Senior Medical Director, Oncology Clinical Development (GI)

Senior Medical Director overseeing clinical development programs in gastrointestinal oncology. Responsible for designing, executing, and interpreting clinical trials while managing cross-functional teams and ensuring regulatory compliance throughout the product development lifecycle.

Responsibilities

• Direct planning, execution, and interpretation of oncology clinical development programs
• Oversee study integrity, safety/efficacy data review, and serious adverse event reporting
• Design, analyze, and report scientific content of protocols and regulatory submissions
• Lead cross-functional teams and may supervise Medical Directors or Clinical Scientists
• Serve as clinical interface with opinion leaders and internal stakeholders on GI oncology programs

Requirements

• M.D., D.O., or non-US equivalent with relevant therapeutic specialty
• Residency program completion strongly preferred; subspecialty fellowship desirable
• Minimum 2 years clinical trial experience in pharmaceutical industry or academia
• Knowledge of clinical trial methodology and regulatory compliance requirements
• Ability to manage moderate-complexity clinical research programs independently
• Excellent oral and written English communication skills
• Experience developing clinical strategy and designing study protocols