;&gt;Position Summary&lt;/u&gt;&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;We are seeking a highly motivated Senior Laboratory Operations Associate with 3–5 years of hands-on experience supporting high-throughput, high-hazard chemistry, vivarium, and GMP operations. This individual will play a critical role in ensuring the smooth operation of a dynamic laboratory environment. The ideal candidate has a deep understanding of management of high-volume high hazard chemicals, asset management, is adaptable, detail-oriented, and a strong cross-functional communicator with a passion for operational excellence.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;K&lt;u&gt;ey Responsibilities&lt;/u&gt;&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;· Under the guidance of the Senior Laboratory Manager, manage day-to-day operations in high-volume chemistry, biology, animal, and GMP laboratories, including supply management, asset management, chemical inventory, and waste handling.&lt;/div&gt;
&lt;div&gt;· Oversee management and administration of laboratory instrument service agreements, remedial repair, scheduling preventative maintenance, and digital asset management system.&lt;/div&gt;
&lt;div&gt;· Manage relationship with select vendors and suppliers.&lt;/div&gt;
&lt;div&gt;· Oversee the receipt, organization, and distribution of reagents and consumables to support chemistry workflows including 55-gallon drums of virgin chemicals and waste.&lt;/div&gt;
&lt;div&gt;· Ensure appropriate segregation, labeling, storage, and disposal of high-hazard chemicals, including Class A, Class B, water reactive materials, organic acids, inorganic acids, bases, and acutely toxic chemicals.&lt;/div&gt;
&lt;div&gt;· Coordinate with chemists to prepare and dispose of solid-phase resins, solvents, and purification materials in compliance with EHS protocols.&lt;/div&gt;
&lt;div&gt;· Monitor and maintain process systems and chemicals in 780 CMR/International Building Code (IBC) §307 designated High-Hazard Group Occupancy (H3 room).&lt;/div&gt;
&lt;div&gt;· Collaborate with vivarium staff to support animal research workflows, including supply delivery, sanitization cycles, live animal deliveries, and carcass disposal in accordance with 105 CMR 480.000.&lt;/div&gt;
&lt;div&gt;· Support cross-functional workflows between R&amp;amp;D and GMP labs.&lt;/div&gt;
&lt;div&gt;· Ensure documentation, materials movement, and environmental monitoring align with GMP compliance expectations.&lt;/div&gt;
&lt;div&gt;· Other responsibilities as required.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;&lt;u&gt;Qualifications&lt;/u&gt;&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Education &amp;amp; Experience&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;· 3–5 years of direct hands-on experience in laboratory operations within a biotechnology environment.&lt;/div&gt;
&lt;div&gt;· Experience supporting high-hazard chemistry, vivarium operations, GMP manufacturing, and BSL-2 biology labs.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Required Skills &amp;amp; Competencies&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;· Experience working in ISO 5, 7, and 8 cleanroom environments.&lt;/div&gt;
&lt;div&gt;· Experience with ‘just-in-time’ supply chain management, KANBAN, 5S/Lean.&lt;/div&gt;
&lt;div&gt;· Familiarity with lab and facility management systems (e.g., LIMS, CMMS, asset management).&lt;/div&gt;
&lt;div&gt;· Comfortable working in environments requiring strict compliance: H3 occupancy, BSL-2, vivarium, and GMP.&lt;/div&gt;
&lt;div&gt;· Strong organizational and multitasking skills with an ability to work independently.&lt;/div&gt;
&lt;div&gt;· Excellent communication skills, both verbal and written.&lt;/div&gt;
&lt;div&gt;· Familiarity with 527 CMR 1.00, RCRA, EPA, DOT, HAZWOPPER, and IATA regulations.&lt;/div&gt;
&lt;div&gt;&amp;nbsp;&lt;/div&gt;
&lt;div&gt;&lt;strong&gt;Physical Requirements&lt;/strong&gt;&lt;/div&gt;
&lt;div&gt;· Ability to be on-call to receive and respond to alarms within 1 hour.&lt;/div&gt;
&lt;div&gt;· Ability to lift 50lbs, stand for extended periods, and perform repetitive physical tasks.&lt;/div&gt;
&lt;div&gt;· Comfortable working with hazardous materials while wearing appropriate PPE including the Advantage 420 Respirator, Tyvek Full GMP Sterile Coverall, lab coat, and ‘silvershield’ gloves.&lt;/div&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$82,010&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$113,300 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-laboratory-operations-associate-prime-medicine/69d3bc53c8e81216cd0b9084</link><guid isPermaLink="true">http://biotechroles.com/senior-laboratory-operations-associate-prime-medicine/69d3bc53c8e81216cd0b9084</guid><pubDate>Mon, 06 Apr 2026 13:59:47 GMT</pubDate><company>Prime Medicine</company><location>Watertown, MA</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director / Vice President Strategy and Operations, Product and Pipeline Innovation (P&PI)]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;About P&amp;amp;PI (P&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;roduct and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;Pipeline&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;&amp;nbsp;Innovation&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;)&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Product and Pipeline Innovation&amp;nbsp;(P&amp;amp;PI) team at Flagship Pioneering plays a critical role in advancing Flagship’s mission to conceive, create, resource, and grow first-in-category life science companies. P&amp;amp;PI partners closely with platform companies and the broader Flagship ecosystem to&amp;nbsp;develop pipeline strategies and&amp;nbsp;guide&amp;nbsp;indication&amp;nbsp;choices that maximize the value of platforms. The team also&amp;nbsp;leads senior-level R&amp;amp;D governance processes to inform portfolio and asset progression choices across the ecosystem.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;About Flagship Pioneering&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category life science platform companies to transform human health and sustainability. Since its founding in 2000, the firm has originated and fostered over 100 scientific ventures, generating more than&amp;nbsp;$34 billion&amp;nbsp;in aggregate value and conducting over 50 clinical trials for novel therapeutic agents.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Position Summary&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Senior Director / Vice President, P&amp;amp;PI Strategy &amp;amp; Operations,&amp;nbsp;is responsible for&amp;nbsp;building&amp;nbsp;and evolving&amp;nbsp;the frameworks, processes, and tools that support pipeline prioritization,&amp;nbsp;indication&amp;nbsp;selection,&amp;nbsp;and cross-functional execution&amp;nbsp;within P&amp;amp;PI.&amp;nbsp;This individual also contributes directly to pipeline and&amp;nbsp;indication&amp;nbsp;strategy development&amp;nbsp;engagements with platform companies.&amp;nbsp;The Senior Director / Vice President&amp;nbsp;is also responsible for&amp;nbsp;the&amp;nbsp;operational&amp;nbsp;effectiveness&amp;nbsp;of the Product &amp;amp; Partnering Review Committee (PPRC),&amp;nbsp;which&amp;nbsp;informs on&amp;nbsp;portfolio choices and asset progression across the ecosystem of Flagship companies.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;Reporting to the COO, Product &amp;amp; Partnering, the&amp;nbsp;Vice President/Senior Director manages the Associate Director, P&amp;amp;PI Strategy &amp;amp; Operations.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Vice President&amp;nbsp;/&amp;nbsp;Senior Director, P&amp;amp;PI Strategy &amp;amp; Operations, co-leads the design and refinement of P&amp;amp;PI’s operating model in collaboration with&amp;nbsp;the platform companies. This includes clarifying engagement models, decision rights, and interfaces to ensure that portfolio strategy and execution are supported by a clear and durable structure.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Vice President / Senior Director&amp;nbsp;co-leads the development of pipeline and indications strategy frameworks, value frameworks, and related portfolio tools. This includes&amp;nbsp;establishing&amp;nbsp;consistent approaches to&amp;nbsp;indication&amp;nbsp;selection, defining stage-appropriate deliverables (including commercial and financial outputs), and supporting value pool mapping.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;Based on portfolio needs,&amp;nbsp;the&amp;nbsp;Vice President / Senior Director&amp;nbsp;will also directly&amp;nbsp;contribute to the&amp;nbsp;development of pipeline and asset strategies in partnership with our platform companies and the broader P&amp;amp;PI team.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;The role&amp;nbsp;drives&amp;nbsp;the strategy, structure, and effectiveness of the Product &amp;amp; Partnering Review Committee (PPRC). Responsibilities include defining&amp;nbsp;objectives&amp;nbsp;and meeting architecture,&amp;nbsp;facilitating&amp;nbsp;discussions,&amp;nbsp;shaping decision outputs, clarifying expectations for materials and analysis, and ensuring that the forum evolves as portfolio needs&amp;nbsp;change.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Vice President / Senior Director&amp;nbsp;oversees management of the broader P&amp;amp;PI body of work, including initiative tracking, prioritization processes, and execution monitoring. They ensure transparency into commitments and progress, elevate emerging risks or bottlenecks, and support informed decision-making&amp;nbsp;regarding&amp;nbsp;sequencing and focus.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;Minimum Qualifications&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Advanced degree in life sciences (PhD, MD, PharmD, or equivalent).&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;7–10+ years of experience in biopharma strategy, portfolio management, R&amp;amp;D strategy, or corporate development.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience as a&amp;nbsp;Principal or Project leader&amp;nbsp;(or equivalent role) at BCG, McKinsey, Bain,&amp;nbsp;Clearview,&amp;nbsp;or another top-tier strategy consulting firm, with&amp;nbsp;demonstrated&amp;nbsp;ability to lead complex engagements&amp;nbsp;particularly&amp;nbsp;in the area of&amp;nbsp;indication&amp;nbsp;strategy development&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Demonstrated ability to structure ambiguous problems, build analytical frameworks, and translate insights into actionable strategic recommendations.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Exercises leadership gravitas and adept at cross-functional&amp;nbsp;collaboratio&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:276,&amp;quot;335559991&amp;quot;:360}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven&amp;nbsp;organizational&amp;nbsp;skills with&amp;nbsp;and&amp;nbsp;ability to&amp;nbsp;manage&amp;nbsp;complex workflows in a fast-paced, evolving environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:276,&amp;quot;335559991&amp;quot;:360}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;10&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;High degree of professionalism, discretion, and accountability.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:1,&amp;quot;335551620&amp;quot;:1,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559737&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:276,&amp;quot;335559991&amp;quot;:360}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;Values and Behaviors&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;11&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Entrepreneurial spirit and mission-oriented toward enabling breakthrough innovation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;11&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Courage to take initiative and drive improvements across teams and processes&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;11&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborative mindset with strong interpersonal and communication skills.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;11&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Commitment to fostering a growth-oriented, high-energy environment.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;11&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559683&amp;quot;:0,&amp;quot;335559684&amp;quot;:-2,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Accountability for high-quality execution and follow-through.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 2&quot;&gt;What We Offer&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134245418&amp;quot;:true,&amp;quot;134245529&amp;quot;:true,&amp;quot;335559738&amp;quot;:200,&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt; Impactful role in a company recognized for transformative contributions to human health and sustainability.&lt;/span&gt;&lt;br&gt;&lt;span data-contrast=&quot;auto&quot;&gt;• Dynamic culture with inspiring colleagues and leaders.&lt;/span&gt;&lt;br&gt;&lt;span data-contrast=&quot;auto&quot;&gt;• Support for professional development and growth in an innovative environment.&lt;/span&gt;&amp;nbsp;&lt;br&gt;&lt;span data-contrast=&quot;auto&quot;&gt;• Comprehensive employee benefits and rewards program.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;br&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TD1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $204,000 - $330,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-director-vice-president-strategy-and-operations-product-and-pipeline-innovation-(pandpi)-flagship-pioneering/69d3bc50c8e81216cd0b9082</link><guid isPermaLink="true">http://biotechroles.com/senior-director-vice-president-strategy-and-operations-product-and-pipeline-innovation-(pandpi)-flagship-pioneering/69d3bc50c8e81216cd0b9082</guid><pubDate>Mon, 06 Apr 2026 13:59:44 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$250000-450000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Quality Assurance – Clinical and Nonclinical Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Position Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span class=&quot;TextRun SCXW5840292 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;Prime&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;Medicine&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;is seeking a&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;Quality Assurance (QA)&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;Director&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;to serve as the company’s primary&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;quality assurance expert across both&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;clinical&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;and nonclinical programs&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;. This&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;role&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;will&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;partner strategically&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;with&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;Clinical&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;Development&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;and Nonclinical functions&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;to&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;establish&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;and maintain&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;pragmatic, risk-based quality frameworks&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;that ensure regulatory compliance and data integrity from early development through clinical execution&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;. The ideal candidate brings hands&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;-&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;on&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;QA&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;experience&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;in&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;gene&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;therap&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;y&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;modalities and&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;a track record&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;of sound judgment, collaborative decision&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;making, and effective partnership with cross&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW5840292 BCX8&quot;&gt;functional teams.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP SCXW5840292 BCX8&quot; data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The ideal candidate will be onsite 2-3 days a week in Watertown, MA.&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Quality Strategy &amp;amp; Governance&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Evolve and deliver the clinical and nonclinical quality strategy for Prime Medicine, embedding ICH E6(R3) and ICH M3(R2)/OECD principles from first-in-human through pivotal stages. &amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Establish and maintain systems and processes (including SOP development) to improve the quality and compliance of both clinical and nonclinical studies, providing oversight and support to CRO GLP studies and internal non-GLP study activities in both the United States and Rest of World (ROW).&amp;nbsp; &lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Partner tightly with Nonclinical, Clinical Operations, CMC, and Regulatory teams to make risk&lt;span data-contrast=&quot;auto&quot;&gt;‑&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;balanced, time&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;‑&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;bound decisions that protect subjects and program timelines.&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Maintain and advance the phase&lt;span data-contrast=&quot;auto&quot;&gt;‑&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;appropriate Quality Management System (QMS) for GCP, applying proportionality to indication, phase, and patient risk. Provide input to and perform reviews of Deviation, CAPA, and Change Management records.&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Ensure data capture, management and analysis is fit for purpose, including audit trail reviews and software assurance approaches to satisfy 21 CFR Part 11/EU Annex 11 compliance requirements.&amp;nbsp; &lt;span data-ccp-props=&quot;{&amp;quot;469777462&amp;quot;:[360],&amp;quot;469777927&amp;quot;:[0],&amp;quot;469777928&amp;quot;:[0]}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Support or lead QA audits and inspections of clinical and nonclinical sites, vendors and studies, ensuring appropriate follow-up and CAPA closure. Contribute to the authoring, review, and revision of SOPs, templates, and procedural documents related to GLP and GCP activities.&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Nonclinical Study Oversight&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure nonclinical study protocols are reviewed and approved on time, and that deviations from approved protocols are properly documented, evaluated, and reported. Implement systems and workflows to ensure that data in study reports are accurate, complete, and traceable through the ELN to raw data and animal subjects where applicable.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Confirm that bioanalytical method qualification and validation studies are conducted in accordance with internal SOPs, ICH M10, and other applicable regulatory guidance. Review bioanalytical method reports for clarity, traceability, and data integrity from source data through final report.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Serve as the quality assurance liaison to CROs conducting GLP studies, providing compliance oversight to ensure adherence to 21 CFR Part 58 and OECD GLP requirements.&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Clinical Study Oversight&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Lead implementation of ICH E6(R3) principles by integrating quality-by-design and Critical-to-Quality (CtQ) factors into study planning, execution, and monitoring. Conduct proportionate risk assessments and maintain defined Quality Tolerance Limits (QTLs) as appropriate to ensure participant safety and data reliability.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Partner with CMC teams as needed to ensure ATMP GMP standards are maintained in accordance with the trial protocol, pharmacy manual(s) and related documents;&amp;nbsp; use manufacturing quality knowledge (e.g., process validation) to support comparability assessments for clinical impact.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Review critical study documents (e.g. clinical protocols, ICFs, monitoring plans, and other essential documents) to ensure compliance with applicable regulations, SOPs, and GCP guidelines.&amp;nbsp;&amp;nbsp;&amp;nbsp; Ensure the maintenance of all QA documentation in the QMS and TMF, if&amp;nbsp; applicable.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Apply a risk-based oversight model that tailors monitoring, deviation management, and data governance to identified risks; ensure timely risk review, communication, and documentation of key quality issues and remedial actions.&amp;nbsp; &lt;span data-ccp-props=&quot;{&amp;quot;469777462&amp;quot;:[360],&amp;quot;469777927&amp;quot;:[0],&amp;quot;469777928&amp;quot;:[0]}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Partner with study teams on vendor selection/qualification; conduct audits, maintain the audit schedule, establish Quality Agreements and provide ongoing oversight of vendor performance. Provide coaching and just-in-time training to study teams and sites on product-specific GCP expectations. &lt;span data-ccp-props=&quot;{&amp;quot;469777462&amp;quot;:[360],&amp;quot;469777927&amp;quot;:[0],&amp;quot;469777928&amp;quot;:[0]}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Receive, investigate, and escalate reports of potential scientific misconduct or serious breaches, ensuring appropriate root&lt;span data-contrast=&quot;auto&quot;&gt;‑&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;cause analysis, documentation, and regulatory reporting.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:360,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;Lead inspection readiness efforts as required.&amp;nbsp; Chair/participate in mock inspections and interview training; storyboard key risks/issues and dossier positions; lead remediation sprints on identified gaps. &lt;span data-ccp-props=&quot;{&amp;quot;469777462&amp;quot;:[360],&amp;quot;469777927&amp;quot;:[0],&amp;quot;469777928&amp;quot;:[0]}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Required Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;10+ years in GCP/Clinical Quality Assurance, including 5+ years in cell &amp;amp; gene therapy; direct experience in gene editing modalities strongly preferred.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Demonstrated success as a primary or sole QA lead supporting early-phase clinical and nonclinical programs.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Deep, current knowledge of ICH E6 (R3), ICH M10, OECD GLP, and FDA/EMA expectations for CGT/ATMPs; practical experience bridging GCP–GLP–GMP interfaces.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Proven decision quality under uncertainty and ability to influence program-level tradeoffs while maintaining compliance and scientific integrity.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Hands-on leadership of audits (CROs, sites, specialty vendors, bioanalytical labs) and inspection readiness with successful outcomes.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Excellent written and verbal communication; clear, concise reporting and executive level briefings.&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;10&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience implementing RBQM, QTLs, and data driven quality metrics in CGT studies.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;10&quot; data-aria-level=&quot;1&quot;&gt;ASQ CQA or equivalent auditor certification.&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$207,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$253,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-quality-assurance-clinical-and-nonclinical-development-prime-medicine/69d3bc4dc8e81216cd0b9081</link><guid isPermaLink="true">http://biotechroles.com/director-quality-assurance-clinical-and-nonclinical-development-prime-medicine/69d3bc4dc8e81216cd0b9081</guid><pubDate>Mon, 06 Apr 2026 13:59:41 GMT</pubDate><company>Prime Medicine</company><location>Watertown, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Pharmacology and Toxicology]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases.&lt;/p&gt;
&lt;p&gt;FL87, Inc was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly experienced nonclinical toxicologist with deep expertise in lipid nanoparticles (LNPs) and nucleic acid therapeutics. The successful candidate will be responsible for leading and executing nonclinical safety strategies across discovery and development programs, and work in a dynamic and fast-paced entrepreneurial environment as part of a highly collaborative team.&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the nonclinical safety lead for lipid nanoparticle (LNP) and nucleic acid–based therapeutic programs from discovery through IND-enabling and early clinical development&lt;/li&gt;
&lt;li&gt;Design, execute, interpret, and report non-GLP and GLP toxicology and safety pharmacology studies, including but not limited to repeat-dose toxicity, local tolerance, immunotoxicity, cytokine release, complement activation, histopathology, and biodistribution&lt;/li&gt;
&lt;li&gt;Oversee, design and direct toxicology, bioanalytical, and biodistribution studies at CROs; conduct site visits for NHP studies and ensuring timely completion of end points and study reports&lt;/li&gt;
&lt;li&gt;Act as the primary nonclinical safety representative on cross-functional teams, providing clear scientific judgment to guide program decisions balancing speed, scientific rigor, and regulatory expectations in a startup environment&lt;/li&gt;
&lt;li&gt;Anticipate, assess, and mitigate modality- and platform-specific safety risks related to LNP delivery of nucleic acid cargoes&lt;/li&gt;
&lt;li&gt;Partner with internal and external study leads to ensure studies are executed with high quality, appropriate timelines, and regulatory compliance&lt;/li&gt;
&lt;li&gt;Review and approve study protocols, amendments, and final reports; ensure submission-ready documentation. Lead authorship of nonclinical sections for regulatory documents&lt;/li&gt;
&lt;li&gt;Integrate nonclinical safety data with PK/PD, biodistribution, and translational findings to support dose selection and clinical starting dose rationale&lt;/li&gt;
&lt;li&gt;Represent the company in interactions with regulatory agencies including FDA and EMA Clearly communicate safety risks, uncertainties, and mitigation strategies to project teams and senior leadership&lt;/li&gt;
&lt;li&gt;Prepare and deliver concise written and verbal summaries to support go/no-go and investment decisions&lt;/li&gt;
&lt;li&gt;Mentor and manage junior pharmacology and bioanalytical scientists and establish platform level safety principles and best practices for non-viral nucleic acid therapeutics&lt;/li&gt;
&lt;li&gt;Operate effectively in a fast-paced, resource-constrained, and highly collaborative startup environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in pharmacology, toxicology, DVM or a related field with at least 10 years of industry experience&lt;/li&gt;
&lt;li&gt;Deep expertise in non-viral delivery platforms including LNPs, nucleic acid therapeutics, with strong knowledge of immunogenicity and biodistribution&lt;/li&gt;
&lt;li&gt;Direct experience supporting FDA regulatory submissions and agency meetings&lt;/li&gt;
&lt;li&gt;Strong written and verbal communication skills with the ability to influence cross-functionally&lt;/li&gt;
&lt;li&gt;Proven track record of project management and mentorship skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $213,000 - $280,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-director-pharmacology-and-toxicology-flagship-pioneering/69d3bc4cc8e81216cd0b907e</link><guid isPermaLink="true">http://biotechroles.com/senior-director-pharmacology-and-toxicology-flagship-pioneering/69d3bc4cc8e81216cd0b907e</guid><pubDate>Mon, 06 Apr 2026 13:59:40 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Director, People and Culture Business Partner]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Director, People and Culture Business Partner&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Location:&lt;/strong&gt; Cambridge and Watertown, MA (between two sites at least 3 days a week)&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Reports To:&lt;/strong&gt; VP, Senior People and Culture Business Partner&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Who We Are&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;At Prime Medicine, we&#39;re not just editing genes — we&#39;re rewriting what&#39;s possible for patients living with debilitating genetic diseases. Built on the groundbreaking Prime Editing platform, a next-generation &quot;search and replace&quot; technology, we are on a mission to deliver potentially curative therapies to patients who have waited long enough.&lt;/p&gt;
&lt;p&gt;Our team of scientists, engineers, and operators is intensely curious, deeply collaborative, and united by a shared belief: that the right science, paired with the right people, can change the course of disease. We move fast, think boldly, and take our work seriously — while making sure we enjoy the journey together.&lt;/p&gt;
&lt;p&gt;This is a pivotal moment for Prime Medicine. We are focused, energized, and building toward breakthroughs that matter. If you want to do the most meaningful work of your career alongside people who feel the same, you&#39;ve found your place.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Opportunity&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a &lt;strong&gt;Director, People and Culture Business Partner&lt;/strong&gt; — a passionate, people-first HR professional who is as comfortable shaping culture as they are rolling up their sleeves on the operational fundamentals that keep a growing biotech humming.&lt;/p&gt;
&lt;p&gt;Reporting to the VP, Senior People and Culture Business Partner, you&#39;ll be a trusted partner to Prime&#39;s management and employees alike - someone who connects deeply with the business, champions our culture, and helps ensure our people strategy keeps pace with our science. At Prime, People &amp;amp; Culture is a strategic driver of our mission.&lt;/p&gt;
&lt;p&gt;This role is for someone who works hard, has fun, and genuinely believes that great organizations are built one person, one team, and one conversation at a time.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;What You&#39;ll Do&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Be a Culture Champion&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Show up as the heart of our employee experience — approachable, credible, and genuinely invested in the people you work with.&lt;/li&gt;
&lt;li&gt;Partner with managers and employees to reinforce and evolve Prime&#39;s culture and values as the company grows.&lt;/li&gt;
&lt;li&gt;Support employee engagement initiatives and translate listening efforts (surveys, conversations, data) into meaningful action.&lt;/li&gt;
&lt;li&gt;Help to continue to make Prime the kind of place where brilliant people do their best, most fulfilling work.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Drive Talent Strategy&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Identify development opportunities that deepen our talent bench and build organizational capability for the long term.&lt;/li&gt;
&lt;li&gt;Support creative career pathing efforts and employee development programs that reflect Prime&#39;s startup spirit and scientific ambition.&lt;/li&gt;
&lt;li&gt;Serve as a true Talent Ambassador — someone employees, management, external vendors and candidates are excited to engage with.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Partner Strategically with the Business&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner closely with management to drive organizational effectiveness, workforce planning, and thoughtful change management.&lt;/li&gt;
&lt;li&gt;Translate Prime&#39;s evolving business priorities and values into people strategies that create real impact.&lt;/li&gt;
&lt;li&gt;Lead organizational design efforts and guide teams through change with clarity and care.&lt;/li&gt;
&lt;li&gt;Provide counsel that&#39;s both candid and compassionate on employee relations and management challenges.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Execute with Excellence&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure flawless execution of core HR cycles: administration, compensation planning, promotions, talent mobility, headcount planning, recruitment, and workforce planning.&lt;/li&gt;
&lt;li&gt;Partner with Total Rewards to navigate compensation cycles effectively and equitably.&lt;/li&gt;
&lt;li&gt;Contribute to policy development and evolving compliance needs as Prime scales — with a pragmatic, startup-savvy lens.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What You Bring&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;An advanced degree in Human Resources, Business, Life Sciences, or a related field.&lt;/li&gt;
&lt;li&gt;10–12+ years of progressive HR experience, with significant HRBP experience supporting managers and employees.&lt;/li&gt;
&lt;li&gt;Deep experience in biotechnology, pharmaceuticals, or life sciences — you understand the cadence, culture, and complexity of science-driven organizations.&lt;/li&gt;
&lt;li&gt;A startup mentality with an operator&#39;s mindset: you know when to build from scratch, when to borrow a best practice, and when to just get it done.&lt;/li&gt;
&lt;li&gt;Demonstrated success juggling multiple priorities in a fast-moving environment without losing sight of the details or the people.&lt;/li&gt;
&lt;li&gt;Strong business acumen and executive presence — you influence at all levels, and people trust your judgment.&lt;/li&gt;
&lt;li&gt;A high tolerance for ambiguity, a bias toward action, and a track record of driving measurable outcomes.&lt;/li&gt;
&lt;li&gt;You work hard, have fun, and make the team around you better.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Why Prime Medicine&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Mission that matters:&lt;/strong&gt; Every program we advance has the potential to change — or save — a life. You&#39;ll feel that every day.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;A team you&#39;ll love:&lt;/strong&gt; brilliant, humble, fun people who take the science seriously&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;A pivotal moment:&lt;/strong&gt; Prime is a focused, forward-moving company with a clear path and bold ambitions. You&#39;ll help shape what comes next.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Cambridge at its best:&lt;/strong&gt; Sit at the epicenter of the world&#39;s most dynamic biotech ecosystem.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;A seat at the table:&lt;/strong&gt; People and Culture is a strategic partner here. Your voice will be heard and your impact will be real.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Prime Medicine is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment where all employees can thrive.&lt;/em&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).&lt;/p&gt;
&lt;p&gt;Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.&lt;/p&gt;
&lt;p&gt;Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$180,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-people-and-culture-business-partner-prime-medicine/69d3bc4ac8e81216cd0b907d</link><guid isPermaLink="true">http://biotechroles.com/director-people-and-culture-business-partner-prime-medicine/69d3bc4ac8e81216cd0b907d</guid><pubDate>Mon, 06 Apr 2026 13:59:38 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA/Watertown, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Head of Biology]]></title><description><![CDATA[&lt;h3&gt;Role Overview&lt;/h3&gt;
&lt;p&gt;Vesalius is seeking a Senior/Executive Director-level Head of Biology to lead biological strategy and target validation across our causality-driven discovery platform. This role is responsible for translating human genetic evidence (including GWAS, rare variants, Mendelian randomization, and functional genomics) into rigorous, disease-relevant biological validation and for shaping preclinical programs across multiple therapeutic areas.&lt;br&gt;&lt;br&gt;The ideal candidate brings deep target validation expertise across therapeutic modalities and disease areas, with particular strength in neurodegeneration (including Parkinson’s disease), genomic perturbation tools, and the ability to contribute meaningfully to cardiovascular and immune-mediated biology. You will build and mentor a high-caliber biology team, establish standards for scientific rigor and decision-quality, and partner closely with data science, chemistry, and platform operations to advance targets toward development readiness.&lt;/p&gt;
&lt;h3&gt;Key Responsibilities&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Own Vesalius’s biological validation strategy from human genetics to disease-relevant cellular phenotypes and translational readouts.&lt;/li&gt;
&lt;li&gt;Translate genetic and functional genomics evidence into testable hypotheses, crisp experimental plans, and clear go/no-go decision points.&lt;/li&gt;
&lt;li&gt;Serve as research project lead for preclinical drug discovery programs (early through established preclinical stages), driving timelines, data quality, and scientific narrative.&lt;/li&gt;
&lt;li&gt;Lead target validation across multiple modalities (small molecules, biologics, oligonucleotides, and emerging modalities), with a modality-agnostic mindset.&lt;/li&gt;
&lt;li&gt;Provide subject-matter leadership in Parkinson’s disease and other neurodegenerative disorders, including immune/neuroinflammatory mechanisms and CNS-relevant cell type dysregulation.&lt;/li&gt;
&lt;li&gt;Oversee design, execution, and interpretation of iPSC-derived and other human-relevant phenotypic assays, including assay development, functional readouts, and orthogonal validation.&lt;/li&gt;
&lt;li&gt;Lead and mentor scientists focused on cell model development and biology enabling capabilities; manage direct reports and coordinate matrixed teams across programs.&lt;/li&gt;
&lt;li&gt;Establish standards for experimental rigor, reproducibility, and data interpretation; drive documentation and best practices to support portfolio prioritization and target nomination.&lt;/li&gt;
&lt;li&gt;Design and manage experiments executed with external partners (CROs and collaborators), including study design, oversight, and troubleshooting.&lt;/li&gt;
&lt;li&gt;Partner closely with data scientists and other subject matter experts to integrate multi-omic datasets with biology, enabling rapid learning cycles and high-quality decisions.&lt;/li&gt;
&lt;li&gt;Collaborate with internal tissue and cell model experts to support target validation and ongoing discovery programs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;Qualifications&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;PhD (or MD/PhD) in neuroscience, biology, immunology, genetics, or related field; or MS/BS with commensurate industry experience.&lt;/li&gt;
&lt;li&gt;10+ years of relevant experience (industry and/or advanced academic), including leadership roles in target validation and assay/model development.&lt;/li&gt;
&lt;li&gt;Demonstrated success validating targets and progressing programs through a preclinical therapeutic pipeline.&lt;/li&gt;
&lt;li&gt;Demonstrated experience in using molecular genomic tools (e.g. genome engineering, RNAi) to interrogate biological systems.&lt;/li&gt;
&lt;li&gt;Proven experience working across multiple therapeutic areas, with emphasis on neurodegeneration and meaningful exposure to cardiovascular and immune biology.&lt;/li&gt;
&lt;li&gt;Deep expertise in human-relevant in vitro systems (e.g., iPSC-derived models), cell culture, molecular biology, genetic manipulation, and functional assay development.&lt;/li&gt;
&lt;li&gt;Track record of impactful scientific contributions (e.g., publications, patents, or delivered programs) and strong scientific judgment.&lt;/li&gt;
&lt;li&gt;Experience leading and mentoring teams, including direct people management and matrix leadership across functions.&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills, including the ability to synthesize complex datasets into clear recommendations for senior stakeholders.&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;Preferred Experience&lt;/h3&gt;
&lt;ul&gt;
&lt;li&gt;Hands-on experience with neuroinflammation/immunology and CNS-relevant cell types (e.g., microglia, astrocytes, neurons, oligodendrocytes).&lt;/li&gt;
&lt;li&gt;Experience designing studies with external CROs and managing vendor relationships for complex assay execution.&lt;/li&gt;
&lt;li&gt;Experience building biology capabilities within a platform or biotech environment and setting organization-wide standards.&lt;/li&gt;
&lt;li&gt;Comfort operating in a fast-paced, ambiguity-tolerant environment with a bias toward action and learning.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $213,000 - $280,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Vesalius Therapeutics currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Vesalius Therapeutics&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-director-head-of-biology-flagship-pioneering/69d3bc48c8e81216cd0b907b</link><guid isPermaLink="true">http://biotechroles.com/senior-director-head-of-biology-flagship-pioneering/69d3bc48c8e81216cd0b907b</guid><pubDate>Mon, 06 Apr 2026 13:59:36 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$280000-420000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Regulatory Affairs]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;(Fall 2025 Cycle: July-Dec 2026)&lt;/p&gt;
&lt;p&gt;Co-Op Assignment Overview&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a co-op for the Fall 2026 semester with experience and/or knowledge in natural science such as Biology, Chemistry or other biotech-related disciplines to join the Regulatory Affairs team. The Prime Medicine Regulatory Affairs team is a tight-knit, closely collaborative, highly creative group working to make the promise of Prime Editing a reality for patients with severe genetic diseases. The qualified candidate will be highly motivated, analytical and collegial. The candidate will support the Regulatory Affairs team in ensuring compliance with relevant regulations and guidelines relevant to the company&#39;s gene editing pipeline programs for patients with genetic diseases. You will assist in researching, interpreting, and implementing regulatory requirements, as well as providing administrative support for regulatory submissions and documentation.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Primary Responsibilities:&lt;/p&gt;
&lt;p&gt;· Conduct research on regulatory requirements pertinent to the company&#39;s product pipeline. Stay updated on changes in regulations and guidelines affecting the industry.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Assist in maintaining regulatory documentation, spreadsheets, and trackers related to the compilation of required inputs for regulatory submissions. Ensure all documents and trackers are organized and up to date.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Support the preparation, compilation, and submission of regulatory documents to FDA and ex-US regulatory agencies. This may include applications for regulatory agency meetings, drug designations, and/or investigational new drug applications.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Assist in monitoring compliance of clinical-stage development programs with regulatory requirements and adherence to regulations.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Cross-functional collaboration with other departments, such as R&amp;amp;D, preclinical, and clinical teams to gather information and help ensure regulatory compliance in product development, testing, and regulatory submission packages.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Assist in preparing regulatory reports and responses to regulatory inquiries.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Participate in training sessions and educational programs to enhance understanding of regulatory requirements and processes.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;· Undertake additional ad-hoc tasks and projects as assigned by the Regulatory Affairs team to support departmental objectives and business needs.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Qualifications:&lt;/p&gt;
&lt;p&gt;· Currently enrolled in a Bachelor&#39;s or Master&#39;s degree program in a relevant field such as Regulatory Affairs, Life Sciences, Pharmacy, Biology, or a related discipline.&lt;/p&gt;
&lt;p&gt;· Strong attention to detail and organizational skills.&lt;/p&gt;
&lt;p&gt;· Excellent analytical, written and verbal communication skills.&lt;/p&gt;
&lt;p&gt;· Ability to work independently and collaboratively in a team environment.&lt;/p&gt;
&lt;p&gt;· Proficiency in Microsoft Office suite (Word, Excel, PowerPoint).&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Preferred Qualifications (but not required):&lt;/p&gt;
&lt;p&gt;· Prior experience, course work, and/or certification in regulatory affairs.&lt;/p&gt;
&lt;p&gt;· Familiarity with medical terminology.&lt;/p&gt;
&lt;p&gt;· Basic understanding of cellular and molecular biology underlying gene therapy.&lt;/p&gt;
&lt;p&gt;· Familiarity with document management systems and spreadsheets (Smartsheet, Excel, etc.).&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;U.S. Pay Range&lt;/p&gt;
&lt;p&gt;$23-$33 USD&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-regulatory-affairs-prime-medicine/69d3bc47c8e81216cd0b9079</link><guid isPermaLink="true">http://biotechroles.com/co-op:-regulatory-affairs-prime-medicine/69d3bc47c8e81216cd0b9079</guid><pubDate>Mon, 06 Apr 2026 13:59:34 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-50000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Director, Data Platform Product Manager]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;About Pioneering Intelligence&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;What if... we could harness science, data, and AI to create breakthroughs and accelerate the creation of new technologies?&lt;/p&gt;
&lt;p&gt;This is the question that Pioneering Intelligence, Flagship Pioneering&#39;s in-house AI initiative, seeks to explore. Joining together cutting edge-research and digital sciences, Pioneering Intelligence is dedicated to developing AI/ML-powered platforms for transformative applications in human health, sustainability and beyond. Pioneering Intelligence builds on Flagship’s legacy of founding companies at the forefront of AI, driving advances across the ecosystem, fueling Flagship’s creation of breakthrough innovations, and pushing the boundaries of the field.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We are a team of computational scientists and engineers from a variety of backgrounds, including applied math, nuclear physics, engineering,&amp;nbsp;and computational biology. We bring together diverse skillsets to draw on the vast reservoir of knowledge from across the scientific spectrum and&amp;nbsp;encourage our team to think beyond what is traditionally accepted in the field of computation.&lt;/p&gt;
&lt;p&gt;We are building a next generation digital foundation that integrates computational science, AI/ML, knowledge engineering, data platforms, and workflow automation. These capabilities support Flagship’s model of exploring the unknown and translating scientific insight into world-changing companies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Flagship Data Platform is a shared data platform that helps Flagship companies move faster by providing secure, well-governed access to trusted data across the portfolio&lt;/p&gt;
&lt;p&gt;As (Senior) Director, Product Manager for the Data Platform, you will own the product strategy, roadmap, and execution from early use cases through scaled adoption. You will work closely with software and ML engineers, UX, scientists, and senior stakeholders across multiple companies to turn ambiguous, high value opportunities into clear, high impact products that accelerate science and decision making.&lt;/p&gt;
&lt;p&gt;You are comfortable operating in a dynamic, highly interdisciplinary environment and can move fluidly between strategy, discovery, and hands-on execution.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Own the end-to-end product vision and roadmap, setting metrics and priorities to maximize impact&lt;/li&gt;
&lt;li&gt;Rapidly drive product discovery, from user research and problem framing to prototyping and validation&lt;/li&gt;
&lt;li&gt;Align priorities with an empowered technical lead&lt;/li&gt;
&lt;li&gt;Use product analytics, qualitative feedback, and experimentation to inform decisions&lt;/li&gt;
&lt;li&gt;Align and communicate results to stakeholders&lt;/li&gt;
&lt;li&gt;Define and use metrics to ensure engagement and user value&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;7+ years product management experience with end-to-end ownership&lt;/li&gt;
&lt;li&gt;Experience building data platforms, APIs, or infrastructure-adjacent products&lt;/li&gt;
&lt;li&gt;Strong understanding of data architectures, pipelines, and governed access&lt;/li&gt;
&lt;li&gt;Proven ability to ship iteratively using product analytics and user research&lt;/li&gt;
&lt;li&gt;Deep skill in discovery, prioritization, and problem framing under ambiguity&lt;/li&gt;
&lt;li&gt;Experience applying LLMs or agentic systems to product definition and prototyping&lt;/li&gt;
&lt;li&gt;Effective collaborator across engineering, science, UX, and ML teams&lt;/li&gt;
&lt;li&gt;Leads through influence and communicates clearly with senior stakeholders&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Experience&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in biotech, computational biology, drug discovery, or scientific software.&lt;/li&gt;
&lt;li&gt;Experience taking products from 0→1 and then scaling them through high growth phases.&lt;/li&gt;
&lt;li&gt;Experience in startup, innovation-intensive, or venture/incubator environments, or in building new product lines inside larger organizations.&lt;/li&gt;
&lt;li&gt;Hands-on experience working with AI/ML, data platforms, or developer/platform products.&lt;/li&gt;
&lt;li&gt;Strength in customer discovery, storytelling, and translating complex technical or scientific concepts for varied audiences.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Near Term Objectives and Outcomes&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;In the first 6–12 months, success looks like:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;The Data Platform is an AI-native platform that delivers clear, differentiated value to teams across the Flagship portfolio.&lt;/li&gt;
&lt;li&gt;The platform integrates proprietary agentic AI systems&lt;/li&gt;
&lt;li&gt;Product priorities are consistently aligned to real usage, governance requirements, and demand, resulting in predictable delivery and measurable adoption&lt;/li&gt;
&lt;li&gt;Product success is measured and managed through a shared, user-centered operating model with PI leadership and key sponsors.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship https://url.us.m.mimecastprotect.com/s/xLXBCqxk3LTk9pwcZf3CEkjif?domain=flagshippioneering.com.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $175,000 - $275,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-director-data-platform-product-manager-flagship-pioneering/69d3bc45c8e81216cd0b9078</link><guid isPermaLink="true">http://biotechroles.com/(senior)-director-data-platform-product-manager-flagship-pioneering/69d3bc45c8e81216cd0b9078</guid><pubDate>Mon, 06 Apr 2026 13:59:33 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Quality Control]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;h1&gt;Fall 2026 Co-op: Quality Control&lt;/h1&gt;
&lt;h2&gt;Co-Op Assignment Overview&lt;/h2&gt;
&lt;p&gt;Prime Medicine is seeking a co-op for the Fall 2026 semester with experience in biological and/or chemical techniques to join the Analytical Development and Quality Control (QC) team. The candidate will gain hands-on experience supporting analytical testing for gene therapy programs, including prime editing components, drug substances, and drug products.&lt;/p&gt;
&lt;p&gt;This co-op will learn cutting-edge analytical technologies, develop an understanding of scientific and regulatory requirements for phase-appropriate analytical testing, and contribute to solving complex technical challenges related to prime editing programs. This is a unique opportunity to directly support the advancement of transformative genetic medicines toward the clinic.&lt;/p&gt;
&lt;p&gt;We are looking for curious problem solvers who enjoy working collaboratively, thrive in a fast-paced environment, and are passionate about advancing genetic editing technologies to improve human health.&lt;/p&gt;
&lt;h2&gt;Primary Responsibilities&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Support product development sample analyses, in-process, release, and stability testing for LNP-based drug products, prime editing component RNAs, and cell-based drug products.&lt;/li&gt;
&lt;li&gt;Execute and support cell-based analytical activities.&lt;/li&gt;
&lt;li&gt;Perform cell-based potency, viability, conduct cell counting.&lt;/li&gt;
&lt;li&gt;Assist with optimization, troubleshooting, validation, and qualification of analytical methods.&lt;/li&gt;
&lt;li&gt;Participate in stability and reference standard programs including protocol/report preparation, data compilation, trending, and analysis.&lt;/li&gt;
&lt;li&gt;Assist with sample management and chain-of-custody documentation.&lt;/li&gt;
&lt;li&gt;Conduct clean room laboratory environmental monitoring for GMP manufacturing suites.&lt;/li&gt;
&lt;li&gt;Document and communicate experimental data in electronic notebooks and quality systems in accordance with cGMP requirements.&lt;/li&gt;
&lt;li&gt;Collaborate cross-functionally with Analytical Development, Manufacturing, MSAT, and Program Teams to support product and method development and qualification/validation.&lt;/li&gt;
&lt;li&gt;Contribute to laboratory functionality, safety compliance, and QC process optimization.&lt;/li&gt;
&lt;li&gt;Identify opportunities for assay optimization, workflow improvements, and automation.&lt;/li&gt;
&lt;li&gt;Demonstrate flexibility in supporting new projects, troubleshooting activities, and evolving program priorities.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Qualifications&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Currently enrolled in a B.S. or M.S. program in Biology, Biochemistry, Biotechnology, Bioengineering, Microbiology, Chemistry, Chemical Engineering, Pharmacology, or related field.&lt;/li&gt;
&lt;li&gt;Completion of foundational biology, biochemistry, microbiology, chemistry, and/or cell biology coursework with laboratory components.&lt;/li&gt;
&lt;li&gt;Experience with aseptic technique and basic cell culture is highly desirable, or liquid nanoparticle technology.&lt;/li&gt;
&lt;li&gt;Ability to work both independently and collaboratively.&lt;/li&gt;
&lt;li&gt;Self-motivated, detail-oriented, and organized with strong problem-solving skills.&lt;/li&gt;
&lt;li&gt;Excellent verbal and written communication skills.&lt;/li&gt;
&lt;li&gt;Eagerness to learn GLP/GMP practices and analytical methodologies.&lt;/li&gt;
&lt;li&gt;Comfortable engaging in cross-functional teamwork.&lt;/li&gt;
&lt;li&gt;Ability to manage multiple projects in a dynamic, fast-paced environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Preferred Qualifications&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Understanding of fundamental principles behind biological and chemical analytical techniques such as UV-Vis, HPLC/UPLC, LC-MS, PCR/qPCR/ddPCR, and potency assays.&lt;/li&gt;
&lt;li&gt;Hands-on experience with biological or chemical analytical techniques including sample preparation, dilution, extraction, and analysis.&lt;/li&gt;
&lt;li&gt;Experience with cell-based assays (e.g., viability assays, flow cytometry, functional assays).&lt;/li&gt;
&lt;li&gt;Familiarity with cell therapy or gene editing technologies.&lt;/li&gt;
&lt;li&gt;Prior internship or co-op experience in the biotechnology industry.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;A cutting-edge, collaborative team committed to mentorship and professional development.&lt;/li&gt;
&lt;li&gt;Exposure to gene and cell therapy analytical strategies in a GMP-regulated environment.&lt;/li&gt;
&lt;li&gt;Participation in seminars with industry experts.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;Note: We are currently not considering co-op candidates outside of the local Boston/Cambridge area.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-quality-control-prime-medicine/69d3bc43c8e81216cd0b9076</link><guid isPermaLink="true">http://biotechroles.com/co-op:-quality-control-prime-medicine/69d3bc43c8e81216cd0b9076</guid><pubDate>Mon, 06 Apr 2026 13:59:30 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-55000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Communications]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a dynamic individual to join the Communications and Public Affairs team to lead the development and execution of communications and brand strategies for a set of companies within Flagship Pioneering’s portfolio. The successful candidate will be a seasoned biotech corporate communications leader who is able to thrive in a fast-paced, start-up environment. This is an exciting opportunity to help shape the growth trajectory for breakthrough life sciences and technology companies in the human health, agriculture, and AI sectors.&lt;/p&gt;
&lt;p&gt;This full-time position reports to the Vice President of Communications and requires in-office presence 4 days per week in Cambridge, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Counsel to Flagship’s company founders and early company leadership, providing strategic guidance to&amp;nbsp;&lt;strong&gt;emergent Flagship companies (Flagship NewCos)&lt;/strong&gt;&amp;nbsp;as they develop brand, voice, foundational messaging and overall communication strategies.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Lead brand development/visual identity and website design and development for NewCos, working with and overseeing outside agencies.&lt;/li&gt;
&lt;li&gt;Design and execute bespoke, integrated communications strategies for company launches, including all written materials, media engagement, and all social media elements. Identify and oversee PR agency support, as needed.&lt;/li&gt;
&lt;li&gt;Design and lead execution of communications strategies for both NewCos and a set of more mature companies (Flagship GrowthCos), including milestone announcements, internal comms, social and digital media, speaking opportunities, and issues management, partnering closely with company leadership.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Work collaboratively with other Communications &amp;amp; Public Affairs team members.&lt;/li&gt;
&lt;li&gt;Participate in weekly Communications &amp;amp; Public Affairs team meetings and collaborate with team members as needed to support broader team priorities that span events, government relations, digital, internal communications, and media relations.&lt;/li&gt;
&lt;li&gt;Manage external resources such as design and agency partners.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree. Advanced degree in a related life sciences field is preferred.&lt;/li&gt;
&lt;li&gt;Extensive leadership-level experience in a public relations agency or corporate communications environment. Experience in pharma and/or biotech, as well as some experience with/exposure to financial and transaction communications.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience working within and across multiple highly complex organizations, while understanding and addressing the needs of both.&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Exceptional research, writing, editing, verbal and interpersonal communication skills.&lt;/li&gt;
&lt;li&gt;Proven media relations track record, as well as the ability to see industry trends and craft insights into effective media relations pitches.&amp;nbsp;Knowledge of and existing relationships with media outside the sphere of traditional media outlets.&lt;/li&gt;
&lt;li&gt;Strong diplomatic and persuasive skills.&lt;/li&gt;
&lt;li&gt;High degree of professional versatility and hands-on capability with a willingness to meet challenges head-on.&lt;/li&gt;
&lt;li&gt;Experience leading in a complex environment that requires skillful engagement of multiple stakeholders and successful, resourceful, and creative navigation of ambiguity.&lt;/li&gt;
&lt;li&gt;Must have the proven ability to advise senior leaders effectively.&lt;/li&gt;
&lt;li&gt;Must have superior interpersonal and organizational skills, along with a demonstrated ability to think strategically and critically and consistently exercise sound judgment.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Proven track record of coordinating multiple programs simultaneously, moving projects forward, and developing and implementing creative, solution-oriented strategies while anticipating future demands and opportunities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The ideal candidate will also have:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;An aptitude for translating complex science into accessible and compelling narratives&lt;/li&gt;
&lt;li&gt;Experience building and leading effective communications campaigns for companies operating at the intersection of technology and science&lt;/li&gt;
&lt;li&gt;Creative mindset with a passion for innovative and impactful communications strategies&lt;/li&gt;
&lt;li&gt;A team player mentality and approach&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $204,000 - $280,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-director-communications-flagship-pioneering/69d3bc41c8e81216cd0b9075</link><guid isPermaLink="true">http://biotechroles.com/senior-director-communications-flagship-pioneering/69d3bc41c8e81216cd0b9075</guid><pubDate>Mon, 06 Apr 2026 13:59:29 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Platform Technologies & Innovation]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;Co-Op Assignment Overview&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a co-op for the Fall 2026 semester with experience in molecular/cell biology-related wet-lab work to join the Prime Editing Platform team. The candidate will contribute to the development of RNA innovations that advance Prime Medicine’s platform capabilities. The qualified candidate will work with a highly collaborative, fast-paced team to design, screen, optimize and validate Prime Editor mRNAs in relevant cell models to support and expand mRNA-based screening efforts. In parallel, the candidate will help drive the exploration and development of RNA modalities across the organization. The candidate will receive consistent mentorship from experienced scientists and learn a variety of different lab-based techniques and skills. Furthermore, the co-op will learn about data analysis and will have an opportunity to present his/her/their work in team meetings. In this position, the candidate will develop a deep understanding of RNA technologies and gene editing and how these efforts fit into the overall drug discovery process.&lt;/p&gt;
&lt;p&gt;Primary Responsibilities:&lt;/p&gt;
&lt;p&gt;· Conduct mRNA production via in-vitro transcription (IVT) and purification.&lt;/p&gt;
&lt;p&gt;· Maintain mammalian cell culture, perform cell passaging.&lt;/p&gt;
&lt;p&gt;· Transfect mammalian cells with Prime Editing reagents to determine gene editing activity.&lt;/p&gt;
&lt;p&gt;· Execute and develop routine cell-based assays to screen for novel mRNA constructs.&lt;/p&gt;
&lt;p&gt;· Perform analytical procedures including ELISA, luciferase assay, qRT-PCR assay and gDNA.&lt;/p&gt;
&lt;p&gt;· Maintain a timely and well-organized electronic lab notebook (ELN).&lt;/p&gt;
&lt;p&gt;· Provide preliminary data analysis, interpretation, and contribute to presentations within Platform team and cross functional teams.&lt;/p&gt;
&lt;p&gt;Required Qualifications:&lt;/p&gt;
&lt;p&gt;· B.S. /M.S. candidate in in Cell &amp;amp; Molecular Biology, Chemical Biology, Biochemistry, or related majors.&lt;/p&gt;
&lt;p&gt;· Firm understanding of, molecular biology, cell biology, and biochemistry. Background understanding of genome editing is a plus.&lt;/p&gt;
&lt;p&gt;· Previous wet-lab (molecular/cell biology) experience.&lt;/p&gt;
&lt;p&gt;· Excellent troubleshooting and communication skills.&lt;/p&gt;
&lt;p&gt;· Interested in solving complex problems in a cross functional collaborative environment.&lt;/p&gt;
&lt;p&gt;Preferred Qualifications:&lt;/p&gt;
&lt;p&gt;· Familiar with cell-based assays, mammalian cell culture and transfection, and nucleic acid biochemistry.&lt;/p&gt;
&lt;p&gt;· Excels at some of the following lab techniques: PCR, nucleotide extraction, molecular cloning, ELISA, etc.&lt;/p&gt;
&lt;p&gt;· Ability to use Word, Excel, PowerPoint, and GraphPad Prism for data documentation, analysis, and presentation.&lt;/p&gt;
&lt;p&gt;· Experience with computational molecular biology tools (e.g., DNA visualization software)&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-platform-technologies-and-innovation-prime-medicine/69d3bc3fc8e81216cd0b9073</link><guid isPermaLink="true">http://biotechroles.com/co-op:-platform-technologies-and-innovation-prime-medicine/69d3bc3fc8e81216cd0b9073</guid><pubDate>Mon, 06 Apr 2026 13:59:27 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$45000-65000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, CMC Development, Biologics]]></title><description><![CDATA[&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Company Description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Metaphore Biotechnologies, Inc. is a privately held biotechnology company building the next generation of biological therapeutics. Inspired by nature, our mission is to transform patient lives by unlocking the power of biological therapeutics with a new mimic-discovery platform.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Role Summary&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Metaphore&amp;nbsp;is seeking a&amp;nbsp;Senior Director, CMC Development &amp;amp; External Manufacturing&amp;nbsp;to&amp;nbsp;lead end-to-end CMC strategy and execution for&amp;nbsp;our&amp;nbsp;biologics&amp;nbsp;programs. This individual will have&amp;nbsp;primary accountability for developing fit-for-stage drug substance and drug product processes&amp;nbsp;with external manufacturing CDMOs. This leader will own the integrated CMC plan (strategy, timeline, budget, and risks),&amp;nbsp;partner with key internal stakeholders to enable seamless transition into&amp;nbsp;late stage&amp;nbsp;CMC work and&amp;nbsp;ensure CMC deliverables support regulatory submissions and clinical supply needs.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Own end-to-end CMC strategy and execution, including governance, integrated plans (timeline/resources/interdependencies), scenario planning, supply forecasting, and risk management to deliver program and company milestones.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Lead external CDMO strategy and oversight for drug substance and drug product (scope setting, operating cadence, deliverables/action tracking, issue escalation/resolution), ensuring execution success.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Provide technical leadership across upstream/downstream, analytical, formulation, fill/finish, and stability, guiding fit-for-stage development decisions (e.g., scale-up strategy, formulation/container strategy, stability approach) and tech transfer readiness.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure phase-appropriate GMP readiness and campaign execution at the CDMO, including deviation/change/CAPA alignment with Quality and ensuring testing and disposition timelines support clinical needs.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Drive CMC regulatory deliverables (CMC sections of submissions/amendments) and executive-level communication of status, decisions, risks, and mitigation plans; build/lead high-performing internal and matrixed teams.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Required Qualifications&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Advanced degree (PhD preferred; MS with&amp;nbsp;significant experience&amp;nbsp;considered) in Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or related discipline.&amp;nbsp;15+ years of&amp;nbsp;biologics&amp;nbsp;CMC experience spanning development through GMP manufacturing and external manufacturing oversight (drug substance and/or drug product).&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven ability to define CMC strategy and translate it into cross-functional deliverables, integrated plans, timelines, and budgets, with strong program leadership and operating rigor.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated success managing external collaborations/CDMOs to deliver CMC development and manufacturing outcomes in fast-paced, matrixed environments.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong technical breadth in at least one major CMC area (and ability to lead across all), including upstream/downstream, analytics, and/or fill/finish/drug product with stability/tech transfer exposure.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Deep working knowledge of cGMP/GxP&amp;nbsp;and quality systems, with clear, concise communication and stakeholder influence skills.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Desired Skills&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335551550&amp;quot;:6,&amp;quot;335551620&amp;quot;:6}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;6&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:1268,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Define and execute strategic vision to advance scientific innovation, translating emerging insights into high-impact initiatives, roadmaps, and measurable outcomes.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:6,&amp;quot;335551620&amp;quot;:6,&amp;quot;335559685&amp;quot;:810,&amp;quot;335559740&amp;quot;:278,&amp;quot;335559991&amp;quot;:450}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;6&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:1268,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Act decisively and own end-to-end accountability, making timely, data-informed decisions, taking responsibility for results, and delivering against commitments in dynamic environments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:6,&amp;quot;335551620&amp;quot;:6,&amp;quot;335559685&amp;quot;:810,&amp;quot;335559740&amp;quot;:278,&amp;quot;335559991&amp;quot;:450}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;6&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:1268,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Build change-agile, high-performing teams and networks, growing others through coaching and development, modeling strong self-awareness, and cultivating relationships with external thought leaders to accelerate learning and partnerships.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:6,&amp;quot;335551620&amp;quot;:6,&amp;quot;335559685&amp;quot;:810,&amp;quot;335559740&amp;quot;:278,&amp;quot;335559991&amp;quot;:450}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&amp;nbsp;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $213,000 - $280,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Metaphore Biotechnologies, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Metaphore Biotechnologies, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-director-cmc-development-biologics-flagship-pioneering/69d3bc3dc8e81216cd0b906e</link><guid isPermaLink="true">http://biotechroles.com/senior-director-cmc-development-biologics-flagship-pioneering/69d3bc3dc8e81216cd0b906e</guid><pubDate>Mon, 06 Apr 2026 13:59:24 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$220000-320000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: LNP Process Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Spring 2026 Co-op: LNP Process Development&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Co-op Assignment Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a co-op for the Spring 2026 semester to work in a cross-functional LNP formulation and process development team. The candidate will work with formulation scientists, process development engineers, and chemical engineers to optimize mRNA and LNP formulation and processes related to the manufacture of LNPs. The candidate will gain hands-on experience with various LNP formulation techniques and processes, analytical and biophysical characterization, and play a critical role in solving challenging problems associated with LNP formulation and process development.&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We want curious problem solvers who enjoy working on exciting projects, working within a team and are passionate about developing genetic editing technologies to better human health and well-being.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate with the LNP formulation and process development team, and cross-functional teams to execute experiments supporting Prime Medicine goals&lt;/li&gt;
&lt;li&gt;Execute experiments to optimize and understand the robustness of LNP formulations and related processes&lt;/li&gt;
&lt;li&gt;Perform analytical testing for assessing LNP formulations and payload quality as it relates to critical process parameters&lt;/li&gt;
&lt;li&gt;Effectively communicate results to internal and external meetings, and present the final summary to the team&lt;/li&gt;
&lt;li&gt;Document and manage all experimental planning and progress in electronic lab notebook in an organized manner, providing statistical analysis and troubleshooting where appropriate.&lt;/li&gt;
&lt;li&gt;Adhere to all laboratory safety requirements and procedures, assist in maintaining general laboratory functionality, including lab equipment maintenance and the ordering, and receiving of lab supplies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;B.S./M.S. candidate in Chemical Engineering, Chemistry, Bioengineering or Biochemistry&lt;/li&gt;
&lt;li&gt;Prior wet lab experience with processes and methods of making and testing LNPs is preferred.&lt;/li&gt;
&lt;li&gt;Prior Co-Op experience(s) is preferred.&lt;/li&gt;
&lt;li&gt;Knowledge of mixing techniques, tangential flow filtration, and characterization techniques (DLS, plate based assays, HPLC) for LNPs&lt;/li&gt;
&lt;li&gt;Familiarity with DOE is a plus&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills.&lt;/li&gt;
&lt;li&gt;Curious, ability to work independently or collaboratively as needed&lt;/li&gt;
&lt;li&gt;Self-motivated, detail-oriented with strong critical thinking skills and excel at identifying and solving problems.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What We Offer:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A cutting-edge team open to mentorship and networking.&lt;/li&gt;
&lt;li&gt;Full reimbursement for monthly commuting costs including MBTA, Commuter Rail, or Bluebikes, etc.&lt;/li&gt;
&lt;li&gt;Participation in regular seminars with industry experts.&lt;/li&gt;
&lt;li&gt;Full participation in employee activities including learning and development offerings, social activities, etc.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;NOTE: We are currently not considering co-op candidates outside of the local Boston/Cambridge area.&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-lnp-process-development-prime-medicine/69d3bc3ac8e81216cd0b906d</link><guid isPermaLink="true">http://biotechroles.com/co-op:-lnp-process-development-prime-medicine/69d3bc3ac8e81216cd0b906d</guid><pubDate>Mon, 06 Apr 2026 13:59:22 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-50000</salary><type>Full-time</type></item><item><title><![CDATA[(Senior) Data Engineer]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;dhkj5-0-0&quot;&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;About ProFound Therapeutics&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound Therapeutics is pioneering the discovery of the expanded human proteome to unlock a new universe of potential therapeutics. By integrating multi-omics, advanced computation, and translational biology, we aim to reveal and characterize thousands of previously uncharted proteins and systematically explore their role in health and disease.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We&#39;re seeking a (Senior) Data Engineer to join our data team. This individual will play a central role in building the data foundation that powers ProFound&#39;s drug discovery platform. You&#39;ll architect systems that integrate diverse biological data—from genomics and proteomics to imaging and perturbation experiments—enabling our scientists to make breakthrough discoveries and our ML models to identify novel therapeutic targets.&lt;/p&gt;
&lt;p&gt;This role offers the unique challenge of working at the intersection of computational biology, machine learning, and modern data engineering, with the impact of accelerating life-saving therapeutics.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Contribute to design and scaling of our multi-modal data platform that integrates public and proprietary biological data (genomics, transcriptomics, proteomics, imaging, perturbation data) across data lakes, graph databases, relational and NoSQL databases, and data warehouses, enabling ML training, computational biology pipelines, and scientific exploration.&lt;/li&gt;
&lt;li&gt;Build production data pipelines and workflows that automate data ingestion and transformation, working with domain experts to optimize analysis pipelines for scientific discovery.&lt;/li&gt;
&lt;li&gt;Partner with computational and wet-lab scientists to model experimental data, manage instrument outputs and electronic lab notebook data, and ensure seamless integration into our data platform.&lt;/li&gt;
&lt;li&gt;Develop and manage cloud infrastructure on AWS following best practices and the Well-Architected framework, with focus on scalability, security, and cost optimization.&lt;/li&gt;
&lt;li&gt;Contribute to the data engineering team’s best practices including comprehensive documentation, monitoring and observability, and robust testing frameworks.&lt;/li&gt;
&lt;li&gt;Collaborate with external partners including CROs, vendors, and consultants to coordinate data transfers and support platform integrations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS, MS, or PhD in Computer Science, Bioinformatics, or related field with 0-4 years of professional data engineering experience.&lt;/li&gt;
&lt;li&gt;Background in scientific domains (biology, chemistry, or related fields).&lt;/li&gt;
&lt;li&gt;Python expertise including data science libraries and testing frameworks.&lt;/li&gt;
&lt;li&gt;AWS experience with storage, database, compute, and analytics services (S3, RDS, DynamoDB, Redshift, Lambda, EC2, Batch, ECS, Glue, Athena).&lt;/li&gt;
&lt;li&gt;Proven experience designing, deploying, and maintaining production data pipelines at scale.&lt;/li&gt;
&lt;li&gt;Hands-on experience with workflow orchestration systems (AWS Step Functions, NextFlow, dbt, Dagster) and event-driven architectures.&lt;/li&gt;
&lt;li&gt;Working knowledge of CI/CD frameworks, infrastructure-as-code (CloudFormation or AWS CDK), and containerization (Docker).&lt;/li&gt;
&lt;li&gt;Strong technical communication skills with ability to translate complex technical concepts for scientific audiences and collaborate effectively across disciplines.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to thrive in dynamic environments, prioritize competing demands, and make pragmatic trade-offs in a fast-paced startup setting.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with data lakes and open table formats (Iceberg preferred).&lt;/li&gt;
&lt;li&gt;Experience with knowledge graph technologies and graph databases (Neo4j).&lt;/li&gt;
&lt;li&gt;Familiarity with lab data management systems (LIMS, ELN, integrated data lakes).&lt;/li&gt;
&lt;li&gt;Experience with MLOps practices and tools for model training pipelines, experiment tracking, and model deployment.&lt;/li&gt;
&lt;li&gt;AWS certification (Associate or Professional level).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Why ProFound&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This role offers the opportunity to shape the technical and scientific foundation of a next-generation drug discovery platform. You will operate with real ownership, influence core architectural decisions, and work directly with leaders in AI, human genetics, and computational biology to expand the human proteome and uncover new therapeutic opportunities&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $74,000 - $176,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. ProFound Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on ProFound Therapeutics, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/(senior)-data-engineer-flagship-pioneering/69d3bc38c8e81216cd0b906b</link><guid isPermaLink="true">http://biotechroles.com/(senior)-data-engineer-flagship-pioneering/69d3bc38c8e81216cd0b906b</guid><pubDate>Mon, 06 Apr 2026 13:59:20 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$140000-200000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: In-Vivo Delivery]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Fall 2026 Co-op Program: July – Dec 2026&lt;/p&gt;
&lt;p&gt;Co-Op Assignment Overview&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a co-op for the Fall 2026 semester with experience in animal- and cellular-based studies to join the Lung Biology team. The candidate will be involved in supporting critical efforts in identifying delivery candidates for lung-directed dosing in animals towards the development of in vivo gene editing therapies that leverage our cutting-edge Prime Editing technologies. The successful candidate will thrive in a fast-paced research program and will enjoy working with colleagues within and across teams from multi-disciplinary backgrounds.&lt;/p&gt;
&lt;p&gt;Primary Responsibilities:&lt;/p&gt;
&lt;p&gt;· Assist and support lung delivery in-vivo studies, include dosing, takedown, tissue processing and antibody staining&lt;/p&gt;
&lt;p&gt;· Plan and execute in vitro assays to evaluate gene editing activity in relevant cell models including primary lung bronchial epithelial cells&lt;/p&gt;
&lt;p&gt;· Follow protocols, standard operating procedures, execute assigned tasks and maintain ELN. Share responsibility in lab reagent inventory and maintaining equipment.&lt;/p&gt;
&lt;p&gt;· Work and collaborate cross-functionally with colleagues. Collect, analyze and present data in team meetings.&lt;/p&gt;
&lt;p&gt;Required Qualifications:&lt;/p&gt;
&lt;p&gt;· Bachelor/Master candidate in Biology related major&lt;/p&gt;
&lt;p&gt;· Direct experience performing routine laboratory procedures and experiments&lt;/p&gt;
&lt;p&gt;· Hands on experience with sterile techniques and culturing of mammalian cell culture including primary cells&lt;/p&gt;
&lt;p&gt;· Comfortable working with rodent models with preliminary techniques or training on animal studies is a plus&lt;/p&gt;
&lt;p&gt;Preferred Qualifications:&lt;/p&gt;
&lt;p&gt;Experience with the following techniques or knowledge familiarities are preferred.&lt;/p&gt;
&lt;p&gt;· Gene editing technologies (Cas9, base editing, prime editing etc)&lt;/p&gt;
&lt;p&gt;· Non-viral delivery&lt;/p&gt;
&lt;p&gt;· Animal dosing techniques (IV, IP, Oral, etc)&lt;/p&gt;
&lt;p&gt;· Lung tissue processing, and cell staining for flow analysis&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-in-vivo-delivery-prime-medicine/69d3bc36c8e81216cd0b9069</link><guid isPermaLink="true">http://biotechroles.com/co-op:-in-vivo-delivery-prime-medicine/69d3bc36c8e81216cd0b9069</guid><pubDate>Mon, 06 Apr 2026 13:59:18 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$45000-65000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Counsel, Legal]]></title><description><![CDATA[&lt;p&gt;&lt;a href=&quot;https://www.flagshippioneering.com/&quot;&gt;Flagship Pioneering&lt;/a&gt;&amp;nbsp;is a bioplatform innovation company&amp;nbsp;that invents and builds platform companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health and sustainability exponentially accelerate scientific progress in areas ranging from cancer detection and treatment to nature-positive agriculture.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt; What sets Flagship apart is our ability to advance biotechnology by uniting life science innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is seeking an experienced Senior Counsel to join a growing Legal Transactions team that serves as the strategic legal business partner to the Business Development, Corporate Development and Pioneering Medicines teams and an integral member of the Legal Team. This role will report to the Vice President, Legal Transactions and will be responsible for managing the process of structuring and negotiating complex pharmaceutical licensing and collaboration agreements and a wide range of other significant transactions across the Flagship ecosystem, as well as managing outside counsel for such matters. The ideal candidate will bring deep expertise in life sciences transactions, a strong foundation of top-tier law firm experience, and the ability to navigate complex, high-value deals in a fast-paced and innovative environment. This role will be tightly integrated into the larger Legal Team with opportunities for broader collaboration and development.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as lead counsel providing full end-to-end support on strategic transactions across the Flagship ecosystem, including pharmaceutical collaborations, licensing transactions, R&amp;amp;D partnerships, M&amp;amp;A and other significant transactions.&lt;/li&gt;
&lt;li&gt;Partner with cross-functional teams—including Business Development, Corporate Development, Pioneering Medicines and Finance —to structure deals that align with Flagship’s innovation strategy and Flagship’s and its portfolio companies’ business objectives.&lt;/li&gt;
&lt;li&gt;Provide support across the Flagship ecosystem as needed to support additional types of corporate transactions, including complex financings, restructuring activities, etc.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Stay ahead of industry trends, evolving regulations, and legal developments impacting pharmaceutical collaborations and biotech transactions.&lt;/li&gt;
&lt;li&gt;Contribute to developing and implementing best practices, templates, and playbooks to streamline relevant legal processes.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Proactively engage and direct external law firm partners and advisors to manage high-stakes negotiations and complex deal structures and legal cost associated with the same.&lt;/li&gt;
&lt;li&gt;Counsel internal stakeholders on legal interpretations, risk management and compliance considerations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications &amp;amp; Experience&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;J.D. from a top-tier law school; licensed to practice in the United States.&lt;/li&gt;
&lt;li&gt;8+ years of experience in complex life sciences transactions, including top-tier law firm experience; previous in-house experience is preferred but not required.&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Deep expertise in pharmaceutical collaborations, licensing agreements, and other significant transactions; expertise in M&amp;amp;A is a plus.&lt;/li&gt;
&lt;li&gt;Proven ability to lead negotiations on complex, high-value deals in the biotech or pharmaceutical industry.&lt;/li&gt;
&lt;li&gt;Excellent executive presence, communication, leadership, and problem-solving skills, with the ability to advise senior executives and drive strategic decision-making.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Why Join Flagship Pioneering?&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This is a rare opportunity to play a critical role in shaping groundbreaking collaborations that drive scientific innovation. As Senior Counsel, Legal, you will operate at the intersection of business, law, and cutting-edge biotechnology, helping to build and support transformational partnerships that advance human health.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;#LI-NM1&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $204,000 - $346,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/senior-counsel-legal-flagship-pioneering/69d3bc34c8e81216cd0b9068</link><guid isPermaLink="true">http://biotechroles.com/senior-counsel-legal-flagship-pioneering/69d3bc34c8e81216cd0b9068</guid><pubDate>Mon, 06 Apr 2026 13:59:16 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: In-Process Analytics]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Fall 2026 Co-op: In-Process Analytics&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Co-op Assignment Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a Fall 2026 co-op to join our Chemistry team, with a focus on in-process analytics and purification of large RNA molecules. The successful candidate will engage in hands-on laboratory work, including UV absorbance measurements using NanoDrop, purification support, sample analysis by UPLC and mass spectrometry (MS), and endotoxin testing of synthetic guide RNA. Through this experience, the co-op will develop proficiency in oligonucleotide characterization, gain exposure to a broad range of in-process analytical techniques, contribute to data generation and documentation, and present findings at weekly team meetings. We welcome curious, collaborative problem solvers who are passionate about advancing gene-editing technologies to improve human health.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support the characterization and purification of Prime&#39;s long guide RNA (gRNA) using a suite of laboratory techniques, including ÄKTA purifier, UPLC, LC-MS, NanoDrop, and endotoxin assays&lt;/li&gt;
&lt;li&gt;Integrate chromatograms for gRNA crude, fraction, and final samples in accordance with Prime&#39;s SOPs to quantify full-length product purity, and tabulate results in the team&#39;s electronic lab notebook&lt;/li&gt;
&lt;li&gt;Learn and contribute to mass analysis of gRNA to identify the molecular weight of the full-length product and related impurities&lt;/li&gt;
&lt;li&gt;Assist senior scientists with buffer preparation, instrument maintenance, and the development of updated analytical methods to expand in-process analytical capacity&lt;/li&gt;
&lt;li&gt;Manage inventory of critical reagents for buffer preparation in support of purification and analytics operations&lt;/li&gt;
&lt;li&gt;Coordinate with scientists to maintain inventory records for final released materials&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Enrolled in a B.S. or M.S. program in Chemistry, Biochemistry, or a related field; basic knowledge of organic chemistry preferred&lt;/li&gt;
&lt;li&gt;Prior completion of general chemistry coursework and associated laboratory courses&lt;/li&gt;
