The Study Optimization Manager (SOM) role is accountable for the development, implementation and oversight of optimal clinical supply strategies using advanced modeling techniques and software for selected high-value clinical trials. This R&D enterprise responsibility impacts optimal design of clinical trials, acceleration of clinical supply, and oversight of strategic, enterprise-level risk mitigation and supply management.

Key Responsibilities:

• Apply strategic, cross-program knowledge of clinical supplies to positively influence clinical trial design and supply chain decisions.
• Accountable for independent development and management of advanced demand and supply models in the N-Side Supply Application or other appropriate tools.
• Builds understanding of the business context, systems, environment, strategy and people assigned to the given area. This also includes an understanding of the relevant and complex internal and external high-volume data sources, validity and domains of such data to align with the intended business objective.
• Leads the creation of required data sets, utilizing understanding of complex business problems, data formats, applicability of the data to the problem and standard modelling techniques. Performs & oversees techniques to validate the quality of the data, and fuse data sources using knowledge of data pre-processing techniques for complex or large-scale use cases.  Identify and access novel internal and external data sources, while ensuring compliance with data security and privacy requirements.
• Utilizes basic and advanced modeling techniques, such as basic statistical methods, predictive modelling, advanced clustering, association rules to create models that perform to particular requirements and specifications. Anticipates how a model’s requirements or the available data, will change over time and designs a product that will be able to cope with these requirements. Brings knowledge and expertise about best practices and current future-focused trends and techniques for data modelling and has experience in delivering solutions to production via Continuous Integration / Continuous Delivery.
• Designs rich data visualizations and uses them to communicate complex messages to business leaders at all levels of the organization in a clear and simple way, with the ability to respond effectively to highly challenging questions.
• Proactively engages with internal stakeholders (Clinical Development, Clinical Operations, Value Evidence and Outcomes, Biostats, Comparators Team, Medicine Development & Industrialization) to obtain needed inputs.
• Ensures optimal supply strategy is identified for assigned studies to include comparators, randomization, blinding, country pre-selection and IRT design requirements.
• Optimizes supply strategies initially and dynamically over the duration of the study to mitigate risk, maximize utilization and identify, assess and act on value opportunities to allow the organization to realize monetary savings and redirect capital to support the R&D pipeline.
• Leads cross-functional matrixed forecasting, planning and scheduling of portfolio working in conjunction with respective CSC WSL / Supply Chain Managers, Planners, and Supply Chain Study Leads.
• Proactively identifies and communicates issues as well as provides proposed solutions.
• Aligns supply strategies across CMC, PM, Regulatory, Analytical, Quality, and CSC.
• Performs monthly assessment of the supply plan impact at the asset and portfolio level, in conjunction with the CSC Demand and Operations Planning cycle.
• Provides ongoing visibility of projected study supply performance, costs and risk levels with clear recommendations for improvement.
• Drives application of value criteria and prioritization of the clinical trial portfolio for identification of advanced demand modeling targets.
• Defines processes for required data integration with Intel Hub, IRT, fusion, and other data platforms.
• Develops and maintains process documentation and data governance standards for advanced demand modeling.

Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelor's degree in pharmacy, Chemistry, Biology, Engineering, Supply Chain, Logistics, Statistics, Bioinformatics, Computer Science or equivalent experience in relevant field
• Understanding of end-to-end CMC, clinical development and clinical supply forecasting, protocol development, dosing, clinical perspectives, financial analysis, risk mitigation, relevant software, data manipulation and analysis.
• Experience in compiling, integrate and analyze data from multiple sources to answer challenging and complex business questions.
• Plan and execute value measurement of data work, in order to demonstrate and improve results.
• Prior experience in communicating complex data science concepts and model outputs to a variety of stakeholders.

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Preferred Qualification
If you have the following characteristics, it would be a plus

• Master's degree in pharmacy, Chemistry, Biology, Engineering, Supply Chain, Logistics, Statistics, Bioinformatics, Computer Science or equivalent experience in relevant field.
• Experience in strategic approaches to optimize utilization, value and risk across multiple programs and multiple modalities.
• Highly collaborative and able to advance adoption and value of advanced demand modelling through highly productive relationships with senior leaders in MDI, Clinical Development, VEO and others.
• Demonstrated competency in managing matrixed and diverse teams including senior level leaders, with an emphasis on diversity, equity and inclusion.
• Highly motivated and strong capability in complex problem solving and risk management involving a range of technical quality, regulatory and operations challenges to ensure delivery to patients without compromising quality or cost.

#LI-GSK

Belgium Salary Range / Fourchette salariale – Belgique: EUR 80,250 to EUR 133,750The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.

Please visit  GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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