Job Description

Role Overview

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An entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including

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adverse event case processing and safety database management.

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Key Responsibilities

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■ Process Individual Case Safety Reports (ICSRs) for adverse events

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■ Perform MedDRA coding of adverse event and medical history terms

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■ Enter and review safety data in pharmacovigilance/drug safety databases

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■ Support signal detection and safety data analysis activities

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■ Assist in preparing periodic safety reports (PSUR/PBRER)

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■ Ensure compliance with GVP (Good Pharmacovigilance Practices) guidelines

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■ Support literature screening for safety-relevant information

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Educational Qualification

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B.Pharm/M.Pharm,



B.Sc/M.Sc Life Sciences, MBBS, BDS, or PG Diploma in Pharmacovigilance.

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Experience Required

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Fresher / 0-1 year. Freshers with the right educational background and a willingness to learn are

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strongly encouraged to apply. On-the-job training will be provided.

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Good to Have

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■ Basic knowledge of MS Office (Word, Excel, PowerPoint)

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■ Good written and verbal communication skills

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■ Attention to detail and documentation discipline

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■ Willingness to learn and work in a regulated, compliance-driven setting

📌 Pharmacovigilance Associate (Bengaluru)
🏢 LLRI - Learning Labb Research Institute
📍 Bengaluru