Associate Director, Global Medical Affairs Lead

Sarepta Therapeutics•Carolina, MA

9h•Hybrid

About The Position

The Associate Director, Global Medical Affairs Lead (GMAL) is a key contributor to the GMAL team within the Global Medical Affairs (GMA) department. As GMALs, we drive medical strategy and tactics to establish and elevate the impact of Sarepta’s science and therapies. This role will contribute to our mission through strategic and tactical scientific support of Sarepta’s gene therapy for Duchenne Muscular Dystrophy (DMD). This role will report to the Global Medical Affairs Lead for DMD Gene Therapy.

Requirements

Doctorate degree (MD, PhD, PharmD) with 5+ years of relevant experience required
Analytical, with a track record of delivering goals while working in high performing diverse teams
Demonstrated success in operating effectively in highly matrixed organizations where influencing skills are critical to day to day success
Experience in building strong and effective relationships with thought leaders and healthcare professionals
Ability to manage multiple tasks and deal effectively with deadlines with cross-functional teams
Proven strategic thinking skills and ability to interpret and implement strategic directions
Articulate with excellent communication and influencing skills
Candidates must be authorized to work in the U.S.

Nice To Haves

Preferred experience in gene therapy, rare neuromuscular disorders or related fields
Recognized by former peers/colleagues/managers for attributes congruent with Sarepta Cultural Values: Patient Mission, Scientific Rigor, Simplicity, Bias to Action, One Sarepta, Trust

Responsibilities

Contribute to the development and execution of GMA strategy for product launch and life-cycle management to bring alignment on key initiatives for the therapeutic area in line with overall Corporate and Medical priorities
Develop medical materials (including slides and talking points) for gene therapy and DMD, ensure cross-functional program alignment, and participate in review processes
Act as SME to review and approve medical and promotional material including congress materials and symposia
Build strong relationships that foster working effectively in close collaboration with cross-functional partners to plan and execute tactics
Remain informed of current developments within pertinent medical and scientific communities through familiarity with current literature and attendance at scientific meetings
Support initiatives to disseminate the scientific and medical impact of our products with key stakeholders (physicians and payers).
Contribute to congress, symposia, advisory board and expert committee strategy development and creation of content
Work effectively and in close collaboration with cross-functional partners to plan and execute tactics
Serves as a role model of integrity and compliance
Perform other related duties as needed
Travel approximately quarterly for internal meetings and/or scientific congresses and meetings.