Associate Medical Director, Pharmacovigilance

Job Summary

A company is looking for an Associate Medical Director, Pharmacovigilance and Risk Management (PVRM).

Key Responsibilities

• Monitor and assess risk/benefit for investigational and marketed products throughout their lifecycle
• Conduct safety surveillance and review clinical trial and post-marketing safety reports
• Generate safety queries and contribute to safety documentation and risk management plans

Required Qualifications and Education

• Medical Degree (MD) with 3-5 years of drug safety experience in a pharmaceutical company
• Experience in oncology is highly desired
• Advanced understanding of pharmacovigilance and risk management regulations
• Expertise in medical review of individual case safety reports and aggregate safety reports
• Knowledge of drug development and global regulatory requirements in the pharmaceutical industry