Senior Pharmacovigilance Associate
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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 and manage Individual Case Safety Reports (ICSRs) in compliance with applicable regulations and client requirements
- Support pharmacovigilance processes and act as the Local Contact Person for Pharmacovigilance as needed
- Perform reconciliation and manage product quality complaints in collaboration with Quality Assurance
Required qualifications
- Life science graduate or equivalent experience in pharmacovigilance
- Minimum 1 year of work experience in pharmacovigilance
- Advanced English proficiency (spoken and written)
- Strong organizational and management skills
- Proficiency in MS Office applications
Complete Job Description
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