Associate Medical Director (PS-MD)

Associate Medical Director responsible for medical safety review of clinical trial serious adverse events, including causality assessment and company analysis development. Provides therapeutic area leadership while ensuring accurate stakeholder communication and regulatory compliance.

Responsibilities

• Conduct medical review of clinical trial serious adverse events and post-marketing safety reports
• Develop company analysis for suspected unexpected serious adverse reactions (SUSARs)
• Lead therapeutic area initiatives and provide overall leadership to assigned therapeutic areas
• Perform causality assessment of adverse events in individual case safety reports
• Communicate accurately and timely with clinical trial stakeholders on safety matters

Requirements

• MD or equivalent medical degree
• 1–2 years drug safety experience with medical assessment and clinical case review
• Understanding of global regulatory processes and practices
• Knowledge of safety profiles for assigned products and therapeutic areas