Associate Pharmacovigilance Specialist
Clarivate(6 days ago)
About this role
An Associate Pharmacovigilance Specialist at Clarivate monitors biomedical literature for adverse events and assesses drug safety information, supporting regulatory compliance and risk management. The role involves analyzing scientific articles, summarizing findings, and ensuring thorough documentation in pharmacovigilance systems.
Required Skills
- Biomedical Literature
- Adverse Events
- Drug Safety
- Data Analysis
- Regulatory Compliance
- Literature Monitoring
- Pharmacovigilance
- Medical Terminology
- Database Management
- Risk Assessment
Qualifications
- Master’s Degree in Life Sciences or related field
About Clarivate
clarivate.comClarivate aims to fuel the world's greatest breakthroughs through enriched data, insights, analytics, workflow solutions and expert services. Find out more.
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