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Role Objectives:
- Execute international adverse event and pharmacovigilance activities per regulatory requirements.
- Coordinate adverse event activities for global sites.
What You'll Do:
- Monitor PV system metrics to ensure compliance and effectiveness.
- Author Safety Monitoring Plans and process adverse events in Argus.
- Provide training and support audits for PV compliance.
What You'll Need:
- Bachelor's in life sciences; advanced degree preferred.
- 3+ years drug safety/pharmacovigilance experience.
- Knowledge of Argus Safety Database and FDA/ICH regulations.
WEP Clinical
WEP Clinical partners with biopharmaceutical sponsors to deliver end-to-end clinical trial and market access solutions, helping bring treatments to patients. Over 15 years of global experience in 150+ countries, we foster a collaborative culture that encourages innovation and growth.