&lt;li&gt;Strong written and oral communication skills, with excellent organizational ability and capacity to work both independently and collaboratively&lt;/li&gt;
&lt;li&gt;Enthusiasm for learning and contributing across multiple aspects of a research program&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior internship or co-op experience in a relevant setting&lt;/li&gt;
&lt;li&gt;Completion of analytical chemistry lecture and laboratory courses&lt;/li&gt;
&lt;li&gt;Hands-on experience in a chemistry laboratory, with familiarity with instrumentation such as HPLC, LC-MS, NanoDrop, and ÄKTA Pure&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What We Offer&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A cutting-edge, mentorship-driven team with strong networking opportunities&lt;/li&gt;
&lt;li&gt;Full reimbursement for monthly commuting costs, including MBTA, Commuter Rail, and Bluebikes&lt;/li&gt;
&lt;li&gt;Access to regular seminars featuring industry experts&lt;/li&gt;
&lt;li&gt;Full participation in company-wide activities, including learning and development programming, social events, and more&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;Please note: We are currently only considering candidates based in the greater Boston/Cambridge area.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-in-process-analytics-prime-medicine/69d3bc32c8e81216cd0b9065</link><guid isPermaLink="true">http://biotechroles.com/co-op:-in-process-analytics-prime-medicine/69d3bc32c8e81216cd0b9065</guid><pubDate>Mon, 06 Apr 2026 13:59:14 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-55000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, Molecular Biology]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are building a new venture, FL122, pioneering genomic technologies at the intersection of human health and assisted reproduction. The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Tessera Therapeutics, and Quotient Therapeutics. We are an equal opportunity employer.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Molecular Biologist to help build the experimental foundation of the company’s scientific platform. As an early scientific team member, you will contribute to the development of core protocols, support the establishment of technical standards, and help execute the experimental strategy, working closely with senior scientists and leadership. We are looking for someone who is resourceful, is open to a rapidly changing, agile environment and has bias to action. The ideal candidate combines deep technical rigor with a growth mindset, pays attention to detail, and has a deep-rooted desire to achieve excellence. Being collaborative is key – the environment is an early stage startup, where all members of the team need to work closely together to break new ground in science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Deliver molecular biology research projects with guidance from senior team members, including experimental execution, troubleshooting, data analysis and clear communication of results&lt;/li&gt;
&lt;li&gt;Support the implementation of appropriate instrumentation, reagents, and consistent workflows to enable scalable and reliable experimental operations&lt;/li&gt;
&lt;li&gt;Handle and process human biospecimen, specifically human gametes, in a BSL2 setting with rigorous adherence to quality and reproducibility standards&lt;/li&gt;
&lt;li&gt;Contribute to the development, optimization, and benchmarking of workflows for extracting and quantifying minute amounts of nucleic acids from single cells and other low-input samples&lt;/li&gt;
&lt;li&gt;Test, compare and implement multiple single cell RNA sequencing methods, including library quantification and QC required for Illumina sequencing&lt;/li&gt;
&lt;li&gt;Collaborate with internal team members and contribute to interactions with external advisors, incorporating feedback into experimental plans&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in biology, molecular biology, genetics or a related discipline with 0–2+ years of postdoctoral or industry experience, with an excellent research track record&lt;/li&gt;
&lt;li&gt;Hands-on experience in the handling of minute amounts of nucleic acids, including rigorous QC and troubleshooting of low-input workflows&lt;/li&gt;
&lt;li&gt;Experience testing and optimizing single cell RNA sequencing methods end-to-end, including library quantification and QC (e.g., yield, size distribution, complexity)&lt;/li&gt;
&lt;li&gt;Demonstrated ability to execute and troubleshoot complex experiments independently, with increasing ownership over time&lt;/li&gt;
&lt;li&gt;Comfort operating in fast-moving, ambiguous startup environments with a collaborative mindset and willingness to take initiative&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background &lt;strong&gt;and interest in Flagship&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $143,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL122 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL122&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/scientist-molecular-biology-flagship-pioneering/69d3bc30c8e81216cd0b9061</link><guid isPermaLink="true">http://biotechroles.com/scientist-molecular-biology-flagship-pioneering/69d3bc30c8e81216cd0b9061</guid><pubDate>Mon, 06 Apr 2026 13:59:12 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Clinical Development - Patient Advocacy and Medical Affairs]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Co-op: Clinical Development - Patient Advocacy and Medical Affairs&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Location:&lt;/strong&gt; Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Co-Op Assignment Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a co-op student to join the Patient Advocacy and Medical Affairs team. This individual will support efforts to build strong relationships with patient communities and collaborate with patient advocacy organizations across Prime’s therapeutic programs. The co-op will contribute to initiatives that integrate the patient perspective into clinical and regulatory strategy. The role will also provide exposure to core medical affairs activities, including conference and publication planning, Key Opinion Leader (KOL) engagement, and clinical study support as it relates to patient engagement. The ideal candidate will be highly motivated, thoughtful, and collaborative, with the ability to engage respectfully with internal and external stakeholders. They will have a strong interest in rare diseases, genetic medicines, and advancing patient-focused drug development.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support Prime Medicine’s patient advocacy strategy and “Patients First” initiatives across therapeutic programs&lt;/li&gt;
&lt;li&gt;Conduct landscape research on patient advocacy organizations, rare disease communities, and relevant stakeholder groups&lt;/li&gt;
&lt;li&gt;Assist in preparing educational materials for patient communities related to genetic medicines and clinical development&lt;/li&gt;
&lt;li&gt;Assist in planning and preparation for Patient Advisory Boards, and synthesis of key insights to help inform patient engagement and clinical development strategies.&lt;/li&gt;
&lt;li&gt;Draft responses to patient and caregiver inquiries, ensuring accurate, timely, and compliant communication.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Assist with KOL engagement, conference/publication and external presentation planning activities as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Participate in cross-functional meetings to gain exposure to clinical strategy, regulatory planning, and stakeholder engagement&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Currently pursuing a B.S. or B.A. in Public Health, Biology, or Health Sciences field&lt;/li&gt;
&lt;li&gt;Strong interpersonal, oral, and written communication skills&lt;/li&gt;
&lt;li&gt;Ability to manage multiple projects and work both independently and within a team environment&lt;/li&gt;
&lt;li&gt;Proficiency in Microsoft Office (PowerPoint, Excel, Word)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Coursework in medical sciences or familiarity with medical terminology&lt;/li&gt;
&lt;li&gt;Interest in rare diseases, genetic therapies, or patient engagement&lt;/li&gt;
&lt;li&gt;Exposure to scientific communication, public health, advocacy, or healthcare policy&lt;/li&gt;
&lt;li&gt;Basic understanding of clinical trials and drug development processes&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$29 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-clinical-development-patient-advocacy-and-medical-affairs-prime-medicine/69d3bc2fc8e81216cd0b905f</link><guid isPermaLink="true">http://biotechroles.com/co-op:-clinical-development-patient-advocacy-and-medical-affairs-prime-medicine/69d3bc2fc8e81216cd0b905f</guid><pubDate>Mon, 06 Apr 2026 13:59:10 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$65000-85000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, In Vivo Biology]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL106 Inc., is a privately held, early-stage biotechnology company focused on developing novel drug delivery modalities. FL106 is backed by Flagship Pioneering, bringing the vision and resources to guide FL106 from platform validation to real-world solutions that meaningfully improve patient care.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL106 is seeking a highly motivated Scientist for In Vivo &amp;amp; Translational biology to lead the design and execution of rigorous &lt;em&gt;in vivo&lt;/em&gt; and &lt;em&gt;ex vivo&lt;/em&gt; assays in support of novel drug delivery technologies. This role will be central to evaluating delivery performance, biodistribution, and biological activity across relevant model systems.&lt;/p&gt;
&lt;p&gt;The ideal candidate is an independent, goal-oriented scientist with strong experimental dexterity and judgment, excellent communication skills, and a bias toward execution. You will work in a highly dynamic, fast-paced, and collaborative entrepreneurial environment, contributing directly to scientific strategy and data-driven decision-making. This is a unique opportunity to help build an early-stage biotechnology company and shape the next frontier of drug delivery.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Core Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, plan and execute mouse and rat studies, including experimental design, protocol development, dosing, tissue collection and processing, and data analysis to evaluate delivery technologies&lt;/li&gt;
&lt;li&gt;Perform readout assays such as flow cytometry, immunofluorescence imaging, bioluminescence, qPCR, and histology&lt;/li&gt;
&lt;li&gt;Manage and collaborate with CROs and external partners to ensure high-quality execution of outsourced studies&lt;/li&gt;
&lt;li&gt;Work closely with interdisciplinary team members (e.g., chemistry, engineering, formulation) to develop integrated experimental plans&lt;/li&gt;
&lt;li&gt;Contribute to the development and refinement of translational and preclinical scientific strategy&lt;/li&gt;
&lt;li&gt;Clearly communicate experimental results and insights through concise presentations, written summaries, and thorough documentation in an electronic lab notebook (ELN)&lt;/li&gt;
&lt;li&gt;Stay current with relevant scientific literature and emerging technologies, proactively sharing insights with the broader team&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications and Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in Biology, Cell Biology, Immunology, or a related field&lt;/li&gt;
&lt;li&gt;2+ years of experience in the biopharmaceutical or biotechnology industry preferred&lt;/li&gt;
&lt;li&gt;Extensive hands-on experience with &lt;em&gt;in vivo&lt;/em&gt; biology in small rodents (mice required; rats preferred)&lt;/li&gt;
&lt;li&gt;Proficiency in high-throughput animal handling, injection techniques, and tissue harvesting and processing (IV, subcutaneous required other routes of administration – e.g. IM, IVT, IT, preferred)&lt;/li&gt;
&lt;li&gt;Experience with non-invasive &lt;em&gt;in vivo&lt;/em&gt; imaging technologies, including bioluminescence and fluorescence imaging, strongly preferred&lt;/li&gt;
&lt;li&gt;Experience performing whole-body perfusion,single cell organ digestion, and cell sorting strongly preferred&lt;/li&gt;
&lt;li&gt;Proven expertise in protein and/or nucleic acid (DNA/RNA) isolation from mammalian cells and tissues, cDNA synthesis, and qPCR&lt;/li&gt;
&lt;li&gt;Experience with histological techniques, including tissue preparation, staining and data analysis&lt;/li&gt;
&lt;li&gt;Hands-on experience with flow cytometry, including sample preparation, panel design or execution, data acquisition, and downstream analysis, strongly preferred&lt;/li&gt;
&lt;li&gt;Proven ability to develop, optimize, and troubleshoot biological assays&lt;/li&gt;
&lt;li&gt;Strong organizational and planning skills, with attention to experimental rigor and reproducibility&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company&amp;nbsp;that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in generation of over 500 patents, initiation of over 50 clinical trials for novel therapeutic agents and an aggregate value of more than $90 billion. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $143,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL106 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL106&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/scientist-in-vivo-biology-flagship-pioneering/69d3bc2cc8e81216cd0b905e</link><guid isPermaLink="true">http://biotechroles.com/scientist-in-vivo-biology-flagship-pioneering/69d3bc2cc8e81216cd0b905e</guid><pubDate>Mon, 06 Apr 2026 13:59:08 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Automation & Assays]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Co-op: &lt;em&gt;Automation &amp;amp; Assays&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;(Fall July-December 2026)&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Co-op Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is seeking a motivated and detail-oriented Co-op Student to join our &lt;strong&gt;Automation &amp;amp; Assays team&lt;/strong&gt; for a 6-month term. This is a hands-on role that offers exposure to cutting-edge automated laboratory systems and a wide range of biochemical and cell-based assays in support of research and process development activities across the company.&lt;/p&gt;
&lt;p&gt;You will work alongside experienced scientists to learn, develop, and execute assays on automated liquid handling platforms, contributing directly to programs that are advancing gene editing therapies toward patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Learn and execute biochemical and cell-based assays (including ELISAs and related methods) to test samples in support of research and process development programs&lt;/li&gt;
&lt;li&gt;Operate and maintain automated liquid handling systems (e.g., Hamilton, Tecan) to run high-throughput workflows&lt;/li&gt;
&lt;li&gt;Maintain accurate and detailed records of experimental work in accordance with good laboratory practices&lt;/li&gt;
&lt;li&gt;Analyze and interpret experimental data, contributing to summaries and reports; scripting experience (Python, R) is a plus for data processing tasks&lt;/li&gt;
&lt;li&gt;Work cross-functionally with research and process development teams to support ongoing project needs&lt;/li&gt;
&lt;li&gt;Contribute to continuous improvement of assay protocols and automation workflows&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Currently enrolled in a Bachelor&#39;s or Master&#39;s program in Biology, Biochemistry, Bioengineering, Biomedical Engineering, or a related field, with at least 2 years of undergraduate coursework completed&lt;/li&gt;
&lt;li&gt;Hands-on wet lab experience, including proficiency in pipetting, cell culture, and aseptic technique&lt;/li&gt;
&lt;li&gt;Strong attention to detail and a commitment to data integrity&lt;/li&gt;
&lt;li&gt;Ability to manage time effectively, prioritize tasks, and work independently in a fast-paced environment&lt;/li&gt;
&lt;li&gt;A collaborative, curious mindset and a genuine passion for science&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice-to-haves:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior experience with automated liquid handling systems (e.g., Hamilton, Tecan)&lt;/li&gt;
&lt;li&gt;Familiarity with ELISA or other biochemical assay formats&lt;/li&gt;
&lt;li&gt;Experience with data analysis or scripting tools (Python, R)&lt;/li&gt;
&lt;li&gt;Previous co-op, internship, or research lab experience in an industry or academic setting&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-automation-and-assays-prime-medicine/69d3bc2bc8e81216cd0b905d</link><guid isPermaLink="true">http://biotechroles.com/co-op:-automation-and-assays-prime-medicine/69d3bc2bc8e81216cd0b905d</guid><pubDate>Mon, 06 Apr 2026 13:59:07 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-50000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, Computational Vaccine Design]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Scientist to join a dynamic team applying computational and data-driven approaches to design novel antigens and evaluate vaccine responses. At Apriori Bio, we have built our biology-enabled AI/ML platform Octavia™ to map viral fitness landscapes, predict immune escape trajectories, and design vaccines to elicit an optimal protective response to future challenges. The successful candidate will contribute to the development and application of computational methods—including structural modeling, machine learning, and statistical inference— that build on Octavia™ insights to support the company’s vaccine design efforts. Experience working with protein engineering and immunological datasets is valuable, as is interest or training in high-throughput functional genomics, virology, or vaccinology.&lt;/p&gt;
&lt;p&gt;The Scientist will work closely with both computational and experimental colleagues to interpret results, generate hypotheses, and support antigen design. This role is ideal for scientists eager for a unique opportunity to learn and innovate within an interdisciplinary, fast-paced startup environment.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Use high-dimensional datasets (e.g., mutational scanning, NGS-based phenotypic screens) and computational approaches—including structural modeling, sequence analysis, and machine learning—to support antigen and immunogen engineering&lt;/li&gt;
&lt;li&gt;Apply and refine computational models that integrate screening data with structural and sequence-based features to guide biomolecule engineering&lt;/li&gt;
&lt;li&gt;Generate hypotheses and design analyses that inform evaluation of novel immunization strategies (in partnership with experimental teams)&lt;/li&gt;
&lt;li&gt;Identify, evaluate, and curate external datasets relevant to vaccine design and antigen optimization&lt;/li&gt;
&lt;li&gt;Develop reproducible computational tools and pipelines for data-driven product design that can be integrated into broader platform workflows&lt;/li&gt;
&lt;li&gt;Collaborate with engineers, computational scientists, and experimentalists to execute project goals and ensure smooth integration of computational findings&lt;/li&gt;
&lt;li&gt;Work with immunology and characterization teams to interpret vaccine immunogenicity using next-generation immune monitoring and antibody profiling tools&lt;/li&gt;
&lt;li&gt;Clearly communicate results and insights to colleagues across scientific and cross-functional teams&lt;/li&gt;
&lt;li&gt;Tackle difficult scientific problems with creativity and resilience while iterating quickly as new data emerges&lt;/li&gt;
&lt;li&gt;Take ownership of complex, open-ended scientific questions, driving analyses forward through ambiguity while balancing speed, rigor, and collaborative problem-solving&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Basic Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in bioengineering, immunology, computational biology, or a related field (or equivalent research experience)&lt;/li&gt;
&lt;li&gt;Experience applying data-driven protein engineering methods to predict and affect protein function, including structural and sequence-based machine-learning approaches&lt;/li&gt;
&lt;li&gt;Experience or training in antigen design leveraging vaccine immune response readouts&lt;/li&gt;
&lt;li&gt;Solid statistical and quantitative foundation, with the ability to translate complex biological datasets into actionable insights&lt;/li&gt;
&lt;li&gt;Strong scientific programming skills (Python preferred) and familiarity with best practices in reproducible scientific computing&lt;/li&gt;
&lt;li&gt;Experience working with high-throughput biological data or NGS-based assays, including modeling and statistical analysis&lt;/li&gt;
&lt;li&gt;Experience using version control and collaborative coding workflows&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in vaccine design&lt;/li&gt;
&lt;li&gt;Experience with deep learning approaches&lt;/li&gt;
&lt;li&gt;Exposure to antibody characterization, immune profiling, or immune repertoire analyses&lt;/li&gt;
&lt;li&gt;Experience with NGS data pipelines, from processing to interpretation&lt;/li&gt;
&lt;li&gt;Familiarity with cloud or distributed computing environments&lt;/li&gt;
&lt;li&gt;Familiarity with storage, analysis and transformation of large tabular datasets and relational databases&lt;/li&gt;
&lt;li&gt;Laboratory experience in molecular biology, biochemistry, or immunology (a plus, not required)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a biotechnology company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.  Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at &lt;a href=&quot;http://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background. &lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies&lt;/strong&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $115,000 - $165,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Apriori Bio, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Apriori Bio, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/scientist-computational-vaccine-design-flagship-pioneering/69d3bc28c8e81216cd0b905b</link><guid isPermaLink="true">http://biotechroles.com/scientist-computational-vaccine-design-flagship-pioneering/69d3bc28c8e81216cd0b905b</guid><pubDate>Mon, 06 Apr 2026 13:59:04 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Co-op: Analytical Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;Company Overview:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology &amp;amp; oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit &lt;a href=&quot;http://www.primemedicine.com/&quot;&gt;www.primemedicine.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;h1&gt;Co-op: Analytical Development&lt;/h1&gt;
&lt;p&gt;(Fall 2026 Cycle)&lt;/p&gt;
&lt;p&gt;Prime Medicine was founded to bring the promise of gene editing to patients. We use Prime Editing, a next-generation technology that can “search and replace” to restore normal genetic function almost anywhere in the genome. Prime Editing searches to find the precise place in the genome to edit and replace the segment of faulty DNA with a correct copy of DNA. A single Prime Editor can correct the individual mutations found across patients, meaning Prime Editing can potentially address more than 90 percent of known disease-causing genetic mutations.&lt;/p&gt;
&lt;p&gt;We envision a world where this technology can cure, halt, and ultimately prevent genetic diseases, providing lifelong benefits to patients. Prime Medicine offers the opportunity to shape the future of gene editing and transform how medicines are used to treat disease. Realizing the promise of Prime Editing requires a talented team with a diversity of viewpoints and expertise. We’re building a group of dedicated, scientifically curious individuals who are passionate about helping patients live longer, healthier lives.&lt;/p&gt;
&lt;h2&gt;Co-op Assignment Overview&lt;/h2&gt;
&lt;p&gt;Prime Medicine is seeking a diligent, motivated, and enthusiastic co-op for the Fall 2026 cycle who has interest in state-of-the-art analytical technologies including HPLC, LC-MS, and capillary electrophoresis to join the analytical development (AD) team. The successful candidate will be able to participate in the development of separation-based analytical methods for the Prime Editor delivery platform and work cross-functionally to advance the Prime pipeline. Also, this co-op student will have hands-on opportunities to gain exposure to a broader range of analytical techniques (such as flow cytometry), gaining familiarity with scientific and regulatory requirements for phase-appropriate analytical testing. There will also be valuable opportunities to participate in other cross-functional projects that are crucial to the success of in vivo and ex vivo gene editing therapeutic drug development.&lt;/p&gt;
&lt;h2&gt;Primary Responsibilities:&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Participate in separation-based method (HPLC, LC-MS) development to assess lipid nanoparticle (LNP) drug products and their components. Assist senior-level scientists with buffer preparation, maintenance of instruments, and developing up-to-date analytical methods that help to increase in-process analytics capacity.&lt;/li&gt;
&lt;li&gt;Participate in cell-based method (flow cytometry) development to assess cell therapy drug products. Support the maintenance of instruments.&lt;/li&gt;
&lt;li&gt;Support the phase-appropriate product development (PD) sample analyses, release testing, and stability studies for the characterization and release of cell and gene therapy drug products, drug substances, and critical raw materials.&lt;/li&gt;
&lt;li&gt;Document, present, and communicate experimental data and conclusions in an electronic notebook, following cGMP documentation practices.&lt;/li&gt;
&lt;li&gt;Data analysis, interpretation, and presentation within the team.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Qualifications:&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Currently enrolled in a B.S. or M.S. program in biochemistry, chemistry, chemical engineering, pharmaceutical science, or a related field.&lt;/li&gt;
&lt;li&gt;Basic knowledge of separation sciences and technologies.&lt;/li&gt;
&lt;li&gt;Ability to handle multiple projects in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Excellent troubleshooting and communication skills.&lt;/li&gt;
&lt;li&gt;Ability to work independently and within a team.&lt;/li&gt;
&lt;li&gt;Skilled in documenting findings and activities in comprehensive reports and ensuring proper inventory of materials and analytical equipment.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Preferred Qualifications:&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Hands-on experience with LC-MS, capillary electrophoresis, and/or cell culture is preferred.&lt;/li&gt;
&lt;li&gt;Previous co-op experience in the biotechnology industry.&lt;/li&gt;
&lt;li&gt;Independently motivated, detail-oriented, and excellent problem-solving abilities.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer:&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;A cutting-edge scientific team dedicated to mentorship and networking&lt;/li&gt;
&lt;li&gt;Experience in the field of gene editing and analytical development/early-stage QC&lt;/li&gt;
&lt;li&gt;Participation in regular scientific seminars with industry experts&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education.&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;
&lt;div class=&quot;title&quot;&gt;U.S. Pay Range&lt;/div&gt;
&lt;div class=&quot;pay-range&quot;&gt;$23&lt;span class=&quot;divider&quot;&gt;—&lt;/span&gt;$33 USD&lt;/div&gt;
&lt;p&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/co-op:-analytical-development-prime-medicine/69d3bc27c8e81216cd0b905a</link><guid isPermaLink="true">http://biotechroles.com/co-op:-analytical-development-prime-medicine/69d3bc27c8e81216cd0b905a</guid><pubDate>Mon, 06 Apr 2026 13:59:03 GMT</pubDate><company>Prime Medicine</company><location>Cambridge, MA</location><salary>$35000-50000</salary><type>Full-time</type></item><item><title><![CDATA[Vice President, Compliance (Biopharma)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Chief Legal Officer, the VP, Compliance, will serve as the company’s senior compliance leader, responsible for designing, implementing, and overseeing a comprehensive and effective global healthcare&amp;nbsp;compliance&amp;nbsp;program aligned with applicable laws, regulations, and industry standards.&amp;nbsp; The role is both strategic and hands-on: ideal for a leader who can set vision while rolling up their sleeves to build processes from the ground up.&amp;nbsp; The VP, Compliance will be a trusted advisor to Nuvalent leadership and a partner across business units.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with the legal team and key stakeholders to build, implement, and maintain a robust and effective U.S. and global comprehensive healthcare compliance program that is right sized for Nuvalent as it transitions to a commercial organization&lt;/li&gt;
&lt;li&gt;Develop, refine and update policies and practices to facilitate global compliance and best practices.&lt;/li&gt;
&lt;li&gt;Advise on compliance matters including interpretation and application of Nuvalent&#39;s Code of Business Conduct, and Company policies.&lt;/li&gt;
&lt;li&gt;Lead implementation of our compliance training program.&lt;/li&gt;
&lt;li&gt;Lead implementation of our monitoring and auditing program, oversee audits and monitor the implementation of our compliance operations.&lt;/li&gt;
&lt;li&gt;Foster a strong internal compliance, ethics, and “speak-up” culture by creating an environment in which employees see Compliance as a strategic partner&lt;/li&gt;
&lt;li&gt;Lead the evaluation, investigation, and resolution of compliance&amp;nbsp;issues/concerns within the organization&lt;/li&gt;
&lt;li&gt;Conduct periodic risk assessments and develop and implement a work plan to address risk.&lt;/li&gt;
&lt;li&gt;Develop process for and oversee compliance with applicable state and federal transparency and aggregate reporting laws (and non-US country laws, as appropriate) and regulations&lt;/li&gt;
&lt;li&gt;Lead and mentor compliance team and ensure appropriate and cooperative allocation of responsibilities.&lt;/li&gt;
&lt;li&gt;Serve as a well-respected, credible subject matter expert throughout the organization, with the ability to provide business-oriented, practical guidance&lt;/li&gt;
&lt;li&gt;Stay current on new laws, regulations, best practices, and enforcement trends.&lt;/li&gt;
&lt;li&gt;Such other responsibilities as assigned from time to time by Chief Legal Officer.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;A professional leadership presence/demeanor, as well as a highly positive and responsible working attitude&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comfortable working in a fast-paced, results-driven, highly accountable environment, with a demonstrated ability to parallel process multiple projects with competing timelines&lt;/li&gt;
&lt;li&gt;Ability to communicate effectively with personnel at all levels of the organization and to inspire confidence and support for&amp;nbsp;compliance&amp;nbsp;initiatives&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Demonstrated ability to think strategically and pay close attention to detail&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to work collaboratively in teams with a practical, solution-oriented approach&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Strong project management skills and ability to handle multiple responsibilities simultaneously and still meet high quality and timeliness standards under pressure&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Self-motivated, able to work independently and be reliable, responsible, and accountable&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Minimum of 15 years of compliance experience in an organization subject to US pharmaceutical regulations; experience in oncology or rare disease business strongly preferred.&lt;/li&gt;
&lt;li&gt;Minimum of 5 years’ experience in an ethics and compliance leadership role.&lt;/li&gt;
&lt;li&gt;Bachelor’s degree required, law degree preferred but not required.&lt;/li&gt;
&lt;li&gt;Prior commercial launch experience is essential; experience guiding a company through its initial commercial launch is preferred.&lt;/li&gt;
&lt;li&gt;Willingness to travel up to 25% of time and conduct in-person training meetings.&lt;/li&gt;
&lt;li&gt;In-depth knowledge of compliance matters related to the launch and subsequent commercialization of branded pharmaceutical products, including a thorough understanding of healthcare laws and regulations and corporate governance issues related to development and commercialization of biopharmaceutical products, including without limitation US Federal healthcare program requirements under the Food, Drug and Cosmetic Act, the False Claims Act, the Anti-Kickback Statute, OIG guidelines and opinions, the Sunshine Act, FCPA. fraud and abuse, transparency, and other healthcare compliance matters&lt;/li&gt;
&lt;li&gt;Experience applying a risk-based analysis to compliance issues and demonstrated creativity in developing solutions that satisfy both our requirements and legal obligations.&lt;/li&gt;
&lt;li&gt;Ability to serve multiple client groups by recognizing and responding quickly and pragmatically to urgent situations.&lt;/li&gt;
&lt;li&gt;Appropriate judgment on when to collaborate with Legal and business colleagues or outside counsel.&lt;/li&gt;
&lt;li&gt;Excellent analytical, written, and verbal communication skills with a track record of preparing and delivering effective and engaging presentations and training programs to teams&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$300,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$335,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vice-president-compliance-(biopharma)-nuvalent/69d3bc25c8e81216cd0b9058</link><guid isPermaLink="true">http://biotechroles.com/vice-president-compliance-(biopharma)-nuvalent/69d3bc25c8e81216cd0b9058</guid><pubDate>Mon, 06 Apr 2026 13:59:00 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, Analytical Development and Quality Control]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases.&lt;/p&gt;
&lt;p&gt;FL87 was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are searching for an experienced and enthusiastic Scientist I/ II, Analytical Development and Quality Control to lead the development of novel methods to characterize novel nucleic acid therapeutics. We are looking for an individual who enjoys hands-on laboratory benchwork and brings scientific rigor and intellectual curiosity to their role. This individual will have the opportunity to work in a dynamic and fast-paced entrepreneurial environment as part of a highly collaborative and rapidly growing team.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Work with the team to drive advancement of platform development and play a vital role in shaping our analytical capabilities. Step into benchwork to execute platform goals with tenacity, agility, and timeliness.&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead the design, development, optimization, and execution of HPLC-based analytical methods (e.g., RP-HPLC, SEC, IEX) to support in-process, release, and stability testing.&lt;/li&gt;
&lt;li&gt;Develop, qualify, validate, and characterize GMP-compliant purity, SEC, and content methods for intermediates and drug products, with a strong emphasis on chromatographic workflows.&lt;/li&gt;
&lt;li&gt;Serve as Subject Matter Expert for chromatography methods during investigations of deviations, OOS/OOT events, assay failures, and other non-conformance issues.&lt;/li&gt;
&lt;li&gt;Provide technical leadership in HPLC troubleshooting, instrument maintenance coordination, data integrity practices, and chromatographic data review.&lt;/li&gt;
&lt;li&gt;Maintain rigorous laboratory documentation and complete, audit-ready analytical records.&lt;/li&gt;
&lt;li&gt;Collaborate effectively with QC, Manufacturing, and Process Development teams to enable program success across phases.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Analyze, troubleshoot, and communicate experimental findings clearly and succinctly in oral, written, and visual formats.&lt;/li&gt;
&lt;li&gt;Work independently and collaboratively in a multidisciplinary team environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD (1+ years) or M.S. (8+ years) in Analytical Chemistry, Biochemistry, or related field.&lt;/li&gt;
&lt;li&gt;Demonstrated in-depth expertise in HPLC, including method development, troubleshooting, system suitability design, chromatographic theory, and data interpretation.&lt;/li&gt;
&lt;li&gt;Hands-on experience with multiple chromatographic techniques (RP-HPLC, SEC, IEX, affinity, gradient optimization, detector setup/maintenance).&lt;/li&gt;
&lt;li&gt;Proven success developing and validating GMP analytical methods and supporting GMP operations.&lt;/li&gt;
&lt;li&gt;Experience with complementary analytical techniques such as UV-Vis, LC-MS, CE, ELISA, or other functional assays is beneficial.&lt;/li&gt;
&lt;li&gt;Experience working in a QC or cGMP laboratory environment with strong understanding of data integrity requirements (&lt;/li&gt;
&lt;li&gt;Strong communication, team leadership, and interpersonal skills.&lt;/li&gt;
&lt;li&gt;Track record of working effectively in a multidisciplinary environment, interacting with teams from other line functions.&lt;/li&gt;
&lt;li&gt;Strong organizational skills, precision in documentation, and ability to manage multiple analytical workflows simultaneously.&lt;/li&gt;
&lt;li&gt;Ability to thrive in a fast-paced, multidisciplinary, and rapidly growing biotech environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background &lt;strong&gt;and interest in Flagship&lt;/strong&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $100,000 - $143,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/scientist-analytical-development-and-quality-control-flagship-pioneering/69d3bc24c8e81216cd0b9057</link><guid isPermaLink="true">http://biotechroles.com/scientist-analytical-development-and-quality-control-flagship-pioneering/69d3bc24c8e81216cd0b9057</guid><pubDate>Mon, 06 Apr 2026 13:59:00 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Scientist, Chemistry]]></title><description><![CDATA[&lt;h4&gt;&lt;strong&gt;COMPANY&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Octant is pioneering a new generation of precision medicines by combining synthetic biology, chemistry, and AI/ML to tackle complex cellular mechanisms driving human disease. We are a small molecule therapeutics company scaling drug discovery to unlock therapies for genetically defined and historically intractable diseases.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;JOB DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Octant is seeking a driven and curious &lt;strong&gt;Scientist&lt;/strong&gt; to join the &lt;a href=&quot;https://openadmet.org/Octant_CYP_blog_post/&quot;&gt;OpenADMET&lt;/a&gt; team. OpenADMET’s mission is to build open predictive models of safety and toxicity for small molecules to improve humanity’s ability to more reliably, cheaply, and effectively treat disease. At a high level, you’ll play a hands-on role in leveraging Octant’s Navigator platform to synthesize and analyze novel small molecules that modulate disease-relevant cellular mechanisms. Specifically, you will support the OpenADMET initiative at Octant by building libraries targeting the “avoidome” to generate high quality data to fuel machine learning model development. You will also expand our platform chemistry capabilities by pioneering novel synthetic and analytical methods. Finally, you will leverage your platform expertise to further Octant’s drug discovery efforts.&lt;/p&gt;
&lt;p&gt;This is an opportunity to revolutionize the way we build drugs.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THIS JOB MIGHT BE GREAT FOR YOU IF YOU HAVE:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in Organic Chemistry, Chemical Biology, or related field with 0-3 years experience post PhD as a post doctoral candidate or industry scientist&lt;/li&gt;
&lt;li&gt;Expertise with multi step organic synthesis, purification and analysis (HPLC, LC/MS, NMR)&lt;/li&gt;
&lt;li&gt;Familiarity with the application of LC-MS methods for proteomics or high throughput screening&lt;/li&gt;
&lt;li&gt;Experience with laboratory automation platforms and high-throughput screening methods&lt;/li&gt;
&lt;li&gt;Excellent problem-solving and communication skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;NICE TO ALSO HAVE:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience coding for data analysis, visualization or lab automation (e.g., Python)&lt;/li&gt;
&lt;li&gt;Familiarity with high-throughput experimentation and direct-to-biology high throughput chemistry approaches&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Optional: Along with your application, please share a paper/preprint/software repo that best highlights your strengths so we can better understand work you&#39;ve led. If there is nothing public, please summarize that work in a few paragraphs. We&#39;d love to also hear about things you&#39;ve been proud to build or lead outside of science.&lt;/p&gt;
&lt;p&gt;The expected annual salary for this role is in the range of $130,000 to $145,000, depending on experience level. We offer health benefits (medical, dental, vision), equity, and 401(k) matching.&lt;/p&gt;
&lt;p&gt;Octant is located in Emeryville, California and we work onsite.&lt;/p&gt;
&lt;p&gt;Octant is an equal opportunity company that values applicants of all backgrounds. We’re committed to fostering an inclusive and supportive work environment. We value less traditional backgrounds, and may consider an equivalent combination of knowledge, skills, education, and experience to meet minimum qualifications. We know that confidence-gap and imposter syndrome can get in the way of meeting spectacular candidates, so please don’t hesitate to apply — we’d love to hear from you.&lt;/p&gt;
&lt;h4&gt;&lt;strong&gt;OCTANT’S NAVIGATOR PLATFORM:&lt;/strong&gt;&lt;/h4&gt;
&lt;p&gt;Octant’s Platform, “The Navigator,” accelerates the design, build, test, and learn iterations across chemistry and biology to build drugs against cellular mechanisms. The Navigator is an expanding set of drug discovery and development capabilities with three interwoven components that operate together:&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Generative Biology – Multiplexed measurements from engineered sensors in human cells to understand cellular mechanisms&lt;/li&gt;
&lt;li&gt;Generative Chemistry – Nanoliter-scale chemical synthesis for rapid exploration of &lt;em&gt;local&lt;/em&gt; &amp;amp; &lt;em&gt;targeted&lt;/em&gt; chemical space&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Generative AI – ML/AI ingests large-scale biological and chemical datasets and drives iteration of experiments to build better molecules faster&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Together, the Navigator platform drives week-to-week progress on our drug programs, generative 3M+ readouts each week across multiple therapeutic areas.&lt;/p&gt;]]></description><link>http://biotechroles.com/scientist-chemistry-octant/69d3bc22c8e81216cd0b9056</link><guid isPermaLink="true">http://biotechroles.com/scientist-chemistry-octant/69d3bc22c8e81216cd0b9056</guid><pubDate>Mon, 06 Apr 2026 13:58:58 GMT</pubDate><company>Octant</company><location>Emeryville, California, United States</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Research Associate/Senior Research Associate, Peptide Chemistry (Contract)]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Abiologics, Inc. is a privately held, early-stage biotechnology company on a mission to make biology better through an innovative therapeutic modality. We are pioneering the development of Synteins™, a transformational class of macromolecular medicines unlocked by novel synthetic and computational technologies. Abiologics is actively seeking exceptional scientists who are passionate about driving therapeutic modality innovation in biotechnology.&lt;/p&gt;
&lt;p&gt;Abiologics was founded in Flagship Pioneering’s venture creation engine, where companies such as Moderna Therapeutics (NASDAQ: MRNA) and Generate Biomedicines were conceived and created. Since Flagship’s founding in 2000, the firm has originated and fostered the development of more than 100 scientific ventures resulting in more than 500 issued patents and more than 50 clinical trials for novel therapeutic agents.&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This contract position offers a terrific opportunity to make a new class of groundbreaking medicines. The successful candidate will work closely with a group of skilled scientists to synthesize, and analyze complex peptides for therapeutic applications. This role requires a deep understanding of organic chemistry and problem-solving skills to develop novel chemistries and creating a new class of macromolecular medicines called Synteins™.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Apply a combination of solid-phase peptide synthesis, conjugation chemistries, and automation technologies to synthesize new macromolecules&lt;/li&gt;
&lt;li&gt;Purify and analyze macromolecules using modern instrumentation&lt;/li&gt;
&lt;li&gt;Independently troubleshoot challenging technical, experimental, and instrumental issues&lt;/li&gt;
&lt;li&gt;Evaluate macromolecular properties using various spectroscopical techniques&lt;/li&gt;
&lt;li&gt;Meticulously record and analyze data with a minimum of oversight&lt;/li&gt;
&lt;li&gt;Prepare and maintain laboratory reagents and instruments&lt;/li&gt;
&lt;li&gt;Regularly summarize progress of work in oral and written format&lt;/li&gt;
&lt;li&gt;Stay informed of the latest developments in peptide chemistry and related fields through continuous learning&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS or MS degree or equivalent experience in chemistry, chemical engineering, or biochemistry and 2+ years of industry experience&lt;/li&gt;
&lt;li&gt;Experience in either or all the following is a plus:
&lt;ul&gt;
&lt;li&gt;organic synthesis including solid-phase peptide synthesis&lt;/li&gt;
&lt;li&gt;reaction design, optimization, and automation&lt;/li&gt;
&lt;li&gt;analytical techniques LCMS, HPLC, FPLC, UV-VIS, CD&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Enthusiasm, independence, and a willingness to learn in a fast-paced, team environment&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills&lt;/li&gt;
&lt;li&gt;Committed to working collaboratively with an interdisciplinary team&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Boston, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&amp;nbsp;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;#LI-MB1&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The pay range for this role is $36 - $46 per hour and the contractor will be employed by a third-party staffing company. Certain employee benefits may be available to the contractor through the staffing company after meeting minimum criteria. Compensation and benefits information is based on Abiologics, Inc&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/research-associatesenior-research-associate-peptide-chemistry-(contract)-flagship-pioneering/69d3bc20c8e81216cd0b9053</link><guid isPermaLink="true">http://biotechroles.com/research-associatesenior-research-associate-peptide-chemistry-(contract)-flagship-pioneering/69d3bc20c8e81216cd0b9053</guid><pubDate>Mon, 06 Apr 2026 13:58:56 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$85000-140000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales): Washington, DC / Baltimore, MD]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The major metro regions for this Southeast territory are Washington DC, / Baltimore, MD&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-washington-dc-baltimore-md-nuvalent/69d3bc20c8e81216cd0b9052</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-washington-dc-baltimore-md-nuvalent/69d3bc20c8e81216cd0b9052</guid><pubDate>Mon, 06 Apr 2026 13:58:56 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Women's Health & Preeclampsia]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;dhkj5-0-0&quot;&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound™ Therapeutics is a biotechnology company discovering novel proteins across the expanded human proteome to unlock first-in-class medicines and transformative drug targets. The company’s proprietary ProFoundry™ Platform integrates state-of-the-art protein detection, validation, and computational technologies to systematically identify and characterize previously inaccessible proteins and validate their therapeutic potential. This approach has generated a rapidly expanding portfolio of novel targets and programs advancing toward the clinic, along with strategic collaborations with leading pharmaceutical partners. Together, these efforts support the development of breakthrough treatments across a broad range of disease areas. For more information, please visit www.profoundtx.com.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;ProFound Therapeutics is seeking an exceptional Principal Scientist to lead and support discovery efforts in Women’s Health, with a focus on preeclampsia and hypertensive disorders of pregnancy. This role contributes to shaping the company’s early-stage pipeline by providing scientific leadership, strategic thinking, and translational rigor across target validation and disease biology.&lt;/p&gt;
&lt;p&gt;The ideal candidate brings deep expertise in preeclampsia and related vascular or placental biology, a passion for uncovering novel disease mechanisms, and a demonstrated ability to design and execute mechanistic studies that bridge in vitro and in vivo models. This is a high-impact, cross-functional role operating with a high degree of scientific autonomy and influence.&lt;/p&gt;
&lt;p&gt;This role works closely with platform scientists, computational biologists, drug discovery teams, and external collaborators to identify, validate, and advance novel therapeutic targets toward drug development.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide scientific leadership for discovery research in preeclampsia and hypertension in pregnancy by designing, executing, and interpreting mechanistic studies using state-of-the-art experimental models and technologies.&lt;/li&gt;
&lt;li&gt;Lead target validation efforts informed by proteomic and computational insights; develop hypotheses, assess risk, and prioritize targets with strong translational potential.&lt;/li&gt;
&lt;li&gt;Partner closely with computational biology and proteomics teams to apply AI-enabled approaches to large-scale datasets (e.g., proteomic, transcriptomic, genetic) and generate novel biological insights.&lt;/li&gt;
&lt;li&gt;Design and oversee in vitro and in vivo disease models to support target biology, biomarker development, and proof-of-concept studies.&lt;/li&gt;
&lt;li&gt;Contribute meaningfully to building and refining the company’s therapeutic strategy in Women’s Health, including scientific decision-making and portfolio discussions.&lt;/li&gt;
&lt;li&gt;Communicate scientific findings clearly and effectively in cross-functional forums, external collaborations, and presentations to senior leadership.&lt;/li&gt;
&lt;li&gt;Support or lead external academic and industry collaborations, including scientific strategy, execution oversight, and data integration.&lt;/li&gt;
&lt;li&gt;Operate in a hybrid role, with approximately 75% focus on scientific leadership, strategy, and collaboration, and 25% hands-on laboratory work, as appropriate.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Physiology, Cell Biology, or a related discipline; postdoctoral training and/or industry experience strongly preferred.&lt;/li&gt;
&lt;li&gt;7+ years of relevant postdoctoral and/or industry experience, consistent with Senior Principal Scientist-level impact and scope.&lt;/li&gt;
&lt;li&gt;Deep understanding of disease mechanisms and translational models in one or more of the following areas: preeclampsia, hypertension, placental development and function, or related biology.&lt;/li&gt;
&lt;li&gt;Hands-on expertise in cellular and molecular biology techniques (e.g., CRISPR, ELISA, qPCR, Western blotting, RNA-seq) and assay development.&lt;/li&gt;
&lt;li&gt;Experience with in vitro and/or in vivo models relevant to the study of pregnancy and related disorders.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to integrate multi-omic and/or genetic data into experimental design and biological interpretation.&lt;/li&gt;
&lt;li&gt;Strong track record of scientific contributions, including publications, patents, and/or scientific presentations.&lt;/li&gt;
&lt;li&gt;Excellent communication, collaboration, and organizational skills, with the ability to operate effectively in a fast-paced, team-oriented environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience working in early-stage biotech or drug discovery environments.&lt;/li&gt;
&lt;li&gt;Familiarity with target identification and validation workflows.&lt;/li&gt;
&lt;li&gt;Experience working with human tissue samples, iPSC-derived systems, and/or organoid models.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&amp;nbsp;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $163,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. ProFound Therapeutics, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on ProFound Therapeutics, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-women&apos;s-health-and-preeclampsia-flagship-pioneering/69d3bc1dc8e81216cd0b904d</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-women&apos;s-health-and-preeclampsia-flagship-pioneering/69d3bc1dc8e81216cd0b904d</guid><pubDate>Mon, 06 Apr 2026 13:58:53 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales): Tampa, FL]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The major metro regions for this Southeast territory are Tampa, St. Petersburg, Fort Myers, FL&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-tampa-fl-nuvalent/69d3bc1cc8e81216cd0b904c</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-tampa-fl-nuvalent/69d3bc1cc8e81216cd0b904c</guid><pubDate>Mon, 06 Apr 2026 13:58:52 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Machine Learning, Origination]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a &lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Principal Scientist (Embedded ML/Computational)&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt; to lead multiple AI/ML or computational projects across early stage ventures, as a part of Flagship’s company origination process. You will define and deliver pragmatic AI strategies, oversee method and platform development (e.g., systems design, drug design, molecular modeling, systems biology, protein design, LLM/agentic workflows), and ensure rigor in model development, benchmarking, scaling, and reporting. You will manage cross functional contributors as applicable, influence company direction, and represent PI to venture teams and external partners. The ideal candidate is a self-directed serial deep diver - someone who can move from protein design one week to mass spec or docking pipelines the next and then spin up LLM based agents that automate scientific workflows.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Program Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Lead development, implementation, control, and reporting of several AI/ML or computational projects within assigned ventures in line with broader strategic plans of PI and Flagship, budgets, and timelines.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Technical Ownership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Take a specialized technical role on project teams to oversee method development, pipeline development, and LLM based agent/workflow design; drive benchmarking, scaling, and implementation into production grade systems.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Best Practices: &lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;promote operational excellence in AI projects by educating cross-functional collaborators.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Team Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Manage and/or coordinate internal and external scientists/engineers and crossfunctional project teams as applicable; mentor early hires; support recruiting and interview.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Planning &amp;amp; Resourcing&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Contribute to project planning, including budgets, resources, and timelines; surface risks and tradeoffs early with clear options.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Landscape &amp;amp; Strategy&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Independently scout emerging literature and the AI/ML landscape; synthesize concepts to propose new development strategies and identify opportunities for PI and venture portfolios.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Representation &amp;amp; Community&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Represent PI to portfolio companies and external partners; act as a recognized subject matter expert; actively participate in scientific conferences and meetings.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Communication &amp;amp; Influence&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Influence the course of projects and technical approaches; adapt and present complex findings to diverse audiences to support meaningful interpretation and action.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Master’s, or PhD in a relevant field (e.g., machine learning, mathematics, statistics, computational sciences) with 5+ years&#39; experience scientific/engineering/computational in academic, pharmaceutical, or biotechnology settings; industry AI/ML experience preferred.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience driving results directly or indirectly through teams of engineers/scientists in dynamic, fastpaced, entrepreneurial, and technical environments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Clear evidence of sustained independent thought and creativity driving high impact, cross disciplinary AI/ML projects.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Successful track record of leadership and contribution to decision making on progression of AI/ML models within projects or programs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Depth across multiple core tools and concepts, including Python; modern ML frameworks (PyTorch or JAX/TensorFlow); version control; databases; deep learning architectures; and relevant informatics software.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Consistent record of outstanding performance reflected in publications, patents, or high impact internal reports where applicable&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Breadth across domains such as protein modeling/design, proteomics/mass spec, cheminformatics/docking/ADMET, biophysics/MD, and LLM/agentic automation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;MLOps expertise: data contracts and lineage (e.g., DVC/LakeFS), experiment tracking (MLflow/W&amp;amp;B), secure AWS infrastructure (S3, Batch/ECS/EKS, SageMaker), Docker, IaC (Terraform/CDK), and CI/CD (GitHub Actions).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Generative modeling (diffusion/flow/VAEs) for sequences, graphs, or 3D structures; docking rescoring (e.g., gnina, DiffDock) and pose quality metrics.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Workflow orchestration (Airflow/Prefect/Argo), data warehouses (Redshift/Snowflake), vector search (FAISS/pgvector), and lightweight internal tools (FastAPI, Streamlit/Gradio).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience mentoring early hires, acting as interim Head of ML, and contributing to hiring plans and interview processes at startups.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;WHY PIONEERING INTELLIGENCE&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Operate at the frontier&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Build and deploy AI/ML that directly powers discovery and decision making across multiple new ventures.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Own the full stack&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: From scoping and data contracts to models, MLOps, and internal UIs—ship endtoend systems that scientists rely on daily.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Compound impact&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Convert one off wins into shared libraries and templates adopted across the PI portfolio.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work with founders&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Partner closely with venture leadership and PI platform engineers; influence strategy through hands on delivery.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Grow fast&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Stretch across domains, take on situational leadership, present at conferences, and help shape first ML teams.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $208,000 - $286,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-machine-learning-origination-flagship-pioneering/69d3bc19c8e81216cd0b904a</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-machine-learning-origination-flagship-pioneering/69d3bc19c8e81216cd0b904a</guid><pubDate>Mon, 06 Apr 2026 13:58:48 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales):  Richmond, VA]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The major metro regions for this Southeast territory are Norfolk, Roanoke, Arlington, Virginia Beach, VA&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-richmond-va-nuvalent/69d3bc18c8e81216cd0b9049</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-richmond-va-nuvalent/69d3bc18c8e81216cd0b9049</guid><pubDate>Mon, 06 Apr 2026 13:58:48 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales): Portland, OR]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The major metro regions for this West territory are Portland, OR / Boise, ID / Billings, MO&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-portland-or-nuvalent/69d3bc14c8e81216cd0b9045</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-portland-or-nuvalent/69d3bc14c8e81216cd0b9045</guid><pubDate>Mon, 06 Apr 2026 13:58:44 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Machine Learning, Genomics]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a &lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Principal Scientist (Embedded ML/Computational)&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt; to lead multiple AI/ML or computational projects across early stage ventures, as a part of Flagship’s company origination process. You will define and deliver pragmatic AI strategies, oversee method and platform development (e.g., systems design, drug design, molecular modeling, systems biology, protein design, LLM/agentic workflows), and ensure rigor in model development, benchmarking, scaling, and reporting. You will manage cross functional contributors as applicable, influence company direction, and represent PI to venture teams and external partners. The ideal candidate is a self-directed serial deep diver - someone who can move from protein design one week to mass spec or docking pipelines the next and then spin up LLM based agents that automate scientific workflows.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Program Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Lead development, implementation, control, and reporting of several AI/ML or computational projects within assigned ventures in line with broader strategic plans of PI and Flagship, budgets, and timelines.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Technical Ownership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Take a specialized technical role on project teams to oversee method development, pipeline development, and LLM based agent/workflow design; drive benchmarking, scaling, and implementation into production grade systems.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Best Practices: &lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;promote operational excellence in AI projects by educating cross-functional collaborators.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Team Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Manage and/or coordinate internal and external scientists/engineers and crossfunctional project teams as applicable; mentor early hires; support recruiting and interview.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Planning &amp;amp; Resourcing&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Contribute to project planning, including budgets, resources, and timelines; surface risks and tradeoffs early with clear options.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Landscape &amp;amp; Strategy&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Independently scout emerging literature and the AI/ML landscape; synthesize concepts to propose new development strategies and identify opportunities for PI and venture portfolios.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Representation &amp;amp; Community&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Represent PI to portfolio companies and external partners; act as a recognized subject matter expert; actively participate in scientific conferences and meetings.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Communication &amp;amp; Influence&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Influence the course of projects and technical approaches; adapt and present complex findings to diverse audiences to support meaningful interpretation and action.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Master’s, or PhD in a relevant field (e.g., machine learning, mathematics, statistics, computational sciences) with 5+ years&#39; experience scientific/engineering/computational in academic, pharmaceutical, or biotechnology settings; industry AI/ML experience preferred.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience driving results directly or indirectly through teams of engineers/scientists in dynamic, fastpaced, entrepreneurial, and technical environments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Clear evidence of sustained independent thought and creativity driving high impact, cross disciplinary AI/ML projects.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Successful track record of leadership and contribution to decision making on progression of AI/ML models within projects or programs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Depth across multiple core tools and concepts, including Python; modern ML frameworks (PyTorch or JAX/TensorFlow); version control; databases; deep learning architectures; and relevant informatics software.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Consistent record of outstanding performance reflected in publications, patents, or high impact internal reports where applicable&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Breadth across domains such as protein modeling/design, proteomics/mass spec, cheminformatics/docking/ADMET, biophysics/MD, and LLM/agentic automation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;MLOps expertise: data contracts and lineage (e.g., DVC/LakeFS), experiment tracking (MLflow/W&amp;amp;B), secure AWS infrastructure (S3, Batch/ECS/EKS, SageMaker), Docker, IaC (Terraform/CDK), and CI/CD (GitHub Actions).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Generative modeling (diffusion/flow/VAEs) for sequences, graphs, or 3D structures; docking rescoring (e.g., gnina, DiffDock) and pose quality metrics.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Workflow orchestration (Airflow/Prefect/Argo), data warehouses (Redshift/Snowflake), vector search (FAISS/pgvector), and lightweight internal tools (FastAPI, Streamlit/Gradio).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience mentoring early hires, acting as interim Head of ML, and contributing to hiring plans and interview processes at startups.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;WHY PIONEERING INTELLIGENCE&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Operate at the frontier&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Build and deploy AI/ML that directly powers discovery and decision making across multiple new ventures.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Own the full stack&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: From scoping and data contracts to models, MLOps, and internal UIs—ship endtoend systems that scientists rely on daily.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Compound impact&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Convert one off wins into shared libraries and templates adopted across the PI portfolio.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work with founders&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Partner closely with venture leadership and PI platform engineers; influence strategy through hands on delivery.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Grow fast&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Stretch across domains, take on situational leadership, present at conferences, and help shape first ML teams.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $208,000 - $286,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-machine-learning-genomics-flagship-pioneering/69d3bc14c8e81216cd0b9044</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-machine-learning-genomics-flagship-pioneering/69d3bc14c8e81216cd0b9044</guid><pubDate>Mon, 06 Apr 2026 13:58:43 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales): Nashville, TN]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The major metro regions for this Great Lakes territory are Nashville, Knoxville, Memphis, TN / Asheville, NC&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-nashville-tn-nuvalent/69d3bc10c8e81216cd0b9042</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-nashville-tn-nuvalent/69d3bc10c8e81216cd0b9042</guid><pubDate>Mon, 06 Apr 2026 13:58:39 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Machine Learning, Biomolecules]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING INTELLIGENCE&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Pioneering Intelligence builds on Flagship Pioneering’s legacy of founding cutting-edge science and computational ventures, harnessing recent advances in AI, machine learning, and data to accelerate fundamental research and create a portfolio of AI-first companies. As part of Flagship’s integrated model of science, entrepreneurship, and capital, it transforms breakthrough ideas into world-changing companies, elevating the AI advances happening across the ecosystem in human health, sustainability, and beyond.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a &lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Principal Scientist (Embedded ML/Computational)&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt; to lead multiple AI/ML or computational projects across early stage ventures, as a part of Flagship’s company origination process. You will define and deliver pragmatic AI strategies, oversee method and platform development (e.g., systems design, drug design, molecular modeling, systems biology, protein design, LLM/agentic workflows), and ensure rigor in model development, benchmarking, scaling, and reporting. You will manage cross functional contributors as applicable, influence company direction, and represent PI to venture teams and external partners. The ideal candidate is a self-directed serial deep diver - someone who can move from protein design one week to mass spec or docking pipelines the next and then spin up LLM based agents that automate scientific workflows.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Program Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Lead development, implementation, control, and reporting of several AI/ML or computational projects within assigned ventures in line with broader strategic plans of PI and Flagship, budgets, and timelines.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Technical Ownership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Take a specialized technical role on project teams to oversee method development, pipeline development, and LLM based agent/workflow design; drive benchmarking, scaling, and implementation into production grade systems.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Best Practices: &lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;promote operational excellence in AI projects by educating cross-functional collaborators.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Team Leadership&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Manage and/or coordinate internal and external scientists/engineers and crossfunctional project teams as applicable; mentor early hires; support recruiting and interview.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Planning &amp;amp; Resourcing&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Contribute to project planning, including budgets, resources, and timelines; surface risks and tradeoffs early with clear options.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Landscape &amp;amp; Strategy&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Independently scout emerging literature and the AI/ML landscape; synthesize concepts to propose new development strategies and identify opportunities for PI and venture portfolios.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Representation &amp;amp; Community&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Represent PI to portfolio companies and external partners; act as a recognized subject matter expert; actively participate in scientific conferences and meetings.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Communication &amp;amp; Influence&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Influence the course of projects and technical approaches; adapt and present complex findings to diverse audiences to support meaningful interpretation and action.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Master’s, or PhD in a relevant field (e.g., machine learning, mathematics, statistics, computational sciences) with 5+ years&#39; experience scientific/engineering/computational in academic, pharmaceutical, or biotechnology settings; industry AI/ML experience preferred.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience driving results directly or indirectly through teams of engineers/scientists in dynamic, fastpaced, entrepreneurial, and technical environments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Clear evidence of sustained independent thought and creativity driving high impact, cross disciplinary AI/ML projects.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Successful track record of leadership and contribution to decision making on progression of AI/ML models within projects or programs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Depth across multiple core tools and concepts, including Python; modern ML frameworks (PyTorch or JAX/TensorFlow); version control; databases; deep learning architectures; and relevant informatics software.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Consistent record of outstanding performance reflected in publications, patents, or high impact internal reports where applicable&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Preferred Qualifications&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Breadth across domains such as protein modeling/design, proteomics/mass spec, cheminformatics/docking/ADMET, biophysics/MD, and LLM/agentic automation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;MLOps expertise: data contracts and lineage (e.g., DVC/LakeFS), experiment tracking (MLflow/W&amp;amp;B), secure AWS infrastructure (S3, Batch/ECS/EKS, SageMaker), Docker, IaC (Terraform/CDK), and CI/CD (GitHub Actions).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Generative modeling (diffusion/flow/VAEs) for sequences, graphs, or 3D structures; docking rescoring (e.g., gnina, DiffDock) and pose quality metrics.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Workflow orchestration (Airflow/Prefect/Argo), data warehouses (Redshift/Snowflake), vector search (FAISS/pgvector), and lightweight internal tools (FastAPI, Streamlit/Gradio).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience mentoring early hires, acting as interim Head of ML, and contributing to hiring plans and interview processes at startups.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;WHY PIONEERING INTELLIGENCE&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Operate at the frontier&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Build and deploy AI/ML that directly powers discovery and decision making across multiple new ventures.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Own the full stack&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: From scoping and data contracts to models, MLOps, and internal UIs—ship endtoend systems that scientists rely on daily.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Compound impact&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Convert one off wins into shared libraries and templates adopted across the PI portfolio.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work with founders&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Partner closely with venture leadership and PI platform engineers; influence strategy through hands on delivery.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Grow fast&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Stretch across domains, take on situational leadership, present at conferences, and help shape first ML teams.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $208,000 - $286,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Intelligence currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Intelligence’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-machine-learning-biomolecules-flagship-pioneering/69d3bc0fc8e81216cd0b9040</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-machine-learning-biomolecules-flagship-pioneering/69d3bc0fc8e81216cd0b9040</guid><pubDate>Mon, 06 Apr 2026 13:58:39 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Account Manager (Sales): Miami, FL]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;em&gt;This role is field-based, and candidates should live within a reasonable distance from the primary city and state to effectively cover the assigned territory.&lt;/em&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The major metro regions for this Southeast territory are Miami, Fort Lauderdale, FL / Puerto Rico&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Regional Business Director, the Senior Oncology Account Manager (Sr. OAM) will contribute to Nuvalent’s overall sales objective by performing assigned sales-related activities. The Sr. OAM will provide physicians, pharmacists, nurses, and all healthcare professionals (HCPs) with products, services, and approved information that enable them to prescribe Nuvalent’s product(s) appropriately.&lt;/p&gt;
&lt;p&gt;The Sr. OAM will implement Nuvalent’s marketing strategies and execute corresponding plans in a compliant and successful manner to achieve both short-term and long-term objectives. The ideal candidate will be capable of managing the territory and administrative requirements efficiently and effectively while maintaining full compliance with drug laws and regulations when representing Nuvalent and Nuvalent’s products to Healthcare Providers. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Achieve the assigned sales objective for the territory&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attain the designated goals for calls on appropriate healthcare professionals to communicate balanced, accurate, and complete information on Nuvalent’s FDA approved products&lt;/li&gt;
&lt;li&gt;Develop and implement a territory business plan to meet customer needs and achieve goals&lt;/li&gt;
&lt;li&gt;Navigate through complex external/customer organizational structures, including hospitals, integrated delivery networks (IDNs), group purchasing organizations (GPOs), and healthcare communities, while aligning with cross-functional commercial partners. Be passionate and motivated through headwinds, driving results in the face of adversity.&lt;/li&gt;
&lt;li&gt;Demonstrate adherence of administrative requirements, including budget management, expense reports management, CRM call reporting and synchronization, etc., within timelines and company guidelines.&lt;/li&gt;
&lt;li&gt;Demonstrate a deep understanding of healthcare professionals (HCP) and account needs, effectively utilizing this knowledge to strategically promote and expand the use of assigned products.&lt;/li&gt;
&lt;li&gt;Operate the territory within the assigned expense budget and demonstrate fiscal responsibility.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Comply with all federal, state, and local laws, regulations, and guidelines, including but not limited to the PhRMA Code on Interactions with Healthcare Professionals, as well as complying with all Nuvalent standards and policies relating to all job activities.&lt;/li&gt;
&lt;li&gt;Successfully complete training and participation in ongoing updates, including but not limited to product knowledge, disease state, market, selling skills, and compliance.&lt;/li&gt;
&lt;li&gt;Assist in the identification and resolution of issues and opportunities while communicating proactively with marketing and sales management. Be disciplined but also willing to challenge norms and processes for continuous improvement. Develop and consistently demonstrate an expert understanding of HCP and Account needs to expand the use of the assigned product appropriately. &lt;/li&gt;
&lt;li&gt;Operate with a strong business owner mentality, taking full accountability for territory outcomes.&lt;/li&gt;
&lt;li&gt;Candidates must demonstrate rare / ultra rare experience and a willingness to navigate highly specialized, challenging markets. Partner seamlessly with Market Access, Medical Affairs (MSLs), Precision Engagement Managers, and Commercial leadership, collaborating cross-functionally, to deliver integrated customer support. Prioritize the collective success of the team and foster a team-oriented environment.&lt;/li&gt;
&lt;li&gt;Utilizing competitive intelligence, identifies and reports shifts in competitor activity, market trends, and customers’ needs to inform strategy and use the data deliberately in all aspects of account and territory management.&lt;/li&gt;
&lt;li&gt;Show diversity of experience, including a range of skillsets and work at previous companies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Customer Focus&lt;/strong&gt;: Builds deep, trust-based relationships with oncologists, infusion centers, nurses, pharmacists, and other decision makers; consistently demonstrates a patient-first mindset.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Territory Management&lt;/strong&gt;: Analyzes market data, prioritizes accounts, and executes strategic call planning to maximize impact and coverage.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Influence &amp;amp; Persuasion&lt;/strong&gt;: Effectively communicates clinical and economic value propositions tailored to the Oncology Market Expertise: Demonstrates a strong understanding of oncology treatment pathways, disease biology, diagnostics/biomarkers, and competitive landscape.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Clinical Fluency&lt;/strong&gt;: Confidently engages in scientific discussions with HCPs, navigating trial data, MOAs, and real-world evidence.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Compliance &amp;amp; Regulatory Adherence&lt;/strong&gt;: Operates within promotional regulations (FDA, OIG, PhRMA) and company compliance boundaries while still driving results.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Business Acumen:&lt;/strong&gt; Understands access, reimbursement, specialty pharmacy distribution, and practice economics to address customer and patient barriers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Data-Driven Decision Making: &lt;/strong&gt;Uses CRM, analytics, and market insights to adapt strategy and demonstrate ROI&lt;strong&gt;.&lt;/strong&gt;&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results Orientation: &lt;/strong&gt;Consistently meets/exceeds sales goals while balancing short-term results with long-term relationship building.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Resilience &amp;amp; Adaptability: &lt;/strong&gt;Thrives in high-change, high-stakes oncology environment; adjusts rapidly to new clinical data, competitive shifts, or access hurdles.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Problem Solving:&lt;/strong&gt; Develops innovative solutions for customer challenges (e.g., access barriers, clinical adoption hesitations).&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Mentorship &amp;amp; Team Contribution: &lt;/strong&gt;Coaches peers, shares best practices, and contributes to a high-performance team culture.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Integrity &amp;amp; Credibility: &lt;/strong&gt;Earns trust through ethical decision-making, transparency, and consistency with company values.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree is required, ideally in business, marketing, healthcare, life science areas of concentration&lt;/li&gt;
&lt;li&gt;9+ years of successful pharmaceutical/biotech sales experience with 3+ in the oncology/hematology and/or rare disease markets, preferably with oral therapeutic selling experience&lt;/li&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Strong computer skills, notably MS Word, MS Excel, and MS PowerPoint&lt;/li&gt;
&lt;li&gt;Periodic overnight travel will be needed for the management of large territories&lt;/li&gt;
&lt;li&gt;Occasional evenings and weekend work may be needed for conferences&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with market-competitive total rewards packages.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The targeted salary range below&amp;nbsp;reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401 (k) retirement savings plan, generous paid time off (including&amp;nbsp;a summer and winter company shutdown), and much more.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$195,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$220,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-account-manager-(sales):-miami-fl-nuvalent/69d3bc0bc8e81216cd0b903e</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-account-manager-(sales):-miami-fl-nuvalent/69d3bc0bc8e81216cd0b903e</guid><pubDate>Mon, 06 Apr 2026 13:58:35 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Machine Learning]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;About Abiologics&lt;/span&gt;&lt;/strong&gt;&amp;nbsp;&lt;br&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Abiologics, Inc. is a privately held, early-stage biotechnology company on a mission to make biology better through chemistry. We are pioneering the development of&amp;nbsp;Synteins&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-fontsize=&quot;12&quot;&gt;TM&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;, a transformational class of&amp;nbsp;synthetic&amp;nbsp;macromolecular medicines&amp;nbsp;composed entirely of non-natural amino acids.&amp;nbsp;Synteins&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-fontsize=&quot;12&quot;&gt;TM&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;are designed to overcome the limitations of traditional biologics, offering programmable stability, delivery, and immune evasion.&amp;nbsp;Abiologics&amp;nbsp;is actively seeking exceptional molecular scientists who are passionate about driving chemical innovation in biotechnology.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Abiologics&amp;nbsp;was founded in Flagship Pioneering’s venture creation engine, where companies such as Moderna Therapeutics (NASDAQ: MRNA) and Generate Biomedicines were conceived and created. Since Flagship’s founding in 2000, the firm has originated and fostered the development of more than 100 scientific ventures resulting in more than 500&amp;nbsp;issued patents&amp;nbsp;and more than 50 clinical trials for novel therapeutic agents.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Position Summary&lt;/span&gt;&lt;/strong&gt;&amp;nbsp;&lt;br&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a Machine Learning&amp;nbsp;scientist&amp;nbsp;to&amp;nbsp;join our computational team&amp;nbsp;to bring SOTA ML models&amp;nbsp;that drive the design and optimization of&amp;nbsp;Synteins&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-fontsize=&quot;12&quot;&gt;TM&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;. You will work at the interface of&amp;nbsp;peptide&amp;nbsp;science, cheminformatics, and AI, collaborating with experimentalists to&amp;nbsp;optimize&amp;nbsp;molecules for affinity, stability, solubility, and&amp;nbsp;other critical&amp;nbsp;developability&amp;nbsp;properties.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;This is a highly interdisciplinary, hands-on role in a fast-moving team. Ideal candidates will have prior experience building or applying ML models to molecular property prediction and optimization in the context of peptides, proteins, or small molecules.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop predictive and generative models to guide&amp;nbsp;Syntein&amp;nbsp;optimization for synthesis efficiency, target binding affinity and selectivity, solubility, thermal stability, and protease resistance.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Integrate large experimental datasets (e.g.,&amp;nbsp;mass, purity, yield, binding, inhibition, activity,&amp;nbsp;structure&amp;nbsp;and stability) to train and refine models in a closed-loop system.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with chemists, biologists, and protein designers to design and prioritize&amp;nbsp;Syntein&amp;nbsp;libraries for synthesis and screening.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Contribute to internal ML pipelines, data infrastructure, and model validation best practices, supporting the scale-up of our discovery platform.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Required&lt;/span&gt;&lt;/em&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;PhD in computational biology, bioengineering, machine learning, or&amp;nbsp;a related field.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;5+ years of industry experience applying ML to protein, peptide, or small molecule modeling.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated&amp;nbsp;experience&amp;nbsp;building models to predict molecular or physicochemical properties (e.g., solubility, stability, binding).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proficiency&amp;nbsp;in Python and ML frameworks (e.g.,&amp;nbsp;PyTorch, scikit-learn,&amp;nbsp;RDKit,&amp;nbsp;PyG).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience in diverse deep learning architectures (e.g.,&amp;nbsp;GNN, RL, VAE, Transformers, GAN)&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication skills with the ability to&amp;nbsp;synthesize AI/ML&amp;nbsp;tools and concepts to team members across many departments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Preferred&lt;/span&gt;&lt;/em&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Familiarity with peptide/protein design concepts (e.g., structure-based optimization, binding site modeling, non-canonical&amp;nbsp;amino acids).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience&amp;nbsp;in the application of ML tools&amp;nbsp;in drug discovery&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with experimental collaboration and designing hypotheses that inform synthesis or screening.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience working in a startup, platform company, or cross-functional discovery team.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Why Join&amp;nbsp;Abiologics&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work on a first-in-class therapeutic modality with unprecedented design flexibility.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Be part of a fast-moving, data-rich platform with real-time feedback from automated synthesis and screening.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with world-class scientists&amp;nbsp;across the&amp;nbsp;Flagship Pioneering&amp;nbsp;ecosystem.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Help build the future of programmable biologics.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
