Pharmacovigilance Specialist

Job Summary

To support pharmacovigilance efforts, the full-time Pharmacovigilance Specialist will manage daily case processing of adverse event cases, perform follow-up activities, and create case narratives while working in a hybrid environment.

Key responsibilities

• Process adverse event cases, including coding and determining seriousness and expectedness
• Conduct case follow-up activities and provide necessary client notifications for case management
• Develop training materials and assist in training delivery while maintaining knowledge of global safety regulations

Required qualifications

• Bachelor's degree in life sciences is required; advanced degree or equivalent preferred
• Two years of related work experience in pharmacovigilance or a similar field
• Basic knowledge of pharmacovigilance practices
• Experience in creating and reviewing case narratives
• Ability to conduct peer reviews for quality and accuracy of cases