Associate Director, Global Medical Affairs 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.

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 Associate Director, Global Medical Affairs Lead (GMAL) is a key contributor to the GMAL team within 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 gene therapy for Duchenne Muscular Dystrophy (DMD).

This role will report to the Global Medical Affairs Lead for DMD Gene Therapy.

• Contribute to the development and execution of GMA strategy for product launch and life‑cycle management to bring alignment on key initiatives for the therapeutic area in line with overall Corporate and Medical priorities
• Develop medical materials (including slides and talking points) for gene therapy and DMD, ensure cross‑functional program alignment, and participate in review processes
• Act as SME to review and approve medical and promotional material including congress materials and symposia
• Build strong relationships that foster working effectively in close collaboration with cross‑functional partners to plan and execute tactics
• Remain informed of current developments within pertinent medical and scientific communities through familiarity with current literature and attendance at scientific meetings
• Support initiatives to disseminate the scientific and medical impact of our products with key stakeholders (physicians and payers).
• Contribute to congress, symposia, advisory board and expert committee strategy development and creation of content
• Work effectively and in close collaboration with cross‑functional partners to plan and execute tactics
• Serves as a role model of integrity and compliance
• Perform other related duties as needed
• Travel approximately quarterly for internal meetings and/or scientific congresses and meetings.

• This is a remote opportunity within the United States of America
• Doctorate degree (MD, PhD, PharmD) with 5+ years of relevant experience required
• Preferred experience in gene therapy, rare neuromuscular disorders or related fields
• Analytical, with a track record of delivering goals while working in high performing diverse teams
• Demonstrated success in operating effectively in highly matrixed organizations where influencing skills are critical to day to day success
• Experience in building strong and effective relationships with thought leaders and healthcare professionals
• Ability to manage multiple tasks and deal effectively with deadlines with cross-functional teams
• Proven strategic thinking…