Senior Pharmacovigilance Associate
Job Summary
Supporting pharmacovigilance processes remotely, the full-time Senior Pharmacovigilance Associate will manage Individual Case Safety Reports (ICSRs), perform follow-ups, and ensure compliance with regulations while collaborating with clients and internal teams.
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 product quality complaints, including unblinding and clinical trial reconciliation
- Support the Pharmacovigilance and Regulatory Affairs Network Department as needed, acting as Local Contact Person for Pharmacovigilance
Required qualifications
- Life science graduate or equivalent qualification in pharmacy, nursing, or a healthcare-related field
- Minimum 1 year of work experience in pharmacovigilance
- Advanced English proficiency (spoken and written)
- Strong organization and management skills, including time management and multitasking
- Proficient in MS Office applications
Complete Job Description
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