Senior Director, Clinical Development

Responsibilities

• Lead multiple late‑stage clinical programs within Sarepta Therapeutics.
• Provide scientific and strategic leadership for activities in clinical development, including regulatory interactions.
• Lead projects under the direction of the Head of Clinical Development, support business development, foster innovation, and external collaboration.
• Manage one or more direct reports and lead the clinical development team for a product.
• Design and execute projects supporting clinical research programs.
• Lead the clinical study team in protocol development, monitoring, study reports, training documents, and other regulatory documents.
• Facilitate clinical development goals and achievement of study quality metrics.
• Contribute to organization, preparation, and execution of investigator and advisory board meetings in collaboration with project teams and stakeholders.
• Stay current on regulations, guidelines, and scientific advances in the therapeutic area.
• Cultivate relationships with external partners such as clinical investigators, clinicians, and scientists to support innovation and business development.
• Assist with due diligence for business development opportunities.
• Travel to field sites, internal and external meetings, and conferences as required.

• Doctorate degree (MD, DO, PhD, or Pharm
  
  D) – MD or DO preferred.
• At least 15 years of clinical/research experience, with 5 years in industry.
• Experience as a practicing physician.
• Strong analytical skills in clinical data (safety and efficacy) and knowledge of biostatistics.
• Working knowledge of GCP and regulatory requirements for clinical studies.
• Ability to make independent, timely, and appropriate decisions.
• Collaborative experience in a fast‑paced, matrix, team‑based environment.
• Excellent written and verbal communication skills.
• Intellectual curiosity, flexibility, and persistence.
• High level of organizational and project management skills.
• Experience interacting with clinical operations, regulatory, QA, and investigators.

Position is hybrid, requiring occasional on‑site presence at a Sarepta facility in the United States and attendance at company‑sponsored events. The role may require travel to field sites, meetings, and conferences.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e‑Verify.

Salary range: $222,400 - $278,000 per year (commensurate with qualifications and market). Benefits include comprehensive wellness, financial support and caregiver assistance.