Medical Director, Oncology Clinical Development (Solid Tumors)

Medical Director for oncology clinical development at AbbVie overseeing solid tumor trial design, execution, and data interpretation. The role manages study protocols, clinical operations oversight, regulatory compliance, and cross-functional collaboration to support product development strategy.

Responsibilities

• Design and implement study protocols aligned with product development plans and regulatory requirements
• Oversee clinical trial execution, study integrity, and enrollment timelines with Clinical Operations
• Review, interpret, and communicate safety and efficacy data; assess and report serious adverse events
• Contribute to scientific content for protocols, reports, regulatory submissions, and clinical strategy
• Ensure adherence to Good Clinical Practices, pharmacovigilance standards, and quality requirements

Requirements

• M.D., D.O., or non-US equivalent with therapeutic specialty background
• Residency program completion strongly preferred; subspecialty fellowship desirable
• Clinical trial experience in pharmaceutical industry, academia, or equivalent
• Knowledge of clinical trial methodology and regulatory compliance requirements
• Demonstrated ability to work collaboratively across functional teams
• Excellent written and oral English communication skills