Associate Director, Global Medical Affairs Lead
Sarepta Therapeutics
August 31, 2026
Remote friendly (Florida, United States)
United States
Medical Affairs
Responsibilities:
- Contribute to development and execution of GMA strategy for product launch and life-cycle management for the therapeutic area aligned with corporate and medical priorities.
- 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 materials, 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 and medical impact with key stakeholders (physicians and payers).
- Contribute to congress, symposia, advisory board, and expert committee strategy development and content.
- Model integrity and compliance; perform related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- Doctorate degree (MD, PhD, PharmD) and 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.
- Demonstrated success in highly matrixed organizations; strong influencing skills.
- Experience building relationships with thought leaders and healthcare professionals.
- Ability to manage multiple tasks and meet deadlines with cross-functional teams.
- Strategic thinking; strong communication and influencing skills.
- Ability to travel domestically and internationally as needed.
Benefits:
- Physical and Emotional Wellness; Financial Wellness; Support for Caregivers (full list on company website).
Application instructions:
- Candidates should apply; remote in the United States; hybrid role with on-site expectation at U.S. facilities and occasional in-person events.
- Contribute to development and execution of GMA strategy for product launch and life-cycle management for the therapeutic area aligned with corporate and medical priorities.
- 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 materials, 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 and medical impact with key stakeholders (physicians and payers).
- Contribute to congress, symposia, advisory board, and expert committee strategy development and content.
- Model integrity and compliance; perform related duties as needed.
- Travel approximately quarterly for internal meetings and/or scientific congresses/meetings.
Qualifications:
- Doctorate degree (MD, PhD, PharmD) and 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.
- Demonstrated success in highly matrixed organizations; strong influencing skills.
- Experience building relationships with thought leaders and healthcare professionals.
- Ability to manage multiple tasks and meet deadlines with cross-functional teams.
- Strategic thinking; strong communication and influencing skills.
- Ability to travel domestically and internationally as needed.
Benefits:
- Physical and Emotional Wellness; Financial Wellness; Support for Caregivers (full list on company website).
Application instructions:
- Candidates should apply; remote in the United States; hybrid role with on-site expectation at U.S. facilities and occasional in-person events.