Pharmacovigilance Scientist

Job Summary

A company is looking for a Pharmacovigilance Scientist to support key pharmacovigilance activities and ensure high-quality delivery of safety and regulatory outputs.

Key Responsibilities

• Author aggregate safety reports including PSURs, PBRERs, PADERs, and DSURs
• Prepare and maintain Risk Management Plans (RMPs) and contribute to Signal Management Reports
• Conduct literature searches, extract and validate safety data, and ensure compliance with global regulatory requirements

Required Qualifications

• Bachelor's or Master's degree in Pharmacy, Nursing, Life Sciences, or a related healthcare/scientific field
• Minimum 2+ years of experience in Pharmacovigilance
• Experience in medical writing, literature search, and signal detection
• Experience in authoring and reviewing aggregate safety reports
• Exposure to quality metrics and client-facing discussions is desirable