Lead the overall strategy, design, and execution of clinical and pre-clinical development programs
Develop scientifically rigorous clinical trial protocols and ensure regulatory and ethical compliance
Oversee preparation of core materials, including clinical development plans, regulatory submissions, and study documentation
Present program strategies and outcomes to internal and external stakeholders, including executive leadership and advisory boards
Collaborate with contract research organizations (CROs), academic partners, and cross-functional teams to ensure successful trial delivery
Partner with regulatory authorities and scientific collaborators to support study progress and milestone achievement
Manage budgets, timelines, and risks to ensure excellence in clinical program execution

Advanced degree required (PhD, PharmD, or equivalent); MD strongly preferred
10+ years of experience in clinical and/or pre-clinical development within biotechnology or pharmaceutical organizations
Proven track record in leading clinical programs and cross-functional teams
Expertise in clinical trial design, regulatory strategy, and stakeholder engagement
Exceptional communication, organizational, and leadership skills

Senior Medical Director, Clinical Development

Key skills