Senior Pharmacovigilance Associate
Job Summary
Providing support for ICSR management activities, the full-time Senior Pharmacovigilance Associate will process Individual Case Safety Reports, manage safety events, and ensure compliance with regulations while working remotely.
Key responsibilities
- Process Individual Case Safety Reports (ICSRs) and manage follow-ups in compliance with regulations and client requirements
- Handle SAE/SUSAR management, including unblinding and clinical trial reconciliation
- Support PV processes and act as the Local Contact Person for Pharmacovigilance as needed
Required qualifications
- Life science graduate or healthcare-related qualification with experience in pharmacovigilance
- Minimum 1 year of work experience in pharmacovigilance
- Advanced English proficiency (spoken and written)
- Strong organizational and management skills, including time and issue management
- Advanced literacy in MS Office
Complete Job Description
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