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&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;#LI-MB1&lt;/p&gt;
&lt;/div&gt;
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&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $212,000 - $291,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Abiologics, Inc currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Abiologics, Inc&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-machine-learning-flagship-pioneering/69d3bc0ac8e81216cd0b903d</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-machine-learning-flagship-pioneering/69d3bc0ac8e81216cd0b903d</guid><pubDate>Mon, 06 Apr 2026 13:58:34 GMT</pubDate><company>Flagship Pioneering</company><location>Boston, MA USA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Formulation Sciences]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Associate Director, Formulation Sciences, the Senior Manager, Formulation Sciences will act as late-stage drug product subject matter expert and will support drug product process validation toward commercialization. The successful candidate needs to demonstrate a proven record of working in a virtual environment with CDMOs to deliver clinical and commercial supplies in support of fast-paced late-stage development programs. Using strategic thinking, the Senior Manager must be able to develop and execute process validation strategies for successful product commercialization.&lt;/p&gt;
&lt;p&gt;This individual has responsibility for support of drug product process validation, scale up, and post-approval changes (SUPAC) and routine commercial manufacturing activities across Nuvalent’s contract research and manufacturing organizations. The primary accountability is being the steward for product development and manufacturing as these programs transition through development and into commercialization. The ultimate goal will be to ensure robust process and manufacture strategies for consistent commercial supply.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support drug product Process Validation activities, Scale up and post-approval changes (SUPAC) and routine commercial manufacturing at CDMOs.&lt;/li&gt;
&lt;li&gt;Identify critical process parameters based on the risk assessment and understanding the impact of material attributes and process parameters on critical quality attributes. Implement appropriate process controls to ensure delivery of consistent batch product quality.&lt;/li&gt;
&lt;li&gt;Draft, coordinate, execute validation protocols, perform data analysis, author/review and approve process validation reports with consistent and effective communication with other functions.&lt;/li&gt;
&lt;li&gt;Provide support to routine process validation studies, assisting with product technology transfers or lifecycle management changes such as process improvement, addition of secondary API and manufacture site change etc.&lt;/li&gt;
&lt;li&gt;Perform technical review of drug product manufacture deviations, change controls, perform process monitoring (manufacturing data summary and analysis, data presentation), perform activities for drug product lot release (assess deviations and process changes).&lt;/li&gt;
&lt;li&gt;Work closely with other team members and cross-functionally with quality assurance, analytical/QC, chemical development, supply chain, and project management team to achieve all project deliverables.&lt;/li&gt;
&lt;li&gt;Provide support for technical decision-making regarding cGMP compliance, validation strategy and regulatory pathway for SUPAC changes etc.&lt;/li&gt;
&lt;li&gt;Familiar with statistical analysis software, such as JMP.&lt;/li&gt;
&lt;li&gt;Perform process capability analysis, identify risk, and make recommendations for process improvement.&lt;/li&gt;
&lt;li&gt;Manage documentation, change controls, material inventory, product complaints, and deviation resolution at CDMOs.&lt;/li&gt;
&lt;li&gt;Represent the drug product group as a Subject Matter Expert to support audits and regulatory inspections.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Support authoring the relevant technical sections of regulatory filings.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Support late-stage validation and post-approval readiness activities and commercial manufacture activities within a virtual working environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong organizational, planning, and multitasking skills in a fast‑paced environment.&lt;/li&gt;
&lt;li&gt;Excellent relationship‑building and communication skills across diverse teams.&lt;/li&gt;
&lt;li&gt;Evidence of effective cross‑functional collaboration with both internal teams and external partners.&lt;/li&gt;
&lt;li&gt;Strong problem‑solving and analytical skills with the ability to break down complex issues.&lt;/li&gt;
&lt;li&gt;Results‑driven mindset with attention to quality and timelines. A strong understanding and knowledge of cGMP/ICH regulations and an ability to apply them to drug product development and manufacturing is required.&lt;/li&gt;
&lt;li&gt;Excellent organization and multi-tasking skills.&lt;/li&gt;
&lt;li&gt;Experience building positive and effective cross functional relationships and the ability to align stakeholders, both internally and externally to Nuvalent.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in pharmaceutics, pharmaceutical sciences, chemical engineering or related field with a minimum of 3+ years or MS with 6+ years /BS with 10+ years of industry experience.&lt;/li&gt;
&lt;li&gt;Proven track record on drug product process validation, scale up and manufacture for solid dosage form (tablets).&lt;/li&gt;
&lt;li&gt;Experience with QbD principles and DOE methodology preferred.&lt;/li&gt;
&lt;li&gt;Manage the outsourcing manufacturing activities at CDMO sites to meet CMC goals.&lt;/li&gt;
&lt;li&gt;Understanding of cGMP/ICH guidelines and the ability to apply them to development and manufacturing.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Experience with solid dosage form (tablet) process development; exposure to late-stage validation is a plus.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Ability to author and critically review relevant development reports as well as regulatory dossiers.&lt;/li&gt;
&lt;li&gt;Up to 25% travel is expected, both domestically and internationally.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$155,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$180,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-formulation-sciences-nuvalent/69d3bc07c8e81216cd0b903c</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-formulation-sciences-nuvalent/69d3bc07c8e81216cd0b903c</guid><pubDate>Mon, 06 Apr 2026 13:58:31 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$150000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, Analytical Development]]></title><description><![CDATA[&lt;h4&gt;COMPANY DESCRIPTION&lt;/h4&gt;
&lt;p&gt;Mirai Bio, Inc is a Flagship backed, privately held biotechnology company on a mission to transform the current approach to information molecule therapeutics to unlock their full therapeutic potential. In recent years, we have begun to experience the power of information molecules in treating historically undruggable diseases and in designing therapies with unprecedented turnaround times. Mirai’s platform integrates nanoparticle development with world-class informatics technologies and a novel pipeline of experimentation and discovery to drive a new generation of highly effective, therapeutically relevant information molecule therapies. We are seeking collaborative, relentless problem solvers that share our passion for impact to join us!&lt;/p&gt;
&lt;p&gt;Mirai was founded by Flagship Pioneering. Flagship Pioneering conceives, creates, resources, and develops first-in-category life sciences companies to transform human health and sustainability. Since its launch in 2000, the firm has applied a unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $30 billion in aggregate value. The current Flagship ecosystem comprises 37 transformative companies, including: Moderna Therapeutics (NASDAQ: MRNA), Rubius Therapeutics (NASDAQ: RUBY), Indigo Agriculture, and Sana Biotechnology (NASDAQ: SANA).&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a highly experienced and innovative Principal Scientist to lead analytical development activities focused on&amp;nbsp;novel lipid nanoparticles (LNPs)&amp;nbsp;and nucleic acid cargos (RNA/DNA) for therapeutics and vaccines. The successful candidate will play a critical role in method development, characterization, and control strategies for novel LNP compositions at different stages of development from platform research to IND+. The role requires deep expertise in analytical chemistry and physicochemical / biophysical analyses for nanoparticle and nucleic acid characterization.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead analytical method development and testing for characterization of LNP-based drug products and nucleic acid drug substances (incl. RNA, DNA).&lt;/li&gt;
&lt;li&gt;Oversee analytical team to provide broad testing support across R&amp;amp;D functions using platform methods including lipid and nucleic acid composition, integrity, purity, particle size, encapsulation, and more.&amp;nbsp; On-site presence and active hands-on involvement in experimental work is expected&lt;/li&gt;
&lt;li&gt;Design and execute complex experiments for in-depth characterization using&amp;nbsp;DLS, HPLC, LC-MS, SEC, FFF/SEC-MALS, CE, UV-Vis, NMR, Cryo-EM and other advanced techniques for nanoparticle characterization.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Collaborate with Formulation, Process Development, and Translational teams to support batch testing, stability characterization, optimization, and troubleshooting.&amp;nbsp; Contribute to establishing acceptable ranges for critical quality attributes (CQAs) and parameters (CPPs).&lt;/li&gt;
&lt;li&gt;Manage/establish methods at external labs / CROs to complement internal capability.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ensure lab instruments are in working condition, manage instrument vendors, and organize demonstrations of new equipment.&lt;/li&gt;
&lt;li&gt;Prepare and review documentation including certificates of analysis, method protocols, laboratory notebooks, and reports.&lt;/li&gt;
&lt;li&gt;Stay current with emerging analytical technologies and industry trends in&amp;nbsp;LNP-based delivery systems, including targeted LNPs.&lt;/li&gt;
&lt;li&gt;Supervise and mentor junior scientists and foster a culture of scientific and operational excellence.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related discipline with&amp;nbsp;8+ years&amp;nbsp;of relevant industry experience; or M.S. with&amp;nbsp;10+ years.&lt;/li&gt;
&lt;li&gt;Demonstrated expertise with analytical methods for&amp;nbsp;lipid nanoparticle characterization, including biochemical / biophysical methods.&lt;/li&gt;
&lt;li&gt;Experience with&amp;nbsp;characterization of nucleic acid-based therapeutics&amp;nbsp;(mRNA, siRNA, DNA).&lt;/li&gt;
&lt;li&gt;Experience with characterization of proteins, mAbs, antibody fragments, and peptides&lt;/li&gt;
&lt;li&gt;Hands-on experience with techniques including&amp;nbsp;HPLC, DLS, NTA, CE, LC-MS/MS, UV-Vis spectroscopy, and single-particle characterization methods.&lt;/li&gt;
&lt;li&gt;Excellent problem-solving, communication, and leadership skills.&lt;/li&gt;
&lt;li&gt;Prior experience in a supervisory role&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Skills:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience working with&amp;nbsp;external labs and/or CDMOs in a&amp;nbsp;matrixed development environment.&lt;/li&gt;
&lt;li&gt;Prior involvement in&amp;nbsp;early stage development and IND filings, preferably for genetic medicines.&lt;/li&gt;
&lt;li&gt;Familiarity with&amp;nbsp;stability studies, forced degradation, and comparability assessments.&lt;/li&gt;
&lt;li&gt;Familiarity with molecular biology and bioconjugation techniques&lt;/li&gt;
&lt;li&gt;Awareness of&amp;nbsp;ICH guidelines,&amp;nbsp;GMP, and&amp;nbsp;regulatory expectations&amp;nbsp;for analytical method validation and CMC submissions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&amp;nbsp;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $163,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Mirai Bio currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Mirai Bio&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-scientist-analytical-development-flagship-pioneering/69d3bc06c8e81216cd0b903a</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-analytical-development-flagship-pioneering/69d3bc06c8e81216cd0b903a</guid><pubDate>Mon, 06 Apr 2026 13:58:30 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Backend Developer]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Extuitive is a Flagship Pioneering–backed startup reimagining product innovation for the AI era. Our mission is to empower entrepreneurs and direct-to-consumer (D2C) brands with AI-driven tools that simplify, accelerate, and scale the launch of new products. Based in Cambridge, MA, we operate like a special ops unit—fast-moving, data-driven, and relentlessly focused on impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;As a &lt;strong&gt;Principal Backend Engineer&lt;/strong&gt;, you’ll be a technical leader responsible for architecting, building, and scaling the core backend systems that power our platform. You’ll drive the design of high-throughput services, resilient data pipelines, and integrations with mission-critical third-party providers. Working closely with product managers, designers, and engineering leadership, you’ll translate complex requirements into robust, elegant systems that support rapid growth. You’ll mentor engineers, influence long-term technical strategy, and help evolve our platform architecture to maintain security and reliability as we scale.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Own Core Backend Systems – Design, build, and maintain scalable services, APIs, and platform infrastructure. Ensure reliability, observability, and maintainability.&lt;/li&gt;
&lt;li&gt;Drive Large-Scale Data Pipelines – Architect and operate high-volume, resilient data pipelines for ingestion, transformation, and analytics.&lt;/li&gt;
&lt;li&gt;Lead Third-Party Integrations – Build and maintain integrations with external vendors, ensuring reliability, observability, and long-term maintainability.&lt;/li&gt;
&lt;li&gt;Influence Architecture &amp;amp; Best Practices – Shape backend architecture, coding standards, testing frameworks, CI/CD pipelines, and operational excellence.&lt;/li&gt;
&lt;li&gt;Mentor &amp;amp; Lead Engineers – Provide guidance on system design, debugging at scale, and engineering practices.&lt;/li&gt;
&lt;li&gt;Wear Multiple Hats – Support DevOps, troubleshooting, or other platform needs when necessary.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;8+ years of backend engineering experience.&lt;/li&gt;
&lt;li&gt;Bachelor’s degree in Computer Science, Software Engineering, or equivalent practical experience.&lt;/li&gt;
&lt;li&gt;Strong expertise in backend languages and frameworks (Node.js/TypeScript, Go, Python, or similar).&lt;/li&gt;
&lt;li&gt;Experience designing scalable distributed systems, microservices, and event-driven architectures.&lt;/li&gt;
&lt;li&gt;Deep experience with third-party integrations, REST/GraphQL APIs, webhooks, and rate-limited services.&lt;/li&gt;
&lt;li&gt;Proficiency with SQL/NoSQL databases, data pipelines, and performance optimization.&lt;/li&gt;
&lt;li&gt;Familiarity with cloud platforms (AWS, GCP) and containerized/deployed systems (Docker, Kubernetes).&lt;/li&gt;
&lt;li&gt;Strong testing, CI/CD, and observability practices.&lt;/li&gt;
&lt;li&gt;Comfortable working in a fast-paced, evolving environment with minimal oversight.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Nice to Have&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience building and shipping features quickly in early-stage startups.&lt;/li&gt;
&lt;li&gt;Exposure to multiple backend domains (analytics, payments, notifications, workflow orchestration).&lt;/li&gt;
&lt;li&gt;Hands-on experience with serverless or edge architectures for rapid iteration.&lt;/li&gt;
&lt;li&gt;Familiarity with low-friction integrations with third-party tools and SaaS platforms.&lt;/li&gt;
&lt;li&gt;Track record of scaling systems from small MVPs to production-ready services.&lt;/li&gt;
&lt;li&gt;Comfort with ambiguity and making trade-offs between speed, quality, and maintainability.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $152,000 - $209,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Extuitive, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Extuitive, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-backend-developer-flagship-pioneering/69d3bc03c8e81216cd0b9037</link><guid isPermaLink="true">http://biotechroles.com/principal-backend-developer-flagship-pioneering/69d3bc03c8e81216cd0b9037</guid><pubDate>Mon, 06 Apr 2026 13:58:27 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Drug Metabolism and Pharmacokinetics (DMPK)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Senior Director, DMPK will serve as the company’s key expert overseeing DMPK strategy across the entire company, including late-stage discovery, development, NDA submission, and commercial readiness, as well as designing, implementing, and interpreting DMPK studies, ensuring high-quality data and regulatory-ready documentation to support IND, CTA, and NDA filings.&lt;/p&gt;
&lt;p&gt;As part of a growing biotech organization, the role requires a hands-on, collaborative leader who can build and guide a high-performing team while working cross-functionally to advance a dynamic portfolio.&lt;/p&gt;
&lt;p&gt;This is a pivotal leadership role in a fast‑growing biotech preparing for its first commercial launch.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide scientific leadership for all DMPK activities across discovery, preclinical, and development-stage programs.&lt;/li&gt;
&lt;li&gt;Develop and execute DMPK strategies, including ADME, bioanalysis, PK/PD modeling, and in vitro/in vivo metabolism studies.&lt;/li&gt;
&lt;li&gt;Serve as the primary DMPK representative on program teams, influencing strategy, timelines, and go/no-go decision‑making.&lt;/li&gt;
&lt;li&gt;Evaluate DMPK liabilities and optimization strategies for new chemical entities.&lt;/li&gt;
&lt;li&gt;Serve as the DMPK lead on cross‑functional program teams (preclinical, clinical, regulatory, CMC, translational medicine).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Study Design &amp;amp; Execution&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee design, outsourcing, and interpretation of ADME, PK, TK, and metabolism studies conducted under GLP and non-GLP conditions.&lt;/li&gt;
&lt;li&gt;Lead bioanalytical method development and validation to support preclinical and clinical studies.&lt;/li&gt;
&lt;li&gt;Ensure integration of PK/PD modeling and simulation to inform dose selection and clinical study design.&lt;/li&gt;
&lt;li&gt;Build and manage relationships with CROs and external partners, ensuring quality, compliance, and scientific rigor.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Regulatory and Documentation&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Author and review DMPK sections of regulatory submissions (IND/CTA, IB, briefing packages, NDAs/MAAs).&lt;/li&gt;
&lt;li&gt;Represent the company in regulatory agency interactions (FDA, EMA, etc.) as the DMPK subject matter expert.&lt;/li&gt;
&lt;li&gt;Ensure compliance with all relevant regulatory guidelines, including GLP and ICH.&lt;/li&gt;
&lt;li&gt;Lead DMPK strategy for Nuvalent’s pipeline ensuring data quality that supports INDs, NDAs, and global regulatory interactions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Competencies&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrated ability to collaborate across matrixed, cross-functional teams in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Proven ability to manage multiple projects simultaneously with attention to timelines and detail.&lt;/li&gt;
&lt;li&gt;Strong communication and interpersonal skills; build trust and foster relationships internally and externally.&lt;/li&gt;
&lt;li&gt;Able to work independently, take initiative, and adapt quickly to evolving priorities.&lt;/li&gt;
&lt;li&gt;Recognized leader who exhibits effective communication, emotional intelligence, and influencing skills, within a matrix operating environment.&lt;/li&gt;
&lt;li&gt;Demonstration of strategic thinking and high-level planning while also balancing the ability to manage and execute operational details.&lt;/li&gt;
&lt;li&gt;Ability to effectively manage multiple projects with competing priorities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;12+ years of industry experience in DMPK, including leadership responsibility.&lt;/li&gt;
&lt;li&gt;D. in Pharmaceutical Sciences, Pharmacokinetics, Biochemistry, Chemistry, or related discipline; postdoctoral training preferred.&lt;/li&gt;
&lt;li&gt;Proven track record supporting programs from discovery through clinical development; experience with IND and NDA/MAA submissions strongly preferred.&lt;/li&gt;
&lt;li&gt;Demonstrated experience supporting small‑molecule oncology therapeutics, ideally kinase inhibitors or targeted therapies.&lt;/li&gt;
&lt;li&gt;Hands‑on expertise with ADME assays and mechanistic metabolism studies and PK/PD modeling and simulation, proficient in Phoenix WinNonlin, preferred: experience with GastroPlus modeling.&lt;/li&gt;
&lt;li&gt;Experience contributing to late‑stage development and NDA filings, preferably in oncology.&lt;/li&gt;
&lt;li&gt;Prior experience supporting products approaching commercial launch.&lt;/li&gt;
&lt;li&gt;Experience with vendor/CRO oversight and budget management.&lt;/li&gt;
&lt;li&gt;Experience working in a small/mid-size biotech environment preferred (rapid decision-making, cross-functional collaboration, matrix leadership).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$270,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$295,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-drug-metabolism-and-pharmacokinetics-(dmpk)-nuvalent/69d3bc02c8e81216cd0b9036</link><guid isPermaLink="true">http://biotechroles.com/senior-director-drug-metabolism-and-pharmacokinetics-(dmpk)-nuvalent/69d3bc02c8e81216cd0b9036</guid><pubDate>Mon, 06 Apr 2026 13:58:26 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Pioneering Medicines: Senior / Principal Scientist, Compound Management]]></title><description><![CDATA[&lt;p&gt;What if…&lt;/p&gt;
&lt;p&gt;We could harness the power of Flagship’s breakthrough scientific platforms to create entirely new therapeutic modalities — and deliver transformative medicines to patients faster?&lt;/p&gt;
&lt;p&gt;Pioneering Medicines, a division of Flagship Pioneering, is building a premier biopharmaceutical R&amp;amp;D organization dedicated to conceiving and advancing life-changing therapies. By integrating and applying Flagship’s innovative platform technologies to serious diseases with high unmet need, we aim to redefine how medicines are discovered and developed. A defining strength of our approach is the ability to combine multiple platforms to generate truly novel and potentially transformative treatments&lt;strong&gt;.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a life sciences innovation company that conceives, creates, resources, and develops first-in-category scientific ventures to transform human health and sustainability. Since its founding in 2000, Flagship has originated and fostered &lt;strong&gt;more than 100 scientific ventures&lt;/strong&gt;, generating &lt;strong&gt;tens of billions in aggregate value&lt;/strong&gt; and advancing breakthroughs across biotechnology and sustainability. Flagship’s unique hypothesis-driven innovation model has enabled the creation and growth of an ecosystem of &lt;strong&gt;40+ companies&lt;/strong&gt;&lt;strong&gt; &lt;/strong&gt;— including high-impact ventures such as &lt;strong&gt;Moderna, Tessera Therapeutics, Generate:Biomedicines, Sana Biotechnology, Indigo Agriculture, and Inari&lt;/strong&gt; — that span cutting-edge platform technologies and therapeutic modalities&lt;/p&gt;
&lt;p&gt;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Compound Manager at Senior Scientist/ Principal Scientist level to join our rapidly evolving Sample Operations and Automation function. This individual will collaborate with operational and scientific teams to manage the registration, storage, and distribution of small molecules, peptides, biologics and additional modalities, while leading the automation of liquid handling, serial dilutions, and assay plate dispensing workflows at Pioneering Medicines. In addition, the individual will collaborate with Information Technology to streamline data collection, analysis, and storage workflows.&lt;/p&gt;
&lt;p&gt;The successful candidate will combine deep operational expertise with a hands-on approach to automation and process development, ensuring high-quality, reproducible data from early discovery programs across multiple therapeutic areas and modalities.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Compound and Sample Management&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee end-to-end compound management workflows through collaboration with the lab operations team, including receipt, registration, storage, tracking, and distribution of small molecules, peptides, biologics, nucleic acids, and other modalities across Pioneering Medicines’ research programs.&lt;/li&gt;
&lt;li&gt;Maintain sample integrity and traceability through robust documentation, inventory systems and adherence to SOPs.&lt;/li&gt;
&lt;li&gt;Manage compound collections in proper storage systems (ambient, refrigerated, cryogenic), and ensure environmental compliance and monitoring, in collaboration with the laboratory operations group.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Automation and Workflow Execution&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with team members to operate, program, and maintain automated liquid handling systems (e.g., Agilent Bravo, Dispendix I.DOT) for high-throughput sample preparation.&lt;/li&gt;
&lt;li&gt;Develop, validate, and optimize serial dilution, reformatting, and assay plate dispensing methods to enable high throughput assays and profiling campaigns.&lt;/li&gt;
&lt;li&gt;Implement automation scheduling software (e.g., VWorks) to coordinate workflows and maximize throughput.&lt;/li&gt;
&lt;li&gt;Drive continuous improvements in automation reliability and process standardization.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Data and Informatics Integration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Interface with informatics platforms (e.g., CDD Vault, Benchling, and compound databases) to ensure accurate data capture and seamless sample tracking.&lt;/li&gt;
&lt;li&gt;Collaborate with data science teams to link sample metadata with experimental results for analytical and decision-support workflows.&lt;/li&gt;
&lt;li&gt;Generate and maintain inventory, utilization, and QC reports across multiple program portfolios.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s or Master’s degree in Chemistry, Biochemistry, Chemical Engineering, or related discipline with 12+ years of experience.&lt;/li&gt;
&lt;li&gt;Strong experience in compound management within pharma, biotech, or high-throughput discovery environments.&lt;/li&gt;
&lt;li&gt;Demonstrated proficiency with liquid handling platforms and compound inventory management systems.&lt;/li&gt;
&lt;li&gt;Deep understanding storage considerations for diverse modalities (e.g., small molecules, peptides, biologics).&lt;/li&gt;
&lt;li&gt;Proven ability to troubleshoot, optimize, and document automated workflows.&lt;/li&gt;
&lt;li&gt;Strong organizational and communication skills, with the ability to manage multiple priorities in a dynamic environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in multi-modal sample management (e.g., nucleic acids, conjugates).&lt;/li&gt;
&lt;li&gt;Prior exposure to early-stage R&amp;amp;D or platform company operations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Core Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Operational excellence and meticulous attention to detail&lt;/li&gt;
&lt;li&gt;Strong technical troubleshooting and analytical mindset&lt;/li&gt;
&lt;li&gt;Collaborative and adaptable in a fast-evolving environment&lt;/li&gt;
&lt;li&gt;Commitment to innovation, data integrity, and process improvement&lt;/li&gt;
&lt;li&gt;Excellent written and interpersonal communication&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering and our ecosystem companies are &lt;strong&gt;committed to equal employment opportunity&lt;/strong&gt; regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TD1&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $126,000 - $214,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Medicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Medicines&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/pioneering-medicines:-senior-principal-scientist-compound-management-flagship-pioneering/69d3bbffc8e81216cd0b9032</link><guid isPermaLink="true">http://biotechroles.com/pioneering-medicines:-senior-principal-scientist-compound-management-flagship-pioneering/69d3bbffc8e81216cd0b9032</guid><pubDate>Mon, 06 Apr 2026 13:58:22 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Counsel, Commercial]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Deputy General Counsel, Commercial, the Senior Counsel, Commercial will be a critical part of Nuvalent’s Legal Department and will contribute significantly to the success of our growing organization. In this role, you will be responsible for advisement on a host of strategic and tactical issues related to the development and future commercialization of prescription drug products. Responsibilities will include advising on matters governed by healthcare fraud and abuse laws, FDA regulations, state and federal drug pricing and transparency laws, access and reimbursement matters, privacy laws and providing legal guidance on patient support programs.&lt;/p&gt;
&lt;p&gt;Senior Counsel, Commercial will act as the brand lawyer and reviewer on the Promotional Materials Review Committee and the Medical Review Committee. This role will also have the opportunity to support cross functional compliance initiatives and other key projects across the organization. We are looking for an attorney with product launch experience and a proactive and solutions-oriented mindset to join the Nuvalent team.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as a legal advisor on a broad range of commercialization-related subjects in support of anticipated launch of company’s first oncology product to the cross functional brand team, including marketing, medical affairs, market access, sales, and other key stakeholders.&lt;/li&gt;
&lt;li&gt;Serve as an experienced subject matter expert and review committee member for advertising, promotional and non-promotional materials, and medical materials, including sales and marketing materials, market access materials, patient support program information, disease education, scientific exchange, press releases, and clinical trial recruitment activities.&lt;/li&gt;
&lt;li&gt;Provide legal advisement on the design and implementation of sales and marketing strategy, market access activities, patient support programs, medical affairs initiatives, media campaigns, and interactions with patients and patient advocacy organizations&lt;/li&gt;
&lt;li&gt;Provide ad-hoc advice on contracts with health care fraud and abuse, FDA or brand related implications.&lt;/li&gt;
&lt;li&gt;Advise on commercialization-related contracts and engagements, including, vendor agreements, service agreements, consulting agreements, statements of work, and sponsorships.&lt;/li&gt;
&lt;li&gt;Serve as a legal representative on cross functional project teams, as assigned, to support business initiatives, identify and mitigate legal risks and to foster collaboration across other legal and compliance disciplines as appropriate.&lt;/li&gt;
&lt;li&gt;Assist in the development of the enterprise-wide compliance program&lt;/li&gt;
&lt;li&gt;Additional responsibilities as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience as the legal representative on a promotional review committee and a medical materials review committee in the pharmaceutical industry&lt;/li&gt;
&lt;li&gt;Experience in advising on healthcare fraud and abuse laws&lt;/li&gt;
&lt;li&gt;Experience advising on matters governed by FDA regulations&lt;/li&gt;
&lt;li&gt;Experience advising on patient support programs and market access initiatives&lt;/li&gt;
&lt;li&gt;Ability to provide responsive, thoughtful, pragmatic and clear advice in support of business&lt;/li&gt;
&lt;li&gt;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Clear communication style that effectively conveys advice and recommendations to key stakeholders&lt;/li&gt;
&lt;li&gt;Experience thriving in a fast-paced environment with a solutions-oriented approach&lt;/li&gt;
&lt;li&gt;A demonstrated track record of acting with integrity and a collegial, solution-oriented mindset&lt;/li&gt;
&lt;li&gt;A champion of a positive and respectful company culture&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of recent relevant legal experience in product support of biotech/pharma, with a strong preference for experience with launching a product in the U.S. market and 3+ years in-house pharmaceutical or biotech oncology experience&lt;/li&gt;
&lt;li&gt;Juris Doctor from an accredited law school; active membership and in good standing in a state bar and either admitted to the Massachusetts bar or eligible for admission to the Massachusetts bar as in-house counsel&lt;/li&gt;
&lt;li&gt;Significant knowledge of enforcement trends, the Federal Food, Drug and Cosmetic Act and related regulations, the False Claims Act, laws related to fraud and abuse in the life science/biotech/pharma industries, transparency laws, and the PhRMA Code.&lt;/li&gt;
&lt;li&gt;Familiarity with ex-US frameworks (e.g., EFPIA, GDPR) preferred&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience with pharmaceutical/biotech commercial contracting preferred&lt;/li&gt;
&lt;li&gt;Team player with strong and effective collaboration and communication skills&lt;/li&gt;
&lt;li&gt;Ability to travel as required to support business activities.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$240,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$270,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-counsel-commercial-nuvalent/69d3bbfec8e81216cd0b9031</link><guid isPermaLink="true">http://biotechroles.com/senior-counsel-commercial-nuvalent/69d3bbfec8e81216cd0b9031</guid><pubDate>Mon, 06 Apr 2026 13:58:22 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Pioneering Medicines: Scientist / Senior Scientist, Invitro Biology / Pharmacology Contractor]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;We are seeking an on-site, lab-based in-vitro scientist in drug discovery who enjoys collaborating with cross-functional teams. Under appropriate guidance, the role involves designing research studies,&amp;nbsp;performing experiments, and analyzing data. The&lt;br&gt;ideal candidate will preferably have expertise in cardiovascular physiology&amp;nbsp;including but not limited to cardio-metabolic or cardiac physiology, along with&amp;nbsp;experience in in-vitro biochemical assays, cell culture, organoid models, hiPSC&amp;nbsp;cultures, cell biology assays, and ex vivo techniques. As and when required, this person will work closely with other stakeholders&amp;nbsp;to help achieve the research goals.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support in vitro screening, characterization, and mechanism of action studies by utilizing various biochemical, biophysical, and cellular techniques to explore signaling pathways for target identification and validation, employing modalities like small molecules, peptides, and other biologics.&amp;nbsp; &amp;nbsp;&lt;/li&gt;
&lt;li&gt;Develop cell-based assays utilizing primary cardiomyocytes, cardiac cell lines, iPSCs, and organoids, along with ex vivo experiments to aid in in vitro pharmacology and translational research.&lt;/li&gt;
&lt;li&gt;Collaborate with key stakeholders of the in vitro, in vivo, and translational teams and other necessary stakeholders to support daily laboratory operations. &amp;nbsp;&lt;/li&gt;
&lt;li&gt;Participate and present data at internal and external meetings&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Basic Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. in biochemistry, biotechnology, biophysics, biology, or a related field.&lt;/li&gt;
&lt;li&gt;3+ years of post-doctoral experience is preferred&lt;/li&gt;
&lt;li&gt;Over three years of experience in academia and/or industry, ideally in the cardiometabolic therapeutic field, is a plus.&lt;/li&gt;
&lt;li&gt;Broad experience in protein and peptide chemistry is preferable&lt;/li&gt;
&lt;li&gt;Have working Skilled in culturing and handling human primary cells, including primary cardiomyocytes and hiPSC-derived cardiomyocytes, is preferable&lt;/li&gt;
&lt;li&gt;Expertise working on molecular biology methods, DNA, RNA isolation, siRNA, and transduction in primary cells.&lt;/li&gt;
&lt;li&gt;Proficiency in common laboratory techniques such as qPCR, flow cytometry, ELISA, Western blotting, plate reader assays, and microscopy.&lt;/li&gt;
&lt;li&gt;Working knowledge of&lt;em&gt; &lt;/em&gt;invitro pharmacology,&amp;nbsp; in cell-based systems.&lt;/li&gt;
&lt;li&gt;Attention to detail and ability to analyze and summarize scientific data, clearly communicate updates and reports to the team and stakeholders, and perform detailed documentation of experimental results via ELN (Electronic Lab Notebook))&lt;/li&gt;
&lt;li&gt;Excellent verbal communication, presentation, and interpersonal skills are required.&lt;/li&gt;
&lt;li&gt;Proficient in scientific software (e.g., GraphPad Prism, FlowJo, etc.)&lt;/li&gt;
&lt;li&gt;Publication record in cardiovascular, cardiometabolic, or related research.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Qualifications&lt;/strong&gt;:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Industrial experience or experience working with academic/industrial collaborators and/or CROs preferred&lt;/li&gt;
&lt;li&gt;Research background in cardiology or metabolism.&lt;/li&gt;
&lt;li&gt;Hands-on experience with gene-based approaches such as CRISPR and RNA interference is a plus&lt;/li&gt;
&lt;li&gt;Understanding of the general drug discovery &amp;nbsp;&amp;amp; development process, from target identification and validation is a bonus.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Job Complexity&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Moderate to high complexity.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;LOCATION:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;br&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-TD1&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $108,000 - $140,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Medicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Medicines&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/pioneering-medicines:-scientist-senior-scientist-invitro-biology-pharmacology-contractor-flagship-pioneering/69d3bbfbc8e81216cd0b9030</link><guid isPermaLink="true">http://biotechroles.com/pioneering-medicines:-scientist-senior-scientist-invitro-biology-pharmacology-contractor-flagship-pioneering/69d3bbfbc8e81216cd0b9030</guid><pubDate>Mon, 06 Apr 2026 13:58:19 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, GMP Quality Assurance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Manager, GMP Quality Assurance, the Manager, GMP Quality Assurance is responsible for maintaining high levels of quality in Nuvalent drug substances, drug products, packaged drug products and finished goods by supporting contract manufacturing organizations (CMOs) and internal partners in Technical Operations.&lt;/p&gt;
&lt;p&gt;Ensure Nuvalent and internal / external stakeholders comply with cGMPs and standards as well as regulations of applicable authorities.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide quality oversight throughout the CMC lifecycle management of Nuvalent’s products. Areas may include Starting Materials, Drug Substance, Drug Product or Finished Goods.&lt;/li&gt;
&lt;li&gt;Conduct product release activities for all phases of development, validation, and commercial production including review and approval of master batch records and executed batch records.&lt;/li&gt;
&lt;li&gt;Provide onsite oversight/monitoring of manufacturing campaigns as appropriate.&lt;/li&gt;
&lt;li&gt;Coordinate QP release as appropriate.&lt;/li&gt;
&lt;li&gt;Effectively interact with external contract manufacturers, testing laboratories, and work as part of an internal multidisciplinary team to conduct, review, and approve manufacturing, testing, and product complaint investigations.&lt;/li&gt;
&lt;li&gt;Assist in preparing or reviewing CMC sections of regulatory submissions.&lt;/li&gt;
&lt;li&gt;Supports associated Investigations, CAPAs, Change Controls, Material Review Boards, OOS, etc.&lt;/li&gt;
&lt;li&gt;Work with team to implement/maintain Quality Agreements with suppliers.&lt;/li&gt;
&lt;li&gt;Represent the QA department on Vendor project teams.&lt;/li&gt;
&lt;li&gt;Assist in conducting audits of CMOs and Testing Laboratories.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ability to drive and deliver multiple projects within project scope and timelines.&lt;/li&gt;
&lt;li&gt;Proven ability to effectively communicate across all functions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in biology, chemistry, life sciences field preferred or related experience.&lt;/li&gt;
&lt;li&gt;5+ years of experience working in Quality functions supporting cGMP manufacturing of pharmaceutical products.&lt;/li&gt;
&lt;li&gt;Direct experience working with the GMP manufacturing of small molecule products is required&lt;/li&gt;
&lt;li&gt;Direct experience working with the GMP manufacturing oversight of small molecule drug substances is a plus&lt;/li&gt;
&lt;li&gt;Working knowledge of MS Word, MS Teams, Veeva Quality Docs, SharePoint and Smartsheet is preferred.&lt;/li&gt;
&lt;li&gt;Strong knowledge of cGMP regulations, practices, and trends pertaining to pharmaceutical product development, manufacturing, testing, and clinical operations is required.&lt;/li&gt;
&lt;li&gt;Knowledge of cGMP regulations, practices, and trends pertaining to commercial product manufacturing and testing is preferred.&lt;/li&gt;
&lt;li&gt;Travel approximately 15%&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$125,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$145,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/manager-gmp-quality-assurance-nuvalent/69d3bbfac8e81216cd0b902b</link><guid isPermaLink="true">http://biotechroles.com/manager-gmp-quality-assurance-nuvalent/69d3bbfac8e81216cd0b902b</guid><pubDate>Mon, 06 Apr 2026 13:58:18 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Pioneering Medicines: Associate Director, Program Management Operations]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;What if...&amp;nbsp;&lt;/strong&gt;We could harness the power of Flagship’s scientific platforms and create novel treatment options that benefit more patients, sooner?&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT PIONEERING MEDICINES &lt;/strong&gt;&lt;/p&gt;
&lt;p class=&quot;p1&quot;&gt;Pioneering Medicines, Flagship Pioneering’s in-house drug development unit, is dedicated to conceiving and developing a broad portfolio of life-changing treatments for patients built from Flagship’s innovative platforms. Harnessing the drug development expertise of its team together with the power of Flagship&#39;s multiple scientific platforms, Pioneering Medicines explores and identifies new product concepts which are then advanced jointly with Flagship’s bioplatform companies. Within Flagship’s Innovation Supply Chain partnerships, Pioneering Medicines works with external collaborators to apply its unique approach to partners’ R&amp;amp;D priorities. These partnerships are highly co-creative strategic alliances that accelerate therapeutic innovation by bringing together partners spanning the full spectrum of drug discovery, development, and production.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Associate Director, Program Management Operations is an individual contributor within the Program Management Group, responsible for establishing and sustaining the &lt;strong&gt;program management operating infrastructure&lt;/strong&gt; that enables effective execution across the R&amp;amp;D portfolio. This role owns program management &lt;strong&gt;processes, systems, tools, reporting, and governance&lt;/strong&gt;, and operates with a high degree of autonomy within a clearly defined functional scope.&lt;/p&gt;
&lt;p&gt;The role partners closely with Program Managers and cross-functional leaders to ensure that programs are planned, governed, and reported in a &lt;strong&gt;consistent, disciplined, and scalable manner&lt;/strong&gt;. This role materially influences program outcomes by strengthening the operating environment in which programs are delivered.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;Program Management Operating Model &amp;amp; Team Enablement&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Establish and maintain fit-for-purpose standards for integrated program planning, milestone and dependency management, risk and issue management, and program reporting across discovery through early clinical development.&lt;/li&gt;
&lt;li&gt;Define clear expectations for how programs are planned, governed, tracked, and communicated, balancing consistency with flexibility based on program stage and complexity.&lt;/li&gt;
&lt;li&gt;Act as an operational partner to Program Managers, enabling focus on asset execution through guidance, training, onboarding, and hands-on support.&lt;/li&gt;
&lt;li&gt;Support onboarding of new Program Managers and cross-functional contributors into the Program Management operating model and systems.&lt;/li&gt;
&lt;li&gt;Continuously improve the Program Management operating model based on execution experience, portfolio needs, and feedback from program teams.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Processes, Tools, Reporting &amp;amp; Data&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Implement and maintain program management processes, tools, and systems that support planning, tracking, and reporting.&lt;/li&gt;
&lt;li&gt;Partner with IT to maintain a secure, intuitive SharePoint-based environment for program documentation, Program Management guidance, and governance materials.&lt;/li&gt;
&lt;li&gt;Develop and maintain concise, leadership-ready dashboards that provide a trusted, single source of truth for program and function-level reporting.&lt;/li&gt;
&lt;li&gt;Ensure accuracy, consistency, and usability of program data across reporting and governance forums.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Governance &amp;amp; Operating Cadence&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure governance forums are prepared with clear, decision-focused materials and documented outcomes.&lt;/li&gt;
&lt;li&gt;Track governance decisions, risks, and action items, ensuring timely follow-through and escalation as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Continuous Improvement &amp;amp; Innovation&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Identify and implement improvements to PM processes, tools, and reporting, including data- and AI-enabled solutions where appropriate.&lt;/li&gt;
&lt;li&gt;Partner with Pioneering Intelligence and IT to pilot efficiency-enhancing approaches that reduce manual effort and improve decision readiness.&lt;/li&gt;
&lt;li&gt;Promote a culture of operational discipline and continuous improvement within Program Management.&lt;/li&gt;
&lt;li&gt;Develop approaches that can be shared and replicated across the Flagship ecosystem, building a modular, repeatable and consistent approach to Program Management.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in life sciences or related discipline; advanced degree and/or PMP certification preferred.&lt;/li&gt;
&lt;li&gt;8–12+ years of experience in program management, PMO operations, or R&amp;amp;D operations within biotech or pharmaceutical development.&lt;/li&gt;
&lt;li&gt;Strong working knowledge of the drug discovery and development process.&lt;/li&gt;
&lt;li&gt;Demonstrated experience establishing and operating PM processes, governance, and reporting across multiple programs.&lt;/li&gt;
&lt;li&gt;Proven ability to influence and drive adoption of standards in a matrixed organization.&lt;/li&gt;
&lt;li&gt;Proficiency with program management tools (e.g., Smartsheet or similar).&lt;/li&gt;
&lt;li&gt;Strong analytical and communication skills, including preparation of executive-ready materials&lt;/li&gt;
&lt;li&gt;Ability to work and adapt in a fast-paced, dynamic environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;#LI-TD1&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $148,000 - $203,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Pioneering Medicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Pioneering Medicines&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/pioneering-medicines:-associate-director-program-management-operations-flagship-pioneering/69d3bbf7c8e81216cd0b9020</link><guid isPermaLink="true">http://biotechroles.com/pioneering-medicines:-associate-director-program-management-operations-flagship-pioneering/69d3bbf7c8e81216cd0b9020</guid><pubDate>Mon, 06 Apr 2026 13:58:15 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Clinical Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Associate Director, Clinical Operations, the Manager, Clinical Operations will ensure excellence in clinical trial planning, execution, and data collection, in accordance with regulatory guidelines. They will be responsible for aspects of clinical study conduct, including site selection, study start-up, conduct and close-out. Providing appropriate escalation of trial specific issues to deliver high quality clinical trial results. Able to adapt to changes in the work environment and manage competing demands.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Manage multiple aspects of clinical studies working under the guidance and direction of the Clinical Program Lead.&lt;/li&gt;
&lt;li&gt;Accountable for the delivery of project(s) to achieve agreed timelines, scope, quality, and budget.&lt;/li&gt;
&lt;li&gt;Perform oversight of CRO and auxiliary vendors; identify risks and broker solutions.&lt;/li&gt;
&lt;li&gt;Provide support and oversight managing the creation, maintenance and close out of TMF activities.&lt;/li&gt;
&lt;li&gt;Ensure appropriate escalation of enrollment, site activation and data collection milestones.&lt;/li&gt;
&lt;li&gt;Support the clinical team to ensure the completeness of clinical protocol, investigator brochure, informed consent forms, clinical study reports and case report forms.&lt;/li&gt;
&lt;li&gt;Ensure site monitoring reports are accurate and thorough, reviewed on a regular basis and that metrics are adhered to.&lt;/li&gt;
&lt;li&gt;Support database lock by ensuring appropriate oversight of sites and by participating in data review/reconciliation efforts.&lt;/li&gt;
&lt;li&gt;Coordinate with Clinical Supply Chain regarding drug forecasting and supply of drug product to sites.&lt;/li&gt;
&lt;li&gt;Establish and maintain effective communication and collaboration with functional area peers to meet study/program objectives and support goals.&lt;/li&gt;
&lt;li&gt;Lead or co-lead department initiatives to support an expanding organization.&lt;/li&gt;
&lt;li&gt;Travel may be required (10% – 15%).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Detail and process orientated, with excellent project management skills, including risk assessment and contingency planning.&lt;/li&gt;
&lt;li&gt;Excellent problem solving, communication and organization skills.&lt;/li&gt;
&lt;li&gt;Flexibility with changing priorities, ability to think critically, strong attention to detail, and ability to work well under pressure.&lt;/li&gt;
&lt;li&gt;Ability to work in a collaborative environment and build effective working relationships across the organization.&lt;/li&gt;
&lt;li&gt;Ability to strategically plan, organize and manage multiple projects simultaneously.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree or higher in a scientific or healthcare discipline preferred with 3+ years relevant experience in clinical operations within the biotech, pharmaceutical or CRO industry.&lt;/li&gt;
&lt;li&gt;Extensive knowledge of ICH-GCP guidelines.&lt;/li&gt;
&lt;li&gt;Relevant experience in early through late Phase clinical trials.&lt;/li&gt;
&lt;li&gt;Knowledge of oncology clinical trials preferred.&lt;/li&gt;
&lt;li&gt;Demonstrated cross-functional leadership fostering team spirit and team motivation.&lt;/li&gt;
&lt;li&gt;Capability to challenge status-quo using risk management approach.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$125,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$145,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/manager-clinical-operations-nuvalent/69d3bbf6c8e81216cd0b901f</link><guid isPermaLink="true">http://biotechroles.com/manager-clinical-operations-nuvalent/69d3bbf6c8e81216cd0b901f</guid><pubDate>Mon, 06 Apr 2026 13:58:14 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$130000-165000</salary><type>Full-time</type></item><item><title><![CDATA[Patent Counsel/Senior Patent Agent]]></title><description><![CDATA[&lt;p&gt;&lt;a href=&quot;https://www.flagshippioneering.com/&quot;&gt;Flagship Pioneering&lt;/a&gt;&amp;nbsp;is a bioplatform innovation company&amp;nbsp;that invents and builds platform companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health and sustainability exponentially accelerate scientific progress in areas ranging from cancer detection and treatment to nature-positive agriculture.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt; What sets Flagship apart is our ability to advance biotechnology by uniting life science innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet.&amp;nbsp; &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. &amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;JOB DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is seeking a savvy, creative, hands-on, Patent Counsel or senior Patent Agent who will work closely with cross-functional teams of Flagship portfolio companies and the Flagship IP team to help develop and execute a comprehensive and global IP strategy.&amp;nbsp; The successful candidate has a passion for science, an ease with multiple and varied life science technologies, excellent patent portfolio development skills, and a demonstrated ability to think strategically.&amp;nbsp;&amp;nbsp;This is an extremely interactive role that requires the ability to mine and identify inventions, guide and educate scientific teams, and communicate succinctly and clearly with both scientific and management teams.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Help build, manage, and execute a global IP strategy for two or more Flagship portfolio companies, including invention mining, patent preparation and prosecution, efficient management of outside counsel, third party patent monitoring, and IP education.&lt;/li&gt;
&lt;li&gt;Provide counsel to, and operationally support, business, corporate and BD efforts&amp;nbsp;of one or more Flagship portfolio companies with&amp;nbsp;due diligence, competitive intelligence, R&amp;amp;D contracting issues, and IP in-licensing efforts, as needed.&lt;/li&gt;
&lt;li&gt;Provide general and directed IP education to company scientists and management.&lt;/li&gt;
&lt;li&gt;Work with science and management teams of portfolio companies to spot issues and work with Flagship legal team to enable effective and efficient resolutions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;QUALIFICATIONS:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;em&gt;Required&lt;/em&gt;: Advanced degree (Ph.D. in a life sciences field; JD preferred).&lt;/li&gt;
&lt;li&gt;&lt;em&gt;Required&lt;/em&gt;: 6+ years of IP experience (patent drafting, prosecution, opinion work, due diligence, strategic development, counseling), including at least 4 years in private law practice&amp;nbsp;&lt;/li&gt;
&lt;li&gt;&lt;em&gt;Required&lt;/em&gt;: Registered to practice before the U.S. Patent and Trademark Office.&lt;/li&gt;
&lt;li&gt;&lt;em&gt;Required&lt;/em&gt;: Sophisticated knowledge of patent law and procedure, including international and foreign patent prosecution procedure.&lt;/li&gt;
&lt;li&gt;IP transactional and/or litigation experience a plus.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PERSONAL CHARACTERISTICS:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Flexible, personable team-player, comfortable in a fast-paced, small company environment, able to think “out-of-the-box,” and proactively counsel clients on IP strategy to contribute to the R&amp;amp;D teams above and beyond assigned projects.&lt;/li&gt;
&lt;li&gt;Proven ability to set and meet ambitious deadlines, handle numerous multifaceted legal issues and see projects through to conclusion.&lt;/li&gt;
&lt;li&gt;Strong written and verbal communication skills, and demonstrated ability to work collaboratively with both scientists and management.&lt;/li&gt;
&lt;li&gt;Ability to distill complexity and to communicate decisively with sound judgment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Why Join Flagship Pioneering?&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;This is a rare opportunity to play a critical role in shaping groundbreaking collaborations that drive scientific innovation. As Senior Counsel, Legal, you will operate at the intersection of business, law, and cutting-edge biotechnology, helping to build and support transformational partnerships that advance human health.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;#LI-NM1&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $128,000 - $258,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/patent-counselsenior-patent-agent-flagship-pioneering/69d3bbf3c8e81216cd0b9019</link><guid isPermaLink="true">http://biotechroles.com/patent-counselsenior-patent-agent-flagship-pioneering/69d3bbf3c8e81216cd0b9019</guid><pubDate>Mon, 06 Apr 2026 13:58:11 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$160000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Market Access Marketing]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Director, Payer &amp;amp; Reimbursement, the Director, Market Access Marketing plays an essential role executing the Market Access strategy, including Payer, Pricing and Patient Support Services strategies, to ensure our upcoming product launches in ROS1 NSCLC and ALK+ NSCLC are strategically positioned to achieve payer coverage, organized customer access, and patient access. This role will be responsible for payer marketing, organized customer marketing, patient support services marketing, and creating market access initiatives to optimize coverage, adoption, and reimbursement of our novel therapies. Given the cross-functional nature of the role, the market access marketer will have a dotted reporting line to the Vice President, Marketing. S/he will also collaborate closely with Sales, HEOR, and Medical Affairs to drive launch readiness and post-launch success.&lt;br&gt;&lt;br&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities: &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Strategic Planning&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Payer &amp;amp; Health Care Decision Maker (HCDM) Messaging Strategy – Develop compelling value propositions and messaging highlighting clinical benefits, cost-effectiveness and differentiation.&lt;/li&gt;
&lt;li&gt;Agency Management – Manage market access marketing AOR to refine and implement strategy, messaging, and materials.&lt;/li&gt;
&lt;li&gt;Work with cross-functional teams to inform and execute pricing, reimbursement and access strategies aligned with business objectives.&lt;/li&gt;
&lt;li&gt;Identify and capitalize on strategic opportunities to best position Nuvalent products at National Accounts (e.g., GPOs, Physician Networks, National and Regional Payers, Pathways and Strategic Partners), including overseeing the execution of marketing tactics at annual meetings&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Market Access &amp;amp; Payer Engagement Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop Market Access Materials – Create tailored account director presentations, digital content and key messaging to deliver to payer and provider HCDMs.&lt;/li&gt;
&lt;li&gt;Pre-Approval Information Exchange (PIE) – Refine and implement PIE strategy, messaging and materials to effectively meet payer expectations and regulatory guidelines.&lt;/li&gt;
&lt;li&gt;Value Proposition – Craft evidence-based messaging to support differentiation story, formulary inclusion, pathway placement, and EHR integration.&lt;/li&gt;
&lt;li&gt;FAQs &amp;amp; Reimbursement Guide – Prepare pricing, coding and coverage documents addressing payer concerns.&lt;/li&gt;
&lt;li&gt;Distribution Selling Sheets – Equip distribution partners with materials on product availability and logistics.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Integrated Delivery Network, GPO Engagement, &amp;amp; Patient Services Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Access Materials for GPO and IDN HCDMs – Educate healthcare professionals on reimbursement and formulary details.&lt;/li&gt;
&lt;li&gt;Patient Support Programs – Develop resources for PSP including patient services website, financial assistance and copay support.&lt;/li&gt;
&lt;li&gt;Patient Access Content and Materials – Ensure patients have clear coverage, affordability, and access guidance.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Internal Training &amp;amp; Strategic Insights&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Training Materials for Market Access Account Director teams – Create and execute training plans for teams to effectively utilize market access marketing materials&lt;/li&gt;
&lt;li&gt;Training Materials for Sales – Provide customized formulary status updates, access and reimbursement guides for sales team&lt;/li&gt;
&lt;li&gt;External Access Communications – Updating external stakeholders on formulary status and changes&lt;/li&gt;
&lt;li&gt;Stakeholder Insights – Organize Payer &amp;amp; Provider Advisory Boards for market insights.&lt;/li&gt;
&lt;li&gt;Competitive &amp;amp; HEOR Analysis – Incorporate relevant HEOR into value messaging and monitor pricing, access strategies and cost-effectiveness data to incorporate.&lt;/li&gt;
&lt;li&gt;Regulatory &amp;amp; Compliance Oversight – Ensure all materials meet FDA, CMS, and payer regulations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Entrepreneurial mindset, and a successful track record working in a fast-paced, rapid-growth environment.&lt;/li&gt;
&lt;li&gt;Proven ability to manage multiple projects, identify and address needs, build internal capabilities and deliver results.&lt;/li&gt;
&lt;li&gt;Excellent interpersonal skills, with the ability to gain alignment by working collaboratively and inclusively across corporate functions.&lt;/li&gt;
&lt;li&gt;Strong verbal and written communication skills.&lt;/li&gt;
&lt;li&gt;Strong analytical skills and ability to translate data into actionable insights.&lt;/li&gt;
&lt;li&gt;Record of achievement, innovation, and compliance.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree required; advanced degree (MBA, PharmD, or PhD) preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in biotechnology, pharmaceuticals, or healthcare with a focus on market access marketing, or payer/organized customer/reimbursement strategy.&lt;/li&gt;
&lt;li&gt;Experience developing market access marketing strategies and executing tactics&lt;/li&gt;
&lt;li&gt;Product launch experience, preferably including oral oncology therapies&lt;/li&gt;
&lt;li&gt;Experience collaborating with external stakeholders to gather and incorporate insights.&lt;/li&gt;
&lt;li&gt;Deep understanding of payer and reimbursement landscape, including Medicare, Medicaid, and Commercial insurers.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$215,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$245,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-market-access-marketing-nuvalent/69d3bbf2c8e81216cd0b9016</link><guid isPermaLink="true">http://biotechroles.com/director-market-access-marketing-nuvalent/69d3bbf2c8e81216cd0b9016</guid><pubDate>Mon, 06 Apr 2026 13:58:10 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$180000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Operating Principal, Summit PBU]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Operating Principal – Summit PBU &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Summit, a Pioneering Business Unit within Flagship, is seeking an &lt;strong&gt;Operating Principal&lt;/strong&gt; to help launch and scale our NewCos. You will work across one or more companies, leading operations and strategy, driving corporate development, and partnering closely with scientific leadership to translate breakthrough ideas into impact.&lt;/p&gt;
&lt;p&gt;This role is ideal for an entrepreneurial leader who thrives in ambiguity, moves seamlessly between science and business, and is energized by building organizations from inception to growth.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategy and operational planning in one or more NewCos.&lt;/li&gt;
&lt;li&gt;Drive corporate development initiatives, including partnerships, financings, and strategic alliances, as well as engagement with Board of Directors and other important stakeholders&lt;/li&gt;
&lt;li&gt;Engage directly with scientists and company leaders to align technical progress with operational goals.&lt;/li&gt;
&lt;li&gt;Recruit, develop, and manage high-performing teams across functions.&lt;/li&gt;
&lt;li&gt;Partner with Flagship central teams (Finance, Talent, Legal/IP, HR) to bring best-in-class infrastructure to each company.&lt;/li&gt;
&lt;li&gt;Shape and execute operating and long-range plans, ensuring milestones are achieved on time and on budget.&lt;/li&gt;
&lt;li&gt;Build strong external relationships with investors, partners, and key opinion leaders.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Who you are:&lt;/strong&gt; You are a dynamic operator and strategist who combines business leadership with scientific fluency. You thrive in fast-moving, entrepreneurial environments and are motivated by building organizations that harness novel science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of experience in biotech, pharma, or life sciences strategy/operations; prior management consulting a plus.&lt;/li&gt;
&lt;li&gt;Proven success in strategic, operational, or corporate development leadership, ideally in early-stage biotech.&lt;/li&gt;
&lt;li&gt;Strong scientific acumen; able to quickly grasp novel science and translate it into plans and execution.&lt;/li&gt;
&lt;li&gt;Track record of building and motivating high-performing teams.&lt;/li&gt;
&lt;li&gt;Skilled communicator, able to influence and inspire across investors, partners, and internal teams.&lt;/li&gt;
&lt;li&gt;Expert problem solver; can bring order to chaos and iterate quickly to find solutions&lt;/li&gt;
&lt;li&gt;Entrepreneurial, resilient, and hands-on; able to adapt and execute with urgency; doesn’t mind rolling up sleeves and doing what needs to be done to move the ball forward&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;How You Lead:&lt;/strong&gt;&lt;br&gt;You set a high bar for yourself and others, balancing precision with agility. You are curious, feedback-driven, and focused on constantly learning how to be the best version of yourself. You face challenges with grit and enthusiasm, while fostering collaboration, shared ownership, and pride in collective achievements.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;EDUCATION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Advanced degree in life sciences or business preferred (PhD, MD, MBA, or equivalent experience).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;LOCATION: &lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-JA2&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $220,000 - $269,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/operating-principal-summit-pbu-flagship-pioneering/69d3bbf0c8e81216cd0b9009</link><guid isPermaLink="true">http://biotechroles.com/operating-principal-summit-pbu-flagship-pioneering/69d3bbf0c8e81216cd0b9009</guid><pubDate>Mon, 06 Apr 2026 13:58:08 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Director, IT Business Partner - Biopharma GXP]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Vice President, Information Technology, the Director, IT Business Partner, GXP will serve as a strategic technology leader responsible for aligning IT capabilities with business objectives across all GXP-regulated departments (GMP, GLP, GCP) as the organization prepares for commercial launch. This role requires deep expertise in pharmaceutical IT systems, regulatory compliance, and the ability to translate complex business requirements into scalable technology solutions that support quality, compliance, and operational excellence.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with GXP business leaders to understand strategic objectives and translate them into comprehensive IT roadmaps that support launch readiness and sustainable operations&lt;/li&gt;
&lt;li&gt;Oversee selection, implementation, and validation of critical GXP systems&lt;/li&gt;
&lt;li&gt;Ensure all IT systems comply with FDA 21 CFR Part 11, EU Annex 11, and data integrity requirements (ALCOA+)&lt;/li&gt;
&lt;li&gt;Lead Computer System Validation (CSV) activities and maintain audit readiness&lt;/li&gt;
&lt;li&gt;Drive IT readiness for commercial launch including system scalability, disaster recovery, and capacity planning&lt;/li&gt;
&lt;li&gt;Build and lead team of IT professionals focused on GXP systems; manage vendor relationships&lt;/li&gt;
&lt;li&gt;Partner with Quality and Regulatory Affairs to support inspections and maintain compliance&lt;/li&gt;
&lt;li&gt;&lt;span data-teams=&quot;true&quot;&gt;Lead project lifecycle activities such as planning, requirement gathering, design, build,&amp;nbsp;testing, implementation and post-implementation support of&amp;nbsp;GxP applications and related business processes.&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;Develop enterprise architecture&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Deep understanding of GXP regulations and their application to IT systems&lt;/li&gt;
&lt;li&gt;Strong knowledge of pharmaceutical manufacturing, quality, and clinical operations&lt;/li&gt;
&lt;li&gt;Experience with GAMP 5, industry standards, and cloud technologies in regulated environments&lt;/li&gt;
&lt;li&gt;Exceptional stakeholder management and communication skills across all organizational levels&lt;/li&gt;
&lt;li&gt;Strategic thinker with strong business acumen and ability to deliver complex projects on time and budget&lt;/li&gt;
&lt;li&gt;Experience in leveraging Enterprise Architecture to deliver business value&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree in Computer Science, Information Technology, Engineering, Life Sciences, or related field required&lt;/li&gt;
&lt;li&gt;10+ years of progressive IT experience in pharmaceutical, biotechnology, or regulated healthcare manufacturing environments&lt;/li&gt;
&lt;li&gt;5+ years in a leadership role managing IT business partnerships, systems implementations, or GXP IT operations&lt;/li&gt;
&lt;li&gt;Demonstrated experience supporting commercial launch activities or significant operational scale-up in a pharmaceutical setting&lt;/li&gt;
&lt;li&gt;Proven track record implementing and managing multiple GXP-regulated systems, especially Veeva systems&lt;/li&gt;
&lt;li&gt;Hands-on experience with Computer System Validation (CSV) and regulatory compliance requirements (21 CFR Part 11, EU Annex 11, data integrity)&lt;/li&gt;
&lt;li&gt;Experience managing IT budgets, vendor relationships, and cross-functional projects&lt;/li&gt;
&lt;li&gt;PMP, ITIL, or relevant IT certifications&lt;/li&gt;
&lt;li&gt;Knowledge of serialization, track-and-trace, and emerging technologies (AI/ML, analytics)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$215,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$235,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-it-business-partner-biopharma-gxp-nuvalent/69d3bbeec8e81216cd0b9004</link><guid isPermaLink="true">http://biotechroles.com/director-it-business-partner-biopharma-gxp-nuvalent/69d3bbeec8e81216cd0b9004</guid><pubDate>Mon, 06 Apr 2026 13:58:06 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Open Call]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 109, Inc. (FL109) is pioneering the use of artificial intelligence, physics and hardware to transform the way we see biology. FL109 is a privately held biotech, conceived by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. Become part of our mission-driven team and help envision the future of science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL109 is seeking innovative and driven professionals to join our interdisciplinary team. As a member of our early-stage company, you will play a pivotal role in developing and deploying state-of-the-art AI solutions that integrate artificial intelligence, physics, and hardware to transform our understanding of molecular biology. Your contributions will be essential in building scalable platforms, managing extensive datasets, and collaborating across diverse teams to achieve groundbreaking results.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We’re looking for amazing talent in these spaces:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;AI&lt;/li&gt;
&lt;li&gt;Software engineering&lt;/li&gt;
&lt;li&gt;Automation&lt;/li&gt;
&lt;li&gt;Physics&lt;/li&gt;
&lt;li&gt;Hardware engineering&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-MB1&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/open-call-flagship-pioneering/69d3bbecc8e81216cd0b8ffd</link><guid isPermaLink="true">http://biotechroles.com/open-call-flagship-pioneering/69d3bbecc8e81216cd0b8ffd</guid><pubDate>Mon, 06 Apr 2026 13:58:04 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$120000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Pricing & Contracting Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Senior Director, Payer &amp;amp; Reimbursement, the&lt;strong&gt; &lt;/strong&gt;Associate Director, Pricing &amp;amp; Contracting Operations plays a critical role in shaping and executing the company’s pricing and contracting strategies to optimize access to Nuvalent’s product portfolio, as well as playing a key part in driving pricing and contracting strategy and management.&lt;/p&gt;
&lt;p&gt;We are a growing pharmaceutical company with a commitment to delivering innovative, oral targeted therapies for oncology patients. &amp;nbsp;We are seeking a dynamic and strategic professional to lead pricing and contracting operations. &amp;nbsp;This individual will support launch planning and execution by preparing strategic pricing frameworks and payer contracting strategies.&amp;nbsp; They will serve as a cross-functional catalyst to optimize market access and net revenue across payer segments, while ensuring operational excellence and compliance in pricing and contract execution.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Strategic Pricing Operations&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Assist in the development and lead implementation and optimization of pricing strategies for in-line and pipeline oncology products&lt;/li&gt;
&lt;li&gt;Serve as the operational manager of the Pricing Committee, including:
&lt;ul&gt;
&lt;li&gt;Managing agenda, preparation and facilitating meetings&lt;/li&gt;
&lt;li&gt;Aligning stakeholders and driving strategic input&lt;/li&gt;
&lt;li&gt;Documenting decisions and actions&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Contracting Execution &amp;amp; Management&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;ul&gt;
&lt;li&gt;Design and manage contracting strategies across key segments: Commercial, Medicare, GPOs, Medicaid, 340B, VA, Payers/PBMs, and IDNs&lt;/li&gt;
&lt;li&gt;Manage day-to-day contract execution and issue resolution&lt;/li&gt;
&lt;li&gt;Submit new contracts and updates to contract terms&lt;/li&gt;
&lt;li&gt;Maintain GPO rosters, updating the 3PL as needed, and prepare quarterly business review (QBR) insights in collaborations with account director teams&lt;/li&gt;
&lt;li&gt;Oversee 340B contract pharmacy vendor partnerships&lt;/li&gt;
&lt;li&gt;Facilitate and resolve escalations from Patient Assistance Program (PAP)&lt;/li&gt;
&lt;/ul&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Data &amp;amp; Insights Collaboration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor competitive pricing intelligence and shifts in market dynamics&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;ul&gt;
&lt;li&gt;Partner with the Commercial Insights &amp;amp; Analytics team to ensure accurate data ingestion, analytics and delivery&lt;/li&gt;
&lt;li&gt;Support Finance-led reporting with analytical and operational coordination&lt;/li&gt;
&lt;/ul&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Access Optimization&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate across internal teams to assess and remove barriers to access:
&lt;ul&gt;
&lt;li&gt;Partner with Finance, Payer National Accounts, Health Systems Strategic Engagement, Patient Services and Field Reimbursement Managers&lt;/li&gt;
&lt;li&gt;Engage with Sales to proactively identify payer policy issues, product formulary status challenges, and denial trends&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;Support rebate dispute resolution and update internal teams on progress&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;VA/FSS Contract Administration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate with Finance and Vendor to facilitate and execute all Requests for Modification (RFM)&lt;/li&gt;
&lt;li&gt;Support the 5-year Contract Solicitation and Interim Agreement&lt;/li&gt;
&lt;li&gt;Collaborate with Finance and Vendor to complete Public Law 102-585 submission and documentation&lt;/li&gt;
&lt;li&gt;Monitor the Tracking Customer and initiate a change if required&lt;/li&gt;
&lt;li&gt;Complete the initial registration and annual renewals of SAM.gov&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrated passion for improving patient access and outcomes.&lt;/li&gt;
&lt;li&gt;Problem-Solving: Proactive approach to resolving complex access issues.&lt;/li&gt;
&lt;li&gt;Analytical Skills: Ability to interpret coverage trends &amp;amp; payer policies to identify barriers and implement solution-oriented strategies to optimize patient access.&lt;/li&gt;
&lt;li&gt;Business Acumen: In-depth understanding prior authorization, coding, billing, patient services, and specialty pharmacy processes.&lt;/li&gt;
&lt;li&gt;Provider Engagement: Building strong relationships with healthcare providers and office Highly responsive; ability to support escalations outside of local time zone working hours, as needed.&lt;/li&gt;
&lt;li&gt;Cross-Functional Collaboration: Partnering with sales, market access, patient services, and medical affairs. Foster a culture of empowerment, collaboration, and a focus on patient impact.&lt;/li&gt;
&lt;li&gt;Team Leadership: Proven leadership&amp;nbsp;and conflict resolution skills.Encourage&amp;nbsp;collaboration,&amp;nbsp;innovation,&amp;nbsp;and&amp;nbsp;new ideas&amp;nbsp;while integrating information from various sources.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Clear Communication: Highly effective presentation, communication, emotional intelligence, and&amp;nbsp;facilitation&amp;nbsp;&amp;amp;&amp;nbsp;interpersonal&amp;nbsp;skills.Ability to explain complex reimbursement processes in simple terms.&lt;/li&gt;
&lt;li&gt;Process Improvement: Identifying opportunities to streamline reimbursement workflows.&lt;/li&gt;
&lt;li&gt;Adaptability: Managing evolving payer landscapes and policy changes.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree required; Master’s degree or MBA preferred&lt;/li&gt;
&lt;li&gt;Minimum of 7+ years of experience in pricing and contract operations within the pharmaceutical or biotech industry&lt;/li&gt;
&lt;li&gt;Management and payer contracting; oral oncology experience preferred&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. reimbursement landscape, regulatory frameworks and government policy developments and their implications&lt;/li&gt;
&lt;li&gt;Self-starter who thrives in a dynamic, entrepreneurial environment&lt;/li&gt;
&lt;li&gt;Successful track record working in a fast-paced companies experiencing rapid-growth&lt;/li&gt;
&lt;li&gt;Excellent interpersonal skills, with the ability to gain alignment by working collaboratively and inclusively across functional teams&lt;/li&gt;
&lt;li&gt;Strong verbal and written communications; Proven ability to grow and collaborate others&lt;/li&gt;
&lt;li&gt;Record of achievement, innovation and compliance&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$175,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$200,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-pricing-and-contracting-operations-nuvalent/69d3bbe9c8e81216cd0b8ff6</link><guid isPermaLink="true">http://biotechroles.com/associate-director-pricing-and-contracting-operations-nuvalent/69d3bbe9c8e81216cd0b8ff6</guid><pubDate>Mon, 06 Apr 2026 13:58:01 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Manager, Growth Marketing]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;THE COMPANY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Extuitive is a Flagship Pioneering–backed startup reimagining product innovation for the AI era. Our mission is to empower entrepreneurs and direct-to-consumer (D2C) brands with AI-driven tools that simplify, accelerate, and scale the launch of new products. Based in Cambridge, MA, we operate like a special ops unit—fast-moving, data-driven, and relentlessly focused on impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We’re seeking a creative, execution-focused Manager of Digital Marketing to build and optimize our full-funnel growth engine from the ground up. You’ll own demand generation, paid acquisition, growth experiments, and martech infrastructure. This is an opportunity to shape our digital strategy, influence product–market fit, and drive exponential customer acquisition for AI-powered SaaS tools.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ol&gt;
&lt;li&gt;&lt;strong&gt;Digital Marketing Strategy &amp;amp; Execution&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Develop and oversee multichannel paid campaigns (Meta, TikTok, Google Search/Display, YouTube)&lt;/li&gt;
&lt;li&gt;Establish and manage awareness, acquisition, and onboarding funnels&lt;/li&gt;
&lt;li&gt;Build and iterate growth loops (referral programs, virality features)&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;&lt;strong&gt;Demand Generation &amp;amp; Lead Funnel Optimization&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Design, launch, and test B2C campaigns targeting Shopify merchants and e-commerce brands&lt;/li&gt;
&lt;li&gt;Optimize cost-per-acquisition (CPA), customer lifetime value (LTV), and conversion rates through data-driven experiments&lt;/li&gt;
&lt;li&gt;Implement automated lead nurturing workflows using email, chat, and retargeting sequences&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;&lt;strong&gt;Go-to-Market (GTM) Campaigns&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Partner with product, content, and sales teams to create and execute launch playbooks for new AI features&lt;/li&gt;
&lt;li&gt;Define target segments, messaging frameworks, and launch timelines&lt;/li&gt;
&lt;li&gt;Analyze post-launch performance and iterate rapidly&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;&lt;strong&gt;Analytics &amp;amp; Martech Infrastructure&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Set up and maintain analytics stack (GA4, Mixpanel, HubSpot, GEO or equivalent)&lt;/li&gt;
&lt;li&gt;Track and report key metrics (CPL, MQL-to-SQL conversion, ROAS, churn)&lt;/li&gt;
&lt;li&gt;Develop dashboards and playbooks to inform strategic decisions&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;&lt;strong&gt;Experimentation &amp;amp; Optimization&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Lead A/B and multivariate tests on landing pages, ad creatives, and email flows&lt;/li&gt;
&lt;li&gt;Prioritize test roadmap based on impact vs. effort&lt;/li&gt;
&lt;li&gt;Document learnings and scale winning experiments&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;&lt;strong&gt;Team Leadership &amp;amp; Collaboration&lt;/strong&gt;&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Grow and mentor a team of performance marketers and lifecycle specialists&lt;/li&gt;
&lt;li&gt;Align cross-functional teams (product, design, engineering, sales) on marketing initiatives&lt;/li&gt;
&lt;li&gt;Present regular updates to executive leadership&lt;/li&gt;
&lt;/ul&gt;
&lt;/ol&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;6+ years of marketing experience focused on digital channels and go-to-market strategies for software/SaaS and consumer brands&lt;/li&gt;
&lt;li&gt;Proven track record developing and executing multi-channel digital campaigns (SEO, SEM, social media, email, content marketing, web analytics) that drive engagement and ROI&lt;/li&gt;
&lt;li&gt;Expert in paid acquisition &amp;amp; demand generation on e-commerce platforms (e.g., Shopify), including search ads, social ads (Meta, LinkedIn), programmatic DSPs, and retargeting workflows&lt;/li&gt;
&lt;li&gt;Experience with GEO (generative engine optimization)&lt;/li&gt;
&lt;li&gt;Proficient with marketing automation &amp;amp; CRM tools (e.g., HubSpot, Marketo, Salesforce Pardot) to architect scalable, personalized customer journeys&lt;/li&gt;
&lt;li&gt;Strong analytical abilities in Excel and BI platforms (Looker, Tableau) to conduct CAC/LTV calculations, cohort analyses, and funnel optimization&lt;/li&gt;
&lt;li&gt;Skilled at structuring digital channel partnerships, from platform integrations to affiliate and influencer programs, to expand reach and acquisition&lt;/li&gt;
&lt;li&gt;Hands-on with go-to-market &amp;amp; product-led growth campaigns, aligning marketing and product for successful launches&lt;/li&gt;
&lt;li&gt;Startup &amp;amp; early-stage SaaS background preferred, thriving in fast-paced, ambiguous environments&lt;/li&gt;
&lt;li&gt;Exceptional communicator &amp;amp; leader, with proven presentation, project-management, and cross-functional team coordination skills&lt;/li&gt;
&lt;li&gt;Advanced PowerPoint proficiency for crafting compelling performance reports and executive decks&lt;/li&gt;
&lt;li&gt;Creative thinker passionate about innovation, consumer-trend spotting, and applying generative AI to marketing initiatives&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $121,000 - $159,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Extuitive, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Extuitive, Inc.’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;
&lt;p style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;#LI-MB1&lt;/p&gt;]]></description><link>http://biotechroles.com/manager-growth-marketing-flagship-pioneering/69d3bbe9c8e81216cd0b8ff5</link><guid isPermaLink="true">http://biotechroles.com/manager-growth-marketing-flagship-pioneering/69d3bbe9c8e81216cd0b8ff5</guid><pubDate>Mon, 06 Apr 2026 13:58:01 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Drug Safety and Pharmacovigilance Scientist]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;The Company:&lt;br&gt;&lt;/strong&gt;With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer.&amp;nbsp; Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the Head of PV Science, the Associate Director, Drug Safety and Pharmacovigilance Scientist is responsible for assessing and interpreting safety data from multiple sources, including clinical trials, spontaneous and solicited reports, aggregate, and literature reports. This individual is expected to provide interpretation and summaries of drug safety information and provide input in the generation of safety reports (e.g., DSURs, PADERs, PBRERs, and clinical safety assessments). This individual may also support the medical assessment of Individual Case Safety Reports (ICSRs) and other drug safety information. The individual will be an integral part of a group of safety professionals within Nuvalent and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Contribute to the generation of aggregate safety reports including development safety update reports, periodic benefit risk evaluation reports, and provide medical input in review of new or existing safety documents to ensure compliance with relevant regulatory requirements, such as protocols, safety summaries and regulatory reports&lt;/li&gt;
&lt;li&gt;Contribute to signaling and safety surveillance processes, including the identification of safety observations, emergent safety concerns and new safety signals, ensure prompt assessment and communication of confirmed safety signals&lt;/li&gt;
&lt;li&gt;Serve as a medical resource for the generation and review of clinical trial protocols, informed consent forms (ICFs) and investigator brochures (IBs) and the development of Reference Safety Information&lt;/li&gt;
&lt;li&gt;Contribute to creation or and updates to Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) and the maintenance of these documents&lt;/li&gt;
&lt;li&gt;Contribute to the development of Standard Operating Procedures, Working Instructions and other guidance documents&lt;/li&gt;
&lt;li&gt;Provide safety and pharmacovigilance training programs as required&lt;/li&gt;
&lt;li&gt;Collaborate cross functionally (e.g., Reg Affairs, Clin Ops, Clin Science) to ensure pharmacovigilance input&lt;/li&gt;
&lt;li&gt;Support the medical assessment of ICSRs as needed&lt;/li&gt;
&lt;li&gt;Support other pharmacovigilance and drug safety responsibilities as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design global risk management frameworks for Nuvalent’s medicines&lt;/li&gt;
&lt;li&gt;Translate safety data into clinical insights&lt;/li&gt;
&lt;li&gt;Adapt visualization tools for safety surveillance&lt;/li&gt;
&lt;li&gt;Influence multidisciplinary teams to prioritize patient safety.&lt;/li&gt;
&lt;li&gt;Strong ability to build relationships, collaborate and influence across disciplines within Nuvalent and with outside stakeholders&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;4+ years’ experience in Drug Safety / Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency&lt;/li&gt;
&lt;li&gt;Degree in a medical or healthcare related discipline like MD, PharmD, RN or PhD.&lt;/li&gt;
&lt;li&gt;Excellent knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines&lt;/li&gt;
&lt;li&gt;Experience with medical drug safety assessments, drug safety surveillance and monitoring activities&lt;/li&gt;
&lt;li&gt;Experience with safety data collection and interpretation from clinical trials, literature and post market&lt;/li&gt;
