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We are looking for a Pharmacovigilance Associate to process and assess adverse event reports within regulatory timelines. You will write case narratives and code events in MedDRA, and support signal detection and periodic safety reports. Required: hands-on experience with Adverse event processing, Case narrative writing, MedDRA coding, Causality assessment, and working knowledge of Argus Safety, ArisGlobal, MedDRA. Preferred: Pharmacovigilance Certification or B.Pharm / M.Pharm. Success in this role is measured by cases processed per day, on-time submission rate, quality error rate.