About this role
The Safety Data Lead I is responsible for analyzing and interpreting adverse experience reports in compliance with regulatory requirements in the pharmacovigilance field. This role involves executing case management activities for investigational and marketed products, collaborating with stakeholders to ensure quality and timeliness.
Required Skills
- ADR Monitoring
- Adverse Reactions
- Pharmacovigilance
- Data Processing
- Clinical Data Management
- Drug Administration
- Life Science
- Biological Sciences
- Medical Sciences
- English Language
About MSD
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