Senior Pharmacovigilance Specialist

Job Summary

Overseeing daily case processing of adverse event cases, the full-time Senior Pharmacovigilance Specialist will manage coding, case follow-up, and narrative creation while ensuring compliance with global safety regulations, all within a hybrid work environment.

Key responsibilities

• Perform daily case processing of adverse event cases, including coding and determining seriousness and expectedness
• Create and review case narratives, providing client notifications as required for case management
• Mentor and train less experienced staff while supporting the development of training materials

Required qualifications

• Bachelor's degree in life sciences is required; an advanced degree, RN, RPh, PharmD, or equivalent is preferred
• Three years of related work experience in pharmacovigilance
• Intermediate knowledge of pharmacovigilance and working knowledge of PV systems such as Oracle Argus Safety or ARISg