Massachusetts Licensed Pharmacovigilance Director

Job Summary

A company is looking for an Associate Director, Pharmacovigilance.

Key Responsibilities

• Oversee day-to-day safety monitoring activities and operations of clinical trials for assigned products
• Provide pharmacovigilance subject matter expertise on program teams and cross-functional platforms
• Facilitate cross-functional Safety Review Committee meetings, including coordinating materials and presentations

Qualifications

• Degree in Pharmacy, Nursing, Epidemiology, Biosciences, or equivalent healthcare degree with pharmaceutical industry experience
• Minimum of 8 years of pharmaceutical industry experience, with at least 5 years directly in pharmacovigilance
• Knowledge of global safety regulations and MedDRA terminology
• Experience in preparing and authoring aggregate safety reports
• Thorough understanding of the drug development process related to safety surveillance activities