Associate Medical Director

Associate Medical Director position focused on medical safety review of clinical trial serious adverse events, including causality assessment and company analysis development. Role provides therapeutic area leadership and may include people management responsibilities.

Responsibilities

• Conduct medical review of clinical serious adverse events and perform causality assessments
• Develop company analyses for suspected unexpected serious adverse reactions
• Lead therapeutic area safety oversight and provide project-level leadership
• Ensure accurate and timely communication with clinical trial stakeholders
• Support post-marketing safety surveillance, audits, and compliance activities as needed

Requirements

• MD or equivalent medical degree
• Drug safety experience preferred (Associate Medical Director I level)
• 1-2 years drug safety experience with medical assessment and clinical case review (Associate Medical Director II level)
• Understanding of global regulations, processes, and safety practices
• Knowledge of disease states and therapeutic area drug safety profiles