&lt;li&gt;Experience with preparation of responses to Regulatory Authorities and experience with IND/NDA submissions and negotiations with Regulatory Authorities as part of marketing approval&lt;/li&gt;
&lt;li&gt;Experience with the development and updates to Reference Safety Information, IB, Company Core Data Sheet and local labels&lt;/li&gt;
&lt;li&gt;Excellent verbal, written and presentation skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Additional Information:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.&lt;/p&gt;
&lt;p&gt;The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors.&amp;nbsp; The range will be reviewed regularly and is subject to change.&lt;/p&gt;
&lt;p&gt;Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;Annual Salary Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$170,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$195,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span style=&quot;font-family: arial, helvetica, sans-serif; font-size: 10pt;&quot;&gt;Nuvalent&amp;nbsp;provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.&lt;/span&gt;&lt;/p&gt;
&lt;hr&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.&lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;word-spacing: 0px; margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;Please be advised that all legitimate correspondence from a Nuvalent employee will come from &quot;@nuvalent.com&quot; email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “&lt;a href=&quot;mailto:no-reply@greenhouse.io&quot;&gt;&lt;span style=&quot;color: black;&quot;&gt;no-reply@greenhouse.io&lt;/span&gt;&lt;/a&gt;” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person. &lt;/span&gt;&lt;/p&gt;
&lt;p style=&quot;margin: 0in 0in 7.5pt 0in;&quot;&gt;&lt;span style=&quot;font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;&quot;&gt;If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-drug-safety-and-pharmacovigilance-scientist-nuvalent/69d3bbe6c8e81216cd0b8fed</link><guid isPermaLink="true">http://biotechroles.com/associate-director-drug-safety-and-pharmacovigilance-scientist-nuvalent/69d3bbe6c8e81216cd0b8fed</guid><pubDate>Mon, 06 Apr 2026 13:57:57 GMT</pubDate><company>Nuvalent</company><location>Cambridge, MA / Remote</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Head of Clinical Development]]></title><description><![CDATA[&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;dhkj5-0-0&quot;&gt;
&lt;p&gt;&lt;strong&gt;What if… &lt;/strong&gt;you could join an organization that creates, resources, and builds life sciences companies that invent breakthrough technologies in order to transform health care and sustainability?&lt;/p&gt;
&lt;p&gt;Montai Therapeutics is a privately held, biotechnology company focused on harnessing AI to decode untapped diverse chemistry to develop breakthrough oral medicines that can address persistent unmet needs in chronic disease. With our CONECTA™ platform, Montai has built the world’s leading foundation models for decoding the complex language between nature’s bioactive chemistry and human biology – supercharging the drug discovery process with unprecedented optionality and predictability.&lt;/p&gt;
&lt;p&gt;The company has curated and annotated a collection of over 1B Anthromolecules™ and Anthrologs™, which are derived from molecules humans have chronically consumed in food, supplements and herbal medicines. This has enabled efficient access to chemistry with vast untapped structural diversity and the potential to selectively and precisely modulate complex biology. Montai is rapidly advancing a pipeline of first-in-class oral medicines for validated biological pathways in inflammation and immunology – focused on biologic replacements and historically difficult to drug transcription factors.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are looking for an experienced Head of Clinical Development, reporting to our Chief Executive Officer, to have overall accountability for the development and implementation of small molecule clinical programs in the therapeutic areas of immunology/inflammation at Montai Therapeutics.&amp;nbsp; We are seeking a highly motivated, collaborative, results-oriented individual with the creativity, resourcefulness, and flexibility to excel in our growing organization.&lt;/p&gt;
&lt;p&gt;Specifically, the Head of Clinical Development will play a pivotal role in driving the successful transition of programs from research to clinical development and will contribute to shaping the clinical strategies that span from candidate discovery to human proof-of-concept.&amp;nbsp; As a leader of our clinical development strategy, this role is responsible for crafting and integrating clinical development plans in alignment with research, translational, nonclinical, regulatory and strategic priorities.&amp;nbsp; This individual will also ultimately oversee those responsible for supporting program operations, resource planning, and interactions with internal governance and external partners.&amp;nbsp; This role is ideal for an experienced individual passionate about translating cutting-edge science into innovative medicines through rigorous, thoughtful and collaborative development planning and execution.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&amp;nbsp;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop programmatic clinical strategy; oversee implementation of clinical programs in line with the clinical strategy and ensure patient safety and data integrity&lt;/li&gt;
&lt;li&gt;Collaborate closely with Project Leaders, Research, Leadership, and external advisors/KOLs to define and refine clinical hypotheses and development strategies.&lt;/li&gt;
&lt;li&gt;Integrate clinical plans with translational, nonclinical, and regulatory development strategies to enable seamless progression from exploratory studies to FIH trials.&lt;/li&gt;
&lt;li&gt;Drive and/or oversee the design, execution, analysis, interpretation, and reporting of clinical studies, both early and more advanced, in collaboration with R&amp;amp;D team members, in a matrixed and highly collaborative team environment&lt;/li&gt;
&lt;li&gt;Incorporate regulatory input, operational feasibility, and real-world data to ensure robust and executable development strategies.&lt;/li&gt;
&lt;li&gt;Serve as a Medical Monitor for early (clinical pharmacology, including first in human, DDI, proof of mechanism/concept) and/or more advanced clinical studies; may serve as Project Team Leader for clinical stage programs&lt;/li&gt;
&lt;li&gt;Assess trade-offs and build alignment with team members to enable informed programmatic decision-making&lt;/li&gt;
&lt;li&gt;Support development and implementation of program biomarker plans and ensure successful implementation at study site(s)&lt;/li&gt;
&lt;li&gt;Lead/author clinical portions of regulatory submissions and responses to regulatory agency questions; as appropriate, serve as a company representative for regulatory interactions&lt;/li&gt;
&lt;li&gt;Identify and address development risks and bottlenecks proactively; drive resolution across functional interfaces.&lt;/li&gt;
&lt;li&gt;Oversight of growing internal and external clinical operations functions and support, including cross-functional leadership and collaboration with quality, CROs, regulatory, and medical writing teams.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Experience:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;M.D. or Ph.D., Ph.D. with 8+ years of relevant experience in biopharmaceutical industry, including significant small molecule drug development experience&lt;/li&gt;
&lt;li&gt;Educational background in a relevant scientific discipline (e.g., biology, biochemistry, immunology) and advanced degree(s), including as Doctor of Medicine and post-graduate medical or scientific training; specific therapeutic experience in immunology/inflammation&lt;/li&gt;
&lt;li&gt;Prior experience as a functional leader (e.g., early clinical development, clinical pharmacology, translational/experimental medicine)&lt;/li&gt;
&lt;li&gt;Broad understanding of biopharmaceutical drug development, including working knowledge of relevant ICH and GCP guidelines and regulations&lt;/li&gt;
&lt;li&gt;Proficiency in developing and nurturing key partnerships and collaborations with external parties, including investigators, KOLs, CROs, and the broader scientific community (including academia, governmental, or nonprofit organizations), as well as internal discovery and preclinical functions&lt;/li&gt;
&lt;li&gt;Record of significant and successful contributions to regulatory submissions, including INDs/CTAs, and regulatory agency interactions&lt;/li&gt;
&lt;li&gt;Experience managing collaborations with consultants, pharmaceutical partners, CROs, and other external organizations is desirable&lt;/li&gt;
&lt;li&gt;Aptitude in serving as a subject matter expert and mentor across the organization&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Desired Skills &amp;amp; Competencies:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Excellent written and oral communication skills&lt;/li&gt;
&lt;li&gt;Experience delivering effective presentations to both technical and non-technical audiences&lt;/li&gt;
&lt;li&gt;Proven leadership skills, with the ability to collaborate and convey strategic implications to diverse stakeholders.&lt;/li&gt;
&lt;li&gt;Strong strategic thinking and critical thinking skills for identifying and addressing bottlenecks while optimizing cross-functional processes.&lt;/li&gt;
&lt;li&gt;Proactive and adaptable in demanding environments, with an operational mindset to improve efficiency and achieve strategic goals.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Location: &lt;/strong&gt;Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;More About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category life sciences companies to transform human health and sustainability. Since its launch in 2000, the firm has, through its Flagship Labs unit, applied its unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $50B in aggregate value. To date, Flagship has deployed over $2.2B in capital toward the founding and growth of its pioneering companies alongside more than $18B of follow-on investments from other institutions. The current Flagship ecosystem comprises 41 transformative companies, including Axcella Health (NASDAQ: AXLA), Denali Therapeutics (NASDAQ: DNLI), Evelo Biosciences (NASDAQ: EVLO), Foghorn Therapeutics (NASDAQ: FHTX), Indigo Ag, Kaleido Biosciences (NASDAQ: KLDO), Moderna (NASDAQ: MRNA), Rubius Therapeutics (NASDAQ: RUBY), Sana Biotechnology, Seres Therapeutics (NASDAQ: MCRB), and Sigilon Therapeutics (NASDAQ: SGTX).&lt;/p&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;Flagship Pioneering and our ecosystem companies are &lt;strong&gt;committed to equal employment opportunity&lt;/strong&gt; regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/div&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;6ni4e-0-0&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;/div&gt;
&lt;div class=&quot;&quot; data-block=&quot;true&quot; data-editor=&quot;c12n7&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;
&lt;div class=&quot;public-DraftStyleDefault-block public-DraftStyleDefault-ltr&quot; data-offset-key=&quot;cpe78-0-0&quot;&gt;&lt;em&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies&lt;/strong&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/div&gt;
&lt;/div&gt;
&lt;/div&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $360,000 - $415,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Montai Therapeutics currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Montai Therapeutics&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/head-of-clinical-development-flagship-pioneering/69d3bbe5c8e81216cd0b8fe4</link><guid isPermaLink="true">http://biotechroles.com/head-of-clinical-development-flagship-pioneering/69d3bbe5c8e81216cd0b8fe4</guid><pubDate>Mon, 06 Apr 2026 13:57:56 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$250000-400000</salary><type>Full-time</type></item><item><title><![CDATA[VP, Customer Experience]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Vice President, Customer Experience leads Dyne’s nationwide field organization, setting strategic direction and driving operational execution for our first commercial launch. This role orchestrates cross-functional collaboration across key accounts, medical affairs, patient services, and reimbursement to ensure patients with neuromuscular diseases, including DMD, DM1, and FSHD, receive optimal care.&lt;/p&gt;
&lt;p&gt;The VP builds and directs a high-performing team focused on delivering Dyne’s innovative therapies to patients, starting with our lead candidate in DMD. Success requires exceptional leadership, deep launch expertise, and a strong understanding of market dynamics, customer insights, and the competitive landscape. This leader ensures seamless coordination across all field functions to position Dyne for sustained growth and impact.&lt;/p&gt;
&lt;p&gt;This is a field-based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Sets the Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Craft a cohesive go-to-market strategy that resonates with the target audience, distinguishes Dyne from competitors, and creates market impact&lt;/li&gt;
&lt;li&gt;Implement business plans to achieve performance goals, including regional launch readiness reviews with senior leadership.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Develop and implement national and regional account and marketing plans to achieve business objectives within the rare disease therapeutic area.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Understand the specific market landscape and trends within each region to identify opportunities and adapt strategies.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Develop and implement long-term strategies for growth and expansion within each region.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Operational Execution &amp;amp; Launch Excellence&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive cross-functional collaboration with Medical Affairs, Patient Services and Distribution, Commercial Operations, Market Access, Corporate Affairs, Human Resources, Compliance, Legal and Patient Advocacy&lt;/li&gt;
&lt;li&gt;Serve as the orchestrator for customer-facing teams to build strong relationships with healthcare providers, KOLs, payers, and other key stakeholders&lt;/li&gt;
&lt;li&gt;Builds and maintains strong relationships with key opinion leaders (KOLs), healthcare professionals (HCPs), and other stakeholders within sites of care&lt;/li&gt;
&lt;li&gt;Manage and grow key accounts across the nation, ensuring the successful adoption of Dyne’s rare disease products.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Navigate the complex US access environment with innovative approaches and patient services support to ensure optimal patient access&lt;/li&gt;
&lt;li&gt;Ensuring customer satisfaction and addressing any issues within the region&lt;/li&gt;
&lt;li&gt;Ensuring that all activities and interactions comply with relevant regulations and guidelines.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Business Performance &amp;amp; Financial Management&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and oversee financial plans for the region, including revenue maximization and budget management.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Deliver on key performance indicators for appropriate KOL/HCP interactions, market access, and product adoption&lt;/li&gt;
&lt;li&gt;Ensure operational efficiency across all aspects of the region&lt;/li&gt;
&lt;li&gt;Allocate resources strategically to maximize impact and ROI&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;People Leadership &amp;amp; Development&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build and inspire high-performing, cross-functional teams that drive innovation, excellence, and an entrepreneurial spirit.&lt;/li&gt;
&lt;li&gt;Motivate, empower and coach the team, delegating tasks and ensuring they meet performance expectations.&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Mentor regional team members to drive performance and development.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Foster strong partnerships across functions to ensure aligned objectives and seamless implementation&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education/Experience/Skills:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree with a minimum 20 years of progressive experience in Pharmaceutical/Biotech&lt;/li&gt;
&lt;li&gt;Rare disease commercial launch experience is required&lt;/li&gt;
&lt;li&gt;Prior experience leading a national sales organization in a biotech or pharma company is strongly preferred&lt;/li&gt;
&lt;li&gt;Culture builder &amp;amp; talent magnet that attracts, hires, develops, retains, and promotes top talent; sets a people-first, performance-driven culture.&lt;/li&gt;
&lt;li&gt;Experience leading cross-functional teams in at least one other discipline (e.g., marketing, market access, patient services, clinical specialty or medical, other) is strongly preferred&lt;/li&gt;
&lt;li&gt;Exceptional leadership ability to lead and motivate teams, set clear goals, and deliver performance.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience managing field organizations through change, innovation, or growth is highly valued.&lt;/li&gt;
&lt;li&gt;Excellent interpersonal and communication skills to build and maintain strong relationships with all stakeholders.&lt;/li&gt;
&lt;li&gt;Strong strategic thinking, business acumen, communication and enterprise leadership and ability to develop and execute operational plans, adapt to changing market conditions, and identify opportunities.&lt;/li&gt;
&lt;li&gt;Experience navigating complex regulatory and compliance environments including strong understanding of relevant policies guiding the Pharmaceutical Industry&lt;/li&gt;
&lt;li&gt;Innovative mindset with ability to drive transformation while delivering results.&lt;/li&gt;
&lt;li&gt;Willingness and ability to travel more than 50% of the time, including frequent overnight stays.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$300,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$355,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vp-customer-experience-dyne-therapeutics/69d3bbe3c8e81216cd0b8fe0</link><guid isPermaLink="true">http://biotechroles.com/vp-customer-experience-dyne-therapeutics/69d3bbe3c8e81216cd0b8fe0</guid><pubDate>Mon, 06 Apr 2026 13:57:54 GMT</pubDate><company>Dyne Therapeutics</company><location>Field Based</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Enterprise Applications Analyst]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Who We Are&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a biotechnology company that invents and builds platform companies that change the world. We bring together the greatest scientific minds with entrepreneurial company builders and assemble the capital to allow them to take courageous leaps. Those big leaps in human health and sustainability exponentially accelerate scientific progress in areas ranging from cancer detection and treatment to nature-positive agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;What sets Flagship apart is our ability to advance biotechnology by uniting life science innovation, company creation, and capital investment under one roof in a way that is largely without precedent. Our scientific founders, entrepreneurial leaders, and professional capital managers are each aligned around an institutionalized process that enables us to innovate and transform for the benefit of people and planet.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;THE ROLE&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are seeking a detail-oriented&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Enterprise Applications Analyst&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;to support the Enterprise Applications team in&amp;nbsp;documenting,&amp;nbsp;managing,&amp;nbsp;optimizing, and evolving Flagship’s business systems landscape. This role will&amp;nbsp;assist&amp;nbsp;with operational support, requirements gathering, reporting,&amp;nbsp;diagraming,&amp;nbsp;and system improvements while also supporting architectural initiatives such as application evaluations, integration support, and documentation of system designs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The analyst will work closely with the&amp;nbsp;Director of Enterprise Applications&amp;nbsp;and cross-functional stakeholders to ensure systems such as UKG, NetSuite, Greenhouse, Cobblestone, Coupa, Notion, and ADP operate effectively and continue to align with business needs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;This role bridges business operations and technical architecture, helping translate business requirements into system improvements and supporting the broader enterprise applications strategy.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;KEY RESPONSIBILITIES&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Business Analysis &amp;amp; Application Support&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support day-to-day operations and troubleshooting across enterprise applications including HCM, ERP, ATS, CLM, Procurement, and Payroll platforms.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Gather, document, and validate business requirements for system enhancements and integrations.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partner with stakeholders across HR, Finance, Procurement, and IT to understand system needs and process improvements.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Assist with testing, configuration validation, and user acceptance testing for system changes and releases.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Provide end-user documentation, training, and ongoing support for enterprise systems.&amp;nbsp;&lt;/span&gt; &amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Architecture &amp;amp; System Design Support&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Assist the&amp;nbsp;Director, Enterprise Applications&amp;nbsp;with architecture and technical design activities, including:&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Documenting system architectures, data flows, and integration patterns across enterprise platforms.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Supporting technical evaluations of new software requests using defined architecture criteria.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Assisting with system integration documentation and configuration validation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Supporting integration development efforts using tools such as Workato or Power Platform.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Helping maintain architectural standards, system documentation, and technical diagrams.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Professional Experience &amp;amp; Qualifications&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Required&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Bachelor’s degree in Information Systems, Business, Computer Science, or related field.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;3+ years of experience in a Business Analyst, Systems Analyst, or Enterprise Applications support role.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience supporting enterprise SaaS platforms such as HCM, ERP, ATS, procurement, or finance systems.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong analytical and documentation skills.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;8&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ability to translate business needs into system requirements.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Preferred&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Exposure to integration platforms such as Workato, Power Platform, or similar tools.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Familiarity with enterprise architecture concepts such as system integration, data governance, or application portfolio management.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;SQL experience for data analysis or validation.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience supporting SaaS application ecosystems.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;ABOUT FLAGSHIP PIONEERING&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these&amp;nbsp;companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.  &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at &lt;/span&gt;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;www.flagshippioneering.com&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;span data-contrast=&quot;auto&quot;&gt;.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&amp;nbsp;&lt;/span&gt;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;core values&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;guide us through uncertainty and toward lasting impact.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We are an equal opportunity employer&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;We recognize that great candidates often bring unique strengths&amp;nbsp;&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;without fulfilling every qualification&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;/span&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;and interest in Flagship.&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Recruitment &amp;amp; Staffing Agencies&lt;/span&gt;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/span&gt;&lt;/em&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;#LI-NM1&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering and our ecosystem companies are committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $76,000 - $104,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/enterprise-applications-analyst-flagship-pioneering/69d3bbe0c8e81216cd0b8fdc</link><guid isPermaLink="true">http://biotechroles.com/enterprise-applications-analyst-flagship-pioneering/69d3bbe0c8e81216cd0b8fdc</guid><pubDate>Mon, 06 Apr 2026 13:57:52 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Manufacturing Engineer]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Principal Manufacturing Engineer is a hands-on technical leader responsible for new product introduction and for defining, validating, and sustaining robust manufacturing processes for electromechanical medical devices. This role supports the development and execution of manufacturing and validation strategies, authors core validation documentation, and collaborates closely with Quality, R&amp;amp;D, Supply Chain, and external manufacturing partners to ensure compliant and scalable production processes. Working knowledge and experience with the processes associated with single use devices (adhesive bonding, thermal welding, injection molding and extrusion) would be considered a strong plus.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead development and execution of manufacturing, test, and validation strategies aligned with regulatory requirements, product risk, and business objectives.&lt;/li&gt;
&lt;li&gt;Serve as a technical authority for manufacturing process development and validation of electromechanical products.&lt;/li&gt;
&lt;li&gt;Develop and maintain Master Validation Plans (MVPs) covering equipment, processes, software, and test methods.&lt;/li&gt;
&lt;li&gt;Lead test method validation (TMV) activities including test strategy development, Gage R&amp;amp;R, robustness studies, and statistical justification of acceptance criteria.&lt;/li&gt;
&lt;li&gt;Ensure all validation activities comply with FDA, ISO 13485, and applicable regulatory standards.&lt;/li&gt;
&lt;li&gt;Apply statistical methods (DOE, Cp/Cpk, MSA) to process characterization, validation, and troubleshooting.&lt;/li&gt;
&lt;li&gt;Analyze data trends to establish control strategies and drive continuous process improvements.&lt;/li&gt;
&lt;li&gt;Author and review technical documentation including validation plans, reports, protocols, work instructions, and risk assessments.&lt;/li&gt;
&lt;li&gt;Support regulatory submissions, audits, and inspections.&lt;/li&gt;
&lt;li&gt;Provide technical leadership to suppliers and contract manufacturers.&lt;/li&gt;
&lt;li&gt;Support new product introduction (NPI), design transfer, and sustaining engineering activities.&lt;/li&gt;
&lt;li&gt;Collaborate cross-functionally with R&amp;amp;D, Quality, Supply Chain, and Operations.&lt;/li&gt;
&lt;li&gt;Mentor manufacturing and validation engineers.&lt;/li&gt;
&lt;li&gt;Ensure compliance with applicable regulations, policies, and procedures.&lt;/li&gt;
&lt;li&gt;Foster a collaborative, solution-oriented team environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Education or Certification Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Mechanical, Electrical, Manufacturing, Biomedical Engineering, or related field.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Professional Work Experience&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Minimum of 10 years of manufacturing engineering experience in a regulated environment.&lt;/li&gt;
&lt;li&gt;Medical device experience preferred (ISO 13485, ISO 14971).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications and Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Expertise in electromechanical manufacturing processes (PCB assembly, cable/harnessing, machining, sheet metal).&lt;/li&gt;
&lt;li&gt;Strong statistical analysis and validation experience.&lt;/li&gt;
&lt;li&gt;Knowledge of regulatory requirements for medical devices.&lt;/li&gt;
&lt;li&gt;Experience with SolidWorks and Minitab preferred.&lt;/li&gt;
&lt;li&gt;Familiarity with schematic tools (e.g., OrCAD) is a plus.&lt;/li&gt;
&lt;li&gt;Experience with single-use device processes is desirable.&lt;/li&gt;
&lt;li&gt;Strong technical writing and documentation skills.&lt;/li&gt;
&lt;li&gt;Ability to manage projects and work cross-functionally.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other Essentials and Key Success Factors&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong technical leadership and problem-solving skills.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication.&lt;/li&gt;
&lt;li&gt;High attention to detail.&lt;/li&gt;
&lt;li&gt;Collaborative and proactive mindset.&lt;/li&gt;
&lt;li&gt;Commitment to continuous improvement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Compensation&lt;/strong&gt; This position offers a competitive salary in the range of $115,000 – $165,000 annually, along with a comprehensive benefits package. Actual compensation will be based on relevant experience, education, and market factors.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In accordance with Massachusetts law, General Laws Chapter 149, Section 19B. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/principal-manufacturing-engineer-fractyl-health/69d3bbe0c8e81216cd0b8fda</link><guid isPermaLink="true">http://biotechroles.com/principal-manufacturing-engineer-fractyl-health/69d3bbe0c8e81216cd0b8fda</guid><pubDate>Mon, 06 Apr 2026 13:57:51 GMT</pubDate><company>Fractyl Health</company><location>Burlington, MA</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Scientist, Process Development - Bioconjugation]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The position is responsible for process development, technology transfer, and management of external CDMO activities to ensure development of robust and reliable GMP manufacturing processes for antibody oligonucleotide conjugates and intermediates. The Senior Scientist will represent CMC Process Sciences as a technical leader and provide guidance to internal process development staff and external vendors on oligonucleotide conjugate development and manufacturing activities from pre-clinical to GMP production for clinical evaluation (Phase 1-3). This includes active oversight of process establishment, process development, scale-down model verification, and process characterization. This person will also have direct oversight of CDMO technology transfer and process development operations.&lt;/p&gt;
&lt;p&gt;This position works closely with key stakeholders including Platform Research, External Manufacturing, Regulatory Affairs, and Project Management to meet the needs of Dyne’s complex clinical supply chain, supporting our preclinical and clinical programs.&lt;/p&gt;
&lt;p&gt;This role is based in Waltham, MA without the possibility of being a remote role. Physical presence onsite is expected on 4-5 days/week.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Responsible for drug substance bioconjugation including process development, tech transfer, scale-up, and process characterization of oligonucleotide conjugates.&lt;/li&gt;
&lt;li&gt;Lead internal CMC Process Development activities via hands-on contribution in the laboratory.&lt;/li&gt;
&lt;li&gt;Work with CDMOs to manage external process development, optimization, and tech transfer of new programs in a stage appropriate manner to ensure key milestones and products are delivered on schedule.&lt;/li&gt;
&lt;li&gt;Partner with Research to support bioconjugation development activities and enhance the tech transfer process to external manufacturing partners.&lt;/li&gt;
&lt;li&gt;Represent bioconjugation Drug Substance process as a technical leader in internal cross-functional CMC teams.&lt;/li&gt;
&lt;li&gt;Establish clear expectations and priorities, set objectives, and effectively apply resources to deliver on program goals.&lt;/li&gt;
&lt;li&gt;Select, qualify and manage external contract development and manufacturing organizations.&lt;/li&gt;
&lt;li&gt;Drive continuous improvement opportunities, adapt to and solve challenges and lead the timely resolution of issues.&lt;/li&gt;
&lt;li&gt;Evaluate and implement emerging technologies/applications to improve conjugation processes and optimize purification methods.&lt;/li&gt;
&lt;li&gt;Partner with internal cross functional teams and serve as the liaison to define suitable, compliant, and defendable CMC strategies.&lt;/li&gt;
&lt;li&gt;Prepare technical source documents, publications, and oral presentations.&lt;/li&gt;
&lt;li&gt;Prepare and review relevant CMC and product related sections and documentation for global regulatory submission.&lt;/li&gt;
&lt;li&gt;Review and approve documents related to development and cGMP operations, including Tech Transfer, Process Characterization, Master Batch Records (MBRs) and Campaign Summary Reports.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education and Skills Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD&amp;nbsp;or equivalent experience&amp;nbsp;in a scientific discipline and a minimum of 5+&amp;nbsp;years&amp;nbsp;related experience working with bioconjugates including a deep understanding of conjugation chemistries, preparative chromatography, and TFF.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience in biopharmaceutical CMC management and/or Research &amp;amp; Development preferably in a clinical-stage biotechnology company.&lt;/li&gt;
&lt;li&gt;Familiarity working with oligonucleotides including but not limited to morpholino oligonucleotides, antisense oligonucleotides, and siRNA is desired.&lt;/li&gt;
&lt;li&gt;Hands on experience with analytical techniques for characterization of conjugates including HPLC/UPLC, SEC, SDS-PAGE, ion exchange chromatography, and UV/vis.&lt;/li&gt;
&lt;li&gt;Experience with oversight of external contract development and manufacturing (CDMO)&lt;/li&gt;
&lt;li&gt;Ability to problem solve emerging issues related to drug substance development.&lt;/li&gt;
&lt;li&gt;A strong understanding of biologics and small molecule manufacturing, analytical development, quality control, quality assurance, and regulatory functions.&lt;/li&gt;
&lt;li&gt;Self-directed individual who is able to work effectively with limited direction in a complex, fast-paced environment.&lt;/li&gt;
&lt;li&gt;Excellent interpersonal, organizational, negotiation, and communication skills; a team member that can work collaboratively with colleagues across functions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$147,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$180,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-scientist-process-development-bioconjugation-dyne-therapeutics/69d3bbdec8e81216cd0b8fd8</link><guid isPermaLink="true">http://biotechroles.com/senior-scientist-process-development-bioconjugation-dyne-therapeutics/69d3bbdec8e81216cd0b8fd8</guid><pubDate>Mon, 06 Apr 2026 13:57:50 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Protein & Cell Sciences]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Metaphore Bio, a generative AI drug design company focused on creating a new class of functional antibodies, is seeking a leader with strong scientific and technical skills to enable the delivery of high-quality therapeutic proteins.&lt;/p&gt;
&lt;p&gt;The Director of Protein &amp;amp; Cell Sciences at Metaphore will lead a focused team responsible for high-throughput production and characterization of antibodies and related proteins, and for cell culture, engineering, and scale-up of antibody/protein production up to the multi-gram scale to support research activities. Responsibilities include delivering high-quality antibodies and protein reagents for multiple simultaneous biologics discovery programs, enabling discovery platform optimization, managing a team of direct and indirect reports, and coordinating both in-house and outsourced protein expression, purification, and characterization activities.&lt;/p&gt;
&lt;p&gt;As a member of the Biotherapeutics &amp;amp; Enabling Technologies leadership team, this scientific leader will work closely with the head of the unit to establish and maintain a Protein &amp;amp; Cell Sciences function that maximizes the ability the potential for Metaphore’s platform to deliver transformative therapeutics to patients.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Scientific and Functional Leadership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead an engaged and entrepreneurial team of 4-5 scientists that contributes significantly to the advancement of the internal and partnered portfolio, develops novel platforms and techniques, and delivers well-characterized, high-quality development candidates.&lt;/li&gt;
&lt;li&gt;Establish, maintain, and communicate best practices for biochemistry and cell biology techniques including expression, production, purification, and analytical and functional characterization of antibodies and related therapeutic proteins.&lt;/li&gt;
&lt;li&gt;Ensure high quality data management including the use of electronic laboratory environments/LIMS for data storage and retrieval, to maximize the potential of AI/ML methods to deliver high-quality leads.&lt;/li&gt;
&lt;li&gt;Partner with research informatics and laboratory automation teams to identify and implement opportunities for improved workflows, more efficient protein production and characterization, and parallelized therapeutic discovery.&lt;/li&gt;
&lt;li&gt;Make highly impactful contributions to programs as a scientific leader and expert on protein therapeutics.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Strategy and Execution&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Implement and manage outsourced protein production and characterization work with CROs that complements internal resourcing.&lt;/li&gt;
&lt;li&gt;Serve as a major interface with downstream CMC functions and external CDMOs to enable seamless progression of molecules into and through DC nomination, process development, and early manufacturing.&lt;/li&gt;
&lt;li&gt;Accountable for resourcing decisions for programs within the HTPP function.&lt;/li&gt;
&lt;li&gt;Partner with peers on the Biotherapeutics leadership team to manage resources, budgets, and operations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Team Building and External Engagement&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Recruit, mentor, and develop a high-performing HTPP unit.&lt;/li&gt;
&lt;li&gt;Foster a culture of collaboration, innovation, and accountability by partnering with other functions within the Biotherapeutics unit and across Metaphore.&lt;/li&gt;
&lt;li&gt;Partner with external collaborators, CROs, and technology providers to expand capabilities and accelerate timelines.&lt;/li&gt;
&lt;li&gt;As a member of the Biotherapeutics leadership team, facilitate group operations and strategic decisions, contribute to the development of the culture and people within the group, and contribute to broader company-wide strategic initiatives.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in Protein Biochemistry, Molecular and Cell Biology, Structural Biology, or a related discipline, or non-PhD with appropriate skills and experience.&lt;/li&gt;
&lt;li&gt;10+ years of experience in biologics drug discovery and development.&lt;/li&gt;
&lt;li&gt;Deep knowledge of antibody expression, purification, and characterization workflows, including the implementation of automation solutions to enable high-throughput protein production.&lt;/li&gt;
&lt;li&gt;Experience managing biologics CROs to expand protein production/characterization capabilities and capacity.&lt;/li&gt;
&lt;li&gt;Strong interpersonal and communication skills, with an established track record of leading and developing people and teams in a fast-paced, entrepreneurial biotech environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Values and Behaviors&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking individuals with an entrepreneurial spirit, strong communication skills, and comfort working in and contributing to a dynamic and cross-functional team environment. The level of the role will be commensurate with the education and years of experience of the identified candidate.&lt;/p&gt;
&lt;p&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $183,000 - $231,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Metaphore Biotechnologies, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Metaphore Biotechnologies, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/director-protein-and-cell-sciences-flagship-pioneering/69d3bbdcc8e81216cd0b8fd4</link><guid isPermaLink="true">http://biotechroles.com/director-protein-and-cell-sciences-flagship-pioneering/69d3bbdcc8e81216cd0b8fd4</guid><pubDate>Mon, 06 Apr 2026 13:57:47 GMT</pubDate><company>Flagship Pioneering</company><location>Somerville, MA USA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Design Assurance Engineer II]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Design Assurance Engineer II to join our team. The ideal candidate is a talented individual who is enthusiastic about learning while making a difference in the world. The DA Engineer will have the opportunity to contribute to a variety of Design Assurance core responsibilities, being the key QA team member on one or more product development projects, working collaboratively with the R&amp;amp;D teams from concept generation through manufacturing transfer, and contributing to risk management process throughout. The role also includes directing cross-functional complaint teams on investigations and root cause analysis to drive product improvement, assisting with complaint metrics and analysis, development of automated metrics system, and managing CAPAs, as required.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Contribute to new product development activity by participating in Design Assurance tasks including risk management activities, V&amp;amp;V planning and execution, statistical analysis, design reviews, and R&amp;amp;D testing.&lt;/li&gt;
&lt;li&gt;Work with cross-functional complaint teams to conduct product malfunction investigations and root cause analysis to drive product improvement.&lt;/li&gt;
&lt;li&gt;Assist with monthly and weekly complaint metrics and analysis. Assist with data analysis, visualization, and reporting using MS Excel and Tableau.&lt;/li&gt;
&lt;li&gt;Assist with the management of the corrective and preventive action system by leading teams through the process, facilitating structured root cause analysis, and keeping CAPAs on track to target timelines&lt;/li&gt;
&lt;li&gt;Execute corrective actions to solve problems and non-conformances based on root cause analysis.&lt;/li&gt;
&lt;li&gt;Assist with the review of document and design changes.&lt;/li&gt;
&lt;li&gt;Perform all activities in compliance with applicable regulations, Fractyl’s policies and guidelines, including, but not limited to, timely documentation of activities and maintaining all required applicable training.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education or Certification Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree in engineering, science, or related field&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;Experience, Qualifications, and Skills&lt;/h4&gt;
&lt;ul&gt;
&lt;li&gt;Minimum of 3-5 years of experience in design assurance/engineering roles within the medical device industry.&lt;/li&gt;
&lt;li&gt;Experience with risk management methodologies (e.g., FMEA, fault tree analysis) and risk management tools.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Solid computer skills essential, including Microsoft Office Suite, Adobe, Minitab, etc.&lt;/li&gt;
&lt;li&gt;Comfortable with basic statistics and data analysis&lt;/li&gt;
&lt;li&gt;Knowledge of FDA regulations and ISO 13485 standards for medical devices&lt;/li&gt;
&lt;li&gt;Experience with project management is a plus&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other Essentials and Key Success Factors&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Strong analytical and problem-solving skills&lt;/li&gt;
&lt;li&gt;Strong attention to detail and ability to prioritize tasks with a passion to deliver quality results&lt;/li&gt;
&lt;li&gt;Ability to lead fast-paced projects&lt;/li&gt;
&lt;li&gt;Proven and successful track record as a team-player and collaborator in small working environments&lt;/li&gt;
&lt;li&gt;Excellent verbal and written communication skills&lt;/li&gt;
&lt;li&gt;Highest levels of professionalism, personal values and ethical standards&lt;/li&gt;
&lt;/ul&gt;
&lt;h4&gt;Compensation&lt;/h4&gt;
&lt;p&gt;This position offers a competitive salary in the range of $62,000 – $90,000 annually, along with a comprehensive benefits package. Actual compensation will be based on relevant experience, education, and market factors.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The description and requirements outlined above are general; additional requirements may apply.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;In accordance with Massachusetts law, General Laws Chapter 149, Section 19B. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h4&gt;&amp;nbsp;&lt;/h4&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;section class=&quot;b_paragraph&quot; data-md-index=&quot;7&quot; data-bm=&quot;101&quot;&gt;&lt;/section&gt;
&lt;section class=&quot;b_paragraph&quot; data-md-index=&quot;8&quot; data-bm=&quot;102&quot;&gt;&lt;/section&gt;]]></description><link>http://biotechroles.com/design-assurance-engineer-ii-fractyl-health/69d3bbdbc8e81216cd0b8fd3</link><guid isPermaLink="true">http://biotechroles.com/design-assurance-engineer-ii-fractyl-health/69d3bbdbc8e81216cd0b8fd3</guid><pubDate>Mon, 06 Apr 2026 13:57:47 GMT</pubDate><company>Fractyl Health</company><location>Burlington, MA</location><salary>$95000-125000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Scientific and Medical Education]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;The Senior Manager, Scientific and Medical Education supports Dyne’s&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;DMD program&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;contribute&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to the execution of publication and medical education activities&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;for&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;programs. This individual&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;help&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;ensure that clinical and non-clinical data from Dyne’s studies are communicated in&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;an accurate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;timely&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, compliant, and compelling manner through high-quality scientific publications, including manuscripts, abstracts, posters, and oral presentations.&lt;/span&gt;&lt;/span&gt;&amp;nbsp;&lt;br&gt;&amp;nbsp;&lt;br&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Additionally, this role supports the creation of internal and external medical education materials such as field medical decks, medical booth collateral, symposia, and onboarding and training resources. The Senior Manager&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;work&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;cross-functionally within Global Medical Affairs and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;more&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;broadly across the DMD program team&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to support aligned planning and execution of Dyne’s scientific and medical education activities.&lt;/span&gt;&lt;/span&gt;&amp;nbsp;&lt;br&gt;&amp;nbsp;&lt;br&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;This role is based in Waltham, MA&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&amp;nbsp;&lt;br&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Support the development and execution of publication and medical education plans aligned with program and corporate strategies&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Contribute to planning Dyne’s congress strategy and presence, including medical booth assets, symposia, and scientific presentations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Execute global medical communications initiatives (&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;i.e.&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;Symposia, roundtables) that support product strategy&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Collaborate with Patient Advocacy to support development of&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;patient-focused&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;educational materials&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Partner with Global and US Medical Affairs Leads to support alignment on program priorities and evidence gaps&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Support the&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;development&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Field Medical Affairs materials, both HCP and payor-focused&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Maintain and update scientific communications platforms and materials&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Maintain strong knowledge of relevant medical literature and data&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Doctorate degree (MD, PhD, PharmD) with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;5&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;+&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;years of relevant experience; rare disease or neuromuscular experience preferred&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Strong analytical skills with ability to deliver against goals in collaborative, team-based environments&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Ability to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;operate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;effectively within matrixed organizations and support cross-functional collaboration&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Demonstrated ability to learn new disease areas or therapeutic modalities&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Experience engaging with external experts and thought leaders&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Experience working with external vendors or agencies&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Excellent written and verbal communication skills&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Proven ability to independently manage multiple complex p&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;rojects&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;in a fast-paced, dynamic environment&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Strong strategic thinking skills with the ability to balance scientific, regulatory, and business considerations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Demonstrated ability to influence cross-functional stakeholders without direct authority&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Highly collaborative team player with a strong cross-functional mindset&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Meticulous attention to detail with a commitment to quality and compliance&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Positive, proactive, and resilient team member who embodies Dyne’s Core Values&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Passion for Dyne’s mission and excitement about contributing to the advancement of therapies for patients with serious diseases&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Ability to drive timelines, meet firm deadlines, and adapt quickly to changing requirements and priorities&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Embrace Dyne’s core values and culture&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Excitement about the vision and mission of Dyne&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Travel up to ~20%&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;#LI-Onsite&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$147,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$180,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-scientific-and-medical-education-dyne-therapeutics/69d3bbd8c8e81216cd0b8fcc</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-scientific-and-medical-education-dyne-therapeutics/69d3bbd8c8e81216cd0b8fcc</guid><pubDate>Mon, 06 Apr 2026 13:57:43 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Director of Sales]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Company overview:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Labs 109, Inc. (FL109) is a privately held, early-stage technology company pioneering the use of artificial intelligence, physics and hardware to transform the way we see biology. FL109 was conceived by Flagship Pioneering, which brings the courage, long-term vision, and resources needed to realize unreasonable results. Become part of our mission-driven team and help envision the future of science.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The &lt;strong&gt;Director of Sales&lt;/strong&gt; will be responsible for driving customer acquisition, building strategic partnerships, and delivering revenue growth across our VaaS, SaaS, and platform offerings.&lt;/p&gt;
&lt;p&gt;This is a hands-on leadership role for a commercially fluent structural biologist or technical sales leader who can operate as both strategist and executor. You will own a defined bookings target, lead end-to-end customer engagement, and act as the commercial “mini-CEO” for client relationships.&lt;/p&gt;
&lt;p&gt;In addition to revenue ownership, you will shape FL109’s market development and outreach strategy, from identifying and cultivating prospective customers to leading participation in key industry events and creating high-impact content that builds awareness and engagement.&lt;/p&gt;
&lt;p&gt;This is a builder role: best suited for a commercially fluent leader who thrives on creating structure, establishing customer relationships, and developing scalable business systems in an emerging market.&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Revenue &amp;amp; Commercial Ownership&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Own and exceed annual bookings and revenue targets for FL109’s commercial offerings.&lt;/li&gt;
&lt;li&gt;Build and manage a qualified pipeline from prospecting through close, leveraging CRM data to ensure forecast accuracy.&lt;/li&gt;
&lt;li&gt;Hold pricing and commercial terms authority within defined guardrails; manage forecasts and deal reviews with leadership.&lt;/li&gt;
&lt;li&gt;Negotiate and structure agreements that create long-term value for customers and for FL109.&lt;/li&gt;
&lt;li&gt;Partner with Finance and Operations to align delivery plans with revenue recognition and margin goals.&lt;/li&gt;
&lt;li&gt;Report regularly on pipeline health, deal progress, and revenue performance to leadership.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Customer Acquisition &amp;amp; Partnership Development&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Identify, engage, and nurture new customers across pharma, biotech, and the Flagship ecosystem.&lt;/li&gt;
&lt;li&gt;Develop tailored account strategies to expand adoption and drive repeat business.&lt;/li&gt;
&lt;li&gt;Build and maintain trusted executive-level relationships with customer stakeholders.&lt;/li&gt;
&lt;li&gt;Represent FL109 externally at key meetings, conferences, and industry events.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Market Development &amp;amp; Outreach&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and oversee FL109’s external engagement strategy, including targeted outreach, event participation, and partnership visibility.&lt;/li&gt;
&lt;li&gt;Partner with leadership and external vendors to execute campaigns, manage event logistics, and track lead conversion.&lt;/li&gt;
&lt;li&gt;Develop and maintain a calendar of high-impact scientific and commercial events aligned with FL109’s growth priorities.&lt;/li&gt;
&lt;li&gt;Contribute to content creation and thought leadership efforts that build FL109’s brand presence across industry channels and social media.&lt;/li&gt;
&lt;li&gt;Manage a modest budget for event participation and outbound initiatives, prioritizing efforts with the highest commercial impact.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Customer Insight &amp;amp; Market Feedback&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Capture key learnings from customer and partner engagements to refine FL109’s value proposition and go-to-market approach.&lt;/li&gt;
&lt;li&gt;Collaborate with the Product and AI teams to share structured insights that inform product strategy and prioritization.&lt;/li&gt;
&lt;li&gt;Represent customer perspectives in internal discussions to ensure solutions align with market needs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Commercial Infrastructure&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with a part-time CRM consultant to finalize implementation, ensure data integrity, and establish effective reporting.&lt;/li&gt;
&lt;li&gt;Own the commercial use and adoption of the CRM system to drive visibility, forecasting accuracy, and pipeline health.&lt;/li&gt;
&lt;li&gt;Define and track key growth metrics and reporting cadence for leadership review.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Cross-Functional Collaboration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with the Client Project Manager to ensure seamless delivery and high customer satisfaction.&lt;/li&gt;
&lt;li&gt;Contribute to pricing, go-to-market, and commercial strategy discussions.&lt;/li&gt;
&lt;li&gt;Work within established templates and tools for contracting, security documentation, and proposal development, with support from internal and external resources as needed.&lt;/li&gt;
&lt;li&gt;Serve as the internal advocate for customer success and external excellence.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;8+ years of experience in commercial, BD, or sales leadership within life sciences, platform technologies, or capital equipment markets.&lt;/li&gt;
&lt;li&gt;Proven record of achieving or exceeding multi-million-dollar sales targets in complex technical environments.&lt;/li&gt;
&lt;li&gt;Experience leading cross-functional commercial efforts in a matrixed organization.&lt;/li&gt;
&lt;li&gt;Deep understanding of cryo-EM or adjacent analytical technologies preferred.&lt;/li&gt;
&lt;li&gt;Experience with outreach, event strategy, and business development in scientific or technology-driven markets.&lt;/li&gt;
&lt;li&gt;Strong negotiation, forecasting, and strategic account planning skills.&lt;/li&gt;
&lt;li&gt;Excellent communication and executive-level presentation abilities.&lt;/li&gt;
&lt;li&gt;Builder mindset: resourceful, analytical, and comfortable with ambiguity in early-stage environments.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;strong&gt;About Flagship&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company&amp;nbsp;that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in generation of over 500 patents, initiation of over 50 clinical trials for novel therapeutic agents and an aggregate value of more than $90 billion. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture. Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The expected base salary range for the role is $100,000 to $140,000, with a target commission of $90,000 to $150,000, for a total on-target range of $230,000 to $290,000 OTE. Actual earnings will vary based on performance. Base salary for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Commission is earned based on defined performance metrics. Flagship Pioneering currently offers healthcare coverage, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering’s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/director-of-sales-flagship-pioneering/69d3bbd7c8e81216cd0b8fcb</link><guid isPermaLink="true">http://biotechroles.com/director-of-sales-flagship-pioneering/69d3bbd7c8e81216cd0b8fcb</guid><pubDate>Mon, 06 Apr 2026 13:57:43 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Discovery Partnerships]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary: &lt;/strong&gt;Quotient is seeking a Director, Discovery Partnerships to lead the company’s discovery partnerships strategy. This is a senior position critical to achieving our company&#39;s objectives in the somatic genomics space. This role is responsible for identifying, developing, and managing strategic partnerships to source human biological samples and associated information essential for our research. The role will be part of the Target Discovery Team and work closely with scientists throughout the company and external collaborators to ensure the successful execution of our research projects.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead the identification and prioritisation of potential academic and commercial collaborators to support the company&#39;s platform and experimental priorities.&lt;/li&gt;
&lt;li&gt;Lead and maintain positive relationships with current active discovery partners&lt;/li&gt;
&lt;li&gt;Drive evaluation of global discovery partnership opportunities, including scientific and strategic rationale, frameworks, and financial assessments.&lt;/li&gt;
&lt;li&gt;Represent the company in negotiating and structuring discovery partnership agreements, ensuring alignment of goals, expectations, and deliverables.&lt;/li&gt;
&lt;li&gt;Define and align biological sample sourcing requirements for somatic genomics studies.&lt;/li&gt;
&lt;li&gt;Oversee the sourcing and timing of biological sample acquisition.&lt;/li&gt;
&lt;li&gt;Establish and maintain a network of external stakeholders, such as key opinion leaders, university teams and tissue banks, to facilitate effective partnerships.&lt;/li&gt;
&lt;li&gt;Collaborate cross-functionally with scientific, legal, operations, and executive teams to align partnership strategy with research and business priorities.&lt;/li&gt;
&lt;li&gt;Lead operational management of partnerships, including coordination of activities, documentation, financial processes, and compliance, to ensure timely delivery against milestones.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Essential&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD in a life science field or equivalent experience in a genomics or biotech setting.&lt;/li&gt;
&lt;li&gt;Experience in partnerships, alliance management, or business development, with a track record of structuring, negotiating, and closing complex external agreements.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to influence and build trust with diverse stakeholders, including scientists, academics, and external partners.&lt;/li&gt;
&lt;li&gt;Proven ability to manage multiple workstreams simultaneously within a matrix environment.&lt;/li&gt;
&lt;li&gt;Working knowledge of relevant contractual agreements (e.g., Material Transfer Agreements, Research Collaboration Agreements, and Service Agreements).&lt;/li&gt;
&lt;li&gt;Strong written and verbal communication, capable of communicating complex scientific concepts to internal and external stakeholders at various levels.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Desirable&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Working knowledge of relevant regulatory and compliance frameworks (e.g., Human Tissue Authority).&lt;/li&gt;
&lt;li&gt;Experience managing procurement processes, including purchase order creation and tracking budgets to support financial processes.&lt;/li&gt;
&lt;li&gt;Previous background evaluating or sourcing biological samples.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Values and Behaviors:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Encourage respectful disagreement and cultivate open-minded, ego-free interactions to continuously push each other towards excellence.&lt;/li&gt;
&lt;li&gt;Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source.&lt;/li&gt;
&lt;li&gt;Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions.&lt;/li&gt;
&lt;li&gt;Use a company-first mindset to guide decision-making; prioritize team over individual success.&lt;/li&gt;
&lt;li&gt;Take calculated risks and challenge convention in the quest for exceptional outcomes.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Quotient: &lt;/strong&gt;Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS).&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies: &lt;/strong&gt;Quotient Therapeutics (“Quotient”) and Flagship Pioneering (“FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient, FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/p&gt;]]></description><link>http://biotechroles.com/director-discovery-partnerships-flagship-pioneering/69d3bbd4c8e81216cd0b8fc7</link><guid isPermaLink="true">http://biotechroles.com/director-discovery-partnerships-flagship-pioneering/69d3bbd4c8e81216cd0b8fc7</guid><pubDate>Mon, 06 Apr 2026 13:57:40 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, UK</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Scientific Communications Lead - DMD]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;br&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot; data-ccp-charstyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;ac0262f4-8a9e-5820-b908-2d943c5f7113|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469777841,&amp;quot;Times New Roman&amp;quot;,469777842,&amp;quot;Times New Roman&amp;quot;,469777843,&amp;quot;Arial Unicode MS&amp;quot;,469777844,&amp;quot;Times New Roman&amp;quot;,469769226,&amp;quot;Times New Roman,Arial Unicode MS&amp;quot;,469775450,&amp;quot;normaltextrun&amp;quot;,201340122,&amp;quot;1&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;normaltextrun&amp;quot;,335572020,&amp;quot;1&amp;quot;,469778324,&amp;quot;Default Paragraph Font&amp;quot;]}&quot;&gt;The Senior Director, Scientific Communications Lead - DMD&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;provide&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;leadership for the planning,&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;development, and execution of&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;an integrated scientific communications&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;strategy&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;for Dyne’s&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Duchenne muscular dystrophy&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;program&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;. This role&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;is responsible for&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;defining long-term strategies that&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;translat&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;e&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;complex scientific&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;,&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;clinical&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;, and real-world&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;data into clear,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;accurate&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;, and compliant communications for internal and external stakeholders, including healthcare professionals&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;and&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;payers&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;The ideal candidate brings deep expertise in strategic&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;scientific communication planning&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;and cross-functional leadership&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;ensuring close partnership with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;other functions withing the Global Medical Affairs team&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;, as well as&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;with&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Clinical Development, Biostatistics, Research,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;HEOR,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;Commercial,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;normaltextrun&quot;&gt;and Corporate Communications to ensure cohesive planning and execution of Dyne’s scientific and medical education strategy.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;335559738&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;This role is based in Waltham, MA.&lt;/span&gt;&lt;/span&gt;&amp;nbsp;&lt;br&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt; &lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;De&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;velop&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and lead the global scientific communications strategy&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;for DMD&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;aligned with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;program and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;corporate objectives&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Develop&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and ensure the execution of&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;a&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;long-term&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;strategic publication&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;plan, including&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;integration of preclinical, clinical, and real-world evidence data into&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;dissemination roadmaps and evidence-generation narratives&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;maintain&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;visibility into timelines,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;dependencies&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and risks to ensure on-time delivery&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Assist&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;in developing Dyne’s overall congress strategy and presence, including planning medical booth assets, symposia, and presentations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Plan and execute global medical communications initiatives (e.g., IME, roundtables) that support product strategy&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serve as strategic a&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;dvisor to cross-functional teams on scientific messaging and data interpretation&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Partner closely with Patient Advocacy and regional medical teams on the development of publications and educational materials for their respective audiences&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Manage agency partners and external vendors to deliver high-quality outputs&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;8&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Manage budgets and resources to support long-term planning and executi&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;on&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;9&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Mentor junior members of the team&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;10&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Doctorate degree (MD, PhD, PharmD) with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;1&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;2+&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;years of experience with a focus on rare diseases, neuromuscular experience, or related discipline&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;11&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Analytical skills, with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;a track record&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;of delivering against goals while working in high performing, diverse teams&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;12&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Demonstrated success in&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;operating&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;effectively in highly matrixed organizations where influencing skills are critical to day-to-day success&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;13&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Experience in building strong and effective relationships with thought leaders&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;14&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Experience in managing vendor partners&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;15&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Excellent written and verbal communication skills&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;16&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Launch experience preferred&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;9&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;17&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Travel up to ~20%&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$233,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$285,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-scientific-communications-lead-dmd-dyne-therapeutics/69d3bbd3c8e81216cd0b8fc6</link><guid isPermaLink="true">http://biotechroles.com/senior-director-scientific-communications-lead-dmd-dyne-therapeutics/69d3bbd3c8e81216cd0b8fc6</guid><pubDate>Mon, 06 Apr 2026 13:57:38 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Business Development & Partnership -South Korea]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;THE ROLE:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship&#39;s Korean subsidiary is focused on bridging Flagship’s innovative ecosystem with the Korean biotech, pharmaceutical and biomedical ecosystem to fostering strategic partnerships in one of the world’s critical healthcare markets. We are seeking an accomplished and dynamic individual to join our &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship APAC &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;team as the Director&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;,&lt;/span&gt; &lt;span data-contrast=&quot;auto&quot;&gt;Alliances and Partnerships for Flagship Pioneering Korea. &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Reporting &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;into&lt;/span&gt; &lt;span data-contrast=&quot;auto&quot;&gt;the &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship APAC&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt; organization&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;,&lt;/span&gt; t&lt;span data-contrast=&quot;auto&quot;&gt;he successful candidate will be responsible for spearheading strategic initiatives, fostering and managing partnerships, and driving business growth in the Korean market. This role requires a visionary leader with a deep understanding of the life sciences industry, exceptional strategic thinking skills, and the ability to build and maintain high-level relationships.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strategic Planning:&lt;/span&gt;&lt;/strong&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Work&lt;span data-contrast=&quot;auto&quot;&gt;ing &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;as&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt; part of Flagship APAC &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;closely &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;to partner&lt;/span&gt; &lt;span data-contrast=&quot;auto&quot;&gt;with Flagship&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;’&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;s Corporate and Business Development &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;team &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;to d&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;efine and execute the partnership strategy in alignment with Flagship Pioneering’s global objectives.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Identify and evaluate new business opportunities, potential partners, and market trends in Korea.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partnership Development:&lt;/span&gt;&lt;/strong&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;Establish and nurture strategic alliances with pharmaceutical companies, biotech firms, research institutions, and other relevant stakeholders in Korea.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;Steward current partnerships in Korea.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;Negotiate and finalize partnership agreements to drive mutual growth and innovation.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Market Expansion:&lt;/span&gt;&lt;/strong&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;Develop strategies to expand Flagship Pioneering’s presence and influence in the Korean market.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborative Initiatives:&lt;/span&gt;&lt;/strong&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Work collaboratively with Flagship Pioneering’s&amp;nbsp;&lt;span data-contrast=&quot;auto&quot;&gt;APAC and &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;g&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;lobal leadership&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;, including the APAC team based in Asia-Pacific and the&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&amp;nbsp;global &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;engagement team &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;based &lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;in Cambridge, MA to align efforts and share best practices.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;Facilitate cross-functional collaboration to support portfolio company growth and development.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Financial Accountability:&lt;/span&gt;&lt;/strong&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;Develop and manage budgets, forecasts, and financial models to support business development activities.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;4&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;Track and report on key performance indicators (KPIs) and milestones.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;A minimum of 8-10 years of experience in business development, partnerships, or related roles within the life sciences sector.&lt;/span&gt;&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Proven track record of successfully developing and managing strategic partnerships in Korea.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Strong understanding of Korean healthcare and regulatory environment.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Exceptional negotiation, communication, and interpersonal skills.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Demonstrated ability to think strategically and drive long-term business growth.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Fluency in Korean and English, both written and spoken.&lt;/li&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;5&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;Advanced degree (MBA, Ph.D., or equivalent) preferred with an emphasis on business or life sciences.&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&lt;strong&gt;LOCATION: &lt;/strong&gt;Seoul, South Korea&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://www.flagshippioneering.com&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our &lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt; guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths &lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt; and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-JR3&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/director-business-development-and-partnership-south-korea-flagship-pioneering/69d3bbd0c8e81216cd0b8fbc</link><guid isPermaLink="true">http://biotechroles.com/director-business-development-and-partnership-south-korea-flagship-pioneering/69d3bbd0c8e81216cd0b8fbc</guid><pubDate>Mon, 06 Apr 2026 13:57:35 GMT</pubDate><company>Flagship Pioneering</company><location>Seoul, South Korea</location><salary>$150000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Program Management]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;h4&gt;Role Summary:&lt;/h4&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Senior&amp;nbsp;Director,&amp;nbsp;Program Management&amp;nbsp;(PM)&amp;nbsp;is&amp;nbsp;a&amp;nbsp;critical role within the cross-functional development team&amp;nbsp;responsible for&amp;nbsp;facilitating&amp;nbsp;and&amp;nbsp;driving execution across the wide spectrum of activities&amp;nbsp;required&amp;nbsp;for successful development of one or more molecules. &amp;nbsp;The&amp;nbsp;PM&amp;nbsp;partners&amp;nbsp;closely&amp;nbsp;with&amp;nbsp;the&amp;nbsp;Program Team Leader (PTL) and&amp;nbsp;functional subject matter experts to ensure that plans are in place with&amp;nbsp;appropriate detail&amp;nbsp;and risk awareness&amp;nbsp;to&amp;nbsp;assure&amp;nbsp;successful achievement of the goals of the development team.&amp;nbsp;&amp;nbsp;The&amp;nbsp;PM&amp;nbsp;ensures integration&amp;nbsp;of&amp;nbsp;these&amp;nbsp;detailed functional plans&amp;nbsp;into a holistic,&amp;nbsp;cohesive,&amp;nbsp;and comprehensive&amp;nbsp;program plan that achieves the strategic goals of the&amp;nbsp;development program. &amp;nbsp;Given the inherent uncertainty associated with drug development in rare disorders,&amp;nbsp;the PM&amp;nbsp;maintains&amp;nbsp;an agile mindset&amp;nbsp;in order to&amp;nbsp;effectively incorporate and react to&amp;nbsp;emerging data and&amp;nbsp;course correct&amp;nbsp;as&amp;nbsp;conditions dictate.&amp;nbsp;&amp;nbsp;Working in&amp;nbsp;close&amp;nbsp;partnership with&amp;nbsp;the&amp;nbsp;PTL, the PM&amp;nbsp;effectively frames and&amp;nbsp;facilitates&amp;nbsp;discussions&amp;nbsp;with&amp;nbsp;team members and external experts&amp;nbsp;to&amp;nbsp;elicit&amp;nbsp;clear&amp;nbsp;recommendations and decisions&amp;nbsp;by fully engaging with team members to consider multiple options with&amp;nbsp;a focus on&amp;nbsp;impact on quality, time,&amp;nbsp;and cost. &amp;nbsp;Their&amp;nbsp;influence&amp;nbsp;and engagement skills allow them to&amp;nbsp;work with&amp;nbsp;a highly motivated team and manage stakeholders&amp;nbsp;at all levels of the company.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This role is based in Waltham, MA without the possibility of being a remote role.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Lead&amp;nbsp;the operations of&amp;nbsp;one or more&amp;nbsp;high performing cross-functional teams, with focus on both the “what”,&amp;nbsp;such as priorities,&amp;nbsp;goal achievement, and resources, and the “how” of&amp;nbsp;maintaining&amp;nbsp;a&amp;nbsp;challenging, collaborative, and sustainable team environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Partner with the PTL to&amp;nbsp;identify&amp;nbsp;short, medium, and long-term team priorities&amp;nbsp;and propose path to address&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Drive&amp;nbsp;execution of&amp;nbsp;the established&amp;nbsp;and&amp;nbsp;aligned Program vision and strategy for bringing a life-changing medicine to patients in need&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Facilitate&amp;nbsp;creation&amp;nbsp;&amp;amp; maintenance of core program strategy documents including&amp;nbsp;Target&amp;nbsp;Product&amp;nbsp;Profile&amp;nbsp;(TPP), Clinical Development Plan, Regulatory Strategy, and Supply Strategy&amp;nbsp;in collaboration with cross-functional representatives&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ensure&amp;nbsp;that non-clinical, clinical, regulatory, and commercialization&amp;nbsp;strategies and plans are aligned with the TPP and the overall Program Strategy&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Inspire development of an efficient plan to&amp;nbsp;achieve development&amp;nbsp;and commercialization&amp;nbsp;strategy,&amp;nbsp;optimizing&amp;nbsp;for quality,&amp;nbsp;speed&amp;nbsp;and cost&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ensure that program decisions are made in&amp;nbsp;a timely,&amp;nbsp;clear&amp;nbsp;and efficient manner through interactions with the PTL, Program Team members, governance&amp;nbsp;forums&amp;nbsp;and other key stakeholders&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Accountable for&amp;nbsp;creation and maintenance of&amp;nbsp;detailed&amp;nbsp;cross-functional&amp;nbsp;plans and effective visual summaries thereof&amp;nbsp;to&amp;nbsp;instill&amp;nbsp;awareness,&amp;nbsp;build&amp;nbsp;accountability and&amp;nbsp;facilitate&amp;nbsp;achievement&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Maintain clear and open communication with&amp;nbsp;Program&amp;nbsp;Team,&amp;nbsp;Dyne Senior Leadership,&amp;nbsp;and other stakeholders&amp;nbsp;regarding&amp;nbsp;program status, priorities,&amp;nbsp;risks&amp;nbsp;and needs, and&amp;nbsp;facilitate&amp;nbsp;appropriate strategic&amp;nbsp;decision-making&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Partner with Head of Program Management to evolve Program Management discipline to meet needs of a growing organization that intends to launch a portfolio of disease products&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Keep abreast of emerging developments&amp;nbsp;regarding&amp;nbsp;research and development in the fields of muscle diseases and oligonucleotide drug discovery and development&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Foster a culture of collaboration, innovation, discovery, and&amp;nbsp;cutting-edge&amp;nbsp;research culture focused on scientific excellence, open communication, and continual improvement&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skill&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Requirements&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Proven and respected team&amp;nbsp;member&amp;nbsp;with:&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Bachelor’s degree in science or related field;&amp;nbsp;Advanced&amp;nbsp;degree in a scientific discipline or MBA&amp;nbsp;preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;15+&amp;nbsp;years of&amp;nbsp;relevant&amp;nbsp;experience in&amp;nbsp;biotech/pharmaceutical industry in positions&amp;nbsp;of increasing responsibility&amp;nbsp;in drug development&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience with late-stage clinical development and commercial stage&amp;nbsp;programs&amp;nbsp;required&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience with neuromuscular diseases a plus&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Exceptional&amp;nbsp;communication skills (verbal, written, presentation) and ability to communicate with across a broad group of&amp;nbsp;stakeholders and teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Proficient with&amp;nbsp;Microsoft Office 365&amp;nbsp;applications,&amp;nbsp;Smartsheet and other PM management workspace collaboration tools&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Expert at&amp;nbsp;cross-functional&amp;nbsp;teamwork&amp;nbsp;and influencing without direct authority&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Demonstrated experience in&amp;nbsp;working with&amp;nbsp;highly effective teams and guiding teams and organizations in making complex and high-stakes data-driven decisions&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Passionate about developing and commercializing life-transforming therapies for patients with severe and life-threatening diseases&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Adept at operating in cross-functional matrix teams, developing effective relationships based on mutual trust and effective communication and thrives in a fast-paced, patient-focused environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Proven ability to&amp;nbsp;establish&amp;nbsp;and maintain credible and trust-based relationships&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Outstanding sense of urgency and ability to&amp;nbsp;help&amp;nbsp;pace&amp;nbsp;the team’s&amp;nbsp;work&amp;nbsp;in highly competitive environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Orientation towards collective achievement and team credit, combined with individual sense of responsibility and accountability for teamwork and product&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Comfort with ambiguity and ability to provide steadiness and consistency in environment of shifting priorities&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ability to lead&amp;nbsp;without authority through&amp;nbsp;complex&amp;nbsp;and ambitious&amp;nbsp;projects in a cross-functional team environment and high-pressure circumstances&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Comfortable in a results-driven, highly accountable environment where you can make a clear impact&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Team player who listens effectively and invites response and discussion&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;A collaborator who communicates in an open, clear, complete,&amp;nbsp;timely&amp;nbsp;and consistent manner&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$233,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$285,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-program-management-dyne-therapeutics/69d3bbcdc8e81216cd0b8fb7</link><guid isPermaLink="true">http://biotechroles.com/senior-director-program-management-dyne-therapeutics/69d3bbcdc8e81216cd0b8fb7</guid><pubDate>Mon, 06 Apr 2026 13:57:32 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Antibody Discovery]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary: &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient is seeking a Director or Senior Director of Antibody Discovery. This role will define and lead Quotient’s antibody discovery strategy; leading the delivery of therapeutic antibody projects in addition to Quotient’s antibody drug discovery platform build through the deployment of cutting-edge technologies. This role will require close involvement in the end-to-end process of translating Somatic Genomics screening outputs (i.e. candidate genes and potential drug targets) into initiation of drug discovery programs. This role will also involve senior project leadership, steering drug discovery matrix teams from early conception through to key inflection points such as development candidate nomination and IND submission.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide balanced expert advice on the feasibility of antibody tractable targets and the conception of high-value drug molecules&lt;/li&gt;
