Director, Global Pharmacovigilance Operations Lead

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.  We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients. What Sarepta Offers At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness ​Financial Wellness Support for Caregivers   For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us   The Importance of the Role This position will oversee Sarepta Pharmacovigilance (PV) case management activities globally for assigned investigational and marketed Sarepta products. This position will also lead strategic PV operational projects and initiatives in collaboration with senior PV management, with minimal guidance. The Director, Pharmacovigilance Operations position requires a highly motivated leader with strong operations, analytical, strategic, and critical thinking skills, and ability to consistently deliver results. The incumbent will join the PV department reporting directly to the Executive Director and Head of Pharmacovigilance Operations and Quality Management. The Opportunity to Make a Difference Primary Responsibilities Include: • Lead pharmacovigilance operations for assigned products and deliver high PV ICSR quality control for intake, case management, safety reporting and follow-up • Oversee PV vendor’s case management activities for assigned products including but not limited to literature reviews, safety data receipt, data entry, case processing, medical evaluation, follow-up, expedited reporting, and closure of Individual Case Safety Reports (ICSRs) • Provide operational support for risk management including contributions to development of risk documents (e.g., RMPs, RARs, etc.) and perform QC of such documents upon request • Conduct functional review of study protocols and escalate challenges/issues for resolution • Manage and maintain direct discussions with license partners to ensure efficiency, compliance, and continuous improvement • Develop and maintain Pharmacovigilance Agreements (PVAs) with license partners • Review and provide input to EDC CRFs and Safety Gateway projects • Lead creation and implementation of safety reporting plans, data entry conventions, and standard operating procedures • Execute PV operational activities for regulatory filings and product registrations • Collaborate cross-functionally with Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Manufacturing, Legal and Commercial in implementing Sarepta PV processes. • Lead weekly case review meetings and guide resolution of ensuing actions • Review product complaints for assigned products • Identify, analyze, develop, and implement continuous improvement opportunities for Sarepta PV operations processes and systems • Delegate for the Head of Pharmacovigilance Operations and Quality Management, upon request More about You Desired Education and Skills: • Advanced degree in Biological Sciences, Nursing, or Healthcare administration • 12+ years of related professional experience • Advanced Argus experience • Advanced knowledge of drug development • Advanced knowledge of global PV regulations