Pharmacovigilance Scientist

Job Summary

A company is looking for a Pharmacovigilance Scientist.

Key Responsibilities

• Lead and support pharmacovigilance activities, overseeing safety operations for clinical trial programs
• Conduct signal management activities, including detection, evaluation, and documentation
• Manage aggregate safety reports and ensure regulatory compliance for timely submissions

Qualifications

• Minimum 7 years of Pharmacovigilance experience, including aggregate safety reports and signal management
• Bachelor's Degree in biologic or natural science; advanced degree preferred
• Knowledge of MedDRA terminology and its application
• Strong computer skills, particularly in MS Excel
• Able to work in a fast-paced environment with multiple competing priorities