Medical Director, Oncology Clinical Development (Solid Tumors)

Medical Director responsible for overseeing clinical trial design, execution, and data interpretation for solid tumor oncology programs. Manages study protocols, investigator coordination, safety reporting, and regulatory compliance while collaborating across functional teams to support product development strategy.

Responsibilities

• Oversee design, implementation, and execution of clinical study protocols aligned with product development plans
• Monitor study integrity, review accumulating safety and efficacy data, and coordinate enrollment and timelines
• Assess and report serious adverse events per corporate policy and regulatory requirements
• Contribute to protocol design, analysis, and regulatory submissions including Clinical Study Reports
• Ensure adherence to Good Clinical Practices, pharmacovigilance standards, and quality requirements

Requirements

• M.D., D.O., or non-US equivalent medical degree with oncology or relevant therapeutic specialty
• Residency program completion strongly preferred; fellowship completion desirable
• Clinical trial experience in pharmaceutical industry, academia, or equivalent setting
• Knowledge of clinical trial methodology, regulatory requirements, and study protocol design
• Ability to manage clinical research studies with appropriate supervision
• Strong cross-functional collaboration and external communication skills
• Excellent oral and written English communication abilities