Senior Medical Director, Oncology Clinical Development (GI)

Senior Medical Director overseeing clinical development programs in gastrointestinal oncology. Directs trial design, execution, and interpretation while managing cross-functional teams and ensuring regulatory compliance and scientific rigor throughout product development.

Responsibilities

• Design, plan, and oversee execution of one or more clinical development programs supporting product development strategy
• Ensure clinical study integrity, safety monitoring, adverse event reporting, and enrollment oversight across assigned protocols
• Develop scientific content for protocols, study reports, regulatory submissions, and other program documentation
• Lead or chair Clinical Strategy Teams to align clinical development plans across functions and manage contingencies
• Serve as clinical expert interface with internal stakeholders, opinion leaders, and regulatory agencies

Requirements

• M.D., D.O., or non-US equivalent with therapeutic specialty in academic or hospital setting
• Minimum 2 years clinical trial experience in pharmaceutical industry or academia
• Ability to manage moderate-complexity clinical research programs independently
• Knowledge of clinical trial methodology, regulatory requirements, and protocol design
• Demonstrated capability leading cross-functional global teams
• Excellent written and oral English communication skills
• Residency completion strongly preferred; subspecialty fellowship desirable