Senior Manager, Global Medical Affairs Strategy, RNA Therapeutics
About this role
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
The Senior Manager, Global Medical Affairs Strategy, RNA Therapeutics , is a key contributor to the GMAL team within the Global Medical Affairs (GMA) department. As GMALs, we drive medical strategy and tactics to establish and elevate the impact of Sarepta’s science and therapies. This role will contribute to our mission through strategic and tactical scientific support of Sarepta’s PMO and siRNA therapies.
The Opportunity to Make a Difference
• Serve as an integral member of the Global Medical Affairs (GMA) team, providing support to: • The development and execution of GMA strategy for product launch and life-cycle management to bring alignment on key initiatives for therapeutic area in line with overall Corporate and Medical priorities in close collaboration with RNA or siRNA Global Medical Affairs • Identifying data gaps and drive data generation initiatives, including participation into IIS/SRA program. • The development of scientific narratives that align the organization on key, scientifically supported messages • Analysis of clinical, non-clinical, real-world data and post-hoc analyses • Contribute to congress, symposia, advisory board and expert committee strategy development and creation of content. Use output to help inform GMA and key organizational activities. • Collaborate with GMA team, to collect, organize, and analyze relevant disease state and competitor data; timely and routinely share new data finding and key learnings across GMA. • Connect insights, data, and technology to enable best decisions for GMA and Program Teams; orchestrate action for GMA on insights. • Deliver training based on identified needs and proactive initiatives to internal stakeholders • Build strong relationships that foster working effectively and in close collaboration with cross-functional partners to plan and execute tactics. • Build DMD and siRNA competency and profile within Sarepta through education and training in line with scientific narratives • Remain informed of current developments within pertinent medical and scientific communities through familiarity with current literature, attendance at scientific meetings, conventions, professional associations of physicians. • Provide end-to-end support for medical content (e.g., slide decks, FAQs, talking points), including development and updates of assigned materials and management of Medical/Legal/Regulatory (MLR) review processes in Veeva. • Manage vendors by providing strategic scientific guidance for the development and updating of medical materials and supporting the review and approval process. • Maintain approved medical materials by reviewing expiring decks, incorporating the latest data, and coordinating MLR review in Veeva. • Participate in medical review process for redacted and/or anonymized clinical trial documents • Serve as the medical lead or reviewer for congress materials, including symposia and booth content. • Address inquiries and requests from Field Medical teams and Medical Information. • Represent Global Medical Affairs (GMA) on cross-functional teams as needed. • Act as a role model for integrity, compliance, and ethical conduct. • Perform additional related duties as required.