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LLRI - Learning Labb Research Institute

Pharmacovigilance Associate

Bangalore, Karnataka, India

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hirly's read of this role

Seniority
Mid level
Country
IN
Work mode
On-site / unstated
First seen by hirly
28 Sept 2026

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the posting

Role Overview 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 …

Original posting on LLRI - Learning Labb Research Institute's site ↗

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