Senior Pharmacovigilance Associate
Job Summary
Supporting pharmacovigilance processes, the full-time Senior Pharmacovigilance Associate will manage Individual Case Safety Reports (ICSRs), perform follow-ups, and ensure compliance with regulations while working remotely.
Key responsibilities
- Process Individual Case Safety Reports (ICSRs) and perform follow-ups in compliance with regulations and client requirements
- Manage Serious Adverse Events (SAE) and Safety Reports, including unblinding and clinical trial reconciliation
- Support pharmacovigilance processes and act as Local Contact Person for Pharmacovigilance as needed
Required qualifications
- Life science graduate or equivalent qualification in pharmacy, nursing, or healthcare
- Minimum of 1 year of work experience in pharmacovigilance
- Advanced English proficiency (spoken and written)
- Strong organizational and management skills, including time and issue management
- Proficiency in MS Office applications
Complete Job Description
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