&lt;li&gt;Present antibody discovery strategies to internal R&amp;amp;D committees to justify capital commitment in new programs&lt;/li&gt;
&lt;li&gt;Drive decision making on construct design, format and developability for new antibody programs according to Target Product Profile specifications&lt;/li&gt;
&lt;li&gt;Independently carry out lead sequence and format optimizations utilizing rational, structure-based and in silico/AI/ML design approaches&lt;/li&gt;
&lt;li&gt;Drive rapid optimization of novel antibody and protein therapeutics through iterative design, build, test, and learn cycles&lt;/li&gt;
&lt;li&gt;As a drug discovery project leader, develop efficient and balanced project plans for one or more biologic drug discovery programs and lead a cross-functional team to execute through lead generation, development candidate nomination and IND submission&lt;/li&gt;
&lt;li&gt;Model best matrix leadership behaviours and support an emphasis on enterprise leadership across the company&lt;/li&gt;
&lt;li&gt;Identify, select, and manage external CROs/vendors, consultants, and academic collaborators to deliver a virtual/outsourced state-of-the-art drug antibody discovery platform for the identification of high-quality mAb molecules at pace&lt;/li&gt;
&lt;li&gt;Build and maintain networks of external experts to pressure-test hypotheses and refine strategies&lt;/li&gt;
&lt;li&gt;Serve as a specialist antibody discovery expert within Quotient’s drug discovery team and across the company.&lt;/li&gt;
&lt;li&gt;Contribute to broader corporate strategy, BD evaluations, and exploratory platform initiatives&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;u&gt;Essential&lt;/u&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Proven experience advancing protein therapeutics through drug discovery phases to development.&lt;/li&gt;
&lt;li&gt;Expertise in structure-based protein engineering and design of antibodies including (multispecifics, Fc engineering, fusion proteins etc)&lt;/li&gt;
&lt;li&gt;Skilled in antibody engineering, including use of in silico, structure-based, and AI/ML approaches to sequence/CDR design, use of display technologies, humanization techniques, sequence liability remediation, analytics, and developability (biophysical) assessment and improvement&lt;/li&gt;
&lt;li&gt;Project leadership experience in pharmaceutical industry R&amp;amp;D environment across multiple therapeutic areas, with a deep understanding of lead identification and optimization through preclinical development of antibody therapeutics&lt;/li&gt;
&lt;li&gt;Track record of advocating for acquisition or creation of new technologies for accelerated antibody design, expression, and characterization&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;u&gt;Desirable&lt;/u&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience in early-stage or start-up biotech environments&lt;/li&gt;
&lt;li&gt;Experience working with genetic and genomics platform-driven drug target discovery&lt;/li&gt;
&lt;li&gt;Broader understanding of protein sciences (expression, developability, and analytical purification and analysis)&lt;/li&gt;
&lt;li&gt;Experience managing the design and validation of cellular assays for the functional characterization of engineered biologics&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Values and Behaviors:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Encourage respectful disagreement and cultivate open-minded, ego-free interactions to continuously push each other towards excellence&lt;/li&gt;
&lt;li&gt;Seek out diverse perspectives; practice active listening and genuine curiosity to ensure all contributions are valued, regardless of source&lt;/li&gt;
&lt;li&gt;Recognize the impact of your behavior, language and attitudes, and strive for balanced, meaningful exchanges that enhance mutual growth and understanding in all interactions&lt;/li&gt;
&lt;li&gt;Use a company-first mindset to guide decision-making; prioritize team over individual success&lt;/li&gt;
&lt;li&gt;Take calculated risks and challenge convention in the quest for exceptional outcomes&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Quotient:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS).&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics and Flagship Pioneering are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics (“Quotient”) and Flagship Pioneering (“FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Quotient, FSP or their employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/p&gt;]]></description><link>http://biotechroles.com/director-antibody-discovery-flagship-pioneering/69d3bbcbc8e81216cd0b8fb6</link><guid isPermaLink="true">http://biotechroles.com/director-antibody-discovery-flagship-pioneering/69d3bbcbc8e81216cd0b8fb6</guid><pubDate>Mon, 06 Apr 2026 13:57:31 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, UK</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Pricing & Reimbursement]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Senior Director, Pricing and Reimbursement is an experienced and strategic leader who is responsible for developing and executing global pricing and market access strategies to ensure optimal market positioning, pricing, and patient access solutions for our innovative products.&lt;/p&gt;
&lt;p&gt;This strategic leader establishes the overarching pricing and reimbursement strategy in alignment with the market access and commercialization strategy and has a proven track record of leading and coordinating strategic activities aimed at building, shaping, and accelerating access, securing reimbursement across global markets. They create effective and productive partnership with cross-functional partners to influence strategic clinical development and commercialization decisions, as well as driving and executing pricing and market access strategies to support the differential value of Dyne assets for payer and HTA stakeholders across all stages of the product lifecycle.&lt;/p&gt;
&lt;p&gt;The person in this role has strong leadership skills, a broad understanding and deep experience of global pharmaceutical markets (US &amp;amp; global markets) and a proven track record of bringing products to market successfully.&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;This role is based in Waltham, MA.&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead the development and implementation of global pricing and market access strategies for our late-stage and early pipeline products, including value proposition and messaging, payer engagement, early access programs, pricing strategies, market access plans, launch sequence optimization, pricing narratives, pricing policy and governance.&lt;/li&gt;
&lt;li&gt;Collaborate cross-functionally with HEOR, R&amp;amp;D, Program Teams, Commercial, Medical Affairs, and other teams to integrate pricing, reimbursement and market access considerations throughout product lifecycles&lt;/li&gt;
&lt;li&gt;Develop and communicate compelling value story narratives and messaging for payers, health technology assessment (HTA) bodies, and other stakeholders&lt;/li&gt;
&lt;li&gt;Develop market access and pricing strategies to optimize product value and patient access globally, including innovative non-traditional market access solutions and contracting approaches to meet evolving payer needs&lt;/li&gt;
&lt;li&gt;Ensure integration of market access and pricing strategies into clinical development plans, brand plans, launch strategies, and launch sequencing decisions&lt;/li&gt;
&lt;li&gt;Provide pricing guidance and assumptions for strategic planning, annual forecasting, and brand budget processes&lt;/li&gt;
&lt;li&gt;Develop resources and materials to be leveraged by the local teams in the engagement with market access stakeholders&lt;/li&gt;
&lt;li&gt;Collect actionable insights through market research, expert input forums, advisory boards, early payer advice, and engagement with external stakeholders&lt;/li&gt;
&lt;li&gt;Represent the company externally on pricing and market access topics with payers, policymakers, and industry groups&lt;/li&gt;
&lt;li&gt;Build, lead and coach a high-performing global pricing and reimbursement team&lt;/li&gt;
&lt;li&gt;Represent Dyne pricing and market access on key senior-level governance forums, working groups, and teams&lt;/li&gt;
&lt;li&gt;Understand and abide by global compliance regulations&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Advanced degree (PhD, PharmD, MD, or MBA) in a relevant field)&lt;/li&gt;
&lt;li&gt;12+ years of experience in pharmaceutical/biotech industry with significant leadership experience in global pricing, reimbursement and market access roles&lt;/li&gt;
&lt;li&gt;5+ years’ experience in people management, with experience building and leading high-performing global teams&lt;/li&gt;
&lt;li&gt;Deep understanding of global healthcare systems, pricing dynamics, and market access requirements&lt;/li&gt;
&lt;li&gt;Proven track record developing successful global pricing and market access strategies for specialty and rare disease products&lt;/li&gt;
&lt;li&gt;Excellent communication and presentation skills, with ability to influence senior leadership&lt;/li&gt;
&lt;li&gt;Experience building and leading high-performing global teams&lt;/li&gt;
&lt;li&gt;Strategic mindset with ability to navigate complex stakeholder environments&lt;/li&gt;
&lt;li&gt;Ability to travel globally on a regular basis&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$241,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$275,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-pricing-and-reimbursement-dyne-therapeutics/69d3bbc8c8e81216cd0b8fb3</link><guid isPermaLink="true">http://biotechroles.com/senior-director-pricing-and-reimbursement-dyne-therapeutics/69d3bbc8c8e81216cd0b8fb3</guid><pubDate>Mon, 06 Apr 2026 13:57:28 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Director, AI Sciences]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics develops breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs.&amp;nbsp; We are a privately held, early-stage company and are an equal opportunity employer.&lt;/p&gt;
&lt;p&gt;Quotient was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;br&gt;We are seeking a Director, AI Sciences to invent and productionize computational capabilities that power target identification, validation, and drug development. The candidate is experienced and excited to operate in a deeply collaborative way with peers in data infrastructure, assay development, biology validation, and drug discovery.&amp;nbsp; They bring enthusiasm, intellectual curiosity, scientific rigor, and a deep-rooted desire to innovate. The candidate will have Director level seniority and report to the head of assay development and data science. This role is based in the vicinity of Cambridge UK and hybrid work arrangements will be considered, but all applicants will require permission to work in UK.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate with key stakeholders to set the technical strategy and roadmap for AI across the platform and drug discovery, then define execution plans and deliver against them.&lt;/li&gt;
&lt;li&gt;Lead, mentor, and grow the AI/ML team, fostering a focus on collaboration and delivery, while maintaining standards for quality and reproducibility.&lt;/li&gt;
&lt;li&gt;Partner with Data Infrastructure to optimize data schemas, metadata, versioning, and access controls for ML training and inference.&lt;/li&gt;
&lt;li&gt;Develop and deploy methods leveraging next-generation sequencing for target discovery and validation.&lt;/li&gt;
&lt;li&gt;Develop and deploy methods leveraging imaging AI of histology images, such as segmentation/detection/classification, weak/self-supervised learning, and rigorous model evaluation tied to biological goals.&lt;/li&gt;
&lt;li&gt;Develop and deploy methods to accelerate the validation of targets using standardised assays and accelerate drug development.&lt;/li&gt;
&lt;li&gt;Communicate results and decisions clearly to technical and non-technical stakeholders.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD or equivalent experience in genomics, computational biology, computer science, or similar discipline is required.&lt;/li&gt;
&lt;li&gt;3–7 years of industry experience delivering AI/ML systems for target discovery and/or drug development, with end-to-end ownership from method development to production.&lt;/li&gt;
&lt;li&gt;Strong leadership and collaboration skills in a matrix environment with a low-ego, high-ownership working style.&lt;/li&gt;
&lt;li&gt;High proficiency in Python and modern ML tooling, cloud computing environments (e.g., AWS), as well as solid software engineering habits (testing, CI/CD, containers, etc.).&lt;/li&gt;
&lt;li&gt;Priority domain experience:&lt;/li&gt;
&lt;ul&gt;
&lt;li&gt;Genomics/NGS: development of methods to leveraging sequencing technologies.&lt;/li&gt;
&lt;li&gt;Imaging AI: microscopy/histology, WSI pipelines, dataset curation/labeling strategies, scalable training and evaluation.&lt;/li&gt;
&lt;li&gt;Validation and drug discovery: development or application of AI tools to target validation using in-vitro models and/or drug discovery in any modality.&lt;/li&gt;
&lt;/ul&gt;
&lt;li&gt;A high degree of energy, accuracy and attention to detail, and a passion for creating transformative medicines for patients with serious diseases.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Recruitment &amp;amp; Staffing Agencies&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/p&gt;]]></description><link>http://biotechroles.com/director-ai-sciences-flagship-pioneering/69d3bbc7c8e81216cd0b8fae</link><guid isPermaLink="true">http://biotechroles.com/director-ai-sciences-flagship-pioneering/69d3bbc7c8e81216cd0b8fae</guid><pubDate>Mon, 06 Apr 2026 13:57:26 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, UK</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Paralegal]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;What if…&lt;/strong&gt;you could tell the story of an organization that creates, resources, and builds bioplatform companies that invent breakthrough technologies in order to transform human health and sustainability?&lt;/p&gt;
&lt;p&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category bioplatform companies to transform human health and sustainability. Since its launch in 2000, the firm has, through its Flagship Labs unit, applied its unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $130 billion in aggregate value. To date, Flagship has deployed over $2.5 billion in capital toward the founding and growth of its pioneering companies alongside more than $19 billion of follow-on investments from other institutions.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering has a new and exciting opportunity for a high-energy, detail-oriented Corporate Paralegal to join its fast-paced, dynamic legal team. This role will report to the Senior Corporate Paralegal and work closely with members of the legal team to support Flagship’s corporate legal function across its growing portfolio of companies.&lt;/p&gt;
&lt;p&gt;The Corporate Paralegal will assist with a range of corporate matters, including financings, corporate governance, equity compensation, and general corporate maintenance for Flagship and its cutting-edge, high-growth companies. This includes providing support on a variety of transactions and day-to-day corporate activities across both private and public companies—such as preparing and organizing documentation for financings; supporting equity compensation processes; and maintaining corporate records and governance materials. This role will also have touchpoints in the Finance, Human Resources, Communications and Flagship Labs groups.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Board Governance Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Assist in preparation of board and stockholder consents&lt;/li&gt;
&lt;li&gt;Maintain board records, minutes, and governance documentation&lt;/li&gt;
&lt;li&gt;Support recurring board cycles across portfolio companies&lt;/li&gt;
&lt;li&gt;Track and organize signature pages; prepare closing binders&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Equity Administration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support equity grant processing and updates in Carta or similar platforms&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Assist with coordination across HR and Finance on equity-related matters&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Respond to routine equity-related inquiries&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Corporate Maintenance &amp;amp; Entity Management&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Maintain and track corporate records, minute books, and entity documentation&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Support entity formations, dissolutions, and ongoing maintenance&lt;/li&gt;
&lt;li&gt;Track officer and director information across entities&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Assist with international entity management&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Process &amp;amp; Infrastructure Support&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support development of governance processes and templates&lt;/li&gt;
&lt;li&gt;Assist with compliance initiatives and cross-functional projects&lt;/li&gt;
&lt;li&gt;Contribute to building scalable governance infrastructure&lt;/li&gt;
&lt;li&gt;Assist with the design and development of AI agentic support for routine corporate matters&lt;/li&gt;
&lt;li&gt;Provide backup and surge support to other paralegals on the Flagship legal team&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Key Qualifications and Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree required&lt;/li&gt;
&lt;li&gt;2–5 years of corporate paralegal experience (law firm and/or in-house)&lt;/li&gt;
&lt;li&gt;Experience with governance, entity management, or equity administration preferred&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Comfortable working in an entrepreneurial environment with compressed timelines and evolving priorities.&lt;/li&gt;
&lt;li&gt;Strong priority-setting, organizational and communication skills&lt;/li&gt;
&lt;li&gt;Exceptional attention to detail and are highly organized&lt;/li&gt;
&lt;li&gt;Ability to prioritize and manage multiple deadlines in a fast-paced, high-volume environment with competing demands.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills.&lt;/li&gt;
&lt;li&gt;Willingness to use and adopt AI tools (ChatGPT, Claude, GC AI) to enhance legal workflows, as well as core legal and business platforms (iManage, SharePoint, Carta, Microsoft Office).&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Flagship Pioneering and our ecosystem companies are committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $88,000 - $121,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/corporate-paralegal-flagship-pioneering/69d3bbc3c8e81216cd0b8fa9</link><guid isPermaLink="true">http://biotechroles.com/corporate-paralegal-flagship-pioneering/69d3bbc3c8e81216cd0b8fa9</guid><pubDate>Mon, 06 Apr 2026 13:57:23 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$85000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Director, Dyne Patient Access and Education]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;The Senior Director, Dyne Patient Access and Education Team leads Dyne’s field-based Nurse Case Managers and Field Reimbursement Managers, who support patients, caregivers, and healthcare providers throughout the treatment journey. This national leader builds, inspires, and develops a high&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;‑&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;performing team responsible for patient and caregiver engagement, navigation of complex access processes, and successful post-prescribing conversion through first infusion and beyond. The Senior Director collaborates cross-functionally and externally to simplify access to patient care through a seamless, compassionate, and compliant support experience.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;This role is critical in shaping how Dyne engages with families, providing education about Dyne therapies and continuous support through the access and onboarding experience. It&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;represents&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;a unique opportunity for a patient&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;‑&lt;/span&gt;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;focused leader to help bring transformative therapies to the patients who need them.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;This is a field-based role.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Lead and develop high-performing&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Field Reimbursement Managers&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Nurse Case Managers&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Oversee the comprehensive field-based Nurse Case Management and Access Program&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;for Dyne&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Foster a coaching culture that enables deeper connection with patients, caregivers, and HCPs.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Set the tone and culture of the team, role model Dyne patient and caregiver, and HCP engagement expectations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Cultivate a&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;“One Dyne”&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;mindset that prioritizes transparency,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;shared&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;ownership&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;and accountability,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;where the success of&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;cross&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;-&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;collaborative field team is central to the success of&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;the individual team&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Develop and execute a national plan that is strategically aligned with the overall US Market Access and Patient Service&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;s objectives&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;and enables execution of regional business goals in partnership with other Field Leadership&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Manage hiring, onboarding, communication, performance,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;training&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;and professional development across the team.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Collaborate with internal cross functional partners and external partners (specialty infusion providers, patient support services program) to ensure ongoing support to patients, and their families / caregivers and HCPs.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Develop and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;maintain&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;strong relationships with HCPs involved with DYNE-251 therapy.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Ensure team&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;in insurance coverage, reimbursement, PA processes, and payer landscapes.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Drive problem-solving to resolve access barriers for patients, caregivers, and HCPs.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Deliver execution plans and manage KPIs supporting post-prescribing performance.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Identify&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;and mitigate risks while ensuring compliance with Dyne policies.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Maintain&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;deep&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;understanding of DMD treatment journeys and adjust tactics accordingly.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Maintain knowledge of rare disease payer policies, including Medicaid.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;E&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;d&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;ucation, Knowledge &amp;amp; Skill Requirements&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;The successful candidate should be a dynamic&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;self-starter&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;with proven abilities as a biopharma commercial leader. S/he will have led successful product launches,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;have a patient focused mindset and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;a strong reputation&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;for excellent cross-functional collaboration and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;possess&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;the following:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;15+ years of experience in the Biotech, Pharmaceutical or Healthcare industry&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;10+ years of field reimbursement and/or nurse case management experience in the Pharmaceutical or Healthcare industries, including rare disease experience and launch experience&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;with&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;HCP-administered therapies, and ideally with home infusion therapies&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;5+ years leading and coaching teams of Field Reimbursement Managers and/or Field Nurse Case Managers&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Has prior experience supporting patients and their caregivers (e.g., nursing, counselor, social work, other allied health positions background) – ideally has worked with pediatric populations and/or within an environment that supported patient in-home visits&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Has prior experience supporting coverage and reimbursement processes for HCP-administered, rare disease products&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Can&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;demonstrate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;a deep understanding of payer policies and processes for obtaining coverage / pre-certification and reimbursement for HCP-administered therapies,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;in particular with&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;State Medicaid FFS and Managed Medicaid policies and processes&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Experience working with IDNs, academic medical centers and large health systems&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Empathetic, friendly, and relatable, with effective communication skills&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Comfortable speaking with patients/families, HCPs&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Willingness to work as leader of and part of an overall commercial team in a demanding environment&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Embraces continuous learning/seeks knowledge&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;Travel is&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;required.&amp;nbsp; It is &lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;expected that the leader will be in field&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;List Bullet&quot;&gt;&amp;nbsp;working with the team and meeting stakeholders on a regular basis.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:200,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$250,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$300,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-director-dyne-patient-access-and-education-dyne-therapeutics/69d3bbc2c8e81216cd0b8fa8</link><guid isPermaLink="true">http://biotechroles.com/senior-director-dyne-patient-access-and-education-dyne-therapeutics/69d3bbc2c8e81216cd0b8fa8</guid><pubDate>Mon, 06 Apr 2026 13:57:21 GMT</pubDate><company>Dyne Therapeutics</company><location>Remote</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Counsel]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;What if…&lt;/strong&gt;you could tell the story of an organization that creates, resources, and builds bioplatform companies that invent breakthrough technologies in order to transform human health and sustainability?&lt;/p&gt;
&lt;p&gt;Flagship Pioneering conceives, creates, resources, and develops first-in-category bioplatform companies to transform human health and sustainability. Since its launch in 2000, the firm has, through its Flagship Labs unit, applied its unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $130 billion in aggregate value. To date, Flagship has deployed over $2.5 billion in capital toward the founding and growth of its pioneering companies alongside more than $19 billion of follow-on investments from other institutions.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Overview&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering has a new and exciting opportunity for a high-energy, self-motivated Corporate Counsel to join its fast-paced, dynamic legal team. The Corporate Counsel will report directly to and collaborate closely with senior corporate attorneys who oversee Flagship’s corporate legal function and advise on legal and operational matters for Flagship and across its portfolio. The Corporate Counsel will concentrate on financings, corporate governance, equity compensation, and general corporate matters for Flagship and its cutting-edge high growth companies. This includes working with Flagship’s private and public companies on a variety of transactions and corporate matters that will range from financings, capital markets transactions and M&amp;amp;A, equity compensation, to general corporate governance.&lt;/p&gt;
&lt;p&gt;The successful candidate will have the requisite experience in corporate transactional matters and corporate governance, which must include venture capital and emerging companies. This individual will join a dedicated team with industry and subject matter expertise. In this role, the Corporate Counsel may interact with members of Flagship’s finance and origination teams and senior members of the legal team.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Counsel will have the following responsibilities and opportunities:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with internal stakeholders and external counsel on a wide range of transactions and corporate matters, including venture financings, capital markets, M&amp;amp;A transactions, corporate governance, and equity issuances.&lt;/li&gt;
&lt;li&gt;Assist with the review, preparation, and negotiation of a range of financing and governance documents, including term sheets, financing documents, and board and stockholder consents, resolutions and minutes.&lt;/li&gt;
&lt;li&gt;Support financing and corporate governance matters across increasingly complex, multi-entity structures, including exposure to LLC governance.&lt;/li&gt;
&lt;li&gt;Work and coordinate with external counsel on transactions, including supporting deal execution, timelines, and deliverables.&lt;/li&gt;
&lt;li&gt;Provide support to Finance, HR, Compensation, and portfolio company teams on corporate governance, equity matters (including option grants, restricted stock, profits interests, and equity plan administration), and related policies and best practices.&lt;/li&gt;
&lt;li&gt;Partner with cross-functional teams to support board composition changes across the Flagship ecosystem, including assisting with documentation for director appointments and resignations, maintaining accurate board records, and facilitating related equity approvals.&lt;/li&gt;
&lt;li&gt;Provide legal counsel for cutting-edge high growth companies in the Flagship ecosystem.&lt;/li&gt;
&lt;li&gt;Support compliance initiatives, process standardization, and form development for the legal group, including designing AI-enabled tools and agentic solutions to improve efficiency in corporate legal workflows.&lt;/li&gt;
&lt;li&gt;Build strong working relationships across Flagship and with external partners.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Key Qualifications and Skills&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;JD degree required and admission to practice law in Massachusetts or another U.S. state bar; outstanding academic credentials.&lt;/li&gt;
&lt;li&gt;2-4 years of relevant experience, preferably in the corporate department of a nationally recognized law firm.&lt;/li&gt;
&lt;li&gt;Foundational understanding of equity financing, equity awards, stock incentive plans, and corporate governance.&lt;/li&gt;
&lt;li&gt;Experience working both collaboratively and independently on components of transactions, with a willingness to take on increasing responsibility over time.&lt;/li&gt;
&lt;li&gt;Ability to prioritize and manage multiple deadlines in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Comfortable working in an entrepreneurial environment with evolving timelines and priorities.&lt;/li&gt;
&lt;li&gt;Experience supporting transactions and working with internal and external stakeholders to meet deadlines.&lt;/li&gt;
&lt;li&gt;Strong interpersonal and client service skills, attention to detail, and ability to work collaboratively as part of a team.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Sound judgment and ability to understand strategic objectives and deliver practical solutions.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills.&lt;/li&gt;
&lt;li&gt;Willingness to use and adopt AI tools (ChatGPT, Claude, GC AI) to enhance legal workflows, as well as core legal and business platforms (iManage, SharePoint, Carta, Microsoft Office).&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Flagship Pioneering and our ecosystem companies are committed to&amp;nbsp;&lt;strong&gt;equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates.&amp;nbsp; The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team.&amp;nbsp;&amp;nbsp; Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $148,000 - $2,035,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/corporate-counsel-flagship-pioneering/69d3bbbfc8e81216cd0b8fa6</link><guid isPermaLink="true">http://biotechroles.com/corporate-counsel-flagship-pioneering/69d3bbbfc8e81216cd0b8fa6</guid><pubDate>Mon, 06 Apr 2026 13:57:19 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Scientist, ADME-PK]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span class=&quot;TextRun SCXW131183527 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;none&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;The&lt;/span&gt;&lt;/span&gt; &lt;span class=&quot;TextRun SCXW131183527 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;none&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;Principal&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;S&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;cientist&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;, ADME-PK&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt; in&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt; Preclinical Development (PCD)&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt; department &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;utilize&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt; their knowledge in drug metabolism, ADME concepts, pharmacokinetics, pharmacodynamic and bioanalytical principles to advance &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;Dyne&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;’s efforts surrounding &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;delivery of therapeutic payloads to muscle and CNS tissues with the FORCE platform&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW131183527 BCX8&quot; data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP SCXW131183527 BCX8&quot; data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;This role is based in Waltham, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Primary Responsibilities Include:&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and execute internal/external preclinical studies to understand the pharmacokinetics (PK) and absorption, metabolism, distribution, and excretion (ADME) of Dyne’s drug candidates&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Represent PCD as the ADME-PK subject matter expert on discovery and program teams&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Partner with and support Research, Toxicology, Translational Biomarkers, Clinical, Regulatory, Project Management and other Dyne departments&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Collaborate with Clinical Pharmacology/Pharmacometrics to develop quantitative tools to translate PK/PD relationship from preclinical to clinical&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Author high quality Regulatory documents including INDs, CTAs, and NDA/BLA filings.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Prepare strategic and science-based ADME strategies that meet regulatory requirements and program goals&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Facilitate strategic scientific communication via meetings, abstracts and manuscripts&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Education and Skill Requirements:&lt;/u&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;PhD in Pharmacokinetics, Pharmacology, Pharmaceutics, Biomedical Sciences or other relevant field with &amp;gt;6 years (MS with &amp;gt;8 years, BS with &amp;gt;12 years) of experience in the biopharmaceutical industry, with evidence of drug development experience&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong knowledge of drug metabolism, ADME concepts, pharmacokinetics, pharmacodynamics and bioanalytical principles&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;F&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;amiliarity with regulatory submission including FIH dosing strategy is highly desirable&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proficient in using WinNonlin or other pharmacokinetic software&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication (verbal and written) and presentation skills, as well as interpersonal skills and the ability to represent PCD in a team environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with PK characterization of protein therapeutics or antibody-drug conjugates (ADCs) is desired&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$159,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$195,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/principal-scientist-adme-pk-dyne-therapeutics/69d3bbbdc8e81216cd0b8f9f</link><guid isPermaLink="true">http://biotechroles.com/principal-scientist-adme-pk-dyne-therapeutics/69d3bbbdc8e81216cd0b8f9f</guid><pubDate>Mon, 06 Apr 2026 13:57:17 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Contracts Systems Manager]]></title><description><![CDATA[&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;h2&gt;Position Summary&lt;/h2&gt;
&lt;p&gt;We are seeking a &lt;strong&gt;Contracts System Manager&lt;/strong&gt; to serve as the primary owner and administrator of Flagship&#39;s Contract Lifecycle Management (CLM) and procurement systems. This individual will be responsible for system configuration, optimization, user support, training, and cross-functional collaboration to ensure the Legal, Procurement, and Finance teams can efficiently manage contracts across Flagship and its portfolio companies. The role requires significant interpersonal engagement—building trusted relationships across business units, influencing stakeholders to adopt new processes, and exercising judgment in navigating competing priorities that require human insight and contextual understanding.&lt;/p&gt;
&lt;p&gt;The ideal candidate will have 3–5 years of experience administering CLM platforms (Cobblestone experience strongly preferred), a solid understanding of procurement workflows, and the ability to translate business requirements into technical system configurations. This role requires strong stakeholder engagement skills, attention to detail, and comfort working in a fast-paced, high-volume environment.&lt;/p&gt;
&lt;p&gt;This is a great opportunity to join a company at the forefront of innovation in technology and science. We are looking for a self-motivated, entrepreneurial, and kind individual who works hard but doesn&#39;t take themselves too seriously. The team you would be joining is tight-knit and committed to helping one another succeed.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Key Responsibilities&lt;/h2&gt;
&lt;p&gt;&lt;strong&gt;System Administration &amp;amp; Configuration&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the primary administrator for Flagship&#39;s CLM system (Cobblestone), including system configuration, user provisioning, role-based access control (RBAC), and permissions management&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Design and configure contract workflows, approval routing logic, and dynamic intake forms based on agreement type, spend thresholds, department, or legal requirements—collaborating directly with business owners to understand their operational needs and secure buy-in on workflow changes&lt;/li&gt;
&lt;li&gt;Manage the company&#39;s contract templates, playbook terms, and clause libraries; configure new templates and process workflows as needed&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Maintain repository accuracy, metadata tagging, and taxonomy; identify inefficiencies in current processes and propose workflow design improvements&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Integration &amp;amp; Technical Operations&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee and troubleshoot API connections and data syncs between the CLM system and downstream systems (e.g., ERP, procurement platforms, HRIS, e-signature tools)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Coordinate with IT on system integrations, security protocols, and technical requirements; serve as a trusted liaison between business functions, IT, and CLM vendor, translating technical constraints into business-friendly explanations and advocating for user needs in system design decisions&lt;/li&gt;
&lt;li&gt;Test and deploy system updates, patches, and new features from vendors; manage change control to minimize disruption to business users&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Configure and maintain vendor management modules, ensuring seamless data capture and risk assessment during vendor onboarding&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;User Support &amp;amp; Training&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide Tier 1 and Tier 2 support for CLM system users, including day-to-day troubleshooting, resolving workflow stalls, and addressing error messages&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Onboard and train new users (both technical and non-technical) on CLM system functionality and related processes through hands-on coaching, live demonstrations, and personalized support; implement train-the-trainer models and adapt training approaches based on individual learning styles and departmental needs&lt;/li&gt;
&lt;li&gt;Develop and maintain CLM training materials, user guides, and Standard Operating Procedures (SOPs); gather user feedback and recommend process improvements&lt;/li&gt;
&lt;li&gt;Support onboarding of new Flagship portfolio companies onto established contract standards and CLM processes, serving as a dedicated point of contact who builds rapport with new teams, addresses concerns with empathy, and guides stakeholders through change management during organizational transitions&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Cross-Functional Collaboration &amp;amp; Stakeholder Engagement&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Act as the primary liaison between IT and Finance, Legal, and Procurement teams, translating business processes into technical system requirements&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Build and maintain strategic relationships with business colleagues across Flagship and portfolio companies to understand evolving contracting needs, anticipate workflow challenges, and influence adoption of standardized processes through trust, credibility, and demonstrated value&lt;/li&gt;
&lt;li&gt;Coordinate directly with external vendors, counterparties, and law firms on contract logistics and system-related clarifications, exercising diplomacy and sound judgment to resolve ambiguities, manage expectations, and maintain productive working relationships&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Reporting &amp;amp; Analytics&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build dashboards and generate contract metrics to inform Legal leadership and cross-functional stakeholders; analyze trends and provide recommendations to improve contract operations efficiency, presenting findings in stakeholder meetings and facilitating discussions to drive consensus on operational improvements&lt;/li&gt;
&lt;li&gt;Conduct regular system audits to monitor data integrity, system health, and key performance metrics (e.g., approval cycle times, contract turnaround)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Track key dates and milestones; proactively identify and escalate potential risks, such as approaching deadlines, renewal windows, or expiring terms requiring action&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Compliance &amp;amp; Process Improvement&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Participate in assessing, refining, and executing on future business requirements for the CLM system; contribute to template and playbook updates based on recurring issues and counterparty redline patterns&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Support compliance with life sciences regulatory requirements (FDA, GxP where applicable) by ensuring contract workflows and documentation meet audit and traceability standards&lt;/li&gt;
&lt;li&gt;Identify and recommend process improvements to enhance efficiency, compliance, and user adoption across the contracting process&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Required Qualifications&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree in Business, Information Systems, Legal Studies, or related discipline&amp;nbsp;&lt;/li&gt;
&lt;li&gt;3–5 years of experience as a CLM systems administrator, legal operations specialist, or similar role&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Proficiency with contract lifecycle management (CLM) systems and associated workflows; hands-on experience with system configuration, workflow design, and user administration&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Understanding of procurement and finance processes, including budgets, payment terms, and vendor engagement&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience developing and implementing system-driven workflows; comfort with Jira or similar tools for user story creation and tracking&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Strong written and verbal communication skills with excellent stakeholder engagement ability, including the capacity to influence without authority, navigate organizational dynamics, and build consensus among diverse business partners&lt;/li&gt;
&lt;li&gt;Ability to exercise independent judgment in prioritizing workflow, escalating appropriately, and making nuanced decisions that balance competing stakeholder interests and business objectives&lt;/li&gt;
&lt;li&gt;Experience troubleshooting CLM or workflow system issues; ability to promptly identify and solve software and process problems&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Detail-oriented with strong organizational and project management skills&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to multi-task and work independently in a fast-paced environment; prioritize workflow based on business objectives&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Preferred Qualifications&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Experience in biotech, life sciences, pharmaceutical, or regulated industries&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience configuring or administering Cobblestone CLM system (taxonomy, permissions, template maintenance, workflow configuration)&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Familiarity with Coupa or other procurement system integration&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience with contract intake and legal operations frameworks&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Exposure to commercial agreements and legal terms and conditions&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Experience leading or actively participating in CLM system implementation projects&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Familiarity with FDA regulations, GxP requirements, or clinical contracting in life sciences environments&lt;/li&gt;
&lt;li&gt;Proficiency with business applications such as Microsoft 365, Coupa, Cobblestone, DocuSign, and Adobe Acrobat&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to work in a scrum/agile environment&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Culture &amp;amp; Values (Flagship)&lt;/h2&gt;
&lt;p&gt;We seek individuals who reflect Flagship&#39;s culture of fearless exploration, entrepreneurial thinking, and collaborative impact. You thrive in environments that require creative problem solving, strong ownership, and alignment with mission-driven outcomes.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Work Environment &amp;amp; Benefits&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Standard office environment in Cambridge with hybrid and remote flexibility options&lt;/li&gt;
&lt;li&gt;Collaborative, interdisciplinary teams engaged in high-impact innovation&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Professional growth opportunities across Flagship Pioneering and its portfolio&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;Equal Opportunity Employer&lt;/h2&gt;
&lt;p&gt;Flagship Pioneering is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected veteran status.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $108,000 - $148,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/contracts-systems-manager-flagship-pioneering/69d3bbbbc8e81216cd0b8f9c</link><guid isPermaLink="true">http://biotechroles.com/contracts-systems-manager-flagship-pioneering/69d3bbbbc8e81216cd0b8f9c</guid><pubDate>Mon, 06 Apr 2026 13:57:15 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$140000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Principal Engineer, Technical Development]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Principal Engineer, Technical Development serves as a technical engineering lead and driver for strategy, conception, optimization, and implementation of innovative manufacturing technologies within the Technical Development organization. This leader blends deep engineering expertise with cross-functional influence to implement innovative manufacturing systems for bioprocess and bioconjugation at clinical and commercial scales and accelerates time to market. The role is ideal for someone who thrives at the intersection of innovation, operations, and process development strategy.&lt;/p&gt;
&lt;p&gt;This is a full-time position based in Waltham, MA with no option for remote work.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Technical Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, optimize and implement engineering for manufacturing processes for new and existing products under current Good Manufacturing Practices (cGMP)&lt;/li&gt;
&lt;li&gt;Lead engineering technology selection, process modeling, equipment specification, and system integration and provide guidance and oversight of outsourced activities at CDMOs.&lt;/li&gt;
&lt;li&gt;Develop and validate process control strategies, including PAT, automation, and real time monitoring.&lt;/li&gt;
&lt;li&gt;Serve as the subject matter expert for engineering across manufacturing, operations, and R&amp;amp;D.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Strategic Impact&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build and execute the long-term engineering roadmap for manufacturing capabilities across all relevant modalities (biologics, oligonucleotides, and bioconjugates).&lt;/li&gt;
&lt;li&gt;Identify opportunities to transition batch processes to innovative platforms, improving throughput and cost-of-goods, while preserving product quality.&lt;/li&gt;
&lt;li&gt;Partner with senior leadership to align manufacturing strategy with business goals and regulatory expectations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional Collaboration&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Work closely with Quality, Supply Chain, and Manufacturing Operations to ensure seamless technology transfer and scaleup.&lt;/li&gt;
&lt;li&gt;Guide technical teams through engineering design reviews, process risk assessments, and regulatory submissions, fostering a culture of innovation and technical excellence.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Operational Excellence&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive continuous improvement initiatives using Lean, Six Sigma, and advanced process analytics.&lt;/li&gt;
&lt;li&gt;Troubleshoot complex manufacturing challenges and implement robust, sustainable solutions.&lt;/li&gt;
&lt;li&gt;Ensure compliance with cGMP, safety standards, and global regulatory requirements.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education, Experience, and Skills Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in chemical or similar engineering discipline with minimum of 7 years relevant experience; advanced degree MS or PhD preferred&lt;/li&gt;
&lt;li&gt;Proven track record designing, implementing, and scaling manufacturing systems&lt;/li&gt;
&lt;li&gt;Hands-on approach for operation of and troubleshooting manufacturing skids&lt;/li&gt;
&lt;li&gt;Development and implementation of PAT technologies&lt;/li&gt;
&lt;li&gt;Experience overseeing outsourced activities at CDMOs&lt;/li&gt;
&lt;li&gt;Expertise in process modeling, control systems, automation, and PAT.&lt;/li&gt;
&lt;li&gt;Experience in Biologics Downstream Purification Process Development and/or Bioconjugation Development preferred&lt;/li&gt;
&lt;li&gt;Familiar with the concepts of Scale-Down Model Qualification (SDMQ), Process Characterization, and defining Process Control Strategy (PCS)&lt;/li&gt;
&lt;li&gt;Strong understanding of current Good Manufacturing Practices (cGMP) and regulatory frameworks (FDA, EMA, ICH) relevant to continuous manufacturing of biologics.&lt;/li&gt;
&lt;li&gt;Attention to detail, exceptional communication skills, and the ability to influence all levels of the organization.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$147,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$180,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/principal-engineer-technical-development-dyne-therapeutics/69d3bbb9c8e81216cd0b8f88</link><guid isPermaLink="true">http://biotechroles.com/principal-engineer-technical-development-dyne-therapeutics/69d3bbb9c8e81216cd0b8f88</guid><pubDate>Mon, 06 Apr 2026 13:57:12 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Connect with Us]]></title><description><![CDATA[&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;div id=&quot;message-list_1759774021.206799&quot; class=&quot;c-virtual_list__item&quot; data-qa=&quot;virtual-list-item&quot; data-item-key=&quot;1759774021.206799&quot;&gt;
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&lt;div class=&quot;p-rich_text_section&quot;&gt;Didn&#39;t find your dream job? Drop your resume for future opportunities!&lt;span class=&quot;c-message__edited_label&quot; data-sk=&quot;tooltip_parent&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&lt;span class=&quot;c-message__edited_label&quot; data-sk=&quot;tooltip_parent&quot;&gt;Please fill out the information below so we understand your interests and capabilities.&lt;/span&gt;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;&amp;nbsp;&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;
&lt;p&gt;&lt;strong&gt;What We Offer:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Make an impact as part of a Fortune “Change the World” company&lt;/li&gt;
&lt;li&gt;Surround yourself with inspirational colleagues and leaders&lt;/li&gt;
&lt;li&gt;A dynamic and innovative work environment, with an exciting startup culture as well as the full support and expertise from Flagship ecosystem&lt;/li&gt;
&lt;li&gt;A platform to grow, learn, and lead&lt;/li&gt;
&lt;/ul&gt;
&lt;/div&gt;
&lt;div class=&quot;p-rich_text_section&quot;&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;MORE ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a biotechnology company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp; Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;http://www.flagshippioneering.com/&quot;&gt;www.flagshippioneering.com&lt;/a&gt;&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;/div&gt;
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&lt;div class=&quot;c-message_actions__container c-message__actions&quot;&gt;&amp;nbsp;&lt;/div&gt;
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&lt;/div&gt;]]></description><link>http://biotechroles.com/connect-with-us-flagship-pioneering/69d3bbb7c8e81216cd0b8f7d</link><guid isPermaLink="true">http://biotechroles.com/connect-with-us-flagship-pioneering/69d3bbb7c8e81216cd0b8f7d</guid><pubDate>Mon, 06 Apr 2026 13:57:10 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Cloud Engineer]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Quotient Therapeutics is a privately-held, early stage company developing breakthrough medicines informed by natural somatic genetic diversity present in patients. Through our work in somatic genomics, we are forging a new status quo for biopharma research and development across a broad pipeline of internal and partnered programs.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The company was founded by Flagship Pioneering, an innovative enterprise that conceives, creates, resources, and grows first-in-category life sciences companies. Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Generate Biomedicines, Sana Biotechnology (SANA), Tessera Therapeutics, Evelo Biosciences (EVLO), Indigo Agriculture, Seres Therapeutics (MCRB), and Syros Pharmaceuticals (SYRS).&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Cloud &amp;amp; Infrastructure Engineer to use their AWS/DevOps/SecOps skills to strengthen and evolve our Unified Digital Platform as we scale our genomics-first drug discovery operations. The candidate will join a collaborative Data Infrastructure team and work closely with biologists, chemists, informaticians, and data scientists to ensure our compute, data, and application environments are secure, reliable, and designed for growth. They bring enthusiasm, curiosity, strong engineering discipline, and a desire to build systems that support cutting-edge biological discovery. This role is based at the Chesterford Research Campus (vicinity of Cambridge) reporting to the Head of Data Engineering. Applicants require permission to work in the UK.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Collaborate with engineers and scientific stakeholders to evolve the cloud infrastructure that supports genomics, imaging, data pipelines, and AI/ML applications across the company.&lt;/li&gt;
&lt;li&gt;Manage and extend our AWS environment using infrastructure-as-code (primarily CDK), enhancing reliability, security, and efficiency across accounts and services.&lt;/li&gt;
&lt;li&gt;Support secure, scalable, and cost-effective use of AWS services including EKS, ECS, EC2, Batch, Lambda, S3, RDS, networking, and IAM.&lt;/li&gt;
&lt;li&gt;Improve observability and operational awareness through logging, alerting, metrics, and dashboards that help maintain system health and control costs.&lt;/li&gt;
&lt;li&gt;Contribute to CI/CD workflows and automation frameworks that underpin data engineering, web applications, and ML/AI systems.&lt;/li&gt;
&lt;li&gt;Strengthen our security posture by improving IAM practices, monitoring, auditing, and compliance alignment, in partnership with colleagues across the company.&lt;/li&gt;
&lt;li&gt;Partner with scientists, software engineers, and ML teams to ensure infrastructure supports modern lab-in-the-loop workflows, high-throughput data ingestion, and scalable analysis environments.&lt;/li&gt;
&lt;li&gt;Communicate technical decisions clearly and pragmatically to peers across scientific and engineering disciplines.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Graduate or post-graduate degree in computer science or a related engineering discipline, or equivalent practical experience.&lt;/li&gt;
&lt;li&gt;Three years or more of hands-on experience with cloud engineering, including AWS services such as EC2, S3, IAM, networking, and container orchestration (EKS or ECS).&lt;/li&gt;
&lt;li&gt;A clear understanding of AWS multi-account architectures and their implementation and management.&lt;/li&gt;
&lt;li&gt;Practical experience with infrastructure-as-code (CDK, CloudFormation, or Terraform).&lt;/li&gt;
&lt;li&gt;Familiarity with observability tooling (CloudWatch, Grafana, or comparable stacks) and cost-awareness in cloud environments.&lt;/li&gt;
&lt;li&gt;Experience with CI/CD pipelines, containerization, and DevOps automation.&lt;/li&gt;
&lt;li&gt;Experience integrating SSO identity platforms such as Okta/Entra.&lt;/li&gt;
&lt;li&gt;A security-minded approach, including understanding of least-privilege IAM, secure networking, and compliance-related workflows.&lt;/li&gt;
&lt;li&gt;Strong collaboration skills and a pragmatic mindset suited to a fast-moving, interdisciplinary biotech environment.&lt;/li&gt;
&lt;li&gt;Awareness of scientific workflows (bioinformatic, cheminformatic, microscopy/histology), including handling large data assets, storage layouts, and performance considerations for downstream analysis.&lt;/li&gt;
&lt;li&gt;Familiarity with common genomic data types such as BAMs, VCFs, etc..&lt;/li&gt;
&lt;li&gt;Experience navigating data governance and patient-confidentiality requirements in biomedical research, including secure access patterns and auditability.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship https://url.us.m.mimecastprotect.com/s/xLXBCqxk3LTk9pwcZf3CEkjif?domain=flagshippioneering.com.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&amp;nbsp;&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;]]></description><link>http://biotechroles.com/cloud-engineer-flagship-pioneering/69d3bbb2c8e81216cd0b8f67</link><guid isPermaLink="true">http://biotechroles.com/cloud-engineer-flagship-pioneering/69d3bbb2c8e81216cd0b8f67</guid><pubDate>Mon, 06 Apr 2026 13:57:06 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, UK</location><salary>$85000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Medical Value Liaison - West / Southwest]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;br&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;The&amp;nbsp;Medical Value&amp;nbsp;Liaison&amp;nbsp;(MVL)&amp;nbsp;is an&amp;nbsp;experienced field medical expert who plays a strategic role&amp;nbsp;in&amp;nbsp;the field medical team with depth and breadth of business acumen, therapeutic knowledge,&amp;nbsp;and leader on the team.&amp;nbsp;The person in this role&amp;nbsp;is&amp;nbsp;a customer&amp;nbsp;facing&lt;/span&gt;&lt;span data-contrast=&quot;none&quot;&gt;,&amp;nbsp;field-based extension of our Medical Affairs team.&amp;nbsp;The&amp;nbsp;MVL’s key&amp;nbsp;objective&amp;nbsp;is to create impact through advancing&amp;nbsp;patient outcomes,&amp;nbsp;medication&amp;nbsp;access, and customer experience&amp;nbsp;within&amp;nbsp;an&amp;nbsp;assigned&amp;nbsp;set of national/regional&amp;nbsp;payer&amp;nbsp;accounts.&amp;nbsp;This individual serves&amp;nbsp;as a key scientific resource, engaging with healthcare decision-makers and&amp;nbsp;other&amp;nbsp;medication access&amp;nbsp;stakeholders to provide scientific, health economic,&amp;nbsp;and&amp;nbsp;clinical support for our&amp;nbsp;portfolio.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This is a field-based role.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Serves as medical lead, engaging&amp;nbsp;in&amp;nbsp;timely&amp;nbsp;and compliant scientific, health&amp;nbsp;economic,&amp;nbsp;disease state exchange with payers and&amp;nbsp;other&amp;nbsp;healthcare decision makers&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develops strategic&amp;nbsp;customer&amp;nbsp;account&amp;nbsp;plans&amp;nbsp;that are aligned with&amp;nbsp;both&amp;nbsp;medical&amp;nbsp;and access&amp;nbsp;strategies, including&amp;nbsp;identifying&amp;nbsp;and building relationships with key&amp;nbsp;customers at&amp;nbsp;payer&amp;nbsp;organizations&amp;nbsp;and&amp;nbsp;other&amp;nbsp;healthcare decision makers&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Gathers high-level&amp;nbsp;customer&amp;nbsp;insights that shape and inform company&amp;nbsp;and access&amp;nbsp;strategy&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Responds to unsolicited&amp;nbsp;medical&amp;nbsp;information requests in&amp;nbsp;a timely,&amp;nbsp;accurate, and compliant manner&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Serves as an internal subject matter expert and provides training&amp;nbsp;as needed for Market Access&amp;nbsp;team&amp;nbsp;and other divisions&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Provides insight, input, and support towards the development of&amp;nbsp;payer facing&amp;nbsp;field tools and resources&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Builds awareness of the company within the payer and access community&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Supports&amp;nbsp;internal&amp;nbsp;health economic and outcomes&amp;nbsp;research&amp;nbsp;(HEOR)&amp;nbsp;initiatives&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrates thorough knowledge of the company, its investigational products&amp;nbsp;and current research,&amp;nbsp;and payer landscapes&amp;nbsp;impacting&amp;nbsp;the&amp;nbsp;company&amp;nbsp;portfolio&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Attends key&amp;nbsp;national and regional&amp;nbsp;payer, HEOR, and medical&amp;nbsp;conferences to gather insights, assess the competitive landscape, and strengthen relationships&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Provides strategic leadership within the team as a peer leader&amp;nbsp;and mentor, motivator, problem solver, and contributes to&amp;nbsp;the overall&amp;nbsp;team strategy&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborates with internal teams&amp;nbsp;including&amp;nbsp;Market&amp;nbsp;Access,&amp;nbsp;HEOR,&amp;nbsp;MSLs,&amp;nbsp;Patient&amp;nbsp;Advocacy,&amp;nbsp;Commercial,&amp;nbsp;Legal,&amp;nbsp;Compliance&amp;nbsp;to&amp;nbsp;maintain&amp;nbsp;a customer-centric, compliant approach&amp;nbsp;within assigned territory&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manages administrative tasks (e.g., Veeva CRM, expense reports, compliance modules) efficiently, including customer profiling and keeping CRM information up to date&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and Skills Requirements&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Advanced scientific degree or equivalent&amp;nbsp;required&amp;nbsp;(e.g.,&amp;nbsp;PharmD,&amp;nbsp;PhD,&amp;nbsp;MD)&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;8+ years of&amp;nbsp;experience&amp;nbsp;in a&amp;nbsp;relevant pharmaceutical&amp;nbsp;industry, managed care,&amp;nbsp;or&amp;nbsp;HEOR&amp;nbsp;role&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience&amp;nbsp;as a payer&amp;nbsp;focused&amp;nbsp;field medical liaison&amp;nbsp;and/or&amp;nbsp;experience in account management, formulary management, trade/rebate, Director of Pharmacy,&amp;nbsp;academic detailing,&amp;nbsp;economic modeling/HEOR, etc.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience with neuromuscular disorders (e.g., DMD, DM1), rare disease, specialty&amp;nbsp;and accelerated approval drugs&amp;nbsp;is highly desired&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Prior launch experience is a plus&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Strong understanding of the US payer system&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Proven ability to work effectively within multidisciplinary teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Skilled in building and&amp;nbsp;maintaining&amp;nbsp;relationships through scientific&amp;nbsp;expertise&amp;nbsp;and follow-through&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Able to&amp;nbsp;master clinical and health economic data and&amp;nbsp;communicate&amp;nbsp;complex information in a concise and effective way&amp;nbsp;across&amp;nbsp;diverse audiences&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Effective communication&amp;nbsp;skills (written, verbal, presentation)&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Expert in planning, prioritizing, and executing tasks efficiently&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Capable of working independently and managing time in a home office&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Adaptable in ambiguous and dynamic environments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Must be willing to travel&amp;nbsp;up to 60%, inclusive of overnight&amp;nbsp;and occasional weekends&amp;nbsp;to meet with customers, internal stakeholders, and attend relevant conferences&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Positive team member who embodies the Dyne Core Values&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;Excitement about Dyne’s vision and mission&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:0,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:0,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:0,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:0,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:0,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$183,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$255,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/medical-value-liaison-west-southwest-dyne-therapeutics/69d3bbb2c8e81216cd0b8f66</link><guid isPermaLink="true">http://biotechroles.com/medical-value-liaison-west-southwest-dyne-therapeutics/69d3bbb2c8e81216cd0b8f66</guid><pubDate>Mon, 06 Apr 2026 13:57:06 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-based</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Associate, Value Realization and Capital Solutions]]></title><description><![CDATA[&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at&amp;nbsp;&lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C02%7Cemccurdy%40flagshippioneering.com%7C8e54295c994c4d440a7b08ddc94a4a72%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638888043086011906%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;amp;sdata=gknIK%2BmYfQpsSi0%2FyQmhzNBo4DurYfmbUQpruIKf6Mc%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;a href=&quot;https://www.flagshippioneering.com/values&quot;&gt;core values&lt;/a&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is growing our Capital Solutions and Value Realizations team and we are looking for an exceptional Associate to join us in building, shaping and crystallizing value across our ecosystem of breakthrough, first in category platform companies designed to transform human health, sustainability and beyond.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;This role is ideal for someone who thrives at the intersection of science, finance, strategy, and M&amp;amp;A and who is energized by working inside one of the most innovative environments in life sciences.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Modelling, valuation and related analyses, and strategic assessments across the Flagship portfolio&lt;/li&gt;
&lt;li&gt;Scientific, clinical, market, and competitive landscape diligence&lt;/li&gt;
&lt;li&gt;Develop high-quality presentation materials and strategic communications&lt;/li&gt;
&lt;li&gt;Supporting initiatives across transaction execution, value realization, and direct private capital financing&lt;/li&gt;
&lt;li&gt;Partnering closely with senior leaders, company executives, and other teams across the Flagship ecosystem&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree in natural sciences and/or business&lt;/li&gt;
&lt;li&gt;Min 3 years of experience as an analyst and/or associate in healthcare investment banking&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Strong exposure to biotech equities and M&amp;amp;A products&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Advanced financial modelling and valuation capabilities&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Ability to distill complex scientific, clinical and market information into clear insights&lt;/li&gt;
&lt;li&gt;Strong verbal and written communication skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;We are an equal opportunity employer&lt;/strong&gt;. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;We recognize that great candidates often bring unique strengths&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;strong&gt;without fulfilling every qualification&lt;/strong&gt;. If you have some of the experience listed above but not all, please apply anyway. We are dedicated to building diverse and inclusive teams and look forward to learning more about your background&lt;strong&gt;&lt;span class=&quot;Apple-converted-space&quot;&gt;&amp;nbsp;&lt;/span&gt;and interest in Flagship.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;#LI-NM1&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $128,000 - $176,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/associate-value-realization-and-capital-solutions-flagship-pioneering/69d3bbafc8e81216cd0b8f64</link><guid isPermaLink="true">http://biotechroles.com/associate-value-realization-and-capital-solutions-flagship-pioneering/69d3bbafc8e81216cd0b8f64</guid><pubDate>Mon, 06 Apr 2026 13:57:02 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$95000-140000</salary><type>Full-time</type></item><item><title><![CDATA[Medical Science Liaison - West]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;br&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;The Medical Science Liaison&amp;nbsp;(MSL)&amp;nbsp;is an&amp;nbsp;experienced field medical expert who plays a strategic role&amp;nbsp;on&amp;nbsp;the field medical team with depth and breadth of business acumen, therapeutic knowledge and serves as an informal leader on the team.&amp;nbsp;The person in this role&amp;nbsp;is&amp;nbsp;a customer&amp;nbsp;facing&lt;/span&gt;&lt;span data-contrast=&quot;none&quot;&gt;,&amp;nbsp;field-based extension of our Medical Affairs team.&amp;nbsp;The MSL’s key&amp;nbsp;objective&amp;nbsp;is to create impact through advancing clinical practice within the assigned territory that leads to improved patient outcomes.&amp;nbsp;This individual serves&amp;nbsp;as a key scientific resource, engaging with healthcare professionals (HCPs), key opinion leaders (KOLs), and other stakeholders to provide scientific and clinical support for our portfolio.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This is a field-based role.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Builds awareness of the company within the medical community and develops strategic KOL/territory engagement plans aligned with the medical strategy&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Supports clinical research (investigator-initiated and company-sponsored), speaker development, and training as needed&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrates thorough knowledge of the company, its investigational products, and current medical research&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Maximizes attendance at national and regional conferences to gather insights, assess the competitive landscape, and strengthen relationships&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborates cross-functionally (clinical, regulatory, market access) to advance business and scientific goals&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develops&amp;nbsp;and&amp;nbsp;executes&amp;nbsp;regional medical strategies in alignment with company goals&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Leads&amp;nbsp;KOL engagement strategies and&amp;nbsp;identifying&amp;nbsp;new scientific leaders&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;8&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrates business acumen within therapeutic area and understands broader organization and competitive landscape&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;9&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Leads identification and mapping of key KOLs within the therapeutic area, driving engagement strategies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;10&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Provides strategic leadership within the MSL team as a peer leader, motivator, and problem solver&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;11&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manages top-tier KOL relationships, synthesizes high-level medical insights, and informs company&amp;nbsp;medical&amp;nbsp;strategies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;12&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Mentors junior MSLs and contributes to team strategy development&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;13&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Acts as a subject matter expert for internal stakeholders, including marketing, sales, and clinical teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;14&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborates with internal teams (HEOR, access, marketing, sales) to&amp;nbsp;maintain&amp;nbsp;a customer-centric, compliant approach&amp;nbsp;within assigned territory&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;15&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Establishes and develops HCP relationships, engaging in activities such as data discussions, clinical trials, and addressing patient journey barriers&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;16&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Responds to unsolicited information requests in&amp;nbsp;a timely,&amp;nbsp;accurate, and compliant manner&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;17&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensures compliant dissemination of scientific&amp;nbsp;and clinical&amp;nbsp;information to healthcare providers&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;18&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manages administrative tasks (e.g., Veeva CRM, expense reports, compliance modules) efficiently, including customer profiling and keeping CRM information up to date&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and Skills Requirements&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;19&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Advanced scientific degree or equivalent&amp;nbsp;required&amp;nbsp;(e.g., MD, PhD,&amp;nbsp;NP, PharmD,&amp;nbsp;PA)&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;20&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;10+ years of MSL&amp;nbsp;experience&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt; is preferred&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;21&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Clinical experience within neuromuscular disorders (e.g., DMD, DM1) preferred; rare disease experience considered&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;22&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Strong knowledge of investigational products and the neuromuscular space, including emerging data&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;23&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;In-depth understanding of clinical trial and investigator-sponsored study processes&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;24&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Proven ability to work effectively within multidisciplinary teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;25&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Clear understanding of MSL role and responsibilities&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;26&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Skilled in building and&amp;nbsp;maintaining&amp;nbsp;relationships with KOLs through scientific&amp;nbsp;expertise&amp;nbsp;and follow-through&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;27&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ability&amp;nbsp;to communicate research results clearly to diverse&amp;nbsp;audiences&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;28&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Strong communication&amp;nbsp;skills (written, verbal, presentation) for building relationships with colleagues&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;29&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Ability to influence without authority at all levels of the organization and externally&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;30&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Expert in planning, prioritizing, and executing tasks efficiently&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;31&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Capable of working independently and managing time in a home office&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;32&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Adaptable in ambiguous and dynamic environments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;33&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Leverages past neuromuscular relationships to support study enrollment and site communication&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;34&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experienced in relationship building to expand company reach&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;35&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Experience with relationship building and expanding a company’s reach&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;36&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Must be willing to travel extensively and occasionally on weekends&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;37&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Positive team member who embodies the Dyne Core Values&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;38&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;Excitement about Dyne’s vision and mission&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:720,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;hybridMultilevel&amp;quot;}&quot; data-aria-posinset=&quot;39&quot; data-aria-level=&quot;1&quot;&gt;Must be willing to travel extensively and occasionally on weekends&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$183,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$250,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/medical-science-liaison-west-dyne-therapeutics/69d3bbaac8e81216cd0b8f60</link><guid isPermaLink="true">http://biotechroles.com/medical-science-liaison-west-dyne-therapeutics/69d3bbaac8e81216cd0b8f60</guid><pubDate>Mon, 06 Apr 2026 13:56:58 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$150000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Associate/ Senior Associate, Molly Gibson’s Pioneering Business Unit (PBU))]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;THE ROLE&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;As an Associate or Senior Associate at Flagship Pioneering&amp;nbsp;in&amp;nbsp;Molly Gibson’s&amp;nbsp;Pioneering Business Unit (PBU), you will&amp;nbsp;ideate, research, and refine novel venture hypotheses,&amp;nbsp;validate&amp;nbsp;key underlying unknowns of biology or technology and transition pressure-tested ideas into building a&amp;nbsp;NewCo&amp;nbsp;around&amp;nbsp;the science.  You will help drive every&amp;nbsp;facet&amp;nbsp;of company origination from the&amp;nbsp;early stages&amp;nbsp;including identification and recruitment of critical partners and advisors, establishment of foundational IP, hiring and leadership of the early scientific team, and establishment of working norms and culture for the team.  In this role you will partner with stakeholders across the broader Flagship ecosystem to bring the full experience of Flagship to support your companies.  A successful candidate will become&amp;nbsp;the&amp;nbsp;expert on the foundational science of the company, frame and clearly communicate the strategy, and translate that strategy into a plan and lead operationalization of that plan alongside a&amp;nbsp;Principal&amp;nbsp;or Partner on the venture creation team.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;THE COMPANY&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Flagship Pioneering (“FSP”) conceives and develops first-in-category&amp;nbsp;bioplatform&amp;nbsp;companies to transform human health and sustainability. FSP has developed over 100 scientific ventures, resulting in more than&amp;nbsp;$130 billion&amp;nbsp;in aggregate value. FSP&amp;nbsp;seeks&amp;nbsp;to change the world by addressing some of humanity’s most urgent challenges: curing intractable diseases, improving human health, and feeding the world by advancing the resiliency and sustainability of agriculture.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;KEY RESPONSIBILITIES&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Contribute to and lead Flagship model explorations to rapidly assess interesting areas of science and develop novel,&amp;nbsp;actionable&amp;nbsp;and high value venture hypotheses&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Outline key scientific questions to enable venture hypotheses and develop experimental plans to rapidly create value and pressure test ideas&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Identify, build, and&amp;nbsp;maintain&amp;nbsp;relationships with&amp;nbsp;appropriate academic&amp;nbsp;KOLs and thought experts,&amp;nbsp;ie, introducing them to the Flagship model, getting early buy-in, vetting/validation and de-risking key concepts of venture hypotheses&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Understand IP landscape, formulate initial strategy, and write seminal applications for the technology and company. Assess patentability of existing IP landscape, including of key competitors and of potentially licensable estate&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop corporate strategy and operations plan for the company. Define value creation,&amp;nbsp;identify&amp;nbsp;application spaces, build out organizational chart, define&amp;nbsp;company goals, timelines and&amp;nbsp;resourcing&amp;nbsp;and&amp;nbsp;identify&amp;nbsp;strategic inflection points to set the company on the path to rapid growth and success&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop audience-specific pitches for company&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support business development activities and continue to evolve the story&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;8&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manage and coordinate early scientific and IP employees. Source,&amp;nbsp;recruit&amp;nbsp;and manage KOLs and early-stage employees as well as relationships with CROs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;9&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manage &amp;amp; lead scientific team (internal or external) and daily research. Manage operational tasks, including establishing lab facilities,&amp;nbsp;purchasing, HR, real estate acquisition, etc.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;10&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Become institutional subject matter expert and transfer to&amp;nbsp;active&amp;nbsp;company team. Stay up to date on the literature, conferences, funding opportunities, and new developments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;1&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;11&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work closely with and&amp;nbsp;leverage&amp;nbsp;Flagship operations teams (Finance, IP, IT, HR, and Talent)&amp;nbsp;expertise&amp;nbsp;for maximal operational excellence&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS &lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The ideal candidate has a STEM-based PhD or MD from a top university and 2 or more years of experience in life sciences biotech,&amp;nbsp;start-up&amp;nbsp;or entrepreneurial activities. The candidate must have a passion for novel science and be operationally savvy.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt; Important skills and capabilities include:&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven ability to rapidly become conversant in new areas of science and capable of engaging thought leaders at the deepest level of technological understanding&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ability to define a clear and compelling value proposition of a given scientific opportunity and effectively and cogently communicate that to technical and non-technical audiences&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Basic understanding of multiple&amp;nbsp;therapeutic&amp;nbsp;modalities of drug&amp;nbsp;discovery&amp;nbsp;including small molecule, ADC, and protein therapeutics&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent analytical skills and ability to synthesize &amp;amp; communicate complex information rapidly and effectively&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Energetic self-starter with strong presence and the ability to work effectively in an entrepreneurial environment&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Open, transparent communication style and&amp;nbsp;demonstrated&amp;nbsp;willingness to engage in difficult conversations in a professional and productive manner&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Passion for growth and development, with clear demonstration of openness to both giving and receiving feedback and&amp;nbsp;track record&amp;nbsp;of acting on feedback&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;8&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Able to work effectively and pleasantly in teams with&amp;nbsp;demonstrated&amp;nbsp;abilities to lead and manage&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;2&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;9&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Unmatched sense of urgency&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering and our ecosystem companies are&amp;nbsp;&lt;strong&gt;committed to equal employment opportunity&lt;/strong&gt;&amp;nbsp;regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;More About Flagship Pioneering:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are creative optimists, and we would love for you to consider joining our team!&amp;nbsp; See &lt;a href=&quot;https://www.flagshippioneering.com/join/roles&quot;&gt;all our open opportunities&lt;/a&gt; across Flagship Pioneering’s Ecosystem!&lt;/p&gt;
