Associate Director, Global Medical Affairs Lead
Sarepta Therapeutics
August 31, 2026
Remote friendly (Illinois, United States)
United States
Medical Affairs
The Associate Director, Global Medical Affairs Lead (GMAL) provides strategic and tactical scientific support for Sarepta’s gene therapy for Duchenne Muscular Dystrophy (DMD). 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, 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 materials and symposia.
- Build and maintain cross-functional relationships to plan and execute tactics.
- Stay current with medical/scientific literature and attend scientific meetings.
- Support dissemination of scientific/medical product impact to physicians and payers.
- Contribute to congress, symposia, advisory board, and expert committee strategy and content creation.
- Model integrity and compliance; perform other related duties as needed.
- Travel approximately quarterly for meetings and/or scientific congresses.
Qualifications:
- Remote (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; proven ability to deliver goals in diverse, high-performing teams.
- Demonstrated success in highly matrixed organizations and strong influencing skills.
- Experience building relationships with thought leaders and healthcare professionals.
- Ability to manage multiple tasks, meet deadlines, and communicate effectively.
- Ability to travel domestically and internationally as needed.
Application instructions:
- Apply if you are solution-oriented, comfortable with ambiguity, and committed to kindness and 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 materials and symposia.
- Build and maintain cross-functional relationships to plan and execute tactics.
- Stay current with medical/scientific literature and attend scientific meetings.
- Support dissemination of scientific/medical product impact to physicians and payers.
- Contribute to congress, symposia, advisory board, and expert committee strategy and content creation.
- Model integrity and compliance; perform other related duties as needed.
- Travel approximately quarterly for meetings and/or scientific congresses.
Qualifications:
- Remote (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; proven ability to deliver goals in diverse, high-performing teams.
- Demonstrated success in highly matrixed organizations and strong influencing skills.
- Experience building relationships with thought leaders and healthcare professionals.
- Ability to manage multiple tasks, meet deadlines, and communicate effectively.
- Ability to travel domestically and internationally as needed.
Application instructions:
- Apply if you are solution-oriented, comfortable with ambiguity, and committed to kindness and integrity.