VISAKHAPATNAM · FULLTIME
Pharmacovigilance Associate
Airvin Skills
Visakhapatnam · hybrid · Posted 1d ago
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Section · 01
About this role
Role & responsibilities
An entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including
adverse event case processing and safety database management.
Key Responsibilities
Process Individual Case Safety Reports (ICSRs) for adverse events
Perform MedDRA coding of adverse event and medical history terms
Enter and review safety data in pharmacovigilance/drug safety databases
Support signal detection and safety data analysis activities
Assist in preparing periodic safety reports (PSUR/PBRER)
Ensure compliance with GVP (Good Pharmacovigilance Practices) guidelines
Support literature screening for safety-relevant information
Preferred candidate profile
Basic knowledge of MS Office (Word, Excel, PowerPoint)
Good written and verbal communication skills
Attention to detail and documentation discipline
Willingness to learn and work in a regulated, compliance-driven environment
Sourced from naukri
Section · 02