&lt;p&gt;&lt;a href=&quot;https://www.flagshippioneering.com/&quot;&gt;Flagship Pioneering&lt;/a&gt; conceives, creates, resources, and develops first-in-category life sciences companies to transform human health and sustainability. Since its launch in 2000, the firm has applied a unique hypothesis-driven innovation process to originate and foster more than 100 scientific ventures, resulting in over $34 billion in aggregate value. To date, Flagship is backed by more than $4.4 billion of aggregate capital commitments, of which over $1.9 billion has been deployed toward the founding and growth of its pioneering companies alongside more than $10 billion of follow-on investments from other institutions. The current Flagship ecosystem comprises 41 transformative companies, including:&amp;nbsp; Axcella Health (NASDAQ: AXLA), Denali Therapeutics (NASDAQ: DNLI), Evelo Biosciences (NASDAQ: EVLO),&amp;nbsp; Foghorn Therapeutics, Indigo Ag, Kaleido Biosciences (NASDAQ: KLDO), Moderna (NASDAQ: MRNA), Rubius Therapeutics (NASDAQ: RUBY), Sana Biotechnology, Seres Therapeutics (NASDAQ: MCRB), and Syros Pharmaceuticals (NASDAQ: SYRS).&lt;/p&gt;
&lt;p&gt;&lt;em&gt;#LI-TD1&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $155,000 - $190,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Flagship Pioneering currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Flagship Pioneering&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/associate-senior-associate-molly-gibson&apos;s-pioneering-business-unit-(pbu))-flagship-pioneering/69d3bbaac8e81216cd0b8f5e</link><guid isPermaLink="true">http://biotechroles.com/associate-senior-associate-molly-gibson&apos;s-pioneering-business-unit-(pbu))-flagship-pioneering/69d3bbaac8e81216cd0b8f5e</guid><pubDate>Mon, 06 Apr 2026 13:56:58 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$110000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Medical Director, US Medical Affairs]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The US Medical Director of Medical Affairs leads&amp;nbsp;Dyne’s medical strategy and execution within the United States, focusing on launch readiness, US-specific KOL engagement, congress planning and execution, and&amp;nbsp;supports&amp;nbsp;real-world evidence (RWE) initiatives. This role ensures alignment with global strategy while tailoring activities to US regulatory, payer, and healthcare landscapes.&amp;nbsp;This role leads efforts to communicate and disseminate scientific and clinical information, engage with medical professionals in the&amp;nbsp;field&amp;nbsp;and contribute to the overall success of the company’s portfolio.&amp;nbsp;The US Medical Director collaborates&amp;nbsp;closely with&amp;nbsp;Global Medical Affairs,&amp;nbsp;US Commercial, Regulatory, Market Access, and Clinical teams to drive successful product introduction and lifecycle management in the US market.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This role is located in our Waltham, MA office.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop and execute&amp;nbsp;US Medical Affairs strategy aligned with global&amp;nbsp;objectives&amp;nbsp;and US market needs&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Act as point person for all&amp;nbsp;US&amp;nbsp;Medical Affairs&amp;nbsp;launch readiness activities, including&amp;nbsp;working closely with&amp;nbsp;global medical director and&amp;nbsp;scientific communications on development of&amp;nbsp;scientific platform development,&amp;nbsp;local&amp;nbsp;congress planning, and&amp;nbsp;local&amp;nbsp;medical education programs&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support congress strategy execution in the US, including booth activities, symposia, and scientific presentations&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work closely and with the Head&amp;nbsp;of the&amp;nbsp;Medical Science Liaison (MSL)&amp;nbsp;team on&amp;nbsp;US KOL engagement strategy:&amp;nbsp;identify, map, and build relationships with key US experts&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support&amp;nbsp;insight collection and synthesis,&amp;nbsp;and supporting the&amp;nbsp;development of field material, working with the MSL team&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Develop US&amp;nbsp;Medical Affairs advisory&amp;nbsp;board&amp;nbsp;strategy and&amp;nbsp;organize&amp;nbsp;and execute&amp;nbsp;advisory boards and expert panels&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Work collaboratively with&amp;nbsp;HCP and Patient&amp;nbsp;Marketing&amp;nbsp;as well as&amp;nbsp;cross-functional stakeholders to integrate medical perspectives into brand strategy, ensuring alignment with scientific and commercial objectives&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partner with Clinical Development&amp;nbsp;and Clinical Operations&amp;nbsp;to support US trial site engagement&amp;nbsp;and recruitment strategies&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Working with&amp;nbsp;the&amp;nbsp;Global Medical Director,&amp;nbsp;identify&amp;nbsp;opportunities to generate&amp;nbsp;real-world evidence (RWE) and&amp;nbsp;phase IV data&amp;nbsp;to address data gaps and support&amp;nbsp;HCP&amp;nbsp;and payer&amp;nbsp;treatment decisions&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure compliance with US regulatory and legal requirements for all medical activities&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Serve as subject matter expert on neuromuscular diseases and Dyne’s therapeutic platforms for US stakeholders&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support&amp;nbsp;the review and approval of externally&amp;nbsp;presented materials through the Medical Review committee and Promotional Review Committee&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Act as a role model for integrity and compliance in all interactions&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and Skills Requirements&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Doctorate degree (MD, PhD, PharmD) with experience in rare diseases; neuromuscular experience preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Minimum&amp;nbsp;8&amp;nbsp;years of relevant experience in Medical Affairs within the US pharmaceutical/biotech industry&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven ability to lead US launch readiness and medical strategy execution&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication and relationship-building skills with US KOLs and cross-functional teams&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ability to interpret and communicate complex scientific data to diverse audiences&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Effective communication skills (written, verbal and presentation)&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Must be willing to travel up to 30%, inclusive of overnight and occasional weekends to meet with customers, internal stakeholders and attend relevant conferences&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Candidates must&amp;nbsp;be authorized to&amp;nbsp;work in the U.S.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Positive team member who embodies Dyne’s Core Values&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excitement about Dyne’s vision and mission&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience managing direct reports&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$196,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$285,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/medical-director-us-medical-affairs-dyne-therapeutics/69d3bba6c8e81216cd0b8f5a</link><guid isPermaLink="true">http://biotechroles.com/medical-director-us-medical-affairs-dyne-therapeutics/69d3bba6c8e81216cd0b8f5a</guid><pubDate>Mon, 06 Apr 2026 13:56:54 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$250000-380000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Scientist, LNP Formulations]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Company description&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL87, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases. It was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;The role&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a motivated Associate Scientist to support the development, preparation, and characterization of Lipid Nanoparticle (LNP) formulations. This role is highly hands-on and focused on formulating, screening, and analyzing LNPs to support discovery and development programs. The ideal candidate works well in a fast-paced, team-oriented environment and is eager to deepen their expertise in formulation science.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prepare and formulate LNPs using established protocols and evolving methods&lt;/li&gt;
&lt;li&gt;Execute formulation experiments to support optimization and screening efforts&lt;/li&gt;
&lt;li&gt;Perform LNP characterization and analytics, including particle size, PDI, encapsulation efficiency, and stability testing&lt;/li&gt;
&lt;li&gt;Accurately document experimental procedures, results, and observations in laboratory records&lt;/li&gt;
&lt;li&gt;Analyze and summarize experimental data and communicate findings to project teams&lt;/li&gt;
&lt;li&gt;Collaborate closely with scientists across formulation, analytics, and biology functions&lt;/li&gt;
&lt;li&gt;Support routine laboratory operations, including reagent preparation, equipment upkeep, and inventory management&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Professional experience and qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BS or MS in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field and 8+ years of industry experience&lt;/li&gt;
&lt;li&gt;Hands-on experience with LNP formulations or lipid-based delivery systems&lt;/li&gt;
&lt;li&gt;Familiarity with LNP analytical techniques (e.g., DLS, encapsulation assays, basic stability studies)&lt;/li&gt;
&lt;li&gt;Strong attention to detail and ability to follow experimental protocols&lt;/li&gt;
&lt;li&gt;Ability to work effectively as part of a team in a fast-paced environment&lt;/li&gt;
&lt;li&gt;Good written and verbal communication skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;What We Offer&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Opportunity to work at the forefront of LNP formulation innovation&lt;/li&gt;
&lt;li&gt;Collaborative, science-driven culture with high impact research&lt;/li&gt;
&lt;li&gt;Competitive compensation and benefits package&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;LOCATION: Cambridge, MA&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;ABOUT FLAGSHIP PIONEERING&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform human health, sustainability and beyond. Since its launch in 2000, Flagship has originated more than 100 companies. Many of these companies have addressed humanity most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&lt;/p&gt;
&lt;p&gt;Flagship has been recognized twice on FORTUNE Change the World list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies and has been twice named to Fast Company annual list of the World Most Innovative Companies. Learn more about Flagship https://url.us.m.mimecastprotect.com/s/xLXBCqxk3LTk9pwcZf3CEkjif?domain=flagshippioneering.com.&lt;/p&gt;
&lt;p&gt;At Flagship, we accept impossible missions to enable bigger leaps. Our core values guide us through uncertainty and toward lasting impact.&lt;/p&gt;
&lt;p&gt;We are an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $96,000 - $126,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL87 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL87&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/associate-scientist-lnp-formulations-flagship-pioneering/69d3bba6c8e81216cd0b8f58</link><guid isPermaLink="true">http://biotechroles.com/associate-scientist-lnp-formulations-flagship-pioneering/69d3bba6c8e81216cd0b8f58</guid><pubDate>Mon, 06 Apr 2026 13:56:53 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$95000-130000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Scientist, in vitro Pharmacology and Assay Development]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Position Summary: &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Metaphore is seeking a highly motivated, detail-oriented, and collaborative Associate Scientist to support in vitro pharmacology and assay development efforts within our Biology team. This role will focus on the design, development, optimization, and execution of cell-based and biochemical assays to support discovery and preclinical programs.&lt;/p&gt;
&lt;p&gt;The ideal candidate will bring strong hands-on experience in assay development and execution, with the ability to independently troubleshoot and refine assays while contributing to broader program goals. This is a primarily pipeline-facing role with opportunities to contribute to platform development efforts involving complex biological systems.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design, develop, optimize, and execute in vitro and ex vivo assays to support discovery and preclinical programs, including functional and phenotypic assays.&lt;/li&gt;
&lt;li&gt;Perform medium-throughput ligand-binding and cell-based assays (e.g., ELISA, MSD, and reporter or proliferation assays) to characterize biological activity and support hit identification and lead optimization.&lt;/li&gt;
&lt;li&gt;Develop and implement assays to evaluate pharmacokinetic (PK) and pharmacodynamic (PD) readouts from in vivo samples.&lt;/li&gt;
&lt;li&gt;Generate custom engineered mammalian cell lines, culture and maintain primary cells, and apply these systems to biologically relevant assay development.&lt;/li&gt;
&lt;li&gt;Analyze, interpret, and clearly communicate experimental data to cross-functional teams to inform program decisions.&lt;/li&gt;
&lt;li&gt;Troubleshoot experimental challenges and independently drive assay improvements to ensure robustness, reproducibility, and scalability.&lt;/li&gt;
&lt;li&gt;Collaborate closely with multidisciplinary teams including Discovery, Protein Sciences and Computational Biology to advance program objectives.&lt;/li&gt;
&lt;li&gt;Contribute to the design and sourcing of critical reagents (e.g., recombinant proteins, cell lines) as needed.&lt;/li&gt;
&lt;li&gt;Coordinate with external vendors and CROs to support assay execution and sample analysis.&lt;/li&gt;
&lt;li&gt;Maintain accurate and timely documentation of experimental work in electronic lab notebooks and contribute to reports and presentations.&lt;/li&gt;
&lt;li&gt;Contribute to a collaborative team environment, including sharing technical expertise and mentoring junior team members where appropriate.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Basic Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s or Master’s degree in biology, biochemistry, pharmacology, or a related field with 8+ years of relevant industry experience.&lt;/li&gt;
&lt;li&gt;Hands-on experience developing and executing in vitro assays, including ligand-binding (e.g., ELISA, MSD) and cell-based functional assays.&lt;/li&gt;
&lt;li&gt;Experience with mammalian cell culture, including maintenance of immortalized cell lines and primary cells.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to troubleshoot and optimize assays independently.&lt;/li&gt;
&lt;li&gt;Experience generating, analyzing, and interpreting experimental data with strong attention to detail.&lt;/li&gt;
&lt;li&gt;Excellent organizational, documentation, and communication skills.&lt;/li&gt;
&lt;li&gt;Proven ability to work effectively in a fast-paced, collaborative, and cross-functional environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred Qualifications: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience working with biologics (e.g., antibodies or related modalities).&lt;/li&gt;
&lt;li&gt;Experience with primary human cell systems or advanced in vitro models (e.g., organoids, microphysiological systems).&lt;/li&gt;
&lt;li&gt;Familiarity with molecular biology and protein biochemistry techniques (e.g., qPCR, Western blotting, recombinant protein expression).&lt;/li&gt;
&lt;li&gt;Experience supporting PK/PD assay development and analysis.&lt;/li&gt;
&lt;li&gt;Prior experience working with or coordinating external CROs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Values and Behaviors &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;We are seeking individuals with an entrepreneurial spirit, strong communication skills, and comfort working in and contributing to a dynamic and cross-functional team environment. The level of the role will be commensurate with the education and years of experience of the identified candidate.&lt;/p&gt;
&lt;p&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt;&amp;nbsp;Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $96,000 - $126,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Metaphore Biotechnologies, Inc. currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Metaphore Biotechnologies, Inc.&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/associate-scientist-in-vitro-pharmacology-and-assay-development-flagship-pioneering/69d3bba2c8e81216cd0b8f53</link><guid isPermaLink="true">http://biotechroles.com/associate-scientist-in-vitro-pharmacology-and-assay-development-flagship-pioneering/69d3bba2c8e81216cd0b8f53</guid><pubDate>Mon, 06 Apr 2026 13:56:50 GMT</pubDate><company>Flagship Pioneering</company><location>Somerville, MA USA</location><salary>$85000-115000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Director, Regulatory Affairs Advertising & Promotion]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;The Executive&amp;nbsp;Director,&amp;nbsp;Regulatory Affairs Advertising &amp;amp; Promotion&amp;nbsp;leads regulatory strategy and compliance for advertising and promotional activities across all external communications.&amp;nbsp;This role serves as the subject matter expert, partnering with&amp;nbsp;the launch team,&amp;nbsp;commercial, medical affairs, R&amp;amp;D, corporate communications, legal, and leadership to ensure messaging aligns with FDA regulations and company&amp;nbsp;objectives.&amp;nbsp;The person in this role&amp;nbsp;provides&amp;nbsp;strategic guidance on complex promotional claims,&amp;nbsp;anticipates&amp;nbsp;market and regulatory factors, and drives innovative, compliant solutions.&amp;nbsp;This role chairs&amp;nbsp;the&amp;nbsp;regulatory review&amp;nbsp;for&amp;nbsp;the Promotion Review Committee&amp;nbsp;(PRC)&amp;nbsp;and&amp;nbsp;for the Medical Review Committee (MRC), balancing legal requirements with business goals while mitigating risk across promotional campaigns and corporate communications.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This role is based in Waltham, MA without the possibility of&amp;nbsp;being a fully remote role.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:2,&amp;quot;335559740&amp;quot;:300}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serves as&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;the&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ubject matter expert for Regulatory Affairs Ad/Promo, providing leadership and development of innovative and compliant strategies to support communication and promotional objectives&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Proactively&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;i&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;dentifies&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and evaluates fundamental issues, providing strategy and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;direction&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;a&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;nticipat&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ing&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;factors that could influence strategies and company position in the market&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;the&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;PRC&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to navigate complicated claims while juggling requirements of laws and regulations, as well as interpreting and implementing FDA Guidance&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;S&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;erves as lead Regulatory Advertising &amp;amp; Promotion expert on&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;MRC&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Accountable for review and approval of external communications materials for promotion and scientific exchange, and corporate messaging in line with relevant goals and deliverables with a broad impact on the organization. When needed, delegates tasks effectively and appropriately to direct focus on strategic planning and execution&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Proposes creative, effective, and compliant regulatory strategies and solutions to challenging promotional concepts that meet business&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;objectives&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and minimize risk&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Supports Commercial&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;lau&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;n&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ch&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;teams&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;,&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;participating&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;in strategy discussions and extended team meetings&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;to&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;provid&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;e&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;regulatory guidance and perspective on marketing strategies and promotion&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;objectives&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and tactics&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Provides promotional regulatory input on concepts and draft materials to ensure they are aligned with promotional regulations, corporate standards and policies and business objectives&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Leads the development and implementation of guidelines and processes for the creation, review,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;approval&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and regulatory submission, where applicable, of external communications content&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Acts as the recognized authority on regulatory advertising and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;promotion&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;matters. Able to work independently and deal with division or corporate functions, or with external agencies.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serves as&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;p&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;rimary Regulatory Advertising &amp;amp; Promotion contact for Regulatory Agencies&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Actively&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;participate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;in labeling and global regulatory team meetings to ensure support for&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;anticipated&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it related to the use of study results in US and global promotion.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Maintains current awareness of evolving FDA regulations and interpretations, FDA advisory letters, enforcement&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;letters&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and policies issues affecting the pharmaceutical/biologics&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;industry and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;C&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ommunicates&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;significant changes in FDA perspective to relevant stakeholders.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Contributes to the development of departmental strategic initiatives to drive effective, compliant promotional regulatory review&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;BS degree in scientific,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;clinical&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;or related area&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;required&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;. Advanced degree&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;highly&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;desirable.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;12+ years pharmaceutical/biotech industry experience with a minimum of 10 years of&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;d&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;irect experience as primary Regulatory reviewer of advertising and promotional materials is&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;required&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;In-depth understanding of strategic regulatory advertising and promotion concepts as well as breadth of regulatory advertising &amp;amp; promotion&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;expertise&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Successful launch experience, preferably including global product launches&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Works comfortably with abstract ideas or situations across functional areas of the business&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Strong&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;track record&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;of implementing successful business strategies for branded and unbranded promotional campaigns&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ability to see impact of decisions across various segments of the organization, including Medical Affairs and Corporate Communications activities.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Strong interpersonal skills&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;p&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;roven negotiator&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;with&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;demonstrated&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;ability to use constructive debate to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;identify&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and move others towards compliant promotional outcomes&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ability to communicate and influence without authority at all levels of the organization and externally&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Well organized with exceptional communication skills, strong influencing skills, strong technical&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;writing&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and documentation skills, as well as strong analytical and problem-solving skills&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Thinks innovatively and creatively,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;identifying&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;the risks surrounding promotional claims and campaigns&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Proficient in computer applications and configurations including Microsoft Office Suite or related software, Veeva&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;PromoMats&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and Veeva&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;MedComms&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;systems&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Demonstrated history of successful interactions with promotional review divisions of FDA (OPDP/APLB) or experience developing/leading the regulatory strategy for a product filing/launch&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Positive team member who&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;embodies the Dyne Core Values&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excitement about&amp;nbsp;Dyne’s&amp;nbsp;vision and mission&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$250,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$305,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/executive-director-regulatory-affairs-advertising-and-promotion-dyne-therapeutics/69d3bba1c8e81216cd0b8f52</link><guid isPermaLink="true">http://biotechroles.com/executive-director-regulatory-affairs-advertising-and-promotion-dyne-therapeutics/69d3bba1c8e81216cd0b8f52</guid><pubDate>Mon, 06 Apr 2026 13:56:49 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director/Director, Medicinal Chemistry]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;COMPANY DESCRIPTION&lt;/strong&gt;&lt;br&gt;&amp;nbsp;&lt;br&gt;Flagship Labs 111 Inc. (FL111) is a privately held, early-stage biotechnology company pioneering a novel platform harnessing innovations in chemistry, computation, and data science to create new therapeutic modalities beyond traditional small molecules. FL111 is backed by Flagship Pioneering, bringing the courage, vision, and resources to guide FL111 from platform validation to patient impact. We are seeking collaborative, creative and relentless problem solvers that share our passion for impact to join us!&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;THE ROLE&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;FL111 is seeking an experienced and highly innovative AD/D, Medicinal Chemistry to lead chemistry efforts for small-molecule drug discovery programs. This role will drive medicinal chemistry strategy from hit identification through lead optimization and candidate selection, working closely with biology, DMPK, computational chemistry, and FSP partners. The ideal candidate is a hands-on scientific leader with deep medicinal chemistry expertise, with a track record of delivering on small molecule heterobifunctional and/or induced proximity programs.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KEY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Design and implement medicinal chemistry strategies from early discovery through candidate selection, leveraging structure- and property-based design principles.&lt;/li&gt;
&lt;li&gt;Drive compound design and optimization by integrating SAR, ADME/DMPK, pharmacology, and safety data to meet target product profiles.&lt;/li&gt;
&lt;li&gt;Partner with computational chemistry teams to apply computational approaches to molecular design and optimization.&lt;/li&gt;
&lt;li&gt;Manage and direct external CRO partnerships, including oversight of complex synthetic routes, timelines, data quality, and compound delivery and registry.&lt;/li&gt;
&lt;li&gt;Collaborate with biology teams to interpret data and guide decision-making in a continuous and iterative design, synthesize, test, learn loop.&lt;/li&gt;
&lt;li&gt;Collaborate with legal and IP teams to draft, review, and support patent filings related to medicinal chemistry innovations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PROFESSIONAL EXPERIENCE &amp;amp; QUALIFICATIONS&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD. in Organic Chemistry or Medicinal Chemistry with &lt;u&gt;8-10+ years&lt;/u&gt; of industry experience in small molecule drug discovery within a pharma or biotech environment.&lt;/li&gt;
&lt;li&gt;Track record of delivering on small molecule heterobifunctional and/or induced proximity programs (e.g., PROTACs).&lt;/li&gt;
&lt;li&gt;Deep expertise in medicinal chemistry, including synthetic organic chemistry, SAR analysis, ADME, pharmacokinetics, and drug design principles.&lt;/li&gt;
&lt;li&gt;Proven ability to lead projects and cross-functional team&lt;/li&gt;
&lt;li&gt;Excellent communication skills with the ability to convey complex scientific concepts.&lt;/li&gt;
&lt;li&gt;Experience managing external CROs and contributing as a chemistry leader&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;About Flagship Pioneering&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is a bioplatform innovation company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity’s most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.&amp;nbsp; Flagship has been recognized twice on FORTUNE’s “Change the World” list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company’s annual list of the World’s Most Innovative Companies. Learn more about Flagship at &lt;a href=&quot;https://nam12.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.flagshippioneering.com%2F&amp;amp;data=05%7C01%7Cemccurdy%40flagshippioneering.com%7C723eebecb4fd441a8d4808dbc3706637%7Cd00b8682fc8b4548b82dda0524788e9b%7C0%7C0%7C638318659764104453%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&amp;amp;sdata=ZLQGwoiIX4KB%2FcilEz8n9NdaOq6EQCJ3GpW8RIYr1Zw%3D&amp;amp;reserved=0&quot;&gt;www.flagshippioneering.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Flagship Pioneering is committed to &lt;strong&gt;equal employment opportunity&lt;/strong&gt; regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;em&gt;Recruitment &amp;amp; Staffing Agencies:&lt;/em&gt;&lt;/strong&gt;&lt;em&gt; Flagship Pioneering and its affiliated Flagship Lab companies (collectively, “FSP”) do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering’s internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;#LI-TL1&lt;/em&gt;&lt;/p&gt;&lt;p id=&quot;pay-transparency&quot; style=&quot;margin: 0 !important; padding: 0 !important; float: none !important; clear: both !important; display: block;&quot;&gt;The salary range for this role is $154,000 - $236,500. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. FL111 currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on FL111&#39;s good faith estimate as of the date of publication and may be modified in the future.&lt;/p&gt;]]></description><link>http://biotechroles.com/associate-directordirector-medicinal-chemistry-flagship-pioneering/69d3bb9ec8e81216cd0b8f51</link><guid isPermaLink="true">http://biotechroles.com/associate-directordirector-medicinal-chemistry-flagship-pioneering/69d3bb9ec8e81216cd0b8f51</guid><pubDate>Mon, 06 Apr 2026 13:56:46 GMT</pubDate><company>Flagship Pioneering</company><location>Cambridge, MA USA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, US Field Effectiveness & Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Director, US Field Effectiveness &amp;amp; Operations is a critical role within the Commercial organization, responsible for driving strategic initiatives and operational excellence to fuel business growth. This individual will build the operational infrastructure for the Key Account Manager (KAM) field force from the ground up, including field analytics and dashboards, territory sizing and alignment, targeting, and the development and execution of field force effectiveness programs.&lt;/p&gt;
&lt;p&gt;This role requires strong cross-functional collaboration across Sales, Marketing, Market Access, Advanced Analytics, Patient Services, Finance, IT, and US Commercial Leadership to ensure launch readiness. The Director will champion innovation and operational efficiency, building scalable processes that enhance collaboration and field productivity with a patient-first mindset.&lt;/p&gt;
&lt;p&gt;This is a remote-based, individual contributor role requiring strong communication, self-initiative, and consultative engagement skills.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Field Effectiveness&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build field reporting and analytics capabilities from the ground up to support KAM performance and decision-making.&lt;/li&gt;
&lt;li&gt;Partner with field leadership to define KPIs and develop analytics and dashboards to track performance and impact.&lt;/li&gt;
&lt;li&gt;Design and lead a Quarterly Business Review (QBR) process to assess commercial effectiveness and outcomes.&lt;/li&gt;
&lt;li&gt;Spend time in the field to understand Dyne’s operating model and translate insights into practical, field-ready solutions.&lt;/li&gt;
&lt;li&gt;Own KAM performance analytics and execution in support of incentive compensation programs.&lt;/li&gt;
&lt;li&gt;Collaborate with the KAM team to design and implement an account planning tool.&lt;/li&gt;
&lt;li&gt;Develop regional and account-level performance dashboards.&lt;/li&gt;
&lt;li&gt;Recommend and drive enhancements to BI and CRM tools to improve KAM effectiveness.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Field Operations&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as the primary point of contact for the VP, Customer Experience, KAM leadership, and the KAM field team.&lt;/li&gt;
&lt;li&gt;Lead field force sizing and structural planning for upcoming launches and ongoing strategic reviews.&lt;/li&gt;
&lt;li&gt;Establish and maintain territory alignment and adjustment processes.&lt;/li&gt;
&lt;li&gt;Lead account and HCP targeting strategy and analytics in partnership with the Data and Advanced Analytics teams.&lt;/li&gt;
&lt;li&gt;Optimize field enablement tools, materials, and processes to maximize field productivity.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education and Skills Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree with 10+ years of experience in biotech, pharma, or life sciences.&lt;/li&gt;
&lt;li&gt;5+ years of experience in field sales, sales leadership, field operations, or consulting roles with deep field operations exposure.&lt;/li&gt;
&lt;li&gt;Proven track record supporting or launching rare disease therapies, preferably in neuromuscular, neurodegenerative, or neurodevelopmental indications.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to build and scale commercial infrastructure, including vendor management.&lt;/li&gt;
&lt;li&gt;Strategic thinker with strong business acumen and a results-oriented mindset.&lt;/li&gt;
&lt;li&gt;Proficiency with commercial technology platforms and data, including CRM, BI tools, Snowflake, Boomi, SP/SIP, and HUB data.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills, with experience presenting to senior leadership.&lt;/li&gt;
&lt;li&gt;Strong problem-solving skills and ability to operate effectively in a fast-paced, evolving environment.&lt;/li&gt;
&lt;li&gt;Travel may be required for this role&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$188,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$230,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-us-field-effectiveness-and-operations-dyne-therapeutics/69d3bb9dc8e81216cd0b8f50</link><guid isPermaLink="true">http://biotechroles.com/director-us-field-effectiveness-and-operations-dyne-therapeutics/69d3bb9dc8e81216cd0b8f50</guid><pubDate>Mon, 06 Apr 2026 13:56:45 GMT</pubDate><company>Dyne Therapeutics</company><location>Remote</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, US Commercial Business Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Director, US Commercial Business Operations is a critical role within the commercial organization, driving strategic initiatives and operational excellence to fuel business growth. Reporting to the Head of US Commercial Operations, this individual is a highly visible commercial leader responsible for building foundational capabilities from the ground up, including operational infrastructure, data strategy, management, and governance; commercial effectiveness program development and execution; and sales enablement.&lt;/p&gt;
&lt;p&gt;This role requires strong cross‑functional collaboration across commercial stakeholders in marketing, market access, patient services, finance, IT, and US Commercial leadership to ensure launch readiness and sustained execution. The Director, US Commercial Business Operations serves as a champion of innovation and operational efficiency, streamlining processes and enhancing collaboration with a patient‑first mindset.&lt;/p&gt;
&lt;p&gt;This is an individual contributor role requiring strong communication, self‑initiative, and consultative engagement skills.&amp;nbsp; This role is based in Waltham, MA &lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities Include:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Operational Excellence and Business Analytics&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Establish scalable processes for forecasting, demand and sales planning, and performance tracking to ensure operational efficiency.&lt;/li&gt;
&lt;li&gt;Manage Veeva, BI tools, and other commercial technology systems to identify market trends, optimize resource allocation, and make data driven-informed decisions.&lt;/li&gt;
&lt;li&gt;In collaboration with Trade and Distribution lead and finance, create channel analytics to inform forecast demand.&lt;/li&gt;
&lt;li&gt;Collaborate with marketing operations for Medical/Legal Review Process logistics&lt;/li&gt;
&lt;li&gt;Partner with marketing operations on National, regional, and local meeting management.&lt;/li&gt;
&lt;li&gt;Lead automation of BI reporting for HQ, executive leadership and field in collaboration with IT commercial business partner.&lt;/li&gt;
&lt;li&gt;Embed AI tools and capabilities into key processes and workflows to improve efficiency, decision-making, and business outcomes.&lt;/li&gt;
&lt;li&gt;Scalable process for alignments, targeting, and Veeva call cycle planning.&lt;/li&gt;
&lt;li&gt;Lead for market access analytics and developing reports through requirement gathering with HUB, SP, SIP and data aggregator.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Data Strategy, Management and Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Implement and refine data strategy as needed.&lt;/li&gt;
&lt;li&gt;Oversee all data channels for US market, ensure quality, and set up processes to identify data issues&lt;/li&gt;
&lt;li&gt;Lead SP and data aggregator data integrity meeting process, setting weekly cross-functional team engagements.&lt;/li&gt;
&lt;li&gt;Ensure data quality and compliance with security and regulatory standards.&lt;/li&gt;
&lt;li&gt;Lead data processes and foster collaboration to align organizational goals while driving continuous improvement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Commercial Effectiveness and Execution-Field Enablement&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead field force programs and services, circle of excellence program development, award trip, and administration.&lt;/li&gt;
&lt;li&gt;Fleet program development and management.&lt;/li&gt;
&lt;li&gt;Optimize field enablement tools and materials for maximum field productivity.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education and Skills Requirements&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree and 10+ years of experience in biotech/pharma/life sciences in field sales, sales leadership, commercial business operations or strategy.&lt;/li&gt;
&lt;li&gt;Proven track record of success in launching rare disease neuromuscular, neurodegenerative or neurodevelopmental therapies.&lt;/li&gt;
&lt;li&gt;Strong leadership experience, managing vendors, and scaling commercial infrastructure.&lt;/li&gt;
&lt;li&gt;Strategic thinker with strong business acumen and results-oriented mindset&lt;/li&gt;
&lt;li&gt;Proficiency with commercial technology and software platforms, and data (CRM, BI tools, Snowflake, Boomi, SP &amp;amp; SIP and HUB data)&lt;/li&gt;
&lt;li&gt;Excellent communication skills and problem-solving skills.&lt;/li&gt;
&lt;li&gt;Strong writing and verbal communication skills, including ability to present to senior management.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$196,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$240,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-us-commercial-business-operations-dyne-therapeutics/69d3bb99c8e81216cd0b8f4b</link><guid isPermaLink="true">http://biotechroles.com/director-us-commercial-business-operations-dyne-therapeutics/69d3bb99c8e81216cd0b8f4b</guid><pubDate>Mon, 06 Apr 2026 13:56:40 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[VP Global Pharmacovigilance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW12482860 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;most commonly mutated&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt; signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&amp;nbsp;&lt;strong&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the CMO, the VP Global Pharmacovigilance has overall responsibility for drug safety activities for early and late phase assets, including furthering the development and implementation of the clinical development strategy. The VP will be accountable for overseeing safety and pharmacovigilance across development and expected global launches and, ultimately, post-marketed products. The VP must possess a strong knowledge of global pharmacovigilance regulations, operational efficiencies, information systems, and best industry practices to effectively solve challenges and facilitate PVG compliance.&lt;/p&gt;
&lt;p&gt;Note this position can be hybrid in our San Diego or South San Francisco locations or fully remote anywhere in the United States.&amp;nbsp;&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Duties and Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide Safety Science leadership for clinical development programs and program teams and integrate safety science strategy with clinical development.&lt;/li&gt;
&lt;li&gt;Represent GPV in communication with health and regulatory authorities.&lt;/li&gt;
&lt;li&gt;Represent GPV at independent Data Safety Monitoring Committee meetings.&lt;/li&gt;
&lt;li&gt;Provide medical oversight of the GPV function including medical review of all cases.&lt;/li&gt;
&lt;li&gt;Provide medical input for maintaining REMS, RMP safety monitoring commitments.&lt;/li&gt;
&lt;li&gt;In collaboration with other members of GPV, create and maintain a signal detection process for Erasca’s products with a clearly defined signal detection strategy for each asset.&lt;/li&gt;
&lt;li&gt;In collaboration with other members of GPV, ensure robust processes are implemented to meet REMS/RMP commitments.&lt;/li&gt;
&lt;li&gt;Overall responsibility for development and implementation of QPV, in collaboration with Quality and GPV Systems.&lt;/li&gt;
&lt;li&gt;Provide periodic benefit-risk assessment reports for internal use.&lt;/li&gt;
&lt;li&gt;Contribute to the preparation of, review, and approve aggregate safety reports required by health authorities.&lt;/li&gt;
&lt;li&gt;Serve as SME author, reviewer, and approver for drug-safety related regulatory reports and clinical study documents (including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), product package labeling, Company Core Safety Information, etc).&lt;/li&gt;
&lt;li&gt;Work with external partners to jointly manage cases, safety reporting, and signal detection across global development for molecule candidates.&lt;/li&gt;
&lt;li&gt;Manage implementation and/or operation of data analytics and data reporting tools to support drug safety compliance and analysis.&lt;/li&gt;
&lt;li&gt;Build and lead highly functioning GPV team including Safety Operations and Safety Science, utilizing internal and external resources.&lt;/li&gt;
&lt;li&gt;Develop operating plans and budgets and allocate resources to ensure budgets, schedules, and performance requirements are met.&lt;/li&gt;
&lt;li&gt;Assess process, systems, and staffing needs to scale for multiple late-stage trials, including oversight of CROs and vendors.&lt;/li&gt;
&lt;li&gt;Develop and maintain relationships across Erasca, particularly in Clinical Development, Clinical Operations, Biometrics, and Regulatory Affairs.&lt;/li&gt;
&lt;li&gt;Perform all duties in keeping with the Company’s core values, policies, and all applicable regulations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Education and Experience:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Doctor of Medicine or x-US equivalent with industry experience in safety science for oncology clinical development required; PharmD or other relevant clinical degree may be considered.&lt;/li&gt;
&lt;li&gt;12 or more years of experience in the biotechnology or pharmaceutical industry with knowledge of GCP, clinical trial conduct, data interpretation, and safety in clinical development. A mix of large and small company experience highly preferred.&lt;/li&gt;
&lt;li&gt;Excellent scientific and clinical and analytical knowledge base, with the ability to assess data and understand safety and medical implications.&lt;/li&gt;
&lt;li&gt;In-depth knowledge of clinical research, including FDA and international regulations, clinical study design, and documentation.&lt;/li&gt;
&lt;li&gt;Experience with early clinical development required; experience in late-stage clinical development and NDA or BLA submission preferred.&lt;/li&gt;
&lt;li&gt;Extensive experience interfacing with US (FDA) and x-US health authorities required. Experience executing clinical trials in China, reporting safety data to China health authorities preferred.&lt;/li&gt;
&lt;li&gt;In depth knowledge of Safety Science and Safety Operations disciplines, with exposure to both internally and externally managed safety systems and databases.&lt;/li&gt;
&lt;li&gt;Direct management experience with proven ability to effectively lead, coach, mentor, and manage others.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to achieve high performance goals and meet deadlines in a fast-paced environment.&lt;/li&gt;
&lt;li&gt;Effective interpersonal, communication and influencing skills, including excellent writing skills; must be a collaborative team player with a can-do attitude and the ability to identify and implement creative solutions to complex technical problems.&lt;/li&gt;
&lt;li&gt;Strong learning orientation, curiosity, and commitment to science and patients.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;wbzude&quot;&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;The&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;anticipated&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;salary&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;range&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;for&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt; this position &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;is&lt;/span&gt; &lt;/span&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;$370,000 to $390,000&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; 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&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;and&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;length&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;of&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;experience&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;within&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;the&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;job,&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;type&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;and&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;length&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;of&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;experience&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;within&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;the&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;industry,&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;education,&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;etc&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;etera.&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt; In addition to base salary, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;the &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;h&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;ired applicant will be eligible to receive &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;an &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;annual bonus and an equity grant at hire and annually in the form of &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;the&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt; option to purchase stock in the future for a specified price.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW233226884 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Along with our casual, collaborative&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; and fun work and the chance to make your mark in our mission to erase cancer, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Erasca&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; offers a comprehensive and competitive benefits package that includes:&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Paid &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Time Off&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, Holiday&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; and Sick &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Leave&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Medical, Dental and Vision Plans&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Short- and Long-Term Disability&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Basic and Voluntary Life/AD&amp;amp;D Coverage&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Flexible Spending Account&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;s&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; (FSA&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;HSA, and Commute&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;)&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, Critical Illness and Accident Coverage&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Pet Insurance, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Employee Assistance Program&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;401(k) Plan with &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Erasca&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; contribution&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, and the opportunity to participate in an &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;E&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;mployee &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;S&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;tock &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;P&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;urchase &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;P&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;rogram.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP SCXW233226884 BCX8&quot; data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vp-global-pharmacovigilance-erasca/69d3bb98c8e81216cd0b8f4a</link><guid isPermaLink="true">http://biotechroles.com/vp-global-pharmacovigilance-erasca/69d3bb98c8e81216cd0b8f4a</guid><pubDate>Mon, 06 Apr 2026 13:56:40 GMT</pubDate><company>Erasca</company><location>San Diego, CA or remote</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Sr Clinical Scientist (contract)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW12482860 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;most commonly mutated&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt; signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Position&amp;nbsp;Summary:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The contract Sr Clinical Scientist will support the clinical aspects of one or more clinical studies and will work closely with cross-functional teams to ensure the successful execution and completion of clinical trials. This is a 12-month contract, renewable, and will require 20-30 hours per week. Some flexibility with working hours will be essential to respond to sites.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Duties and Responsibilities: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Key clinical deliverables include:
&lt;ul&gt;
&lt;li&gt;timely screening of patient enrollment packages from sites&lt;/li&gt;
&lt;li&gt;addressing site inquiries&lt;/li&gt;
&lt;li&gt;data review and cleaning&lt;/li&gt;
&lt;li&gt;medical and scientific input into the development of deliverables required for study activation and conduct (CRFs, SAP, data listings, etc.)&lt;/li&gt;
&lt;li&gt;document development (INDs, Protocols, IBs, applicable regulatory documents, etc.)&lt;/li&gt;
&lt;li&gt;other support and deliverables as needed&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;In collaboration with other functions and stakeholders, develop responses to Health Authorities and IRBs on clinical or medical questions.&lt;/li&gt;
&lt;li&gt;Perform all duties in keeping with the Company’s core values, policies and all applicable regulations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Education and Experience:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Undergraduate degree required; PhD, PharmD, or other relevant advanced degree in a health science field preferred.&lt;/li&gt;
&lt;li&gt;At least 10 years of biotech or pharmaceutical industry experience as a clinical scientist or in a closely related clinical development function.&lt;/li&gt;
&lt;li&gt;Experience in oncology clinical trials required, early development experience a plus.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to evaluate, interpret, and present complex scientific data.&lt;/li&gt;
&lt;li&gt;Knowledge of biostatistics, GCP, and regulatory requirements for clinical studies; extensive experience with data analysis and interpretation; understanding of principles of safety and pharmacovigilance.&lt;/li&gt;
&lt;li&gt;Strong verbal and written communication and presentation skills.&lt;/li&gt;
&lt;li&gt;This person must be flexible, responsive, and self-sufficient.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to meet deadlines in a fast-paced environment; a collaborative team player with a can-do attitude and the ability to identify and implement creative solutions to complex problems.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW233226884 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Along with our casual, collaborative&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; and fun work and the chance to make your mark in our mission to erase cancer, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Erasca&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; offers a comprehensive and competitive benefits package that includes:&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Paid &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Time Off&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, Holiday&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; and Sick &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Leave&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Medical, Dental and Vision Plans&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Short- and Long-Term Disability&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Basic and Voluntary Life/AD&amp;amp;D Coverage&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Flexible Spending Account&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;s&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; (FSA&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;HSA, and Commute&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;)&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, Critical Illness and Accident Coverage&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Pet Insurance, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Employee Assistance Program&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;401(k) Plan with &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Erasca&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; contribution&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, and the opportunity to participate in an &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;E&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;mployee &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;S&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;tock &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;P&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;urchase &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;P&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;rogram.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP SCXW233226884 BCX8&quot; data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:259}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr-clinical-scientist-(contract)-erasca/69d3bb94c8e81216cd0b8f48</link><guid isPermaLink="true">http://biotechroles.com/sr-clinical-scientist-(contract)-erasca/69d3bb94c8e81216cd0b8f48</guid><pubDate>Mon, 06 Apr 2026 13:56:36 GMT</pubDate><company>Erasca</company><location>San Diego, CA</location><salary>$130000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Director, QA GMP Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Director of&amp;nbsp;QA GMP&amp;nbsp;Operations&amp;nbsp;is responsible&amp;nbsp;for&amp;nbsp;management&amp;nbsp;of&amp;nbsp;GMP quality within our&amp;nbsp;external&amp;nbsp;manufacturing operations&amp;nbsp;globally&amp;nbsp;and internal GMP operations&amp;nbsp;for development and commercial&amp;nbsp;programs.&amp;nbsp;The Director will also work closely with internal business stakeholders as well as internal Quality function to deliver outcomes&amp;nbsp;to advance programs within compliance.&amp;nbsp;&amp;nbsp;The Director&amp;nbsp;is responsible for&amp;nbsp;oversight of&amp;nbsp;QA&amp;nbsp;activities&amp;nbsp;and&amp;nbsp;ensuring the quality of deliverables within the role&#39;s purview.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;This is an onsite role based in Waltham, MA.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:true,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Management of&amp;nbsp;external quality operations in support of GMP manufacturing (clinical&amp;nbsp;and&amp;nbsp;commercial) activities.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manage deviations, OOS and OOTs investigations while adhering to cGMP principles and ICH guidelines.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Review batch records, analytical method reports and technical reports including regulatory sections of IND/IMPD and BLA/MAAs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;QA support&amp;nbsp;of&amp;nbsp;Tech Transfer and Process Validation activities.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Disposition of&amp;nbsp;GMP&amp;nbsp;batches&amp;nbsp;and interfacing with the Qualified Person (QP).&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Change&amp;nbsp;management to ensure proper evaluation of&amp;nbsp;manufacturing and testing&amp;nbsp;related changes&amp;nbsp;by&amp;nbsp;Quality, Regulatory, and Subject Matter Experts.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Manage&amp;nbsp;CDMO performance&amp;nbsp;within&amp;nbsp;Quality Agreement expectations&amp;nbsp;and GMP compliance.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Drive&amp;nbsp;continuous&amp;nbsp;improvement&amp;nbsp;and&amp;nbsp;inspection&amp;nbsp;readiness.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate cross functionally to ensure pre-approval inspection and commercial readiness activities&amp;nbsp;are&amp;nbsp;completed&amp;nbsp;at the CDMOs&amp;nbsp;and internally.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Adjudicate on&amp;nbsp;compliance discussions and negotiate any required corrective actions.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Create and foster a culture of collaboration and engagement for advancing quality outcomes and operational excellence.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559685&amp;quot;:630,&amp;quot;335559740&amp;quot;:259,&amp;quot;335559991&amp;quot;:450,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469777462&amp;quot;:[360,630],&amp;quot;469777927&amp;quot;:[0,0],&amp;quot;469777928&amp;quot;:[0,8],&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Minimum of a BA/BS degree&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Minimum of 10+ years of experience&amp;nbsp;in GMP Quality Operations&amp;nbsp;in a&amp;nbsp;&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;clinical late stage and/or commercial biotechnology&amp;nbsp;company&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Leadership experience managing cross-functional teams with an ability to influence teams to prioritize activities and&amp;nbsp;allocate&amp;nbsp;resources&amp;nbsp;without direct authority&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience implementing and&amp;nbsp;utilizing&amp;nbsp;various outsourcing and support models&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with&amp;nbsp;disposition of&amp;nbsp;product batches and interfacing with a&amp;nbsp;Qualified Person&amp;nbsp;(QP)&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent written and oral communication skills, including well-developed presentation skills&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent organizational skills&amp;nbsp;and&amp;nbsp;ability to manage multiple priorities&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong collaboration&amp;nbsp;and interpersonal&amp;nbsp;skills to effectively interact with internal or external stakeholders at all levels in the organization&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;General business management knowledge to assess the impact of project decisions on financial and corporate objectives&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ability to drive&amp;nbsp;timelines, meet firm&amp;nbsp;deadlines,&amp;nbsp;and adapt quickly to changing requirements and priorities&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Embrace Dyne’s core values and culture&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:540,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$188,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$230,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-qa-gmp-operations-dyne-therapeutics/69d3bb92c8e81216cd0b8f46</link><guid isPermaLink="true">http://biotechroles.com/director-qa-gmp-operations-dyne-therapeutics/69d3bb92c8e81216cd0b8f46</guid><pubDate>Mon, 06 Apr 2026 13:56:34 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Manager or Director, Clinical Pharmacology]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW12482860 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer’s&amp;nbsp;&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt;most commonly mutated&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW12482860 BCX8&quot;&gt; signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer.&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Position Summary:&lt;/span&gt;&lt;/strong&gt;&lt;span data-contrast=&quot;none&quot;&gt; &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:160,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Clinical Pharmacology Lead is responsible for providing clinical pharmacology expertise to the cross functional product development team and contributing to clinical development through advancing MIDD (Model Informed Drug Development) initiatives. The core job responsibilities include analysis, interpretation and reporting of clinical PK and PK/PD data, preparation and review clinical pharmacology data for regulatory submissions. In addition to the Clinical Pharmacology Lead responsibilities, this position also serves as DMPK Lead through collaboration with research team on non-clinical DMPK, and translational pharmacology activities.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential Duties and Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Provide clinical pharmacology expertise to the cross functional product development team.&lt;/li&gt;
&lt;li&gt;Conduct data analyses including non-compartmental PK analyses, pop PK, and ER analyses.&lt;/li&gt;
&lt;li&gt;Design and execute clinical pharmacology studies (eg, food effect, DDI, AME/Mass Balance studies).&lt;/li&gt;
&lt;li&gt;Co-author regulatory documents such as protocol, study report, healthy authority briefing book, and IB.&lt;/li&gt;
&lt;li&gt;Collaborate with research team on non-clinical DMPK and translational pharmacology activities.&lt;/li&gt;
&lt;li&gt;Manage external CROs to ensure compliance with planned study protocols, deliverables, internal quality control standards, and timelines.&lt;/li&gt;
&lt;li&gt;Perform all duties in keeping with the Company’s core values, policies and all applicable regulations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Required Education and Experience:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;PhD or PharmD with training in relevant fields such as pharmaceutical sciences, clinical pharmacology, and/or engineering. No prior industrial working experience is required for the Manager level position; a minimum of 7 years of relevant working experience is required for the Director level position.&lt;/li&gt;
&lt;li&gt;Solid knowledge and experience in pharmacokinetics, pharmacodynamics, and drug metabolism.&lt;/li&gt;
&lt;li&gt;Proficient in using WinNonlin, NONMEM, R, and other modeling and simulation software.&lt;/li&gt;
&lt;li&gt;Working experience in preclinical and clinical development of investigational drugs in diverse platforms including small molecules and biologics.&lt;/li&gt;
&lt;li&gt;Proven track record in authoring DMPK and Clinical Pharmacology components of regulatory documents.&lt;/li&gt;
&lt;li&gt;Excellent collaboration, communication, and interpersonal skills.&lt;/li&gt;
&lt;li&gt;Must be a highly flexible, results oriented, independent self-starter who enjoys working in a fast-paced and dynamic, team-oriented environment.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-charstyle=&quot;wbzude&quot;&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;The&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;anticipated&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;salary&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;range&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;for&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt; this position &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;is&lt;/span&gt; &lt;/span&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;$190,000 to $245,000&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;TextRun SCXW198344204 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;.&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;The&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;final&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;salary&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;offered&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;to&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;a&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;successful&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;candidate&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;will&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;be&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW198344204 BCX8&quot;&gt;dependent&lt;/span&gt; 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option to purchase stock in the future for a specified price.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span class=&quot;TextRun SCXW233226884 BCX8&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Along with our casual, collaborative&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; and fun work and the chance to make your mark in our mission to erase cancer, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Erasca&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; offers a comprehensive and competitive benefits package that includes:&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Paid &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;Time Off&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;, Holiday&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt;,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW233226884 BCX8&quot;&gt; 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&lt;p&gt;Erasca, Inc., is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of sex , race, religion, national origin, ancestry, physical or mental disability, protected medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/manager-or-director-clinical-pharmacology-erasca/69d3bb8fc8e81216cd0b8f44</link><guid isPermaLink="true">http://biotechroles.com/manager-or-director-clinical-pharmacology-erasca/69d3bb8fc8e81216cd0b8f44</guid><pubDate>Mon, 06 Apr 2026 13:56:31 GMT</pubDate><company>Erasca</company><location>San Diego, CA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Patient Marketing]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;The Director, Patient Marketing leads the development and execution of patient-focused strategies and initiatives that empower individuals and families affected by Duchenne Muscular Dystrophy. In an active launch environment, this role is pivotal in driving rapid, impactful patient engagement programs that support successful market entry and adoption. It blends strategic vision with hands-on execution, ensuring Dyne delivers meaningful engagement, education, and advocacy programs aligned with our mission and brand objectives. You operate with agility to meet critical launch milestones, leveraging innovative technologies and omni-channel tactics to maximize patient reach. Collaboration across Marketing, Patient Advocacy, Medical Affairs, Market Access, and Field teams is essential to create a cohesive patient experience from awareness through treatment, while continuously optimizing based on real-time insights and launch KPIs.&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;This role is based in Waltham, MA&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt; &lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Patient-Centric Strategy &amp;amp; Execution&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and implement comprehensive patient engagement strategies across Dyne’s therapeutic areas, grounded in deep understanding of the patient journey and unmet needs.&lt;/li&gt;
&lt;li&gt;Lead the development and rapid execution of launch-focused DSE and branded patient campaigns, ensuring alignment with brand objectives and critical timelines.&lt;/li&gt;
&lt;li&gt;Design and execute omni-channel campaigns (digital, social, email, events) to educate and empower patients and caregivers.&lt;/li&gt;
&lt;li&gt;Design and execute Patient Support Services branding and field resource pull through.&lt;/li&gt;
&lt;li&gt;Partner with creative agencies to develop patient-facing materials, websites, and educational resources.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Community Engagement &amp;amp; Advocacy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Build and manage patient ambassador programs, including recruitment, training, and event participation.&lt;/li&gt;
&lt;li&gt;Collaborate with advocacy organizations and patient advisory boards to ensure authentic representation and feedback.&lt;/li&gt;
&lt;li&gt;Support national and regional advocacy events, conferences, and community programs, including occasional evenings/weekends.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Education &amp;amp; Compliance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all patient marketing initiatives adhere to FDA regulations, privacy standards, and Dyne’s compliance policies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Insights &amp;amp; Innovation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Leverage market research and patient insights to inform strategy and optimize engagement tactics.&lt;/li&gt;
&lt;li&gt;Identify emerging trends and technologies to enhance patient experience and access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross-Functional Collaboration&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Work closely with US Marketing Brand Lead and Patient Advocacy teams to align patient initiatives with overall brand strategy.&lt;/li&gt;
&lt;li&gt;Coordinate with Medical Affairs and Market Access to ensure integrated support for patients and caregivers.&lt;/li&gt;
&lt;li&gt;Represent marketing function as the PRC reviewer for all promotional material.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;E&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;d&lt;/span&gt;&lt;span data-ccp-charstyle=&quot;Strong&quot;&gt;ucation, Knowledge &amp;amp; Skill Requirements&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:0,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;BA/BS degree required; advanced degree (MBA, MPH) preferred&lt;/li&gt;
&lt;li&gt;10+ years in biopharma marketing, with at least 5 years focused on patient engagement or advocacy&lt;/li&gt;
&lt;li&gt;Proven track record in rare disease or specialty markets; neuromuscular experience is a plus&lt;/li&gt;
&lt;li&gt;Strong understanding of patient literacy and ability to translate complex science into accessible language&lt;/li&gt;
&lt;li&gt;Excellent communication and cultural competency skills&lt;/li&gt;
&lt;li&gt;Ability to lead cross-functional teams and manage agency partners&lt;/li&gt;
&lt;li&gt;Familiarity with FDA regulations and compliance requirements&lt;/li&gt;
&lt;li&gt;Experience in a small, rapidly growing biotech with the ability to operate and maneuver in a start-up environment while keeping a solutions-oriented mentality&lt;/li&gt;
&lt;li&gt;Demonstrated strength in digital marketing, media strategy, and leveraging innovative technologies (including AI-driven solutions) to enhance patient engagement and education.&lt;/li&gt;
&lt;li&gt;Motivated by an unwavering commitment to patients&lt;/li&gt;
&lt;li&gt;Ability to travel up to 25%&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-BJ&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$188,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$230,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-patient-marketing-dyne-therapeutics/69d3bb8ec8e81216cd0b8f42</link><guid isPermaLink="true">http://biotechroles.com/director-patient-marketing-dyne-therapeutics/69d3bb8ec8e81216cd0b8f42</guid><pubDate>Mon, 06 Apr 2026 13:56:30 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Executive Director, Investor Relations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;The Organization&lt;/h2&gt;
&lt;p&gt;What&#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).&lt;/p&gt;
&lt;p&gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).&lt;/p&gt;
&lt;p&gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;The Perfect Addition to Our Team&lt;/h2&gt;
&lt;p&gt;You are intellectually curious and can bring new ideas and perspectives to lead the development, implementation, and management of our investor relations function. You follow up and follow through, efficiently connecting problems with solutions. You work successfully in a fast-paced team environment and have strong interpersonal skills, effectively building working relationships with leaders across the Company and with outside parties.&lt;/p&gt;
&lt;h2&gt;The Opportunity&lt;/h2&gt;
&lt;p&gt;The Executive Director, Investor Relations will be responsible for developing and executing a comprehensive investor relations strategy that enhances Entrada’s visibility, credibility, and positioning within the financial community and broader stakeholder landscape. Reporting to the Chief Financial Officer, the ideal candidate will combine deep investor relations and financial expertise with strong scientific and clinical fluency to build investor confidence, drive awareness, and support long-term shareholder value creation for a NASDAQ-listed biotechnology company with an expanding portfolio of clinical-stage programs.&lt;/p&gt;
&lt;h2&gt;Responsibilities&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Drive the strategic direction, planning, and execution of the investor relations function, including financial communications, while building and continuously strengthening a best-in-class investor relations program.&lt;/li&gt;
&lt;li&gt;Serve as a trusted advisor to senior leadership by providing insight and guidance on investor messaging, communications effectiveness, market dynamics, and investor sentiment.&lt;/li&gt;
&lt;li&gt;Act as the primary point of contact to the investment community, responding to external inquiries in an accurate, appropriate, and timely manner; establish and maintain strong relationships with biotechnology-focused buy-side and sell-side analysts and institutional investors.&lt;/li&gt;
&lt;li&gt;Develop and maintain proactive engagement with investors and analysts to clearly communicate the Company’s long-term vision, clinical and platform strategy, differentiation, opportunity, risk factors, and key milestones.&lt;/li&gt;
&lt;li&gt;Lead the development and coordination of financial and investor communications—including earnings releases, investor webcasts, investor presentations, Company corporate presentations and investor relations section of the Company website&lt;/li&gt;
&lt;li&gt;Coordinate cross-functionally with Finance and Legal to support the timely and compliant execution of external financial disclosures and investor communications including periodic reports (Form 10-K and Form 10-Q), annual proxy statements and other reports.&lt;/li&gt;
&lt;li&gt;Lead the Company’s participation in investment community events, including investor conferences, non-deal roadshows, analyst days, and targeted investor meetings.&lt;/li&gt;
&lt;li&gt;Develop, track, and report key investor relations metrics in our Irwin investor relations system to assess program effectiveness and inform continuous improvement.&lt;/li&gt;
&lt;li&gt;Monitor published research analyst reports covering the Company and analyze biopharmaceutical industry trends, investor perceptions, and competitor communications to inform strategic positioning and messaging.&lt;/li&gt;
&lt;li&gt;Support capital markets activities, including potential financings and strategic transactions, in close partnership with the CFO and senior leadership.&lt;/li&gt;
&lt;li&gt;Partner closely with the Chief Corporate Affairs Officer to ensure alignment with the broader corporate communications strategy and Entrada brand.&lt;/li&gt;
&lt;li&gt;Manage external agencies and vendors, as needed, ensuring high-quality deliverables and disciplined management of external spend.&lt;/li&gt;
&lt;li&gt;Ensure all investor communications and activities fully comply with SEC regulations and disclosure requirements, including Regulation FD and NASDAQ listing standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;The Necessities&lt;/h2&gt;
&lt;p&gt;At Entrada, our passion for science, our devotion to patients and our values drives our&amp;nbsp;behavior:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Humanity&lt;/strong&gt; - We genuinely care about patients and about one another.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Tenacity&lt;/strong&gt; - We are relentless and persistent in the pursuit of developing therapies&amp;nbsp;for patients.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Creativity&lt;/strong&gt; - We are creative problem solvers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Collaboration&lt;/strong&gt; - We are more than the sum of our parts.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Curiosity&lt;/strong&gt; - We have a growth mindset and push conventional thought and theory.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;To thrive on our team, you will need to come with:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree required; advanced degree (PhD, MD, MBA, or MS in life sciences, biotechnology, or finance-related discipline) preferred.&lt;/li&gt;
&lt;li&gt;10+ years of progressive experience in investor relations within the biotechnology or pharmaceutical industry.&lt;/li&gt;
&lt;li&gt;Experience supporting investor relations for a publicly traded biotechnology or pharmaceutical company, preferably NASDAQ-listed.&lt;/li&gt;
&lt;li&gt;Experience in a clinical-stage or pre-commercial biotechnology environment strongly preferred.&lt;/li&gt;
&lt;li&gt;Established relationships within the biotechnology buy-side and sell-side community strongly preferred.&lt;/li&gt;
&lt;li&gt;Proven ability to develop and execute investor relations strategies that effectively reach and influence target audiences.&lt;/li&gt;
&lt;li&gt;Strong financial acumen and financial modeling familiarity, with the ability to clearly communicate complex financial and clinical information to diverse external stakeholders.&lt;/li&gt;
&lt;li&gt;Develop clear and compelling PowerPoint presentations for earnings calls, investor meetings, and board discussions that translate complex financial and strategic information into concise, visually compelling narratives.&lt;/li&gt;
&lt;li&gt;Demonstrated experience supporting equity offerings, capital markets transactions, or other strategic financings preferred.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to lead the use of investor relations software solutions to support investor engagement, shareholder monitoring and analytics, Irwin experience preferred.&lt;/li&gt;
&lt;li&gt;Excellent written and verbal communication skills, with exceptional attention to detail.&lt;/li&gt;
&lt;li&gt;Highly self-directed with exceptional project management and organizational skills, and the ability to prioritize multiple high-impact workstreams and deadlines.&lt;/li&gt;
&lt;li&gt;Experience building, managing, and scaling investor relations capabilities across internal teams and external partners (e.g., agencies, vendors, consultants).&lt;/li&gt;
&lt;li&gt;Demonstrated ability to work collaboratively and influence across functions and with senior executives to support the achievement of business objectives.&lt;/li&gt;
&lt;li&gt;Deep understanding of the drug development lifecycle and the regulatory and disclosure environment for biopharmaceutical companies, including SEC and Regulation FD requirements.&lt;/li&gt;
&lt;li&gt;Experience preparing senior executives and Board members for investor engagement and earnings communications preferred.&lt;/li&gt;
&lt;li&gt;Ability to travel approximately 25% as required to support investor engagement and key industry events.&lt;/li&gt;
&lt;li&gt;This is a US based remote position, with preference given to local New England based candidates who can be in office 1 day per week to the Entrada Therapeutics Headquarters located in Boston, MA.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support&lt;/h2&gt;
&lt;p&gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.&lt;/p&gt;
&lt;p&gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;— Kerry Robert, SVP of People&lt;/p&gt;
&lt;p&gt;The salary for this opportunity ranges from $292,000-$335,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range.&lt;span style=&quot;color: rgb(255, 255, 255);&quot;&gt;#LI-GG1 #LI-Remote&lt;/span&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;Equal Opportunity Employer&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Third Party Staffing Agencies&lt;/h2&gt;
&lt;p&gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.&lt;/p&gt;
&lt;h2&gt;Privacy Statement&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics, Inc. (the “&lt;strong&gt;Entrada&lt;/strong&gt;,” “&lt;strong&gt;we,&lt;/strong&gt;” “&lt;strong&gt;us,&lt;/strong&gt;” or “&lt;strong&gt;our&lt;/strong&gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement &lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://www.entradatx.com/privacy-notice&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;here &lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;to understand how and when your data is being used.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/executive-director-investor-relations-entrada-therapeutics/69d3bb8bc8e81216cd0b8f40</link><guid isPermaLink="true">http://biotechroles.com/executive-director-investor-relations-entrada-therapeutics/69d3bb8bc8e81216cd0b8f40</guid><pubDate>Mon, 06 Apr 2026 13:56:27 GMT</pubDate><company>Entrada Therapeutics</company><location>Boston, MA</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Director of Training]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Director of Training leads the vision, strategy, and execution of Dyne’s training programs, ensuring all field-facing teams are equipped with the knowledge, skills, and capabilities needed to excel. This role oversees the development, integration, and continuous enhancement of training frameworks, curricula, digital learning assets, and capability-building initiatives that support both initial onboarding and ongoing professional development across all functions required for Account Management.&lt;/p&gt;
&lt;p&gt;The Director provides strategic oversight of vendors and training partners to ensure consistency, quality, and alignment across the commercial field. Working cross-functionally with Commercial Leadership, Medical Leadership, Compliance, Marketing, HR, and Field Leadership, this role translates strategic business priorities into high-impact learning solutions that elevate field performance and drive commercial excellence.&lt;/p&gt;
&lt;p&gt;This leader guides the development of modern learning systems and processes, identifying capability gaps through data, field insights, and performance metrics. The Director plays a key role in supporting product launches, enhancing field readiness, and strengthening leadership capabilities throughout the organization. Through innovative training strategies and disciplined execution, this role ensures Dyne’s field teams are prepared to deliver exceptional customer experiences and achieve business goals.&lt;/p&gt;
&lt;p&gt;This role is located at our office in Waltham, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Coordination of the new hire training and ongoing skills/knowledge training across all cross functional field-facing facing teams.&lt;/li&gt;
&lt;li&gt;Ensure that the training curriculum and on-boarding processes meet the current and emerging needs of the field-facing employees.&lt;/li&gt;
&lt;li&gt;Oversee the development, updating, and use of all training modules that are appropriate for field employees.&lt;/li&gt;
&lt;li&gt;Create training materials that enhance the learning process; including study guides, home study materials, assessments, frequently asked questions, competitive overviews, etc.&lt;/li&gt;
&lt;li&gt;Lead field employee training across all settings which include 1:1 meetings, conference calls, live classroom, etc.&lt;/li&gt;
&lt;li&gt;Gather and analyze data from direct field observations, focus groups, and other methods to identify potential training gaps and suggest areas for improvement that will enhance performance and achieve Dyne’s goals.&lt;/li&gt;
&lt;li&gt;Manage the training of field employees on cross functional business rules (ie. Veeva CRM, Concur, Patient Services data/CRM, etc.).&lt;/li&gt;
&lt;li&gt;Work closely with cross functional Leadership to ensure that the development of training initiatives is designed to strengthen the&amp;nbsp;pull through of Dyne’s Field Leader capabilities and competencies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional Collaboration&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support leadership in leading content development workstreams across field meetings from an objective, content, and agenda standpoint. &amp;nbsp;&lt;/li&gt;
&lt;li&gt;Work with the cross-functional teams to gather feedback on training needs and development of necessary meeting workshops to meet those needs.&lt;/li&gt;
&lt;li&gt;Work with account leadership to facilitate management-level “train-the-trainer” sessions.&lt;/li&gt;
&lt;li&gt;Assist field teams and account leadership with field coaching, recruiting, and interviewing as needed.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Systems and Employee On-going Personal Development&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Create and manage the Learning Management System (LMS), and all vendors related to field training and development resources.&lt;/li&gt;
