California Licensed Pharmacovigilance Consultant

Job Summary

A company is looking for a Medical Director, Pharmacovigilance (Consultant).

Key Responsibilities

• Perform medical review of adverse events from clinical trials to assess severity and causality
• Monitor safety data for emerging patterns or trends and conduct further analysis on safety signals
• Contribute to the development and implementation of risk management plans and communication strategies

Required Qualifications

• Medical degree (MD) with a strong clinical background
• Experience in clinical practice or clinical research is preferred
• Experience in oncology and/or cell therapy is strongly preferred
• Thorough understanding of pharmacovigilance principles and global regulatory requirements
• Proficiency in Argus is required