Pharmacovigilance Executive

A pharmacovigilance job description involves monitoring, detecting, assessing, and preventing adverse drug reactions (ADRs) and safety issues across a medication's lifecycle to protect patient health and ensure compliance with global health authorities

Core Role & Responsibilities

• Case Processing: Collect, triage, and process Individual Case Safety Reports (ICSRs) for adverse events
• Medical Coding: Code adverse events and medical history using standardized terminology like MedDRA and WHO dictionaries.
• Narrative Writing: Write clear patient event timelines and clinical summaries from drug initiation to reaction onset.
• Causality & Compliance Assessment: Evaluate the causal relationship between a drug and an adverse event, ensuring strict adherence to 7-to-15-day reporting timelines for serious cases.