&lt;li&gt;Work with corporate compliance and/or our compliance agency partner to ensure field employees are trained and up to date on policies and procedures that affect their respective functional areas.&lt;/li&gt;
&lt;li&gt;Other duties as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education, Experience, &amp;amp; Skills:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree (science or business preferred) or equivalent combination of relevant education and applicable job experience may be considered. MBA preferred.&lt;/li&gt;
&lt;li&gt;A minimum of 12 years’ progressively responsible experience in pharmaceutical or medical sales and training, with a minimum of 6 years in a training or field leadership role.&lt;/li&gt;
&lt;li&gt;A focus on neuroscience and Rare Disease preferred.&lt;/li&gt;
&lt;li&gt;Requires prior pharmaceutical field experience, first-line pharmaceutical/biotech field management experience, and vendor and contract management.&lt;/li&gt;
&lt;li&gt;Experience with product launches and Account Management experience is highly desired.&lt;/li&gt;
&lt;li&gt;Demonstrated leadership and teaching/facilitation ability.&lt;/li&gt;
&lt;li&gt;Proven ability in creating effective training materials.&lt;/li&gt;
&lt;li&gt;Proven application of adult learning principles.&lt;/li&gt;
&lt;li&gt;The ability to successfully navigate challenging situations and conversations with diplomacy, respect and flexibility when required.&lt;/li&gt;
&lt;li&gt;Experience in launching a product in a rare disease&lt;/li&gt;
&lt;li&gt;Excellent interpersonal and communication skills.&lt;/li&gt;
&lt;li&gt;Ability to complete verbal and written evaluations of others.&lt;/li&gt;
&lt;li&gt;Organization, initiative, and self-motivation.&lt;/li&gt;
&lt;li&gt;Project and vendor management experience.&lt;/li&gt;
&lt;li&gt;Professionalism, integrity, and the ability to comply with strict policy, work in a highly regulated environment and maintain confidential information and data.&lt;/li&gt;
&lt;li&gt;Skilled at negotiating with business partners or management and influencing senior level leaders regarding matters of significance to the organization.&lt;/li&gt;
&lt;li&gt;Proficient at creating and communicating a clear vision among team members effectively aligning resources and activities to achieve functional area and/or organizational goals.&lt;/li&gt;
&lt;li&gt;Ability to travel up to 30% overnight.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$188,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$230,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-of-training-dyne-therapeutics/69d3bb8bc8e81216cd0b8f3f</link><guid isPermaLink="true">http://biotechroles.com/director-of-training-dyne-therapeutics/69d3bb8bc8e81216cd0b8f3f</guid><pubDate>Mon, 06 Apr 2026 13:56:26 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[VP,  Chief Information Security Officer (CISO)]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Vice President, Chief Information Security Officer (CISO)&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Location: SF Bay Area or Austin, TX&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Position Summary&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Vice President, Chief Information Security Officer (CISO) is responsible for defining, building, and operating the company’s global cybersecurity program as a core business function. This leader will own the end-to-end security strategy, risk posture, and investment roadmap to protect the organization’s technology platforms, intellectual property, and sensitive clinical and patient data.&lt;/p&gt;
&lt;p&gt;This role combines technical expertise with executive leadership, requiring deep knowledge in cybersecurity architecture, cloud security, and AI-driven platforms, with the ability to embed security directly into systems, data pipelines, and product development lifecycles. The CISO will translate complex cybersecurity risks into clear business terms, enabling informed decision-making at the executive and Board levels.&lt;/p&gt;
&lt;p&gt;This role will champion the use of AI-assisted security operations, intelligent automation, and advanced analytics to transform how cybersecurity is delivered across the enterprise. The CISO will drive the adoption of modern AI-enabled security tooling and architectures to improve detection fidelity, accelerate response times, and increase operational efficiency—while reducing noise, manual effort, and overall risk exposure.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Own and operate the end-to-end enterprise cybersecurity program, including strategy, architecture, operations, governance, and compliance.&lt;/li&gt;
&lt;li&gt;Establish a multi-year security roadmap aligned with business priorities, technology evolution, and regulatory requirements.&lt;/li&gt;
&lt;li&gt;Drive program maturity, ensuring continuous improvement across all domains of cybersecurity. Ensure security is integrated into enterprise planning, product development, and operational execution.&lt;/li&gt;
&lt;li&gt;Develop and maintain a risk-based cybersecurity investment framework to prioritize initiatives and allocate resources effectively.&lt;/li&gt;
&lt;li&gt;Lead architectural decisions across: identity and access systems, data protection and encryption strategies, network and zero-trust architectures, secure platform design for clinical and genomic systems and for agentic workflows.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Present regular updates to executive leadership on cyber risk posture, threat landscape, program maturity, incident readiness and response. Lead Board-level discussions on cybersecurity strategy, risk tolerance, and investment priorities.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Define and execute a strategy for AI-assisted cybersecurity operations, leveraging machine learning, automation, and advanced analytics to enhance detection and response capabilities.&lt;/li&gt;
&lt;li&gt;Build a highly automated, intelligence-driven SecOps function that minimizes manual intervention and improves speed and accuracy of threat identification and remediation.&lt;/li&gt;
&lt;li&gt;Drive adoption and optimization of modern security platforms, including: Next-generation SIEM/SOAR, CNAPP / CSPM, EDR/XDR, Identity intelligence platforms. Leverage AI/ML to improve signal-to-noise ratio in security alerts, detect anomalous behavior across security domains, and&amp;nbsp; automate triage, investigation, and response workflows&lt;/li&gt;
&lt;li&gt;Integrate AI capabilities into threat intelligence, vulnerability management, and risk analysis processes. Continuously evaluate emerging AI security tools and capabilities, balancing innovation, risk, and operational value.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Oversee enterprise security operations including monitoring, detection, and response.&amp;nbsp; Lead incident response and crisis management, ensuring rapid containment and recovery.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Own compliance strategy across frameworks including SOC 2, ISO 27001, and NIST.&amp;nbsp; Ensure alignment with healthcare and global data protection regulations (HIPAA, GDPR, CCPA).&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;20+ years of progressive cybersecurity leadership experience.&lt;/li&gt;
&lt;li&gt;Bachelor’s degree in Computer Science, Cybersecurity, Engineering, or a related technical field required.&amp;nbsp; Advanced degree (Master’s or PhD) is strongly preferred.&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Proven experience owning and operating an enterprise-wide cybersecurity program, including strategy, execution, and governance. Strong track record of building modern, engineering-led security organizations in cloud-native environments.&lt;/li&gt;
&lt;li&gt;Comfortable operating in high-growth, high-complexity environments. Experience building and scaling security programs in cloud-native, high-growth environments.&lt;/li&gt;
&lt;li&gt;Deep, practical expertise across: Cloud security architecture (CSPM, CNAPP, workload security), Identity and access management (IAM, SSO, zero trust), Detection &amp;amp; response (SIEM, SOAR, EDR/XDR), Application and API security, Data security, encryption, and DLP, DevSecOps and secure SDLC practice&lt;/li&gt;
&lt;li&gt;Strong balance of: technical depth (architecture, cloud, security engineering), and strategic leadership (program ownership, executive influence)&lt;/li&gt;
&lt;li&gt;Hands-on experience implementing or operating AI-assisted security tools and automation frameworks.&lt;/li&gt;
&lt;li&gt;Demonstrated success engaging with executive leadership and Boards on cybersecurity risk and investment decisions.&lt;/li&gt;
&lt;li&gt;Experience developing risk-based investment strategies and prioritization frameworks.&amp;nbsp; Ability to translate cybersecurity complexities into executive and Board-level communications.&lt;/li&gt;
&lt;li&gt;Exceptional executive communication and storytelling skills.&lt;/li&gt;
&lt;li&gt;Proven ability to influence senior leadership and drive alignment on complex risk and investment decisions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Compensation &amp;amp; Total Rewards&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;This range reflects a good-faith estimate of the base pay we reasonably&amp;nbsp;expect to offer at the time of&amp;nbsp; hire.&amp;nbsp;Final compensation will vary based on experience, qualifications, and internal equity considerations.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;This position&amp;nbsp;is also eligible for additional compensation and benefits through&amp;nbsp;Natera’s robust Total Rewards program, including:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Annual performance incentive bonus&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Long-term equity awards&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Comprehensive health benefits (medical, dental, vision)&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;401(k) with company match&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Generous paid time off and company holidays&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Additional wellness and work-life benefits&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Compensation Range &lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$257,600&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$322,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/vp-chief-information-security-officer-(ciso)-natera/69d3bb89c8e81216cd0b8f38</link><guid isPermaLink="true">http://biotechroles.com/vp-chief-information-security-officer-(ciso)-natera/69d3bb89c8e81216cd0b8f38</guid><pubDate>Mon, 06 Apr 2026 13:56:24 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$220000-350000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Drug Substance Development & Manufacturing]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;The Organization&lt;/h2&gt;
&lt;p&gt;What&#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).&lt;/p&gt;
&lt;p&gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).&lt;/p&gt;
&lt;p&gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;The Perfect Addition to Our Team&lt;/h2&gt;
&lt;p&gt;You are a motivated, resourceful, and enthusiastic Drug Substance Development &amp;amp; Manufacturing expert excited to support the company at a critical stage in its growth trajectory. You excel at peptide and/or oligonucleotide late-stage process development, GMP manufacturing and supply chain of drug substances. You thrive when performing these activities with minimal supervision in a collaborative matrix environment. At Entrada, you will not be siloed, but rather expected to interact across different functional groups, including Chemistry, Analytical, Drug Product, Quality, and CDMOs. Your ability and desire to thrive in a nimble, fast-paced results-driven environment will set you up for success.&lt;/p&gt;
&lt;h2&gt;The Opportunity&lt;/h2&gt;
&lt;p&gt;The Associate Director of Drug Substance Development and Manufacturing will lead and manage late-stage drug substance development for Entrada’s novel pipeline programs. This role will be instrumental in supporting development activities for clinical and commercial batches and ensuring validation parameters for manufacturing batches.&lt;/p&gt;
&lt;h2&gt;Responsibilities&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Facilitate timely execution, disposition, and release of intermediate/drug substance batches through detailed technical review of master batch records, executed batch records and other cGMP documentation.&lt;/li&gt;
&lt;li&gt;Partner with internal and external Quality Assurance, Quality Control and Technical Operations teams to execute late-stage development activities such as Process Characterization and Process Performance Qualifications.&lt;/li&gt;
&lt;li&gt;Act as a person-in-plant for smooth execution of critical manufacturing activities for clinical and commercial batches.&lt;/li&gt;
&lt;li&gt;Conduct risk assessments and develop mitigation strategies for manufacturing-related issues.&lt;/li&gt;
&lt;li&gt;Identify and resolve manufacturing issues and escalate appropriately to internal and/or joint governance if required.&lt;/li&gt;
&lt;li&gt;Implement and manage the Continuous Process Verification (CPV) program to ensure manufacturing process remain in a constant state of control and meet validated parameters.&lt;/li&gt;
&lt;li&gt;Author/review change controls to introduce process improvements through the lifecycle of programs from Phase 1 through Phase 3/validation and commercialization&lt;/li&gt;
&lt;li&gt;Work closely with other internal functions including chemistry, analytical, quality control, quality assurance, DP, and regulatory affairs to ensure programs are effectively supported and high-quality standard maintained.&lt;/li&gt;
&lt;li&gt;Partner with Entrada team for CDMO due diligence during new CDMO selection to vet capabilities, risks and investments required.&lt;/li&gt;
&lt;li&gt;Author/review related sections in regulatory filing documents (IND, IMPD, NDA, BLA, MAA, etc.).&lt;/li&gt;
&lt;li&gt;Other tasks as assigned or as required for a given program.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;The Necessities&lt;/h2&gt;
&lt;p&gt;At Entrada, our passion for science, our devotion to patients and our values drives our&amp;nbsp;behavior:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Humanity&lt;/strong&gt; - We genuinely care about patients and about one another.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Tenacity&lt;/strong&gt; - We are relentless and persistent in the pursuit of developing therapies&amp;nbsp;for patients.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Creativity&lt;/strong&gt; - We are creative problem solvers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Collaboration&lt;/strong&gt; - We are more than the sum of our parts.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Curiosity&lt;/strong&gt; - We have a growth mindset and push conventional thought and theory.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;To thrive on our team, you will need to come with:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Master’s or suitable advanced degree in organic chemistry or other scientific or engineering discipline with 8+ years of related experience in pharmaceutical industry.&lt;/li&gt;
&lt;li&gt;Demonstrated proficiency in process development, tech transfer, scale-up, GMP manufacturing DS for clinical, and commercial supplies.&lt;/li&gt;
&lt;li&gt;Proficient in managing activities and resolving manufacturing challenges at CDMOs during routine cGMP manufacturing and process validations.&lt;/li&gt;
&lt;li&gt;Experienced in onboarding/managing/collaborating with CDMOs, raw material suppliers, testing partners, and other production partners.&lt;/li&gt;
&lt;li&gt;Hands-on experience in SPPS/SPOS, downstream purification and lyophilization is highly preferred.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to develop and maintain production timelines and budgets.&lt;/li&gt;
&lt;li&gt;Up-to-date with industry practices and regulations (e.g. GxP, ISO, ICH, etc.) across multiple health authorities (e.g. FDA and EMA).&lt;/li&gt;
&lt;li&gt;Ability to interpret and relate Quality standards for implementation and review.&lt;/li&gt;
&lt;li&gt;Strong project management, interpersonal, communication, and problem-solving skills preferable.&lt;/li&gt;
&lt;li&gt;Ability to communicate clearly and professionally both in writing and verbally.&lt;/li&gt;
&lt;li&gt;Ability to travel up to 20% (domestic and international).&lt;/li&gt;
&lt;li&gt;This is a US based remote position with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support&lt;/h2&gt;
&lt;p&gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.&lt;/p&gt;
&lt;p&gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;— Kerry Robert, SVP of People&lt;/p&gt;
&lt;p&gt;The salary for this opportunity ranges from $172,000-$202,000 The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. &lt;span style=&quot;color: rgb(255, 255, 255);&quot;&gt;#LI-JF1 #LI-Remote&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;Equal Opportunity Employer&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Third Party Staffing Agencies&lt;/h2&gt;
&lt;p&gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.&lt;/p&gt;
&lt;h2&gt;Privacy Statement&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics, Inc. (the “&lt;strong&gt;Entrada&lt;/strong&gt;,” “&lt;strong&gt;we,&lt;/strong&gt;” “&lt;strong&gt;us,&lt;/strong&gt;” or “&lt;strong&gt;our&lt;/strong&gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement &lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://www.entradatx.com/privacy-notice&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;here &lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;to understand how and when your data is being used.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-drug-substance-development-and-manufacturing-entrada-therapeutics/69d3bb87c8e81216cd0b8f32</link><guid isPermaLink="true">http://biotechroles.com/associate-director-drug-substance-development-and-manufacturing-entrada-therapeutics/69d3bb87c8e81216cd0b8f32</guid><pubDate>Mon, 06 Apr 2026 13:56:23 GMT</pubDate><company>Entrada Therapeutics</company><location>Boston, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Imaging Biomarkers]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;The Director of Imaging Biomarkers lead&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;the development and execution of innovative imaging strategies across Dyne’s therapeutic programs.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;This&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;pivotal&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;role&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;will&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;ensur&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;e&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;that imaging biomarker strategies are scientifically rigorous, clinically relevant, and condu&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;cive to robust therapeutic development. The person in this&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;role focuses on enhancing the understanding of disease&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;mechanisms&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;patient populations,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;evaluating therapeutic efficacy, and supporting clinical&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;trial&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;designs through innovative imaging approaches.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;This role is cri&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;tical to linking early phase research to clinical development,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;providing&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;essential insights that drive decision making.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;The person in this role&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;leverages&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;their&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;in various imaging modalities to develop novel biomarker applications that assess therapeutic efficacy, drive patient-centric trial designs, and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;facilitate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;regulatory approval processes.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;This role combines scientific depth with strategic vision, driving the discovery, validation, and application of advanced imaging modalities to enable precision medicine and accelerate drug development. The&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;person in this role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;serve&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;as a trusted expert and collaborative leader, fostering innovation and ensuring scientific rigor in both preclinical and clinical settings&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;.&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559740&amp;quot;:276,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;This role is based in Waltham, MA.&amp;nbsp; &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Collaborate with cross-&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;functional&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;teams including clinical development, biostatistics, and regulatory affairs to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ensure&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;that imaging biomarkers are effectively integrated into clinical trial protocols&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Enable the delivery of high-quality data supporting both internal decision making and external communications with stakeholders, including regulatory authorities&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Define and execute the imaging biomarker strategy aligned with clinical and translational objectives&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serve as the subject matter expert for imaging biomarkers across&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;pre-clinical&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and clinical programs&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead the&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;development&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, validation, and qualification of imaging biomarkers for disease characterization, patient stratification, and pharmacodynamic assessment&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Partner with Clinical Development, Translational Biomarkers, Biostatistics, Data Management and Regulatory teams to integrate imaging biomarkers into Dyne clinical trials&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Evaluate and implement&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;cutting-edge&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;imaging technologies (e.g., MRI, PET, CT, ultrasound, optical imaging)&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ensure compliance with regulatory standards for imaging biomarker development and qualification&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Collaborate with external imaging CROs, academic institutions, and technology vendors to deploy imaging biomarkers into Dyne clinical trials&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Oversee vendor selection and budget management for imaging-related activities&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Manage imaging biomarker operations in clinical studies including protocol development, support site training, and data quality assurance&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Foster a culture of innovation and scientific rigor&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skill&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;Requirements&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ph.D., M.D., or equivalent in Biomedical&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Engineering,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Medical Physics&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, Radiology, or related&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;scientific disciplines&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;10+ years of experience in imaging biomarker development within pharma, biotech, or academic research&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Blend of technical knowledge, scientific acumen, and strategic vision to foster collaborations with academic institutions, industry partners, and clinical&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;experts&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Deep scientific&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;in at least one major imaging modality&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;(&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;preferably MRI&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;)&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and a strong understanding of image acquisition, processing, and analysis&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Proven&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;track record&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;in applying imaging biomarkers in clinical trials and regulatory submissions&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Expertise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;in&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;quantitative imaging method&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ologies&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, image analysis software, and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;imaging&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;data interpretation&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Strong leadership and project management skills with ability to influence across functions&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Excellent communication and presentation skills&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Preferred Experience:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559739&amp;quot;:120,&amp;quot;335559740&amp;quot;:360,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Familiarity with AI/ML approaches for image analysis&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to improve efficiency, accuracy, and uncover complex patterns in imaging data&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Understanding and implementation of digital biomarkers using wearables, sensors, or other digital health technologies&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Knowledge of disease-specific imaging biomarkers (&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;e.g., neurology&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, cardiology&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;or neuromuscular&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;)&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$196,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$240,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-imaging-biomarkers-dyne-therapeutics/69d3bb86c8e81216cd0b8f31</link><guid isPermaLink="true">http://biotechroles.com/director-imaging-biomarkers-dyne-therapeutics/69d3bb86c8e81216cd0b8f31</guid><pubDate>Mon, 06 Apr 2026 13:56:21 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Staff Salesforce Architect, Sales & Service Cloud]]></title><description><![CDATA[&lt;h2&gt;&lt;strong&gt;The Opportunity&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;We are seeking an exceptional Staff Salesforce Architect to lead the design and evolution of our Sales Cloud and Service Cloud platforms. In this strategic role, you&#39;ll own the technical architecture, govern platform standards, and drive transformation initiatives that impact thousands of users across go-to-market and customer success functions. You&#39;ll be our technical authority on Salesforce best practices, scalability, and innovation.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;What You&#39;ll Do&lt;/strong&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Platform Architecture &amp;amp; Governance (35%)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Design end-to-end solutions integrating Sales and Service Cloud; establish metadata frameworks, custom objects, and data models for scalability&lt;/p&gt;
&lt;p&gt;Define platform standards, coding guidelines, and integration patterns; ensure compliance with Salesforce Governor Limits and platform constraints&lt;/p&gt;
&lt;p&gt;Lead org hygiene initiatives, technical debt reduction, and long-term roadmap evolution&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Solution Design &amp;amp; Implementation (40%&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Architect complex workflows, automation, omni-channel, and AI-driven capabilities (Einstein Analytics, Einstein Copilot)&lt;/p&gt;
&lt;p&gt;Design secure integrations (MuleSoft, AWS, REST/OAuth) between Salesforce and enterprise systems&lt;/p&gt;
&lt;p&gt;Lead implementation of key initiatives (data cloud, person accounts, skill-based routing) from design through production&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Mentorship &amp;amp; Technical Leadership (25%&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Guide Salesforce developers and admins; conduct design reviews and architecture validation&lt;/p&gt;
&lt;p&gt;Partner with product, business systems, and engineering leadership on roadmap alignment&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;What You&#39;ll Bring&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Required:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;10+ years of Salesforce architecture and implementation experience, with deep expertise in Sales and Service Cloud&lt;/li&gt;
&lt;li&gt;Expert-level knowledge of Apex, Lightning Web Components (LWC), Flows, and SOQL optimization&lt;/li&gt;
&lt;li&gt;Proven ability to design secure, scalable integrations (REST APIs, OAuth, SSO, MuleSoft)&lt;/li&gt;
&lt;li&gt;Experience architecting multi-org, multi-cloud solutions in enterprise environments&lt;/li&gt;
&lt;li&gt;Strong knowledge of Salesforce Governor Limits, performance optimization, and data modeling&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Preferred:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;AWS, MuleSoft, or Heroku integration experience&lt;/li&gt;
&lt;li&gt;Experience with Einstein Analytics, Einstein Copilot, or AI-driven Salesforce capabilities&lt;/li&gt;
&lt;li&gt;Salesforce Certified Application Architect or System Architect (or both)&lt;/li&gt;
&lt;li&gt;Healthcare or regulated industry experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Knowledge, Skills &amp;amp; Abilities&lt;/strong&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Strategic Design: Ability to balance innovation with pragmatic delivery; make trade-offs between technical perfection and business velocity&lt;/li&gt;
&lt;li&gt;Security Mindset: Deep understanding of data governance, OAuth, SAML, multi-tenancy, and compliance frameworks&lt;/li&gt;
&lt;li&gt;Executive Communication: Translate technical architecture into compelling business value for C-suite and product stakeholders&lt;/li&gt;
&lt;li&gt;Mentorship: Ability to elevate team capability through code review, design collaboration, and knowledge sharing&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Why Join Natera&lt;/strong&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Impact: Work on healthcare technology transformations that directly improve patient outcomes&lt;/li&gt;
&lt;li&gt;Scale: Lead large-scale transformation (Sales &amp;amp; Service Vision 2026) across 8 product delivery teams&lt;/li&gt;
&lt;li&gt;Growth: Invest in cutting-edge tools (AWS, Salesforce Data Cloud, AI/ML)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;strong&gt;Compensation &amp;amp; Benefits&lt;/strong&gt;&lt;/h2&gt;
&lt;p&gt;Natera offers competitive compensation including base salary, performance bonuses, and equity. Comprehensive benefits include health insurance, 401(k) matching, flexible PTO, professional development budget, and more.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Austin, TX&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$152,800&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$191,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/staff-salesforce-architect-sales-and-service-cloud-natera/69d3bb83c8e81216cd0b8f2e</link><guid isPermaLink="true">http://biotechroles.com/staff-salesforce-architect-sales-and-service-cloud-natera/69d3bb83c8e81216cd0b8f2e</guid><pubDate>Mon, 06 Apr 2026 13:56:19 GMT</pubDate><company>Natera</company><location>Austin, TX</location><salary>$160000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Clinical Outsourcing]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;The Organization&lt;/h2&gt;
&lt;p&gt;What&#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).&lt;/p&gt;
&lt;p&gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).&lt;/p&gt;
&lt;p&gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;The Perfect Addition to Our Team&lt;/h2&gt;
&lt;p&gt;You are a seasoned leader in the pharmaceutical industry who is eager to shape and implement clinical outsourcing strategies for clinical trials. You are well organized and collaborative, able to work seamlessly with teams to drive our clinical activities. You thrive in a fast-paced environment, juggling priorities, and stepping in wherever needed. With a proven track record in scaling operations within biotech or pharmaceutical settings, you are a results-driven problem solver who efficiently connects problems with solutions. Your strong interpersonal skills enable you to build effective relationships inside and outside the company. If you&#39;re passionate about making a difference and driving results, we want to hear from you!&lt;/p&gt;
&lt;h2&gt;The Opportunity&lt;/h2&gt;
&lt;p&gt;The Associate Director, Clinical Outsourcing, will be responsible for development and execution of Entrada’s clinical outsourcing strategy and will manage vendor outsourcing, negotiation, and contracting for Entrada clinical studies. This role reports to the Executive Director, Clinical Business Operations, and sits within the Clinical and Business Operations and Biometrics department.&amp;nbsp; The successful candidate for this role will demonstrate an in-depth knowledge of outsourcing models and strategies, negotiations and contracting, study financials, and cost-effective best practices, as well as a thorough understanding of clinical operations, clinical trial services, and clinical technologies.&lt;/p&gt;
&lt;h2&gt;Responsibilities&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Develop Entrada’s long-term Outsourcing strategy in support of the DMD and Ocular Franchises, inclusive of full-service CROs, functional service providers, bioanalytical laboratories, ancillary services and technology service providers.&lt;/li&gt;
&lt;li&gt;Independently lead and be accountable for the vendor selection and onboarding process, including preparing RFPs, leading the review of proposal responses, conducting complex budget analysis comparisons and negotiations, and coordinating vendor qualification with QA.&lt;/li&gt;
&lt;li&gt;Identify opportunities to reduce costs, increase efficiency, and mitigate risk related to outsourced services across the portfolio.&lt;/li&gt;
&lt;li&gt;Lead and manage large, complex contract and financial negotiations with external service providers (including detailed scopes of work, exhibits, payment terms, budgets, and change orders) to ensure favorable terms and risk mitigations.&lt;/li&gt;
&lt;li&gt;Manage review and negotiation of contract business terms and partner with internal stakeholders, Legal, and Finance as needed to finalize terms and obtain approvals.&lt;/li&gt;
&lt;li&gt;Support development and negotiation of MSAs, quality agreements, and vendor oversight plans.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;The Necessities&lt;/h2&gt;
&lt;p&gt;At Entrada, our passion for science, our devotion to patients and our values drives our&amp;nbsp;behavior:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Humanity&lt;/strong&gt; - We genuinely care about patients and about one another.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Tenacity&lt;/strong&gt; - We are relentless and persistent in the pursuit of developing therapies&amp;nbsp;for patients.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Creativity&lt;/strong&gt; - We are creative problem solvers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Collaboration&lt;/strong&gt; - We are more than the sum of our parts.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Curiosity&lt;/strong&gt; - We have a growth mindset and push conventional thought and theory.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;To thrive on our team, you will need to come with:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in life sciences, business, or a related field; advanced degree preferred.&lt;/li&gt;
&lt;li&gt;10+ years of progressive leadership experience in clinical operations or related areas, with at least eight years of clinical operations or outsourcing experience.&lt;/li&gt;
&lt;li&gt;Expert in outsourcing and contracting best practices for all phases of clinical research with an in-depth understanding of the drug development process and cross-functional responsibilities, including clinical trial design, study start-up and execution, monitoring, and site management, safety reporting, data management, and biometrics.&lt;/li&gt;
&lt;li&gt;In-depth experience soliciting and critically evaluating CRO and service provider proposals, negotiating contractual terms, and growing and fostering long-term, healthy vendor relationships.&lt;/li&gt;
&lt;li&gt;Strong attention to detail, analytical, negotiation, and business communication skills.&lt;/li&gt;
&lt;li&gt;Ability to interact and influence effectively with multi-functional teams at all internal and external organization levels.&lt;/li&gt;
&lt;li&gt;Forward-thinking and creative with high ethical standards.&lt;/li&gt;
&lt;li&gt;Ability to work in a fast-paced professional environment with changing priorities and business needs.&lt;/li&gt;
&lt;li&gt;Strong problem-solving and multi-tasking skills.&lt;/li&gt;
&lt;li&gt;Well-organized and self-directed.&lt;/li&gt;
&lt;li&gt;This is a US based remote position with preference given to local New England based candidates. This role will require minimum monthly or quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support&lt;/h2&gt;
&lt;p&gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.&lt;/p&gt;
&lt;p&gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;— Kerry Robert, SVP of People&lt;/p&gt;
&lt;p&gt;The salary for this opportunity ranges from $173,000-$203,000. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. &lt;span style=&quot;color: rgb(255, 255, 255);&quot;&gt;#LI-JF1 #LI-Remote&lt;/span&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;Equal Opportunity Employer&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Third Party Staffing Agencies&lt;/h2&gt;
&lt;p&gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.&lt;/p&gt;
&lt;h2&gt;Privacy Statement&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics, Inc. (the “&lt;strong&gt;Entrada&lt;/strong&gt;,” “&lt;strong&gt;we,&lt;/strong&gt;” “&lt;strong&gt;us,&lt;/strong&gt;” or “&lt;strong&gt;our&lt;/strong&gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement &lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://www.entradatx.com/privacy-notice&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;here &lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;to understand how and when your data is being used.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-clinical-outsourcing-entrada-therapeutics/69d3bb82c8e81216cd0b8f2d</link><guid isPermaLink="true">http://biotechroles.com/associate-director-clinical-outsourcing-entrada-therapeutics/69d3bb82c8e81216cd0b8f2d</guid><pubDate>Mon, 06 Apr 2026 13:56:18 GMT</pubDate><company>Entrada Therapeutics</company><location>Boston, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Global Health Economics & Outcomes Research (HEOR)]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;We are seeking a Director, Global HEOR, to lead the strategy and execution of how we define, substantiate, and communicate the value of one or more medicines approaching commercialization. This role is responsible for ensuring that, from clinical development through real-world evidence generation and payer engagement, we are making the strongest and best-supported arguments to secure access to our medicines. Accordingly, the Director, Global HEOR, helps shape development plans, evidence strategies, and value narratives so that they align with how payers and health technology assessment (HTA) bodies make decisions, balancing analytical rigor with a clear focus on what is relevant for decision-making.&lt;/p&gt;
&lt;p&gt;This is a highly cross-functional, hands-on role for someone who combines deep analytical thinking with sound judgment, intellectual curiosity with pragmatism, and a strong orientation toward results. The role directly influences how our medicines are developed, positioned, and ultimately accessed by patients worldwide. Success in this role requires continually asking not just “Is this analysis methodologically defensible?” but “Does this help us make a better case for access, and if not, what would?”&lt;/p&gt;
&lt;p&gt;This role is based in Waltham, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Informing development strategies from HEOR / market access perspective&lt;/li&gt;
&lt;li&gt;Represent the HEOR and market access perspective in internal clinical development and regulatory forums&lt;/li&gt;
&lt;li&gt;Provide critical input into clinical development plans, including protocol design, endpoint selection, and other aspects of clinical trial evidence generation, to ensure alignment with future payer and HTA expectations&lt;/li&gt;
&lt;li&gt;Communication of value to payers and HTA bodies&lt;/li&gt;
&lt;li&gt;Lead development of AMCP dossiers for US payers&lt;/li&gt;
&lt;li&gt;Lead development of cost-effectiveness models for NICE and other HTA bodies requiring formal cost-effectiveness analyses&lt;/li&gt;
&lt;li&gt;Serve as a core team member for HTA submissions outside the US, with responsibility for shaping and stress-testing value narratives included in pricing and reimbursement dossiers and interpreting and recommending evidence to support such narratives, in a way that optimizes both credibility and relevance for payer decision-making&lt;/li&gt;
&lt;li&gt;Make substantial contributions to other payer communication materials (e.g., Medical Value Liaison slide decks) and launch readiness activities as needed&lt;/li&gt;
&lt;li&gt;Leading real-world evidence strategy and execution of real-world analyses&lt;/li&gt;
&lt;li&gt;Lead planning of real-world evidence generation activities to address evidence gaps as needed for informing decision-making by payers, HTA bodies, and clinicians&lt;/li&gt;
&lt;li&gt;Oversee execution of real-world data analyses, ensuring analytical rigor and fitness for purpose&lt;/li&gt;
&lt;li&gt;Interpret and translate results from real-world analyses into peer-reviewed publications and other external communications intended to meaningfully inform clinical practice and payer/HTA decision-making&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Education and Skills Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree or equivalent experience in a relevant field such as economics, public health, epidemiology, biostatistics, health policy, life sciences, or a related discipline.&lt;/li&gt;
&lt;li&gt;Advanced degrees (Master’s, PhD, PharmD, MD) are welcome but not required.&lt;/li&gt;
&lt;li&gt;10+ years of progressive experience in HEOR, health analytics, value demonstration, market access, or a closely related quantitative or scientific field.&lt;/li&gt;
&lt;li&gt;Demonstrated success leading complex evidence‑generation, modeling, or analytical programs within biopharma, healthcare consulting, payer organizations, or academic research environments.&lt;/li&gt;
&lt;li&gt;Experience influencing senior leaders and driving strategic decisions through evidence and structured analysis.&lt;/li&gt;
&lt;li&gt;We are looking for candidates who demonstrate the following skills and qualities:
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Analytical ability:&lt;/strong&gt; Strong reasoning and structured problem‑solving capabilities, with curiosity, persistence, and creativity to tackle complex, open‑ended problems.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Sophisticated understanding of evidence:&lt;/strong&gt; Clear judgment about what different analytical methodologies can and cannot tell you, and what makes an analysis more or less robust.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Understanding of value frameworks:&lt;/strong&gt; Familiarity with decision‑making frameworks that inform how medicines are valued, priced, and reimbursed.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Strong mathematical intuition:&lt;/strong&gt; Deep understanding of how numbers work, how models behave, and how assumptions propagate through analyses.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Critical evaluation of scientific literature:&lt;/strong&gt; Ability to read, interpret, and rigorously critique medical, scientific, and health economics publications.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Biological and clinical literacy:&lt;/strong&gt; Sufficient grounding in biology and clinical science to engage effectively with development teams and external clinical experts.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Results orientation:&lt;/strong&gt; Focus on organizational priorities—balancing rigor with pragmatism and avoiding analysis for analysis’ sake.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Bias toward solutions and progress:&lt;/strong&gt; Mindset oriented toward finding solutions, offering alternatives, and maintaining momentum.&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$210,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$252,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-global-health-economics-and-outcomes-research-(heor)-dyne-therapeutics/69d3bb81c8e81216cd0b8f2a</link><guid isPermaLink="true">http://biotechroles.com/director-global-health-economics-and-outcomes-research-(heor)-dyne-therapeutics/69d3bb81c8e81216cd0b8f2a</guid><pubDate>Mon, 06 Apr 2026 13:56:17 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Clinical Biomarkers]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h2&gt;The Organization&lt;/h2&gt;
&lt;p&gt;What&#39;s happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1).&lt;/p&gt;
&lt;p&gt;2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670).&lt;/p&gt;
&lt;p&gt;We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.&lt;/p&gt;&lt;/div&gt;&lt;h2&gt;The Perfect Addition to Our Team&lt;/h2&gt;
&lt;p&gt;You are excited about the opportunity to lead clinical biomarker development and strategy at Entrada. You enjoy a fast-paced environment and juggling competing priorities. You bring an in-depth knowledge of biomarker development and strategy, as well as a broad understanding of regulatory expectations supporting assay performance across various stages of clinical development. You follow up and follow through, efficiently connecting problems with solutions. You work successfully in a team environment, with strong people skills to effectively build working relationships inside and outside of the company.&lt;/p&gt;
&lt;h2&gt;The Opportunity&lt;/h2&gt;
&lt;p&gt;The Associate Director, Clinical Biomarkers, will lead scientific efforts to develop and execute biomarker strategies in support of ongoing and future clinical trials. This individual will oversee biomarker activities across external CROs and specialty laboratories, while also conducting technical and strategic evaluations of emerging and innovative biomarker platforms to support Entrada’s drug development pipeline.&lt;/p&gt;
&lt;p&gt;In addition, this role will provide leadership and mentorship to the internal biomarker team, supporting the growth and development of team members across varying levels of experience and expertise. The ideal candidate will demonstrate strong project management capabilities and effectively communicate progress, risks, and timelines to ensure the successful and timely delivery of biomarker assays in support of clinical programs.&lt;/p&gt;
&lt;h2&gt;Responsibilities&lt;/h2&gt;
&lt;ul&gt;
&lt;li&gt;Lead internal clinical biomarker initiatives in the development, transfer, and execution of stage-appropriate biomarker assays for clinical development.&lt;/li&gt;
&lt;li&gt;Effectively manage on-going activities for biomarker testing and identify technology solutions to support ongoing and planned clinical trials.&lt;/li&gt;
&lt;li&gt;Demonstrate an established depth and/or breadth of expertise in biomarker assays and provide strong technical guidance; managing the assay development/transfer and oversee fit-for-purpose validation at selected vendors.&lt;/li&gt;
&lt;li&gt;Contribute to biomarker-related sections of clinical study protocols and health authority submission document, where applicable.&lt;/li&gt;
&lt;li&gt;Operationalize biomarker tests and ensure results are delivered and archived per clinical development needs.&lt;/li&gt;
&lt;li&gt;Collaborate with Program Team Leaders, Regulatory, and Medical Directors in the review of clinical protocols, investigator training documents, lab manuals, clinical sample analysis, and regulatory submission activities for clinical development.&lt;/li&gt;
&lt;li&gt;Partner with Discovery and Non-clinical Development teams in the evaluation and development of clinical biomarker assays and vendor selection for early projects.&lt;/li&gt;
&lt;li&gt;Manage, identify, and communicate risks to stakeholders in a clear and timely fashion.&lt;/li&gt;
&lt;li&gt;Manage and guide junior level staff for successful assay development and execution within the biomarker function.&lt;/li&gt;
&lt;li&gt;Actively engage with industry professionals via attendance and delivery of presentations in conferences, workshops, focus groups, and literature/publications to guide best practices for biomarker development and clinical implementation.&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;The Necessities&lt;/h2&gt;
&lt;p&gt;At Entrada, our passion for science, our devotion to patients and our values drives our&amp;nbsp;behavior:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;strong&gt;Humanity&lt;/strong&gt; - We genuinely care about patients and about one another.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Tenacity&lt;/strong&gt; - We are relentless and persistent in the pursuit of developing therapies&amp;nbsp;for patients.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Creativity&lt;/strong&gt; - We are creative problem solvers.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Collaboration&lt;/strong&gt; - We are more than the sum of our parts.&lt;/li&gt;
&lt;li&gt;&lt;strong&gt;Curiosity&lt;/strong&gt; - We have a growth mindset and push conventional thought and theory.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;To thrive on our team, you will need to come with:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ph.D. with 6 + years of relevant experience or Master&#39;s in a scientific discipline with 8+ years relevant experience.&lt;/li&gt;
&lt;li&gt;Previous experience defining and executing “fit-for-purpose” clinical biomarker assays to address key scientific and clinical questions.&lt;/li&gt;
&lt;li&gt;Broad understanding of FDA and EMA requirements for biomarker regulatory sections.&lt;/li&gt;
&lt;li&gt;Extensive understanding in developing, performing, and optimizing ligand binding assay technologies (e.g. ELISA, MSD) and molecular assays (e.g. qPCR, ddPCR, western blot) and related software for data analysis.&lt;/li&gt;
&lt;li&gt;Experience in outsourcing and managing activities at CROs (e.g. managing timelines and technical troubleshooting) and overseeing development and validation of clinical biomarker assays in a GLP and GCP(GXP) environment.&lt;/li&gt;
&lt;li&gt;Strong verbal and written communication and presentation skills.&lt;/li&gt;
&lt;li&gt;Strong interpersonal skills and knowledge of intercultural differences; adept at working across multiple functions to drive decision making.&lt;/li&gt;
&lt;li&gt;Experience working in a fast-paced, cross-functional environment with multiple competing priorities.&lt;/li&gt;
&lt;li&gt;This role follows a hybrid working model, with in office attendance 2-3 days per week minimum at the Entrada Therapeutics Headquarters in Boston, MA.&amp;nbsp;&lt;/li&gt;
&lt;/ul&gt;
&lt;h2&gt;What We Offer: Meaningful Work, Fair Rewards, and Real Support&lt;/h2&gt;
&lt;p&gt;At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity. We believe in transparency and equity and are committed to sharing salary ranges for every position, along with insight into our compensation philosophy, in accordance with certain state requirements in the United States and fostering a fair and open environment at the onset.&lt;/p&gt;
&lt;p&gt;But we also know it is more than just pay. When you join Entrada, you’ll be part of a mission-driven team with access to comprehensive health, dental and vision coverage; life and disability insurance; with a 401(k) match. We pride ourselves on offering competitive benefits that empower our employees and reflect the value of their contributions – offering paid, gender-inclusive parental leave, holistic support for your health and well-being, education reimbursement, discretionary time off and commuting benefits aligned to your working model. If you find yourself working from our office in Boston’s Seaport District, this puts you steps away from some of the best the city has to offer.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;“Our approach to compensation is grounded in transparency, equity and performance for the unique contributions each person brings. At Entrada, we know that meaningful work deserves meaningful reward — and we view compensation as one way we show appreciation for the collaboration, curiosity and commitment that drive our mission forward.”&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;— Kerry Robert, SVP of People&lt;/p&gt;
&lt;p&gt;The salary for this opportunity ranges from $&lt;span data-teams=&quot;true&quot;&gt;173,000 - $206,000&lt;/span&gt;. The final base compensation offered will depend on several considerations which include but may not be limited to a candidate’s skills, competencies, experience and other job-related factors permitted by law. The final salary offered may fall outside of this range. &lt;span style=&quot;color: rgb(255, 255, 255);&quot;&gt;#LI-JF1 #LI-Hybrid&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;h2&gt;Equal Opportunity Employer&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;Third Party Staffing Agencies&lt;/h2&gt;
&lt;p&gt;Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.&lt;/p&gt;
&lt;h2&gt;Privacy Statement&lt;/h2&gt;
&lt;p&gt;Entrada Therapeutics, Inc. (the “&lt;strong&gt;Entrada&lt;/strong&gt;,” “&lt;strong&gt;we,&lt;/strong&gt;” “&lt;strong&gt;us,&lt;/strong&gt;” or “&lt;strong&gt;our&lt;/strong&gt;”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement &lt;span style=&quot;text-decoration: underline;&quot;&gt;&lt;a href=&quot;https://www.entradatx.com/privacy-notice&quot; target=&quot;_blank&quot;&gt;&lt;strong&gt;here &lt;/strong&gt;&lt;/a&gt;&lt;/span&gt;to understand how and when your data is being used.&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-clinical-biomarkers-entrada-therapeutics/69d3bb7ec8e81216cd0b8f27</link><guid isPermaLink="true">http://biotechroles.com/associate-director-clinical-biomarkers-entrada-therapeutics/69d3bb7ec8e81216cd0b8f27</guid><pubDate>Mon, 06 Apr 2026 13:56:13 GMT</pubDate><company>Entrada Therapeutics</company><location>Boston, MA</location><salary>$180000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Staff AI-Native Platform Engineer]]></title><description><![CDATA[&lt;h1&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Staff AI-Native Platform Engineer (L5)&lt;/span&gt;&lt;/h1&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Location:&lt;/strong&gt; US - Remote&lt;br&gt;&lt;strong&gt;Experience:&lt;/strong&gt; 8+ years in Cloud/Platform Engineering or Infrastructure, with a proven track record of leading cross-functional initiatives and influencing organizational AI strategy.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;About the Role&lt;/span&gt;&lt;/h2&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;We are looking for a visionary &lt;strong&gt;Staff AI-Native Platform Engineer&lt;/strong&gt; to lead the evolution of our technical foundation. In this high-impact role, you will move beyond traditional automation to architect &lt;em&gt;an AI-native ecosystem&lt;/em&gt; that integrates Generative AI into every layer of our Development Platform.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;As a technical leader within the Platform organization, you won’t just be maintaining infrastructure, you will be reimagining &lt;em&gt;the developer experience (DevEx)&lt;/em&gt;. You will be the primary advocate for GenAI, fostering a culture of “AI-first” engineering by building agentic workflows that accelerate Cloud Orchestration, CI/CD, Observability, and FinOps. We need a creative engineer who can bridge the gap between cutting-edge LLM capabilities and robust, production-grade platform tooling.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;What You’ll Do&lt;/span&gt;&lt;/h2&gt;
&lt;h3&gt;&lt;span style=&quot;color: #434343;&quot;&gt;Architect AI-Integrated Infrastructure&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;AI-First Development Platform:&lt;/strong&gt; Design and build unified interfaces where AI agents manage complex tasks like environment provisioning, automated PR reviews, and self-documenting codebases.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Intelligent Orchestration:&lt;/strong&gt; Embed AI-driven intelligence into CI/CD pipelines and Observability stacks to enable predictive scaling, automated incident triage, and self-healing systems.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Autonomous FinOps:&lt;/strong&gt; Evolve AI-assisted FinOps workflows to automate cost attribution, anomaly detection, and optimization recommendations across AWS and other cloud environments.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Governance &amp;amp; Guardrails:&lt;/strong&gt; Implement AI-driven governance to ensure architectural standards and security policies are met without slowing down developer velocity.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #434343;&quot;&gt;Elevate Developer Experience (DevEx)&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Agentic Tooling:&lt;/strong&gt; Develop production-grade internal tools that use agentic reasoning to solve &quot;day two&quot; operational challenges for product teams.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Internal Developer Portal (IDP):&lt;/strong&gt; Integrate natural language interfaces into our IDP, allowing developers to interact with the platform through conversational AI.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Actionable Insights:&lt;/strong&gt; Transform raw telemetry into “executive-ready” insights using advanced data modeling and AI-driven visualization.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #434343;&quot;&gt;Lead AI Mentorship &amp;amp; Evangelism&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Strategic Advisory: &lt;/strong&gt;Partner with senior leadership to model the technical and operational trade-offs of various AI architectural decisions (e.g., Build vs. Buy, Model Selection).&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Team Upskilling:&lt;/strong&gt; Act as a force multiplier by mentoring engineers on advanced AI tooling, prompt engineering for infrastructure, and the deployment of agentic systems.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Community Building:&lt;/strong&gt; Stay at the forefront of the GenAI landscape, regularly sharing insights and driving the adoption of emerging tools and patterns across the organization.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;What You Bring&lt;/span&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Platform Expertise:&lt;/strong&gt; 8+ years of experience in Cloud Engineering (AWS preferred), with deep knowledge of Kubernetes, Terraform/CloudFormation, and modern CI/CD patterns.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;AI/ML Applied Logic:&lt;/strong&gt; Expert-level experience applying AI techniques (summarization, RAG, agentic reasoning) to real-world operational workflows. You understand how to make LLMs &quot;useful&quot; in a production environment.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Advanced Programming:&lt;/strong&gt; Expert Python skills and experience with AWS SDKs. You are comfortable building complex integrations and custom CLI/API tools.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;The &quot;Staff&quot; Mindset:&lt;/strong&gt; A history of leading large-scale, cross-functional projects. You can navigate ambiguity, build consensus across teams, and deliver measurable business impact.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Creative Evangelism:&lt;/strong&gt; The ability to present complex AI concepts to both technical and non-technical stakeholders, inspiring teams to shift toward AI-native workflows.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Product Thinking:&lt;/strong&gt; Experience building Internal Developer Portals (IDP) with a focus on &quot;Platform as a Product&quot; and user-centric design.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #434343;&quot;&gt;Bonus Points&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Experience with LangChain, LlamaIndex, or other AI orchestration frameworks.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Contributions to open-source platforms or AI projects.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Experience with vector databases and fine-tuning models for domain-specific tasks.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Remote USA&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$152,100&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$190,100 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/staff-ai-native-platform-engineer-natera/69d3bb7dc8e81216cd0b8f26</link><guid isPermaLink="true">http://biotechroles.com/staff-ai-native-platform-engineer-natera/69d3bb7dc8e81216cd0b8f26</guid><pubDate>Mon, 06 Apr 2026 13:56:13 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Compliance]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Director of Compliance&amp;nbsp;provides&amp;nbsp;compliance guidance on a wide range of commercialization issues as Dyne scales and prepares for the&amp;nbsp;anticipated&amp;nbsp;launch of its first therapies. These topics include HCP and patient engagement, disease‑state education, compliance with FDA regulations, health care fraud and abuse laws, Value &amp;amp; Access matters, patient support programs, data privacy, and various federal and state laws governing the pharmaceutical industry.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Director of Compliance helps design and implement a global compliance program to ensure that Dyne&amp;nbsp;complies with&amp;nbsp;all applicable laws, regulations, and ethical codes where the company&amp;nbsp;operates. The Director of Compliance works closely with Medical, Commercial, Regulatory Affairs, and G&amp;amp;A colleagues. We&amp;nbsp;seek&amp;nbsp;a strategic, collaborative, solutions‑oriented leader with deep knowledge and experience. Prior rare‑disease and launch experience enables the Director of Compliance to help Dyne navigate the challenges of our first therapy launches.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;This role is based&amp;nbsp;in&amp;nbsp;Waltham, MA,&amp;nbsp;without the possibility of being a remote role.&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;Primary Responsibilities&amp;nbsp;Include:&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Design and implement a comprehensive health care compliance program consistent with all laws, regulations,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;policies&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and industry standards.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559740&amp;quot;:276}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Establish and refresh corporate policies,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;procedures&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and guidelines to ensure compliant operations across all Commercial, Medical and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;research&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;activities.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead risk assessments to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;identify&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and prioritize compliance risks&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Develop and deliver risk-based compliance training for employee&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Develop and implement auditing &amp;amp; monitoring plans and related dashboards&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead confidential, thorough investigations into potential violations&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Establish Compliance as an approachable, knowledgeable, practical, helpful, solutions-oriented business partner&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Collaborate closely with the Franchise Counsel to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;align on&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;consistent, actionable legal and compliance solution&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;s.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Champion Dyne’s core values and culture of integrity&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serve as a trusted advisor to senior leadership and cross-functional teams on business and compliance strategies&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Perform&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;additional&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;duties as&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;required&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, Experience,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Advanced degree in law, business&amp;nbsp;administration&amp;nbsp;or related field.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;10+ years of overall professional experience, including at least 7+ years of healthcare compliance experience, ideally within a global rare disease biotechnology company.&lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Deep&amp;nbsp;expertise&amp;nbsp;in U.S. health care laws, federal health care programs, and therapy launches.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong understanding of PhRMA Code, Anti-Kickback Statute, False Claims Act, data privacy,&amp;nbsp;and transparency laws.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience supporting&amp;nbsp;compliant patient engagement, HCP engagement, scientific exchange, and innovative patient support programs.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven success advising cross-functional teams (Medical, Commercial, Regulatory, Technical Operations, and G&amp;amp;A) on complex, time-sensitive matters.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Skilled at balancing strategic&amp;nbsp;compliance&amp;nbsp;guidance with practical business judgment in fast-paced, evolving environments.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Exceptional communication, analytical, and project management skills with attention to detail&amp;nbsp;and execution&amp;nbsp;excellence.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborative leadership style and enterprise&amp;nbsp;mindset that&amp;nbsp;reinforces organizational culture and values.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience thriving in a small, rapidly growing biotech or start-up environment with a solutions-oriented approach.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$200,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$240,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-compliance-dyne-therapeutics/69d3bb7bc8e81216cd0b8f25</link><guid isPermaLink="true">http://biotechroles.com/director-compliance-dyne-therapeutics/69d3bb7bc8e81216cd0b8f25</guid><pubDate>Mon, 06 Apr 2026 13:56:10 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Sr Software Engineer in Test]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;POSITION SUMMARY:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Senior Software Engineer in Test is responsible for developing and maintaining software automation test frameworks and tools using programming languages and test automation libraries.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;PRIMARY RESPONSIBILITIES:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Responsible for supporting test infrastructure of Natera software systems and components.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Design, build, and maintain test automation tools and frameworks using clean coding practices and functional programming methodologies.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Perform complete end-to-end validation of Natera software applications.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Perform system analysis, assess risk, and develop strong test strategies by analyzing product design and technical specifications, and by collaborating with product managers and developers.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Evangelize new testing methodologies, best practices and tools with goals to continuously improve test coverage through automation.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Integrate with deployment infrastructure to establish a continuous build and test cycle.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Work closely with developers in all phases of SDLC to build quality into our development process.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Report, document, and communicate failures discovered through testing with the affected teams.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;This role works with PHI on a regular basis both in paper and electronic form and has access to various technologies to access PHI (paper and electronic) in order to perform the job&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure&amp;nbsp;Compliance&amp;nbsp;training and security training as soon as possible but not later than the first 30&amp;nbsp;days of hire.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Must maintain a current status on Natera training requirements.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Employee must pass post offer criminal background check.&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;QUALIFICATIONS:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;5+ years of experience developing test automation frameworks and harnesses using programming and scripting languages.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;BS degree in Computer Science or equivalent work experience.&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KNOWLEDGE, SKILLS, AND ABILITIES:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Strong working knowledge of Scala and/or Java.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Recent hands-on experience of REST API testing and test automation&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Recent hands-on experience with front-end test automation tools and libraries such as Selenium, TestNG, Junit, ScalaTest, Gatling and others.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Extensive working knowledge of relational databases, strong SQL skills.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Strong knowledge of Linux and command line shell scripting.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Strong knowledge of QA methodologies, test planning, system dependencies, and product integration phases.&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Remote USA&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$122,900&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$153,600 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr-software-engineer-in-test-natera/69d3bb79c8e81216cd0b8f23</link><guid isPermaLink="true">http://biotechroles.com/sr-software-engineer-in-test-natera/69d3bb79c8e81216cd0b8f23</guid><pubDate>Mon, 06 Apr 2026 13:56:09 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Director, Business & Operations – US Affiliate]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Director, Business &amp;amp; Operations – US Affiliate will serve as a key strategic and operational partner to the SVP, Head of US Affiliate, supporting the effectiveness, execution, and scalability of the US Affiliate organization. This role will provide operational leadership and continuity across the function, enabling the SVP and US Affiliate Leadership Team to remain focused on the highest‑impact priorities as Dyne builds and grows its US presence.&lt;/p&gt;
&lt;p&gt;The Director will be responsible for business operations across the US Affiliate, including budget ownership and financial planning, vendor and contract management, operating rhythm and governance, and the execution of function‑wide initiatives. Acting as a connective hub across Commercial, Medical, Finance, Legal, HR, and other G&amp;amp;A partners, this leader will translate strategic priorities into well‑structured plans, drive execution, and ensure visibility into progress, risks, and resource needs.&lt;/p&gt;
&lt;p&gt;The ideal candidate is highly organized, proactive, and comfortable operating in a fast‑paced, evolving environment. They bring strong judgment, executive presence, and the ability to influence without authority, paired with a hands‑on approach to getting work done.&lt;/p&gt;
&lt;p&gt;This role is based in Waltham, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Strategic &amp;amp; Operational Partnership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Serve as a trusted thought partner to the SVP, Head of US Affiliate, helping translate affiliate strategy and priorities into clear, actionable, and measurable operating plans.&lt;/li&gt;
&lt;li&gt;Support the US Affiliate Leadership Team with structured problem solving, prioritization, and follow‑through across key initiatives.&lt;/li&gt;
&lt;li&gt;Anticipate organizational needs and proactively bring recommendations, options, and solutions to leadership.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Business Operations &amp;amp; Operating Rhythm&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Establish and manage the operating rhythm for the US Affiliate, including leadership meetings, business reviews, planning cycles, and governance forums.&lt;/li&gt;
&lt;li&gt;Drive clarity on goals, ownership, timelines, and success metrics across affiliate initiatives.&lt;/li&gt;
&lt;li&gt;Develop and maintain dashboards and tracking tools that provide transparency into performance, risks, dependencies, and decision points.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Budget, Financial Planning &amp;amp; Resource Management&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support development and management of the US Affiliate budget in close partnership with Finance, including annual planning, forecasting, tracking, and variance management.&lt;/li&gt;
&lt;li&gt;Support headcount planning, resource allocation, and investment prioritization to ensure alignment with affiliate and enterprise objectives.&lt;/li&gt;
&lt;li&gt;Prepare budget materials, analyses, and recommendations for affiliate leadership and enterprise review forums.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Vendor, Contract &amp;amp; External Partner Management&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Oversee vendor strategy and management for the US Affiliate, including agency partners, consultants, and other external service providers.&lt;/li&gt;
&lt;li&gt;Partner with Legal, Finance, and Procurement to manage contracts, statements of work, renewals, and compliance.&lt;/li&gt;
&lt;li&gt;Ensure vendors are delivering against scope, timelines, and value expectations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross‑Functional &amp;amp; Enterprise Initiatives&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead and coordinate high‑priority, function‑wide and cross‑functional initiatives impacting the US Affiliate.&lt;/li&gt;
&lt;li&gt;Act as a central point of integration between the US Affiliate and partner functions to ensure alignment and execution.&lt;/li&gt;
&lt;li&gt;Track initiative progress, identify risks, and escalate issues with proposed solutions.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Leadership Enablement &amp;amp; Execution&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drive coordination across HQ and field‑based roles spanning Commercial, Medical, and partner functions to maintain momentum and alignment on priority initiatives.&lt;/li&gt;
&lt;li&gt;Design and manage the US Affiliate “Cadence of the Business,” including Leadership Team meetings, offsites, business reviews, and short‑ and long‑term planning cycles.&lt;/li&gt;
&lt;li&gt;Serve as a leader for high‑priority initiatives that do not have a natural functional home (e.g., ways of working, launch KPI management, executive reporting).&lt;/li&gt;
&lt;li&gt;Support change management and organization‑wide communication for new processes, initiatives, and ways of working.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications &amp;amp; Experience&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree required; advanced degree (MBA or equivalent) preferred.&lt;/li&gt;
&lt;li&gt;10+ years of progressive experience in commercialization strategy, commercial operations, program management, or related roles within biotechnology or pharmaceuticals, or relevant experience from a biotech or life sciences consulting firm focused on commercialization or commercial planning.&lt;/li&gt;
&lt;li&gt;Experience supporting senior leaders and leadership teams in high‑growth or launch‑stage environments.&lt;/li&gt;
&lt;li&gt;Demonstrated experience with budget management, financial planning, and vendor/contract oversight.&lt;/li&gt;
&lt;li&gt;Strong cross‑functional leadership skills with the ability to influence without formal authority.&lt;/li&gt;
&lt;li&gt;Exceptional written and verbal communication skills; able to synthesize complexity into clear, executive‑ready thinking.&lt;/li&gt;
&lt;li&gt;Highly organized, detail‑oriented, and comfortable managing multiple priorities simultaneously.&lt;/li&gt;
&lt;li&gt;High integrity and discretion in handling sensitive and confidential information.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$188,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$240,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/director-business-and-operations-us-affiliate-dyne-therapeutics/69d3bb77c8e81216cd0b8f20</link><guid isPermaLink="true">http://biotechroles.com/director-business-and-operations-us-affiliate-dyne-therapeutics/69d3bb77c8e81216cd0b8f20</guid><pubDate>Mon, 06 Apr 2026 13:56:06 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$180000-260000</salary><type>Full-time</type></item><item><title><![CDATA[Sr Product Analyst]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Job Title&lt;/strong&gt;: Senior Product Analyst - Real World Data&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Job Description&lt;/strong&gt;:&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;We are seeking a highly skilled and experienced &lt;strong&gt;Senior Product Analyst&lt;/strong&gt; to join our Real World Data team.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Your primary responsibility will be to become an expert in our multimodal data and to deliver insights and analyses on this data to our customers. You’ll support end-to-end analytical product development in Amazon QuickSight, Snowflake, and Plotly Dash—translating stakeholder needs into the first versions of customer-facing software. You will also help define the semantic layer (metrics and definitions), establish analytics workflows and quality standards, and mentor other analysts through review and best practices.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Responsibilities&lt;/strong&gt;:.&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Data Analysis: Use SQL (and Python/R) to extract insights, generate reports and conduct deep-dive analysis from multimodal data.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Analytical Tool Development &amp;amp; Visualization: Maintain and build analytical tools and customer-facing dashboards (QuickSight) plus internal apps/prototypes (Plotly Dash/Streamlit strongly preferred) to accelerate exploration and stakeholder decision-making.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Cross-functional Partnership: Collaborate with stakeholders, domain experts, Product, and Data Engineering to understand needs, align on definitions, and deliver analytical products.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Analytical Process: Define best practices, processes, and methodologies (intake/prioritization, QA, documentation, release notes). Create standards for the analytics team code style, improve code/dashboard performance, and own documentation of data and logic.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Intermediate Data Modeling &amp;amp; Semantic Layer&lt;strong&gt;:&lt;/strong&gt; Design and document intermediate analytical models that power dashboards and self-serve analysis. Own metric definitions, calculation standards, and a shared “source of truth” for business logic.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Required Qualifications&lt;/strong&gt;:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Bachelor&#39;s or Master&#39;s degree in Computer Science, Data Science, Business Analytics, Mathematics, Healthcare, or a related field.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Proven experience (5+ years) as a Product Analyst, Data Analyst, Business Analyst or similar role, with a strong focus on analytics and development of visualization tools.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Proficiency with data analysis tools including SQL and Excel and data warehouses such as Redshift, BigQuery or Snowflake.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience with analytical data modeling and/or semantic layers (metric definitions, dimensional models, governed datasets).&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience with Python or R.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Demonstrated experience shipping customer-facing dashboards (QuickSight or similar), including requirements gathering and iteration based on user feedback.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Strong communication and presentation skills, with the ability to convey complex analytical findings to technical and non-technical stakeholders.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Preferred Qualifications&lt;/strong&gt;:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience building analytical apps using Plotly Dash, Streamlit or equivalent&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Knowledge of statistical analysis, predictive modeling and machine learning techniques.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #202124;&quot;&gt;Understanding of ETL technologies, Connector Management, Data Management &amp;amp; Analytics platforms.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #202124 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #202124;&quot;&gt;Prior experience working with complex healthcare data modalities, such as claims data, electronic health records (EHR), omics data (e.g., genomics, proteomics), and other healthcare-related datasets.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #202124 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #202124;&quot;&gt;Prior work evaluating or enabling AI/LLM analytics interfaces with emphasis on semantic correctness, guardrails, and trustworthy outputs.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Remote USA&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$117,600&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$147,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr-product-analyst-natera/69d3bb75c8e81216cd0b8f1e</link><guid isPermaLink="true">http://biotechroles.com/sr-product-analyst-natera/69d3bb75c8e81216cd0b8f1e</guid><pubDate>Mon, 06 Apr 2026 13:56:05 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - Public Payer]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across Medicaid (fee‑for‑service and managed care), select Medicare segments, and key federal payer channels. This role serves as the enterprise lead for assigned public payer accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions supporting Dyne’s rare and specialty therapeutic portfolio, including launch‑stage products.&lt;/p&gt;
&lt;p&gt;The CAD must excel at strategic navigation of complex state and federal programs, thrive in fast‑paced, growth‑oriented environments, and build trusted, high‑impact relationships with diverse payer stakeholders.&lt;/p&gt;
&lt;p&gt;This is a field-based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Public Payer Strategy &amp;amp; Policy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute Medicaid and public payer access strategies aligned with regulatory, budgetary, and policy requirements.&lt;/li&gt;
&lt;li&gt;Navigate Medicaid Drug Rebate Program requirements and state-specific access pathways.&lt;/li&gt;
&lt;li&gt;Serve as the internal subject-matter expert on public payer coverage, reimbursement, and health equity considerations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Government Account Management&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead engagement with state Medicaid agencies, Medicaid MCOs, and federal payer organizations (e.g., VA, DoD, TRICARE, Indian Health Services).&lt;/li&gt;
&lt;li&gt;Support P&amp;amp;T committee reviews, coverage determinations, and utilization management discussions.&lt;/li&gt;
&lt;li&gt;Educate public payer stakeholders on disease state, clinical value, and anticipated budget impact in preparation for and through launch.&lt;/li&gt;
&lt;li&gt;Develop and execute national and public payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate and respond to evolving payer dynamics, policy changes, benefit design trends, and specialty drug management strategies.&lt;/li&gt;
&lt;li&gt;Serve as the internal subject-matter expert on payer access, reimbursement models, channel economics, and rare/specialty disease policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Contracting &amp;amp; Access Solutions&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Partner with Contracts &amp;amp; Pricing, Legal, and Finance to support rebate or innovative contracting approaches when appropriate.&lt;/li&gt;
&lt;li&gt;Collaborate on public payer-specific distribution, specialty pharmacy, and affordability strategies/considerations.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross-Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead and coordinate cross-functional account teams (Market Access, Sales, Medical Affairs, HEOR, Trade, Marketing, Legal, Finance, Patient Services).&lt;/li&gt;
&lt;li&gt;Translate complex clinical, economic, and health equity data into clear, compliant payer communications.&lt;/li&gt;
&lt;li&gt;Partner closely with Patient Services, Trade and Field teams to support rapid patient access.&lt;/li&gt;
&lt;li&gt;Support organizational readiness and pull-through across pre-launch and post-launch phases.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Insight Generation &amp;amp; External Influence&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor and synthesize payer, policy, reimbursement, and competitive insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Representing the organization at payer meetings, industry forums, and trade associations.&lt;/li&gt;
&lt;li&gt;Identify opportunities for strategic partnerships, policy engagement, and innovative access programs.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Compliance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all public payer engagements comply with applicable laws, regulations, and internal compliance policies.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree (MBA, MPH, MS, PharmD) preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Medicaid, public payer, or managed markets roles.&lt;/li&gt;
&lt;li&gt;Strong understanding of Medicaid structures, state policy environments, reimbursement mechanics, and public payer decision‑making.&lt;/li&gt;
&lt;li&gt;Experience supporting access for specialty, rare disease, or high‑cost therapies.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Excellent communication, stakeholder engagement, and cross‑functional leadership skills.&lt;/li&gt;
&lt;li&gt;Strong negotiation and strategic planning abilities with executive presence.&lt;/li&gt;
