Senior Pharmacovigilance Associate
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Job Summary
Providing support for ICSR management activities, the full-time Senior Pharmacovigilance Associate will process Individual Case Safety Reports, manage 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 SAE/SUSAR activities including unblinding, clinical trial reconciliation, and protocol reviews
- Support PV processes and act as Local Contact Person for Pharmacovigilance as needed
Required qualifications
- Life science graduate, pharmacy, nursing, or other healthcare-related qualification or experience in pharmacovigilance
- Minimum 1 year of work experience in pharmacovigilance
- Advanced English proficiency (spoken and written)
- Strong organization and management skills
- Proficiency in MS Office
Complete Job Description
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