Associate Director, Global Medical Affairs Lead
Sarepta Therapeutics
August 31, 2026
Remote friendly (Pennsylvania, United States)
United States
Medical Affairs
The Associate Director, Global Medical Affairs Lead (GMAL) is a key contributor to the Global Medical Affairs (GMA) team, driving medical strategy and tactics to establish and elevate the impact of Sarepta’s science and therapies. Reports to the Global Medical Affairs Lead for DMD Gene Therapy.
Responsibilities:
- Contribute to development and execution of GMA strategy for product launch and life-cycle management
- Develop medical materials (slides and talking points) for gene therapy and DMD; ensure cross-functional program alignment; participate in review processes
- Act as SME to review and approve medical and promotional materials (including congress/symposia materials)
- Build relationships with cross-functional partners; plan and execute tactics
- Stay current on medical/scientific developments via literature and scientific meetings
- Support dissemination of scientific/medical product impact with physicians and payers
- Contribute to congress, symposia, advisory board, and expert committee strategy and content
- 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: gene therapy experience; rare neuromuscular disorders or related fields
Skills:
- Analytical; delivers goals in diverse teams
- Strong influencing skills in highly matrixed organizations
- Builds relationships with thought leaders/healthcare professionals
- Manages multiple tasks and deadlines with cross-functional teams
- Strategic thinking; interprets and implements strategy
- Excellent communication and influencing skills
- Ability to travel domestically and internationally as needed
Application/Work setup:
- Hybrid role: expected to work on-site at a U.S. facility and/or attend in-person company-sponsored events from time to time.
- Candidates must be authorized to work in the U.S.
Responsibilities:
- Contribute to development and execution of GMA strategy for product launch and life-cycle management
- Develop medical materials (slides and talking points) for gene therapy and DMD; ensure cross-functional program alignment; participate in review processes
- Act as SME to review and approve medical and promotional materials (including congress/symposia materials)
- Build relationships with cross-functional partners; plan and execute tactics
- Stay current on medical/scientific developments via literature and scientific meetings
- Support dissemination of scientific/medical product impact with physicians and payers
- Contribute to congress, symposia, advisory board, and expert committee strategy and content
- 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: gene therapy experience; rare neuromuscular disorders or related fields
Skills:
- Analytical; delivers goals in diverse teams
- Strong influencing skills in highly matrixed organizations
- Builds relationships with thought leaders/healthcare professionals
- Manages multiple tasks and deadlines with cross-functional teams
- Strategic thinking; interprets and implements strategy
- Excellent communication and influencing skills
- Ability to travel domestically and internationally as needed
Application/Work setup:
- Hybrid role: expected to work on-site at a U.S. facility and/or attend in-person company-sponsored events from time to time.
- Candidates must be authorized to work in the U.S.