Associate Director, Global Medical Affairs Lead
Sarepta Therapeutics
August 31, 2026
Remote friendly (Cambridge, MA)
United States
Medical Affairs
Responsibilities:
- Contribute to the 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.
- Serve as SME to review and approve medical and promotional material, including congress materials and symposia.
- Build strong relationships with cross-functional partners 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 strategy development and content creation for congresses, symposia, advisory boards, and expert committees.
- Model integrity and compliance; perform other related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- 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 teams.
- Success in highly matrixed organizations; strong influencing and communication skills.
- Ability to build relationships with thought leaders/healthcare professionals.
- Ability to manage multiple tasks, meet deadlines, and implement strategic directions.
- Ability to travel domestically and internationally as needed.
Benefits:
- Physical and Emotional Wellness; Financial Wellness; Support for Caregivers.
Application instructions:
- Apply if you are comfortable with ambiguity and candor and place kindness and integrity at the forefront of your work.
- Contribute to the 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.
- Serve as SME to review and approve medical and promotional material, including congress materials and symposia.
- Build strong relationships with cross-functional partners 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 strategy development and content creation for congresses, symposia, advisory boards, and expert committees.
- Model integrity and compliance; perform other related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- 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 teams.
- Success in highly matrixed organizations; strong influencing and communication skills.
- Ability to build relationships with thought leaders/healthcare professionals.
- Ability to manage multiple tasks, meet deadlines, and implement strategic directions.
- Ability to travel domestically and internationally as needed.
Benefits:
- Physical and Emotional Wellness; Financial Wellness; Support for Caregivers.
Application instructions:
- Apply if you are comfortable with ambiguity and candor and place kindness and integrity at the forefront of your work.