Associate Director, Global Medical Affairs Lead
Sarepta Therapeutics
August 31, 2026
Remote friendly (California, United States)
United States
Medical Affairs
The Associate Director, Global Medical Affairs Lead (GMAL) will contribute to Sarepta’s gene therapy program for Duchenne Muscular Dystrophy (DMD).
Responsibilities:
- Contribute to development and execution of GMA strategy for product launch and life-cycle management.
- Develop medical materials (slides, talking points) for gene therapy and DMD; ensure cross-functional alignment and participate in reviews.
- Serve as SME to review and approve medical and promotional materials, including congress/symposia materials.
- Build relationships and collaborate with cross-functional partners to plan and execute tactics.
- Stay current on medical/scientific literature and attend scientific meetings.
- Support dissemination of scientific/medical impact to key stakeholders (physicians and payers).
- Support congress, symposia, advisory board, and expert committee strategy and content creation.
- Serve as a role model of integrity and compliance.
- Perform other related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- Remote opportunity within the United States.
- Doctorate degree (MD, PhD, PharmD) with 5+ years of relevant experience (required).
- Preferred: experience in gene therapy, rare neuromuscular disorders, or related fields.
- Analytical; delivers goals in diverse teams.
- Proven ability to operate in highly matrixed organizations; strong influencing skills.
- Relationship-building experience with thought leaders and healthcare professionals.
- Ability to manage multiple tasks and meet deadlines with cross-functional teams.
- Strategic thinking and ability to interpret/implement strategy.
- Excellent communication and influencing skills.
- Ability to travel domestically and internationally as needed.
Salary/Benefits/Application:
- Targeted salary range: $173,200–$216,500 per year.
- Candidates must be authorized to work in the U.S.
- Apply if you’re solution-oriented, comfortable with ambiguity, and value kindness/integrity.
Responsibilities:
- Contribute to development and execution of GMA strategy for product launch and life-cycle management.
- Develop medical materials (slides, talking points) for gene therapy and DMD; ensure cross-functional alignment and participate in reviews.
- Serve as SME to review and approve medical and promotional materials, including congress/symposia materials.
- Build relationships and collaborate with cross-functional partners to plan and execute tactics.
- Stay current on medical/scientific literature and attend scientific meetings.
- Support dissemination of scientific/medical impact to key stakeholders (physicians and payers).
- Support congress, symposia, advisory board, and expert committee strategy and content creation.
- Serve as a role model of integrity and compliance.
- Perform other related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- Remote opportunity within the United States.
- Doctorate degree (MD, PhD, PharmD) with 5+ years of relevant experience (required).
- Preferred: experience in gene therapy, rare neuromuscular disorders, or related fields.
- Analytical; delivers goals in diverse teams.
- Proven ability to operate in highly matrixed organizations; strong influencing skills.
- Relationship-building experience with thought leaders and healthcare professionals.
- Ability to manage multiple tasks and meet deadlines with cross-functional teams.
- Strategic thinking and ability to interpret/implement strategy.
- Excellent communication and influencing skills.
- Ability to travel domestically and internationally as needed.
Salary/Benefits/Application:
- Targeted salary range: $173,200–$216,500 per year.
- Candidates must be authorized to work in the U.S.
- Apply if you’re solution-oriented, comfortable with ambiguity, and value kindness/integrity.