Pharmacovigilance Associate
Job Summary
Providing support to project teams, the full-time Pharmacovigilance Associate will process Individual Case Safety Reports (ICSRs), manage safety data, and ensure compliance with regulations while working remotely.
Key responsibilities
- Process Individual Case Safety Reports (ICSRs) in accordance with regulations and client requirements
- Perform follow-up on ICSR and manage Serious Adverse Events (SAE) and Suspected Unexpected Serious Adverse Reactions (SUSAR)
- Support pharmacovigilance processes and act as the Local Contact Person for Pharmacovigilance as needed
Required qualifications
- Life science graduate, pharmacy, nursing, or other healthcare-related qualification
- 0-1 year of experience in pharmacovigilance is desirable but not required
- Advanced English proficiency (spoken and written)
- Proficiency in MS Office
- Strong organizational and time management skills
Complete Job Description
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