Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.
Summary of Position:
The Sr. Medical Director, Drug Safety & 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 & with high quality.
Position Responsibilities:
Lead and support development of pharmacovigilance strategies for products within Therapeutic area, to ensure compliance with corporate clinical development and commercial goals.
Oversight and conducting of signal detection activities include monitoring, evaluation, interpretation, management and communication of safety information.
Responsible for oversight and conduct of Product Safety Committee (PSC) meeting(s) to evaluate risk-benefit for the compounds with support from cross-functional teams. Escalate and present safety issues to the Executive Safety Committee.
Medical safety review including causality assessment of all available safety data generated from various sources (e.g. pre-clinical, clinical trial data, post-marketing and literature) throughout the development process for assigned compounds/projects.
Provides medical expert safety review input into all critical documents for products in clinical development (e.g., INDs/NDA/BLA submissions, protocols and amendments, ICFs, IBs, and clinical research reports (CSR))
Oversight of aggregate reports and signal evaluation reports for assigned projects.
Responsible for the Clinical content of responses to inquiries from regulatory authorities related to Safety topics.
Provide leadership and support to Contract Research Organization (CRO) staff to ensure overall delivery of services. Ensures vendor oversight of outsourced Medical activities, as applicable.
Oversee and collaborate with internal safety scientists within TA
Assist with the writing and development of SOPs as required to ensure compliance to regulations and local laws.
Lead high quality planning and execution of external meetings and internal stakeholder meetings (e.g., DMCs, Vendor oversight meetings, etc.)
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.
Support process improvement and functional training at departmental & company level
Ensure that the highest quality, ethical & professional values are demonstrated in all aspects of work.
Ensures compliance with corporate policies and procedures, as well as all related healthcare laws and regulations
Candidate Requirements:
MD or MBBS or MD-PhD or equivalent medical degree
5 or more years of pharmaceutical experience in Drug Safety & Pharmacovigilance.
Strong understanding of pharmacovigilance regulations in the US and EU.
Experience in supporting drug safety activities in registrational clinical studies
High level of medical competence, with an ability to balance this with industry standards to achieve business goals
Demonstrated skills in scientific analysis and reasoning.
Sound knowledge of overall drug development process from discovery to registration and post marketing requirements & surveillance.
Prior IND, as well as NDA/BLA (filing/submission) and other regulatory interaction experience is highly desirable
Strong track record of delivering results through effective team and peer leadership in matrix
Excellent leadership & organizational skills, analytical skills, presentation skills, and strong experience in translating important data into clinical strategies.
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
