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Job Description: Pharmacovigilance Services Associate
Key Responsibilities:
โ Case Processing: Identify, enter, and manage Individual Case Safety Reports (ICSRs) in the safety database.
โ MedDRA Coding: Ensure accurate coding of adverse events using MedDRA terminology.
โ Follow-ups: Perform written follow-ups for both serious and non-serious cases.
โ Regulatory Compliance: Adhere to global pharmacovigilance regulations and client-specific guidelines.
โ Affiliate Mailbox Management: Handle case reconciliation and ensure timely reporting.
Skills Required:
- Basic knowledge of pharmacovigilance operations & drug safety surveillance.
- Strong attention to detail for data entry and case processing.
- Ability to work in rotational shifts (if required).
Who Should Apply?
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Fresh graduates (B.Pharm, M.Pharm) looking to start a career in pharmacovigilance.
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Professionals with 0-2 years of experience in drug safety or clinical research.
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Candidates with strong English communication skills.