Pharmacovigilance Specialist
Job Summary
Managing individual case safety reports, the full-time Pharmacovigilance Specialist will perform case-level assessments, compose medical narratives, and ensure regulatory compliance while working in a hybrid environment.
Key responsibilities
- Process daily adverse event cases, including coding and assessing seriousness and expectedness
- Conduct case follow-up activities and create/review case narratives
- Maintain knowledge of global safety regulations and perform peer reviews for quality assurance
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 and regulations
Complete Job Description
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