&lt;li&gt;Demonstrated success operating in launch‑stage, high‑growth, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-public-payer-dyne-therapeutics/69d3bb72c8e81216cd0b8f1d</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-public-payer-dyne-therapeutics/69d3bb72c8e81216cd0b8f1d</guid><pubDate>Mon, 06 Apr 2026 13:56:02 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Sr Phlebotomist - Elkton, MD]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;color: #a33600;&quot;&gt;&lt;strong&gt;*THIS IS NOT A REMOTE POSITION, THIS IS AN IOP IN ELKTON, MARYLAND*&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;POSITION SUMMARY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;A&amp;nbsp;&lt;strong&gt;Sr Phlebotomist&amp;nbsp;&lt;/strong&gt;serves patients by identifying the best method for retrieving blood; preparing specimens for laboratory testing; and performing screening procedures.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;PRIMARY RESPONSIBILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Verifies test requisitions by comparing information with nursing station log; bringing discrepancies to the attention of unit personnel.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Verifies patient by reading patient identification.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Obtains blood specimens by performing venipunctures and finger sticks.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Maintains specimen integrity by using aseptic technique, following department procedures; observing isolation procedures.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily tallies of collections performed.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Maintains quality results by following department procedures and testing schedule; recording results in the quality-control log; identifying and reporting needed changes.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Maintains safe, secure, and healthy work environment by following standards and procedures; complying with legal regulations.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Resolves unusual test orders by contacting the physician, pathologist, nursing station, or reference laboratory; referring unresolved orders back to the originator for further clarification; notifying supervisor of unresolved orders.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Updates job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Enhances phlebotomy department and hospital reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Must maintain a current status on Natera training requirements&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Logistical management/printing of patient reports for that area&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Billing question answering/triaging and follow-up with patients&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Scheduling pick ups from courier services - FedEx or Medspeed.&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;QUALIFICATIONS&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Minimum of 5 years of phlebotomy experience&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;BS/BA degree (preferred)&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;High School Diploma (or equivalent) required&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;Phlebotomy Certificate (if required by State)&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;KNOWLEDGE, SKILLS, AND ABILITIES&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Ability to serve and protect the hospital community by adhering to professional standards, hospital policies and procedures, federal, state, and local requirements, and JCAHO standards.&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;PHYSICAL DEMANDS AND WORK ENVIRONMENT&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;Work in an office setting with scrubs required&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;The position requires tracking of each draw&amp;nbsp;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr-phlebotomist-elkton-md-natera/69d3bb70c8e81216cd0b8f1b</link><guid isPermaLink="true">http://biotechroles.com/sr-phlebotomist-elkton-md-natera/69d3bb70c8e81216cd0b8f1b</guid><pubDate>Mon, 06 Apr 2026 13:56:00 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - Optum/United Healthcare]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director (CAD) is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across priority national and regional payer accounts, PBMs, Medicaid, Medicare, and federal payer channels. This role serves as the enterprise lead for assigned accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions across Dyne’s neuromuscular portfolio.&lt;/p&gt;
&lt;p&gt;The CAD collaborates closely with Market Access, HEOR, Medical Affairs, Trade, Sales, Patient Services, Legal, and Finance to ensure rapid and equitable patient access. This is a field‑based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Market Access &amp;amp; Payer Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute account specific payer strategies that optimize‑specific payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate evolving payer dynamics, benefit design changes, policy shifts, and specialty management trends.&lt;/li&gt;
&lt;li&gt;Serve as an internal subject-matter expert on access pathways, ‑matter expert on access pathways, rare‑disease reimbursement, channel economics, and payer policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;National Account Leadership &amp;amp; Contracting&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic engagement and negotiations with national and regional payers, PBMs, Medicaid MCOs, and federal payers.&lt;/li&gt;
&lt;li&gt;Secure favorable coverage policies, UM criteria, and contracting arrangements—including value-based models where appropriate‑based models where appropriate.&lt;/li&gt;
&lt;li&gt;Identify account-specific access barriers and develop compliant, specific access barriers and develop compliant, data‑driven solutions in partnership with HEOR, Medical, Policy, Trade, and Patient Services.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional‑Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional account planning and coordination across Market Access, Medical Affairs, HEOR, Trade, Commercial, Legal, and Finance.&lt;/li&gt;
&lt;li&gt;Translate payer insights into actionable recommendations for launch execution, forecasting, brand positioning, and pipeline strategy.&lt;/li&gt;
&lt;li&gt;Support organizational readiness across pre‑launch, launch, and post‑launch phases to enable rapid patient access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;External Influence &amp;amp; Insight Generation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor payer, policy, and competitive developments; synthesize insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Represent Dyne at payer engagements, industry associations, and strategic forums.&lt;/li&gt;
&lt;li&gt;Identify opportunities for partnerships, innovative access programs, and policy engagement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Compliance &amp;amp; Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all interactions, materials, and contracting activities comply with Dyne policies, legal, regulatory, and compliance standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree such as MBA, MPH, MS, or PharmD preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Market Access, National Accounts, Managed Markets, or Trade.&lt;/li&gt;
&lt;li&gt;Proven success securing access for specialty, rare‑disease, or high‑cost therapies across commercial and/or public payer segments.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty pharmacy distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Strong negotiation skills and executive presence, with the ability to influence across complex, cross‑functional organizations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to operate effectively in high‑growth, launch‑stage, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Alignment with Dyne’s values, including a patient‑centric mindset, integrity, collaboration, and accountability.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-optumunited-healthcare-dyne-therapeutics/69d3bb6ec8e81216cd0b8f1a</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-optumunited-healthcare-dyne-therapeutics/69d3bb6ec8e81216cd0b8f1a</guid><pubDate>Mon, 06 Apr 2026 13:55:58 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$140000-220000</salary><type>Full-time</type></item><item><title><![CDATA[Sr Payroll Manager/Associate Director, Payroll Operations]]></title><description><![CDATA[&lt;p&gt;The Senior Payroll Manager/Associate Director, Payroll Operations is responsible for overseeing the end-to-end payroll function for a large, multi-state workforce, ensuring compliance, accuracy, and efficiency across all payroll operations. This strategic role manages the payroll team and partners closely with HR, Accounting and Finance, Legal, and external vendors to optimize systems, processes, and service delivery. The Senior Payroll Manager/Associate Director, Payroll Operations plays a key role in payroll and tax compliance risk mitigation, audit readiness, and driving process innovation to support the company’s growth and scalability. This individual will serve as the company’s top payroll subject matter expert, accountable for leading high-impact projects such as system integrations, tax compliance initiatives, internal process redesign, and policy governance.&lt;/p&gt;
&lt;p&gt;PRIMARY RESPONSIBILITIES:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead, coach, and develop a high-performing payroll team, ensuring accurate and timely processing of payroll for a workforce of 5,000+ employees across multiple states and business units.&lt;/li&gt;
&lt;li&gt;Own the payroll strategy and roadmap, driving continuous improvement, automation, and alignment with enterprise priorities.&lt;/li&gt;
&lt;li&gt;Oversee and refine internal controls, data integrity practices, and payroll compliance to mitigate risk and ensure audit readiness.&lt;/li&gt;
&lt;li&gt;Serve as a strategic partner to Finance, Accounting, HR, and Legal, providing payroll insights and aligning payroll processes with business and regulatory requirements.&lt;/li&gt;
&lt;li&gt;Manage vendor relationships, including third-party payroll providers, tax agencies, and system vendors, ensuring accountability and service excellence.&lt;/li&gt;
&lt;li&gt;Lead or co-lead payroll system implementations, upgrades, and integrations with timekeeping, HRIS, and financial systems.&lt;/li&gt;
&lt;li&gt;Ensure accurate calculation and application of complex pay components including bonuses, equity, commissions, retro pay, garnishments, and various leave types.&lt;/li&gt;
&lt;li&gt;Stay up to date on evolving payroll legislation and translate regulatory changes into clear, compliant policies and workflows.&lt;/li&gt;
&lt;li&gt;Develop and deliver KPIs and executive-level reporting to support strategic decision-making and resource planning.&lt;/li&gt;
&lt;li&gt;Act as escalation point for complex or sensitive payroll issues requiring judgment, cross-functional coordination, or executive visibility.&lt;/li&gt;
&lt;li&gt;Management of the payroll team.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;QUALIFICATIONS:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor&#39;s degree in Accounting, Finance, Business, or a related field required; Master’s degree or MBA a plus.&lt;/li&gt;
&lt;li&gt;Minimum of 8–10 years of progressive payroll experience, including 3+ years in a people management role.&lt;/li&gt;
&lt;li&gt;Strong experience managing payroll operations in a high-growth, multi-state environment with 5,000+ employees.&lt;/li&gt;
&lt;li&gt;Expertise with Workday Payroll, UltiPro (UKG Pro) or a comparable enterprise payroll platform is required; system implementation experience highly preferred.&lt;/li&gt;
&lt;li&gt;Certified Payroll Professional (CPP) strongly preferred.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;KNOWLEDGE, SKILLS, AND ABILITIES:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Expert-level knowledge of federal, state, and local payroll regulations, tax compliance, and reporting requirements.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to lead through ambiguity, drive results, and influence stakeholders across departments.&lt;/li&gt;
&lt;li&gt;Strong analytical and critical thinking skills; able to diagnose complex issues and implement sustainable solutions.&lt;/li&gt;
&lt;li&gt;Proven ability to manage confidential information with discretion and integrity.&lt;/li&gt;
&lt;li&gt;Exceptional communication skills, with experience presenting to senior leadership and external auditors.&lt;/li&gt;
&lt;li&gt;Process improvement and systems-savvy mindset, with a track record of streamlining payroll operations and leveraging technology.&lt;/li&gt;
&lt;li&gt;Will be overseeing payroll team.&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Compensation &amp;amp; Total Rewards&amp;nbsp;&lt;/span&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;This range reflects a good-faith estimate of the base pay we reasonably&amp;nbsp;expect to offer at the time of&amp;nbsp; hire.&amp;nbsp;Final compensation will vary based on experience, qualifications, and internal equity considerations.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;This position&amp;nbsp;is also eligible for additional compensation and benefits through&amp;nbsp;Natera’s robust Total Rewards program, including:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Annual performance incentive bonus&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Long-term equity awards&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Comprehensive health benefits (medical, dental, vision)&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;401(k) with company match&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Generous paid time off and company holidays&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Additional wellness and work-life benefits&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;/p&gt;&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Compensation Range &lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$132,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$165,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr-payroll-managerassociate-director-payroll-operations-natera/69d3bb6dc8e81216cd0b8f19</link><guid isPermaLink="true">http://biotechroles.com/sr-payroll-managerassociate-director-payroll-operations-natera/69d3bb6dc8e81216cd0b8f19</guid><pubDate>Mon, 06 Apr 2026 13:55:56 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - ESI/Cigna/Prime]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director (CAD) is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across priority national and regional payer accounts, PBMs, Medicaid, Medicare, and federal payer channels. This role serves as the enterprise lead for assigned accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions across Dyne’s neuromuscular portfolio.&lt;/p&gt;
&lt;p&gt;The CAD collaborates closely with Market Access, HEOR, Medical Affairs, Trade, Sales, Patient Services, Legal, and Finance to ensure rapid and equitable patient access. This is a field‑based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Market Access &amp;amp; Payer Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute account specific payer strategies that optimize‑specific payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate evolving payer dynamics, benefit design changes, policy shifts, and specialty management trends.&lt;/li&gt;
&lt;li&gt;Serve as an internal subject-matter expert on access pathways, ‑matter expert on access pathways, rare‑disease reimbursement, channel economics, and payer policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;National Account Leadership &amp;amp; Contracting&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic engagement and negotiations with national and regional payers, PBMs, Medicaid MCOs, and federal payers.&lt;/li&gt;
&lt;li&gt;Secure favorable coverage policies, UM criteria, and contracting arrangements—including value-based models where appropriate‑based models where appropriate.&lt;/li&gt;
&lt;li&gt;Identify account-specific access barriers and develop compliant, specific access barriers and develop compliant, data‑driven solutions in partnership with HEOR, Medical, Policy, Trade, and Patient Services.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional‑Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional account planning and coordination across Market Access, Medical Affairs, HEOR, Trade, Commercial, Legal, and Finance.&lt;/li&gt;
&lt;li&gt;Translate payer insights into actionable recommendations for launch execution, forecasting, brand positioning, and pipeline strategy.&lt;/li&gt;
&lt;li&gt;Support organizational readiness across pre‑launch, launch, and post‑launch phases to enable rapid patient access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;External Influence &amp;amp; Insight Generation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor payer, policy, and competitive developments; synthesize insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Represent Dyne at payer engagements, industry associations, and strategic forums.&lt;/li&gt;
&lt;li&gt;Identify opportunities for partnerships, innovative access programs, and policy engagement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Compliance &amp;amp; Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all interactions, materials, and contracting activities comply with Dyne policies, legal, regulatory, and compliance standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree such as MBA, MPH, MS, or PharmD preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Market Access, National Accounts, Managed Markets, or Trade.&lt;/li&gt;
&lt;li&gt;Proven success securing access for specialty, rare‑disease, or high‑cost therapies across commercial and/or public payer segments.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty pharmacy distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Strong negotiation skills and executive presence, with the ability to influence across complex, cross‑functional organizations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to operate effectively in high‑growth, launch‑stage, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Alignment with Dyne’s values, including a patient‑centric mindset, integrity, collaboration, and accountability.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-esicignaprime-dyne-therapeutics/69d3bb6ac8e81216cd0b8f16</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-esicignaprime-dyne-therapeutics/69d3bb6ac8e81216cd0b8f16</guid><pubDate>Mon, 06 Apr 2026 13:55:54 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$160000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Marketing Manager, Health Systems]]></title><description><![CDATA[&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Senior Marketing Manager, Health Systems&amp;nbsp;&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;About the Role:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;&lt;br&gt;&lt;/strong&gt;Join Natera as an Senior Marketing Manager for Health Systems to play a critical role in an innovative new business unit supporting our largest customers, health systems. This is an exciting time at Natera and we are actively building capabilities and solutions to partner strategically with these large customers. This role will be critical to helping us shape the way we go-to-market. Reporting to the Head of Marketing, Health Systems, you will oversee marketing efforts that support marketing communications, marketing operations and sales B2B assets development.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Primary Responsibilities:&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Marketing B2B assets development: &lt;/strong&gt;Partner with the Strategic Account Management (SAM) team, and cross functionally, to build out assets to support our B2B strategy with health system customers.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Marketing communications:&lt;/strong&gt; Drive all marketing communications efforts for the Health Systems BU, interfacing across the organization to make sure the organization is updated on Health System progress.&amp;nbsp; Coordinate all communications for SAMs, work with our social media and website teams to update those areas and help the organization infuse Health System messaging across the company.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Marketing operations: &lt;/strong&gt;Responsible for overseeing the budget, medical legal review efforts, vendor and legal oversight, graphic design and agency collaboration and sales analytics and applications as they pertain to marketing efforts.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Conference and non-personal promotion&lt;/strong&gt;:&amp;nbsp; Oversee all operations in regards to national trade associations and societies memberships, conference and event activities and promotional content through these entities.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Change agent: &lt;/strong&gt;Stay abreast of health care trends that are impacting these large Health System customers and be the agent of change across Natera to educate others about these unique customers.&amp;nbsp;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Education:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Bachelor’s degree in a related field required (B.A. or B.S.); advanced degree (MBA, M.S.) preferred.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience:&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Minimum of 5 years in healthcare product marketing, product management, sales, medical affairs, or strategic consulting.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience in life sciences, health technology, or diagnostics is required.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Oncology experience is preferred.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Experience with health system marketing is strongly preferred.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Knowledge, Skills, and Abilities:&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;High integrity and strong interpersonal skills to build lasting relationships with stakeholders.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Excellent project management skills with strong attention to detail and ability to manage timelines effectively.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Proven ability to synthesize health care trends and clinical information and develop concise, impactful promotional materials.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Strong written and verbal communication skills, including proficiency in presenting technical content to diverse audiences.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Collaborative mindset with the ability to lead and align cross-functional teams.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Analytical, problem-solving mindset with experience gathering customer insights and translating them into actionable strategies.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Familiarity with digital marketing channels and field marketing tactics is a plus.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #222222 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;Proficiency in Google Suite, Microsoft PowerPoint, Excel, and CRM platforms like Salesforce.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #222222;&quot;&gt;&lt;strong&gt;Location: Remote - Must be willing to travel up to 20% &lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Remote USA&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$133,600&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$167,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr.-marketing-manager-health-systems-natera/69d3bb69c8e81216cd0b8f15</link><guid isPermaLink="true">http://biotechroles.com/sr.-marketing-manager-health-systems-natera/69d3bb69c8e81216cd0b8f15</guid><pubDate>Mon, 06 Apr 2026 13:55:53 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$140000-180000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - CVS/Aetna]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director (CAD) is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across priority national and regional payer accounts, PBMs, Medicaid, Medicare, and federal payer channels. This role serves as the enterprise lead for assigned accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions across Dyne’s neuromuscular portfolio.&lt;/p&gt;
&lt;p&gt;The CAD collaborates closely with Market Access, HEOR, Medical Affairs, Trade, Sales, Patient Services, Legal, and Finance to ensure rapid and equitable patient access. This is a field‑based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Market Access &amp;amp; Payer Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute account specific payer strategies that optimize‑specific payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate evolving payer dynamics, benefit design changes, policy shifts, and specialty management trends.&lt;/li&gt;
&lt;li&gt;Serve as an internal subject-matter expert on access pathways, ‑matter expert on access pathways, rare‑disease reimbursement, channel economics, and payer policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;National Account Leadership &amp;amp; Contracting&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic engagement and negotiations with national and regional payers, PBMs, Medicaid MCOs, and federal payers.&lt;/li&gt;
&lt;li&gt;Secure favorable coverage policies, UM criteria, and contracting arrangements—including value-based models where appropriate‑based models where appropriate.&lt;/li&gt;
&lt;li&gt;Identify account-specific access barriers and develop compliant, specific access barriers and develop compliant, data‑driven solutions in partnership with HEOR, Medical, Policy, Trade, and Patient Services.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional‑Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional account planning and coordination across Market Access, Medical Affairs, HEOR, Trade, Commercial, Legal, and Finance.&lt;/li&gt;
&lt;li&gt;Translate payer insights into actionable recommendations for launch execution, forecasting, brand positioning, and pipeline strategy.&lt;/li&gt;
&lt;li&gt;Support organizational readiness across pre‑launch, launch, and post‑launch phases to enable rapid patient access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;External Influence &amp;amp; Insight Generation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor payer, policy, and competitive developments; synthesize insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Represent Dyne at payer engagements, industry associations, and strategic forums.&lt;/li&gt;
&lt;li&gt;Identify opportunities for partnerships, innovative access programs, and policy engagement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Compliance &amp;amp; Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all interactions, materials, and contracting activities comply with Dyne policies, legal, regulatory, and compliance standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree such as MBA, MPH, MS, or PharmD preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Market Access, National Accounts, Managed Markets, or Trade.&lt;/li&gt;
&lt;li&gt;Proven success securing access for specialty, rare‑disease, or high‑cost therapies across commercial and/or public payer segments.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty pharmacy distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Strong negotiation skills and executive presence, with the ability to influence across complex, cross‑functional organizations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to operate effectively in high‑growth, launch‑stage, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Alignment with Dyne’s values, including a patient‑centric mindset, integrity, collaboration, and accountability.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-cvsaetna-dyne-therapeutics/69d3bb66c8e81216cd0b8f12</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-cvsaetna-dyne-therapeutics/69d3bb66c8e81216cd0b8f12</guid><pubDate>Mon, 06 Apr 2026 13:55:50 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$180000-250000</salary><type>Full-time</type></item><item><title><![CDATA[Sr. Manager, Biopharma Real World Data Analyst]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;Sr. Manager, Real World Data Analyst&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Natera is the global leader in the development of blood-based diagnostics and has built considerable momentum in the utilization of our Signatera (tumor informed) and Latitude (tumor naïve) assays.&amp;nbsp; 2025 reflected a significant increase in the utilization of Signatera with &amp;gt;700k samples processed across our labs.&amp;nbsp; Our WGS/WES repertoire and the integration of Foresight’s phased variants technique and expertise in Lymphomas have enabled Natera to offer the most experienced, published, and highest ordered MRD test available with global reach.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;In addition, our best-in-class MRD assays combined with ultra-sensitivity has positioned Natera to lead this area of diagnostics.&amp;nbsp; Our business model has adapted and expanded to offer our customers real world data and insights to support their research objectives.&amp;nbsp; We believe that our unique, multi-time point molecular data, matched with curated clinical data from the EHR and matched H&amp;amp;E digital pathology provides our customers with the most biologically informed dataset for Oncology.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;These insights are ideally suited to support translational and clinical development teams with the evidence necessary to improve trial design, select the right patients and understand the correlation across treatments, outcomes and molecular signatures across several data modalities (MRD / ctDNA, WGS, WES &amp;amp; WTS, Claims, EMR curated clinical data and digpath).&amp;nbsp; In addition, our multi-modal datasets are uniquely designed to understand response, quantify resistance and build models defining recurrence and the time horizons when high risk patients may relapse/recur.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Natera’s Mission for Life Science Companies&lt;/strong&gt;:&lt;/p&gt;
&lt;p&gt;Integrate and utilize Natera’s portfolio of products, services and solutions to transform the R&amp;amp;D methodology and improve the probability of success across all of pharma’s primary verticals (Discovery, Development &amp;amp; Commercial) while bringing new products to market faster while compressing costs.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Summary Of The Role:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Real-World Data &amp;amp; Analytics (RWDA) group within the Biopharma team at Natera works with major Biopharmaceutical partners to provide best-in-class data, analysis, and methodological guidance for Natera’s real-world data offering.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We are seeking a highly motivated and solutions-oriented RWDA / Data Scientist with experience and interest in oncology, molecular analysis and epidemiological study design to join our team. This role requires the individual engage customers to generate new hypotheses and research questions, iterate and interrogate existing hypotheses and research questions, design research projects, conduct and iterate on the analysis as well as derive insights from complex real-world multi-modal, multi-time point molecular and clinical data. The individual will also implement advanced statistical methods, and utilize internal analytical tools, interfaces as well as AI tools to generate, visualize and enhance insights.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Team Reporting: data analysts will report directly to the Sr. Manager.&amp;nbsp; This role will be responsible for identifying, hiring, mentoring, training and supervising the team across a number of customers.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Biopharma Partnerships: design, prepare data and conduct analysis and delivery of RWE analyses for biopharma clients. You will be responsible for translating complex clinical development and translational research questions into actionable research plans and insights utilizing Natera data for trial design, outcomes research and other bespoke projects.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Multi-modal Real World Data Expertise: generate insights from complex real-world endpoints using extensive coding, demonstrating deep comprehension of Natera clinical and molecular data structures and complexity, while also serving as an expert on the methodological nuances and limitations of real-world data.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Methodological Standards &amp;amp; Mentorship: Build technical standards by implementing advanced methods in survival analysis, machine learning and predictive modeling.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; AI-Enhanced Applications: Integrate practical adoption of Natera tools including: LLMs and agentic tools into your own daily workflow. Your focus will be on using these technologies to improve the speed and accuracy of code development, documentation, and review.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Scientific Leadership &amp;amp; Influence: Own the communication of high impact/value results to internal stakeholders and external partners. You will be responsible for the scientific integrity of all deliverables, including manuscripts, conference abstracts, and technical reports where appropriate.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Cross-Functional Collaboration: Collaborate with internal product, oncology, and clinical abstraction, medical, scientific, business development and consortia teams to continually enhance Natera data quality, products, and analytical best practices.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Product / Work-Flow Enhancement: Proactively identify gaps in current products and ensure that customer feedback is collected and integrated into the Natera product road map.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Oncology &amp;amp; RWE Domain Expertise: Maintain deep expertise in oncology clinical guidelines (e.g., NCCN) and emerging RWE methodologies. You will be responsible for translating these external shifts into internal strategy, ensuring that our research designs and data modeling stay ahead of the evolving oncology landscape and reflect the most current standard of care.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Education: Advanced education in epidemiology, biostatistics, data science, public health, or related fields, to the level of either:&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Master’s degree, or PhD and 4+ years of additional work experience&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Technical &amp;amp; Statistical Mastery:&amp;nbsp;&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Expert-level proficiency in observational real-world healthcare data, specifically in designing and implementing complex time-to-event methodologies (survival analysis).&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Track record of leading RWD analytical studies from initial scoping through to publication or dissemination.&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Proficient in using R and SQL, especially statistical tools and packages.&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Proficiency applying machine learning, LLM-based coding assistants (e.g., Copilot, Cursor) and agentic frameworks to support data analysis, code review, or scientific documentation workflows.&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Adherence to good software engineering practices (version control, modular code, documentation).&lt;/p&gt;
&lt;p&gt;o&amp;nbsp;&amp;nbsp; Experience with code review.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Communication &amp;amp; Client Ownership: Experience as a primary technical point of communication for biopharma clients, with a proven ability to collaborate on study design and translate highly technical findings into strategic recommendations for senior-level stakeholders.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Leadership &amp;amp; Soft Skills: Strong project leadership and the ability to manage multiple high-priority workstreams simultaneously in a fast-paced environment.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Soft Skills: Strong project leadership with excellent written and verbal communication skills. Ability to thrive in a fast-paced, dynamic environment working with multi-disciplinary scientists on complex problems.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Solution Oriented: Ability to see through initial research questions to the high impact / valuable insights customers require (need vs. want). Understand the question behind the question as well as identify solutions to generate meaningful insights when the data does not exist.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred Skillsets:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Experience working with Pharma or drug development.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Experience in clinical trial design in the clinical development space.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Extensive proficiency with EMR raw and curated data, claims, and registry data.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Practical experience building, fine-tuning, or configuring LLM-based tools and agentic workflows specifically for scientific discovery.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; High-level familiarity with NCCN guidelines and the ability to interpret real-world outcomes within the context of the current oncology standard of care.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Significant experience analyzing multi-modal data including biomarker, genomic, or other high-dimensional molecular data alongside clinical datasets.&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp;&amp;nbsp; Proficiency in managing large-scale data projects within cloud environments such as AWS or Google Cloud Platform (GCP).&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Travel: As necessary (up to 20%)&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;This is a remote position.&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;description&quot;&gt;The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp;amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.&lt;/div&gt;&lt;div class=&quot;title&quot;&gt;Remote USA&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$143,100&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$178,900 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/sr.-manager-biopharma-real-world-data-analyst-natera/69d3bb65c8e81216cd0b8f11</link><guid isPermaLink="true">http://biotechroles.com/sr.-manager-biopharma-real-world-data-analyst-natera/69d3bb65c8e81216cd0b8f11</guid><pubDate>Mon, 06 Apr 2026 13:55:49 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$150000-190000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - Centene / Humana]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director (CAD) is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across priority national and regional payer accounts, PBMs, Medicaid, Medicare, and federal payer channels. This role serves as the enterprise lead for assigned accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions across Dyne’s neuromuscular portfolio.&lt;/p&gt;
&lt;p&gt;The CAD collaborates closely with Market Access, HEOR, Medical Affairs, Trade, Sales, Patient Services, Legal, and Finance to ensure rapid and equitable patient access. This is a field‑based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Market Access &amp;amp; Payer Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute account specific payer strategies that optimize‑specific payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate evolving payer dynamics, benefit design changes, policy shifts, and specialty management trends.&lt;/li&gt;
&lt;li&gt;Serve as an internal subject-matter expert on access pathways, ‑matter expert on access pathways, rare‑disease reimbursement, channel economics, and payer policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;National Account Leadership &amp;amp; Contracting&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic engagement and negotiations with national and regional payers, PBMs, Medicaid MCOs, and federal payers.&lt;/li&gt;
&lt;li&gt;Secure favorable coverage policies, UM criteria, and contracting arrangements—including value-based models where appropriate‑based models where appropriate.&lt;/li&gt;
&lt;li&gt;Identify account-specific access barriers and develop compliant, specific access barriers and develop compliant, data‑driven solutions in partnership with HEOR, Medical, Policy, Trade, and Patient Services.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional‑Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional account planning and coordination across Market Access, Medical Affairs, HEOR, Trade, Commercial, Legal, and Finance.&lt;/li&gt;
&lt;li&gt;Translate payer insights into actionable recommendations for launch execution, forecasting, brand positioning, and pipeline strategy.&lt;/li&gt;
&lt;li&gt;Support organizational readiness across pre‑launch, launch, and post‑launch phases to enable rapid patient access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;External Influence &amp;amp; Insight Generation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor payer, policy, and competitive developments; synthesize insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Represent Dyne at payer engagements, industry associations, and strategic forums.&lt;/li&gt;
&lt;li&gt;Identify opportunities for partnerships, innovative access programs, and policy engagement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Compliance &amp;amp; Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all interactions, materials, and contracting activities comply with Dyne policies, legal, regulatory, and compliance standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree such as MBA, MPH, MS, or PharmD preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Market Access, National Accounts, Managed Markets, or Trade.&lt;/li&gt;
&lt;li&gt;Proven success securing access for specialty, rare‑disease, or high‑cost therapies across commercial and/or public payer segments.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty pharmacy distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Strong negotiation skills and executive presence, with the ability to influence across complex, cross‑functional organizations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to operate effectively in high‑growth, launch‑stage, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Alignment with Dyne’s values, including a patient‑centric mindset, integrity, collaboration, and accountability.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-centene-humana-dyne-therapeutics/69d3bb63c8e81216cd0b8f0d</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-centene-humana-dyne-therapeutics/69d3bb63c8e81216cd0b8f0d</guid><pubDate>Mon, 06 Apr 2026 13:55:47 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$160000-240000</salary><type>Full-time</type></item><item><title><![CDATA[Corporate Account Director - Anthem / Kaiser]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Corporate Account Director (CAD) is a senior commercial leader responsible for shaping and executing Dyne’s U.S. market access strategy across priority national and regional payer accounts, PBMs, Medicaid, Medicare, and federal payer channels. This role serves as the enterprise lead for assigned accounts, driving coverage, reimbursement, formulary positioning, and innovative access solutions across Dyne’s neuromuscular portfolio.&lt;/p&gt;
&lt;p&gt;The CAD collaborates closely with Market Access, HEOR, Medical Affairs, Trade, Sales, Patient Services, Legal, and Finance to ensure rapid and equitable patient access. This is a field‑based role.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key Responsibilities&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;em&gt;Market Access &amp;amp; Payer Strategy&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Develop and execute account specific payer strategies that optimize‑specific payer strategies that optimize coverage, reimbursement, and formulary access across commercial, PBM, Medicaid, Medicare, and federal payer segments.&lt;/li&gt;
&lt;li&gt;Anticipate evolving payer dynamics, benefit design changes, policy shifts, and specialty management trends.&lt;/li&gt;
&lt;li&gt;Serve as an internal subject-matter expert on access pathways, ‑matter expert on access pathways, rare‑disease reimbursement, channel economics, and payer policy.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;National Account Leadership &amp;amp; Contracting&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead strategic engagement and negotiations with national and regional payers, PBMs, Medicaid MCOs, and federal payers.&lt;/li&gt;
&lt;li&gt;Secure favorable coverage policies, UM criteria, and contracting arrangements—including value-based models where appropriate‑based models where appropriate.&lt;/li&gt;
&lt;li&gt;Identify account-specific access barriers and develop compliant, specific access barriers and develop compliant, data‑driven solutions in partnership with HEOR, Medical, Policy, Trade, and Patient Services.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;Cross Functional‑Functional Commercial Leadership&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Lead cross-functional account planning and coordination across Market Access, Medical Affairs, HEOR, Trade, Commercial, Legal, and Finance.&lt;/li&gt;
&lt;li&gt;Translate payer insights into actionable recommendations for launch execution, forecasting, brand positioning, and pipeline strategy.&lt;/li&gt;
&lt;li&gt;Support organizational readiness across pre‑launch, launch, and post‑launch phases to enable rapid patient access.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;External Influence &amp;amp; Insight Generation&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Monitor payer, policy, and competitive developments; synthesize insights for senior leadership.&lt;/li&gt;
&lt;li&gt;Represent Dyne at payer engagements, industry associations, and strategic forums.&lt;/li&gt;
&lt;li&gt;Identify opportunities for partnerships, innovative access programs, and policy engagement.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;&lt;em&gt;Compliance &amp;amp; Governance&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Ensure all interactions, materials, and contracting activities comply with Dyne policies, legal, regulatory, and compliance standards.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree: advanced degree such as MBA, MPH, MS, or PharmD preferred.&lt;/li&gt;
&lt;li&gt;10+ years of experience in the biopharma industry, including at least 8 years in Market Access, National Accounts, Managed Markets, or Trade.&lt;/li&gt;
&lt;li&gt;Proven success securing access for specialty, rare‑disease, or high‑cost therapies across commercial and/or public payer segments.&lt;/li&gt;
&lt;li&gt;Deep understanding of U.S. payer systems, reimbursement pathways, specialty pharmacy distribution, and Medicaid/federal payer dynamics.&lt;/li&gt;
&lt;li&gt;Strong negotiation skills and executive presence, with the ability to influence across complex, cross‑functional organizations.&lt;/li&gt;
&lt;li&gt;Demonstrated ability to operate effectively in high‑growth, launch‑stage, or ambiguous environments.&lt;/li&gt;
&lt;li&gt;Alignment with Dyne’s values, including a patient‑centric mindset, integrity, collaboration, and accountability.&lt;/li&gt;
&lt;li&gt;Ability to travel domestically, including overnight travel.&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:720,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$238,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$260,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/corporate-account-director-anthem-kaiser-dyne-therapeutics/69d3bb5fc8e81216cd0b8f0b</link><guid isPermaLink="true">http://biotechroles.com/corporate-account-director-anthem-kaiser-dyne-therapeutics/69d3bb5fc8e81216cd0b8f0b</guid><pubDate>Mon, 06 Apr 2026 13:55:43 GMT</pubDate><company>Dyne Therapeutics</company><location>Field-Based</location><salary>$180000-280000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Oncology Trial Navigator]]></title><description><![CDATA[&lt;h1&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Oncology Trial Navigator&lt;/strong&gt;&lt;/span&gt;&lt;/h1&gt;
&lt;h3&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;&lt;br&gt;About the Role&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;br&gt;The &lt;strong&gt;Oncology Trial Navigator&lt;/strong&gt; will play a critical role in connecting Signatera patients to life-changing clinical trial opportunities. As a front-line clinical expert, you will be responsible for the end-to-end execution of patient matching workflows—from initial AI-enabled screening to successful enrollment at a clinical trial site.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;br&gt;You will serve as the primary clinical point of contact for external stakeholders, including treating oncologists, principal investigators (PIs), and research coordinators. This role combines deep oncology clinical knowledge with high-touch stakeholder engagement in a fast-scaling, mission-driven environment. You will work closely with the Senior Manager of Oncology Trial Navigation to pilot and refine the navigation service, providing the &quot;on-the-ground&quot; insights necessary to scale this function across the oncology domain.&lt;/span&gt;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;&lt;br&gt;What You’ll Do&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Physician &amp;amp; Site Engagement&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Conduct high-volume, structured outreach to oncologists, PIs, and research coordinators regarding trial-eligible patients identified through Natera’s platforms.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Act as a clinical consultant to research sites, delivering patient eligibility notifications and facilitating seamless referral workflows.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Track patient progression from initial identification through referral and enrollment, ensuring timely follow-up and resolution of site-level bottlenecks.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Trial Matching &amp;amp; Medical Review&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Operationalize outputs from Natera’s AI-enabled trial matching platform to manage a daily priority queue of potential matches.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Perform rigorous clinical reviews, reconciling patient molecular data (e.g., MRD status, biomarkers) and exome results with trial-specific inclusion/exclusion criteria.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Collaborate with the Clinical Product team to provide real-time feedback on matching accuracy, helping to refine AI algorithms and data filters.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Patient &amp;amp; Caregiver Support (as applicable)&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Provide high-level, empathetic, and compliant education to patients regarding specific clinical trial opportunities and the clinical significance of their molecular results.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Coordinate warm handoffs to site research teams, ensuring patients feel supported and informed throughout the referral process.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;br&gt;&lt;br&gt;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Operational Excellence&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Maintain meticulous documentation of all outreach and referral activities within CRM and tracking tools.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Contribute to the continuous improvement of Standard Operating Procedures (SOPs).&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Participate in cross-functional collaboration with internal partners to optimize the field.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h3&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Education &amp;amp; Licensure:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Current, active licensure as a &lt;strong&gt;Registered Nurse (RN), Certified Genetic Counselor (CGC), Nurse Practitioner (NP), or Physician Assistant (PA)&lt;/strong&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Must maintain licensure in good standing throughout employment.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Board Certification (e.g., OCN, CCRC, or similar) is highly preferred.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;A master’s degree in a clinical or scientific field is preferred.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Professional Experience:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;3–5 years of oncology clinical experience, with at least 2 years specifically in &lt;strong&gt;oncology clinical research&lt;/strong&gt; (e.g., as a Research Nurse, Coordinator, or Navigator).&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Proven experience in patient identification and trial matching services, ideally within a molecular diagnostics or biotech environment.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Experience communicating complex clinical and genomic information to physicians, PIs, and patients.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Clinical Expertise:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Strong clinical knowledge of oncology, with a focus on biomarker-driven therapies and MRD-based clinical trial landscapes.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Expert-level understanding of clinical trial design and the ability to interpret complex inclusion/exclusion criteria.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Technical &amp;amp; Data Proficiency:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Technology Adoption:&lt;/strong&gt; Ability to quickly master new AI-enabled matching tools and digital health platforms.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Data Literacy:&lt;/strong&gt; Comfort navigating large clinical datasets and translating patient records into structured eligibility requirements.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Systems Advocacy:&lt;/strong&gt; Proactive in identifying workflow inefficiencies and suggesting technological or process-based solutions.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Core Competencies:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Exceptional communication and interpersonal skills.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;High degree of empathy and professionalism in patient-facing interactions.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Strong organizational skills and follow through discipline.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-oncology-trial-navigator-natera/69d3bb5ec8e81216cd0b8f0a</link><guid isPermaLink="true">http://biotechroles.com/senior-oncology-trial-navigator-natera/69d3bb5ec8e81216cd0b8f0a</guid><pubDate>Mon, 06 Apr 2026 13:55:42 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$110000-150000</salary><type>Full-time</type></item><item><title><![CDATA[Contracts Manager]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Contracts Manager is responsible for managing a wide range of contract negotiations and agreements to support Dyne Therapeutics&#39; business operations and collaborations. This role focuses on drafting and negotiating service agreements, clinical trial agreements, consulting agreements, pharmacy benefit manager agreements, license agreements, confidential disclosure agreements. Additionally, the Contracts Manager handles other commercial phase agreements and mitigates risk.&amp;nbsp;The person in this role will be able to manage multiple priorities and work collaboratively in an environment with multiple stakeholders.&lt;br&gt;&lt;br&gt;This role is based in Waltham, MA.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Primary Responsibilities Include:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Drafts, reviews, and negotiates a wide range of contracts&lt;/li&gt;
&lt;li&gt;Ensure contracts align with company policies, legal standards, and business objectives&lt;/li&gt;
&lt;li&gt;Assist with the maintenance of a centralized contract repository; ensuring all contracts are properly filed, tracked, and accessible; monitoring contract deadlines and renewals; and assisting with the contracts execution process&lt;/li&gt;
&lt;li&gt;Identify and mitigate potential risks in contract terms and conditions in partnership with Contracts leadership&lt;/li&gt;
&lt;li&gt;Work closely with internal departments (e.g., Sales, Finance, IT, Clinical Operations, Commercial, and Medical Affairs) to understand their contract needs and provide support&lt;/li&gt;
&lt;li&gt;Assist in developing and updating contract templates, policies, and procedures to improve efficiency and reduce risk&lt;/li&gt;
&lt;li&gt;Assist in training and educating employees on contract-related processes and best practices&lt;/li&gt;
&lt;li&gt;As needed, prepare reports on contract status and key metric&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Education and Skills Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in Law, Business Administration, or a related field preferred Paralegal certification or equivalent experience may be considered.&lt;/li&gt;
&lt;li&gt;Minimum of 5 years of experience in contract management, preferably in the biotechnology or pharmaceutical setting&lt;/li&gt;
&lt;li&gt;Experience with Conga Contracts preferred&lt;/li&gt;
&lt;li&gt;Proven experience drafting, reviewing, and negotiating complex contracts&lt;/li&gt;
&lt;li&gt;Strong understanding of contract law and legal terminology&lt;/li&gt;
&lt;li&gt;Excellent negotiation, communication, and interpersonal skills&lt;/li&gt;
&lt;li&gt;High attention to detail and organizational skills&lt;/li&gt;
&lt;li&gt;Proficiency in contract management software and Microsoft Office Suite.&lt;/li&gt;
&lt;li&gt;Ability to work with minimal supervision and manage multiple priorities in a fast-paced environment&lt;/li&gt;
&lt;li&gt;Certified Commercial Contracts Manager (CCCM) or equivalent certification is strongly preferred.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;#LI-Onsite&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$118,340&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$145,500 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/contracts-manager-dyne-therapeutics/69d3bb5bc8e81216cd0b8f09</link><guid isPermaLink="true">http://biotechroles.com/contracts-manager-dyne-therapeutics/69d3bb5bc8e81216cd0b8f09</guid><pubDate>Mon, 06 Apr 2026 13:55:39 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham, MA</location><salary>$120000-160000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Manager, Oncology Trial Navigation]]></title><description><![CDATA[&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Senior Manager, Oncology Trial Navigation&lt;br&gt;&lt;/strong&gt;&lt;/span&gt;&lt;/h2&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;About the Role&lt;/strong&gt;&lt;/span&gt;&lt;/h2&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;The &lt;strong&gt;Senior Manager of Oncology Trial Navigation &lt;/strong&gt;will play a critical role in connecting Signatera patients to appropriate clinical trial opportunities, sponsored by biopharma partners, academia, or by Natera itself. &lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;The Senior Manager will initially serve as the lead individual contributor to establish ground truth for the oncology navigation workflow with the expectation that the role will evolve as the program scales to focus on strategic program growth and team leadership.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;You will serve as the operational bridge between Natera’s centralized patient screening team and external stakeholders—including treating oncologists, principal investigators (PIs), research coordinators, and, when appropriate, patients themselves.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;You will play a key role in operationalizing and scaling the oncology focused trial navigation program, partnering with internal stakeholders to harmonize best practices, refine clinical workflows, and scale the team’s reach. This is a unique opportunity for an experienced clinician to drive strategic development of a function that directly accelerates oncology clinical trial enrollment in a fast-scaling, mission driven environment. This role demands exceptional communication and cross functional collaboration to successfully deliver and expand clinical trial support in the oncology domain.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;What You’ll Do&lt;/strong&gt;&lt;/span&gt;&lt;/h2&gt;
&lt;h3&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Physician &amp;amp; Site Engagement&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Conduct structured outreach to oncologists, PIs, and research coordinators regarding trial-eligible patients.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Deliver patient eligibility notifications and facilitate referral workflows.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Support site prioritization and activation strategies.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Ensure timely follow-up and outcome tracking.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Trial Matching Coordination&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Operationalize outputs from Natera’s AI-enabled trial matching platform.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Support eligibility review by aligning molecular and clinical data with trial inclusion/exclusion criteria.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Track patient progression from identification through referral and enrollment.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Patient &amp;amp; Caregiver Support (as applicable)&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Provide high-level, compliant education about trial opportunities.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Coordinate seamless handoffs to site research teams.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Approach all patient interactions with empathy and professionalism.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Operational Excellence&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Support business development by providing clinical feasibility insights.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Maintain accurate documentation of outreach and referral activities.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Use tracking tools to monitor performance metrics.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Develop SOPs and continuous process improvement to support and scale operational excellence in Oncology Trial Navigation that are harmonized with existing Natera departments.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Participate in cross-functional collaboration with Clinical Ops, Medical, Data Science, and Business Development.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Proactively identify opportunities for process optimization, communication strategies, and contribute to organizational growth through development and implementation of operational strategy and best practices.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;h3&gt;&lt;span style=&quot;color: #494949;&quot;&gt;&lt;strong&gt;Leadership and Team Building&lt;/strong&gt;&lt;/span&gt;&lt;/h3&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Lead the hiring, onboarding, and professional development of Oncology Trial Navigation IC roles to scale this function.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Provide direct coaching on clinical navigation, complex stakeholder management, and empathy-led patient outreach.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Define performance metrics and drive a culture of continuous improvement, ensuring the team is equipped to meet growing trial demand.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Qualifications&lt;/strong&gt;&lt;/span&gt;&lt;/h2&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Education &amp;amp; Licensure:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Current, active licensure as a Registered Nurse, Certified Genetic Counselor, Nurse Practitioner, Physician Assistant or other advanced clinical licensure.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Required to maintain licensure in good standing throughout employment.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Board Certification (e.g. OCN, CCRC or similar) is highly preferred.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;A master&#39;s degree in a clinical or scientific field is highly preferred.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Professional Experience:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;5+ years of oncology clinical experience, with at least 3 years specifically in oncology clinical research.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Preference for experience specifically in patient identification and trial matching services at a leading molecular diagnostics laboratory or independent clinical trial matching company.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Leadership Experience:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Proven experience in building and scaling a clinical program.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Demonstrated ability to manage direct reports and mentor team members in a fast paced environment.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Strong initiative and follow through discipline.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;&lt;strong&gt;Clinical Expertise:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Advanced clinical knowledge in oncology with deep understanding of biomarker driven oncology, MRD based clinical trial landscapes&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Expert-level understanding of clinical trial design and the ability to interpret complex inclusion/exclusion criteria.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Familiarity with centralized screening or trial referral models.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Experience communicating with patients, physicians, PIs, and research coordinators.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;&lt;strong&gt;Technical &amp;amp; Data Proficiency:&lt;/strong&gt;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Ability to quickly learn new technologies and serve as primary business stakeholder for technological solutions utilized in Oncology Trial Navigation.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Proactive in identifying inefficiencies and partnering with technology teams to facilitate solution development.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #000000 !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Comfortable navigating large datasets and&amp;nbsp; translating complex clinical trial protocols into structured data requirements.&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;h2&gt;&lt;span style=&quot;color: #000000;&quot;&gt;Core Competencies&amp;nbsp;&lt;/span&gt;&lt;/h2&gt;
&lt;ul&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Ability to design, implement, and scale clinical navigation workflows.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Proven success as both an individual contributor and effective people leader.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Exceptional communication and interpersonal skills.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;High degree of empathy and professionalism in patient-facing interactions.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;li style=&quot;color: #1f1f1f !important;&quot;&gt;
&lt;p&gt;&lt;span style=&quot;color: #1f1f1f;&quot;&gt;Strong organizational skills and follow through discipline.&lt;/span&gt;&lt;/p&gt;
&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-manager-oncology-trial-navigation-natera/69d3bb58c8e81216cd0b8f08</link><guid isPermaLink="true">http://biotechroles.com/senior-manager-oncology-trial-navigation-natera/69d3bb58c8e81216cd0b8f08</guid><pubDate>Mon, 06 Apr 2026 13:55:35 GMT</pubDate><company>Natera</company><location>US Remote</location><salary>$130000-170000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, US Marketing Operations]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;Role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt; Summary&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The&amp;nbsp;Associate Director,&amp;nbsp;US Marketing Operations&amp;nbsp;establishes&amp;nbsp;and leads the tactical execution of marketing operations, with an immediate focus on launch readiness for Dyne’s lead assets in Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1). As Dyne transitions into a fully integrated biotechnology company, this role plays a critical part in building the systems, processes, and operational infrastructure&amp;nbsp;required&amp;nbsp;to enable compliant, impactful, and efficient delivery of therapeutic education to US external stakeholders.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The Associate Director serves as a key partner across Marketing, Commercial Operations, Medical Affairs, Market Access, Patient Services, Regulatory, Legal, Compliance, and Information Technology, driving operational excellence and enabling speed to market in highly regulated and complex therapeutic landscapes.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;This role is located in our Waltham, MA office.&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-bottom=&quot;0px none #000000&quot; data-ccp-padding-bottom=&quot;0px&quot; data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:246,&amp;quot;335559739&amp;quot;:246,&amp;quot;335559740&amp;quot;:240,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;Commercial MLR Review Committee Leadership&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:246,&amp;quot;335559739&amp;quot;:246,&amp;quot;335559740&amp;quot;:240,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;Chair the Dyne Commercial Medical, Legal, and Regulatory review committee and manage the end-to-end content review and approval process for Commercial-led therapeutic education&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:246,&amp;quot;335559739&amp;quot;:246,&amp;quot;335559740&amp;quot;:240,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partner closely with Marketing, Medical, Legal, and Regulatory teams to foster a collaborative, solution-oriented review culture&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure&amp;nbsp;timely, compliant review of HCP, payer, and patient-facing materials and&amp;nbsp;optimize&amp;nbsp;systems supporting content workflows such as Veeva Vault&amp;nbsp;PromoMats&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Collaborate with Regulatory, Legal, and Compliance to&amp;nbsp;maintain&amp;nbsp;policies, procedures, and governance aligned with evolving regulatory standards&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 4&quot;&gt;HCP and Consumer Engagement&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:279,&amp;quot;335559739&amp;quot;:279,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Design and implement a fit-for-purpose HCP and consumer peer-to-peer engagement model that meets the unique educational needs of rare disease launches in DMD and DM1&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Oversee HCP and consumer engagement operations across the Commercial organization, including nomination, contracting, onboarding, training,&amp;nbsp;logistics, and relationship management&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure compliance with all applicable industry regulations and internal policies, including&amp;nbsp;fair market value&amp;nbsp;requirements and Sunshine reporting&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 4&quot;&gt;Marketing Excellence and Performance&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:279,&amp;quot;335559739&amp;quot;:279,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Serve as a strategic partner to Dyne Brand Teams, aligning Marketing Operations capabilities to commercial&amp;nbsp;objectives&amp;nbsp;to enhance executional effectiveness&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Drive continuous improvement across marketing operations processes to support agility, scalability, and compliance&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Oversee print fulfillment operations and manage promotional asset lifecycle planning&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partner with Commercial Operations, Information Technology, and Analytics teams to enable systems that track performance and integrate insights into campaign design and optimization&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure personalized and precise customer engagement through effective use of data, segmentation, and targeting strategies&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 4&quot;&gt;Congress and Meeting Management&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:279,&amp;quot;335559739&amp;quot;:279,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Lead planning and execution of US HCP and consumer-facing congresses, conventions, and field-sponsored events to maximize Dyne’s presence and engagement impact&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Partner closely with Marketing, field-facing teams, and Medical Affairs to coordinate KOL engagement strategies at congresses, ensuring operational excellence, brand alignment, and compliance&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;heading 3&quot;&gt;Qualifications&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559685&amp;quot;:0,&amp;quot;335559738&amp;quot;:246,&amp;quot;335559739&amp;quot;:246,&amp;quot;335559740&amp;quot;:240,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Bachelor’s degree&amp;nbsp;required; advanced degree such as MBA or MPH preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;8+ years of experience in the pharmaceutical or biotechnology industry, with experience supporting rare disease or accelerated approval launches preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Demonstrated ability to thrive in fast-paced environments with strong prioritization and problem-solving skills&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proactive, adaptable, and solution oriented, with&amp;nbsp;a track record&amp;nbsp;of delivering results under tight timelines&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven experience leading promotional review processes in regulated environments&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Deep understanding of US regulatory requirements and compliance standards governing promotional activity&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication, interpersonal, and stakeholder management skills&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong business acumen with the ability to translate strategic&amp;nbsp;objectives&amp;nbsp;into operating execution&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience with commercial systems and platforms such as Veeva Vault&amp;nbsp;PromoMats&amp;nbsp;highly preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience&amp;nbsp;operating&amp;nbsp;effectively in a small, rapidly growing biotech environment with comfort navigating ambiguity&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:false,&amp;quot;134233118&amp;quot;:false,&amp;quot;134233279&amp;quot;:false,&amp;quot;134245418&amp;quot;:false,&amp;quot;134245529&amp;quot;:false,&amp;quot;201341983&amp;quot;:0,&amp;quot;335551550&amp;quot;:0,&amp;quot;335551620&amp;quot;:0,&amp;quot;335559738&amp;quot;:210,&amp;quot;335559739&amp;quot;:210,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$155,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$190,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-us-marketing-operations-dyne-therapeutics/69d3bb56c8e81216cd0b8f06</link><guid isPermaLink="true">http://biotechroles.com/associate-director-us-marketing-operations-dyne-therapeutics/69d3bb56c8e81216cd0b8f06</guid><pubDate>Mon, 06 Apr 2026 13:55:34 GMT</pubDate><company>Dyne Therapeutics</company><location>Remote</location><salary>$160000-210000</salary><type>Full-time</type></item><item><title><![CDATA[Senior Lab Equipment Tech]]></title><description><![CDATA[&lt;p&gt;&lt;strong&gt;POSITION SUMMARY:&lt;/strong&gt;&lt;br&gt;The Senior Lab Equipment Tech supports the CQV (Commissioning, Qualification, and Validation) team by maintaining, calibrating, and troubleshooting laboratory equipment used in genetic testing. This entry-level role is ideal for individuals with a strong attention to detail and an interest in laboratory operations, equipment maintenance, and regulatory compliance.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;PRIMARY RESPONSIBILITIES:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Perform routine cleaning, maintenance, and inspections of laboratory equipment (e.g., pipettes, centrifuges, cold storage units).&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Assist in calibrating lab instruments under supervision and perform preventive maintenance.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Monitor and document equipment performance using logbooks and electronic records in compliance with GDP (Good Documentation Practices).&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Support CQV engineers during commissioning and qualification (IQ/OQ/PQ) activities.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Assist with vendor coordination for equipment repairs and service.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Maintain laboratory tools and spare parts and ensure workspace organization.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Conduct inventory checks and manage equipment availability.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Adhere to lab safety protocols and regulatory requirements.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;QUALIFICATIONS:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp; High school diploma or equivalent (associate degree preferred).&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;0–2 years of experience in a laboratory or regulated environment.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Basic understanding of laboratory equipment and calibration procedures.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Proficiency with basic computer applications (e.g., Microsoft Word, Excel)&lt;br&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;KNOWLEDGE, SKILLS, AND ABILITIES:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Strong organizational skills and attention to detail.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Ability to follow protocols and regulatory guidelines.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Willingness to learn and adapt to new tasks and technologies.&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Team-oriented with strong communication skills.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;PHYSICAL DEMANDS &amp;amp; WORK ENVIRONMENT:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;This position requires the ability to use a computer keyboard, communicate over the telephone and read printed material.&amp;nbsp;&lt;br&gt;●&amp;nbsp;&amp;nbsp; &amp;nbsp;Duties may require working outside normal working hours (evenings and weekends) at times.&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;strong&gt;OUR OPPORTUNITY&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.&lt;/p&gt;
&lt;p&gt;The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;WHAT WE OFFER&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!&lt;/p&gt;
&lt;p&gt;For more information, visit &lt;a href=&quot;http://www.natera.com/&quot; data-cke-saved-href=&quot;http://www.natera.com/&quot;&gt;www.natera.com&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.&lt;/p&gt;
&lt;p&gt;All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.&lt;/p&gt;
&lt;p&gt;&lt;em&gt;If you are based in California, we encourage you to read this important information for California residents.&amp;nbsp;&lt;/em&gt;&lt;/p&gt;
&lt;p&gt;Link: &lt;a href=&quot;https://www.natera.com/notice-of-data-collection-california-residents&quot; target=&quot;_blank&quot;&gt;https://www.natera.com/notice-of-data-collection-california-residents/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;Please be advised that Natera will reach out to candidates with a @&lt;a href=&quot;http://natera.com/&quot; target=&quot;_blank&quot; data-saferedirecturl=&quot;https://www.google.com/url?q=http://natera.com&amp;amp;source=gmail&amp;amp;ust=1657718972773000&amp;amp;usg=AOvVaw3zRwaIiu7070kJKNG4hjRm&quot;&gt;natera.com&lt;/a&gt;&amp;nbsp;email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.&lt;/p&gt;
&lt;p&gt;For more information:&lt;br&gt;- &lt;a href=&quot;https://www.bbb.org/article/tips/12261-bbb-tip-employment-scams&quot; target=&quot;_blank&quot;&gt;BBB announcement on job scams&lt;/a&gt;&amp;nbsp;&lt;br&gt;- &lt;a href=&quot;https://www.fbi.gov/investigate/cyber&quot; target=&quot;_blank&quot;&gt;FBI Cyber Crime resource page&lt;/a&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/senior-lab-equipment-tech-natera/69d3bb52c8e81216cd0b8efe</link><guid isPermaLink="true">http://biotechroles.com/senior-lab-equipment-tech-natera/69d3bb52c8e81216cd0b8efe</guid><pubDate>Mon, 06 Apr 2026 13:55:30 GMT</pubDate><company>Natera</company><location>Austin, TX</location><salary>$55000-75000</salary><type>Full-time</type></item><item><title><![CDATA[Associate Director, Trial Master File Lead]]></title><description><![CDATA[&lt;div class=&quot;content-intro&quot;&gt;&lt;h3&gt;Company Overview:&lt;/h3&gt;
&lt;p&gt;Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at &lt;a href=&quot;https://www.dyne-tx.com/&quot;&gt;https://www.dyne-tx.com/&lt;/a&gt;, and follow us on &lt;a href=&quot;https://x.com/dyne_tx&quot;&gt;X&lt;/a&gt;, &lt;a href=&quot;https://www.linkedin.com/company/dynetx/&quot;&gt;LinkedIn&lt;/a&gt;&amp;nbsp;and &lt;a href=&quot;https://www.facebook.com/DyneTherapeutic/&quot;&gt;Facebook&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;Role Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;The Associate Director, T&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;rial&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;M&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;aster&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;F&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;ile (TMF) Lead&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;is responsible for&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;developing and driving the global TMF strategy,&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;establishing&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;and maintaining robust governance frameworks, and ensuring end&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;to&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;end oversight of the Trial Master File across the clinical portfolio. This role serves as the enterprise owner of TMF processes, quality standards, and inspection readiness, ensuring that TMF operations meet regulatory requirements, support high&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;quality clinical execution, and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;operate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;efficiently at scale.&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;This&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;role&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;partners closely with Clinical Operations, Quality, Regulatory, and external vendors to ensure a unified, proactive approach to TMF health, completeness, and compliance&lt;/span&gt;&lt;/span&gt;&amp;nbsp;&lt;br&gt;&amp;nbsp;&lt;br&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;Primary Responsibilities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;&amp;nbsp;Include&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Normal (Web)&quot;&gt;:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;134233117&amp;quot;:true,&amp;quot;134233118&amp;quot;:true,&amp;quot;335572071&amp;quot;:0,&amp;quot;335572072&amp;quot;:0,&amp;quot;335572073&amp;quot;:4278190080,&amp;quot;335572075&amp;quot;:0,&amp;quot;335572076&amp;quot;:0,&amp;quot;335572077&amp;quot;:4278190080,&amp;quot;335572079&amp;quot;:0,&amp;quot;335572080&amp;quot;:0,&amp;quot;335572081&amp;quot;:4278190080,&amp;quot;335572083&amp;quot;:0,&amp;quot;335572084&amp;quot;:0,&amp;quot;335572085&amp;quot;:4278190080,&amp;quot;335572087&amp;quot;:0,&amp;quot;335572088&amp;quot;:0,&amp;quot;335572089&amp;quot;:4278190080,&amp;quot;469789798&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789802&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789806&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789810&amp;quot;:&amp;quot;none&amp;quot;,&amp;quot;469789814&amp;quot;:&amp;quot;none&amp;quot;}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot; data-ccp-parastyle-defn=&quot;{&amp;quot;ObjectId&amp;quot;:&amp;quot;b669530d-9cee-5fd4-8da3-4cdbed7bfaa2|1&amp;quot;,&amp;quot;ClassId&amp;quot;:1073872969,&amp;quot;Properties&amp;quot;:[469775450,&amp;quot;Body&amp;quot;,201340122,&amp;quot;2&amp;quot;,134233614,&amp;quot;true&amp;quot;,469778129,&amp;quot;Body&amp;quot;,335572020,&amp;quot;1&amp;quot;,469777841,&amp;quot;Helvetica&amp;quot;,469777842,&amp;quot;Helvetica&amp;quot;,469777843,&amp;quot;Helvetica&amp;quot;,469777844,&amp;quot;Helvetica&amp;quot;,469769226,&amp;quot;Helvetica&amp;quot;,335551500,&amp;quot;0&amp;quot;,268442635,&amp;quot;22&amp;quot;]}&quot;&gt;TMF Strategy &amp;amp; Leadership:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:360,&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Define and own the company’s TMF strategy,&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;including&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;innovation opportunities and continuous improvement initiatives&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead the development and implementation of scalable TMF operating models, ensuring alignment with clinical development goals&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Serve as the internal subject matter expert on TMF best practices, regulations, and inspection trends&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Represent TMF leadership in cross&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;functional forums, governance committees, and senior&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;level operational discussions&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Governance &amp;amp; Process Ownership:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:360,&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Establish and maintain TMF governance frameworks, including policies, SOPs, work instructions, and quality standards&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Oversee TMF lifecycle management—from planning and setup through&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;closeout&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;and archival&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Define TMF roles, responsibilities, and RACI structures across internal teams and vendors&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Monitor adherence to processes and drive corrective and preventive actions (CAPAs) related to TMF quality issues&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ensure&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;timely&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;collection, review, and management of TMF documents from&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;clinical&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;study teams and external partners&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;TMF Oversight &amp;amp; Compliance:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:360,&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Provide strategic oversight of TMF operations, including ongoing quality reviews, completeness assessments, and key performance indicators (KPIs&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;)&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ensure TMFs across the portfolio remain inspection&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;ready&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Lead TMF&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;related preparation for audits, inspections, and regulatory submissions&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;, ensuring all documentation is complete and&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;accurate&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Analyze TMF metrics and trends to proactively&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;identify&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;risks, gaps, and improvement opportunities&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to implement proactively&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Vendor &amp;amp; Technology Management:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:360,&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Oversee TMF service providers, CRO partners, and technology platforms to ensure alignment with TMF requirements&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Partner with IT and business stakeholders to&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;optimize&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;the eTMF system, workflows, and integrations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Ensure vendors adhere to contractual obligations, performance expectations, and quality standards related to TMF&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Stay up to date with industry trends and regulatory requirements related to TMF management and documentation practices&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;em&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Cross&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Functional Partnership &amp;amp; Support:&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559685&amp;quot;:360,&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Collaborate with&amp;nbsp;&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;cross-functional study teams&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;to guide TMF planning, milestones, and document management expectations&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Provide training, coaching, and strategic direction to internal and external partners on TMF processes and regulatory requirements&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Advise&lt;/span&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;&amp;nbsp;leadership on TMF health and organizational readiness for key regulatory events&lt;/span&gt;&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p data-ccp-border-between=&quot;0px none #000000&quot; data-ccp-padding-between=&quot;0px&quot;&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span data-ccp-parastyle=&quot;Body&quot;&gt;Education and Skills Requirements:&lt;/span&gt;&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:120}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Bachelor’s degree in life sciences or related field; advanced degree preferred&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;8+ years of experience in clinical operations, document management, or related&amp;nbsp;GxP&amp;nbsp;environment, with significant TMF&amp;nbsp;expertise&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong knowledge of&amp;nbsp;ICHGCP, TMF Reference Model, and global regulatory expectations&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Proven experience developing TMF strategy, governance frameworks, or enterprise&amp;nbsp;level processes&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ability to lead cross-functionally without authority&amp;nbsp;Demonstrated leadership in managing TMF operations or oversight at a portfolio level&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience working with eTMF systems and CRO/vendor oversight&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication, influencing, and stakeholder&amp;nbsp;management skills&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335557856&amp;quot;:16777215}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-pay-transparency&quot;&gt;&lt;div class=&quot;pay-input&quot;&gt;&lt;div class=&quot;title&quot;&gt;MA Pay Range&lt;/div&gt;&lt;div class=&quot;pay-range&quot;&gt;&lt;span&gt;$155,000&lt;/span&gt;&lt;span class=&quot;divider&quot;&gt;&amp;mdash;&lt;/span&gt;&lt;span&gt;$190,000 USD&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.&lt;/p&gt;
&lt;p&gt;The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements.&amp;nbsp; Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.&lt;/p&gt;
&lt;p class=&quot;Body&quot;&gt;&lt;em&gt;&lt;span style=&quot;font-family: &#39;Arial&#39;,sans-serif; color: #626262;&quot;&gt;Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.&lt;/span&gt;&lt;/em&gt;&lt;/p&gt;&lt;/div&gt;]]></description><link>http://biotechroles.com/associate-director-trial-master-file-lead-dyne-therapeutics/69d3bb51c8e81216cd0b8efd</link><guid isPermaLink="true">http://biotechroles.com/associate-director-trial-master-file-lead-dyne-therapeutics/69d3bb51c8e81216cd0b8efd</guid><pubDate>Mon, 06 Apr 2026 13:55:29 GMT</pubDate><company>Dyne Therapeutics</company><location>Waltham</location><salary>$140000-180000</salary><type>Full-time</type></item></channel></rss>