Global Medical Affairs Lead-RNA

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.

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:

The Global Medical Affairs Lead (GMAL) - RNA, 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 RNA therapies for Duchenne Muscular Dystrophy (DMD).

• Serve as an integral member of the GMAL team, contributing to:
  • Contribute 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 GMAL
  • Often represents GMA on key committees & governance teams to provide medical and scientific advice on Sarepta product development strategies and bring output and insight back to GMA. Is seen as SME and ensures external stakeholder's needs are considered.
  • Identify data gaps and drive data generation initiatives, including participation into IIS/SRA program. Driving of data generation and dissemination initiatives.
  • Develop scientific narratives that align the organization on key, scientifically supported messages
  • Analysis of clinical, non-clinical, real-world data and post-hoc analyses
  • Provide medical input on real-world evidence generation initiatives including IIS/SRA, registries, and HEOR studies
• Co-lead program publication plans to bridge research/clinical plans to commercialization. Co-develop and review abstracts and manuscripts.
• 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. Occasionally represent GMA on cross-functional teams.
• Develop medical materials (including slides and field materials) for PMO and DMD, ensure cross-program alignment, and participate in review processes.
• Collaborate with GMAL team, to collect, organize, and analyze relevant disease state and competitor data for RNA therapies; 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 PMO and DMD 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.
• Act as SME to review and/or approve medical and promotional material, prepare and deliver presentations,…