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We are looking for a Pharmacovigilance Officer to process and code adverse event cases within regulatory timelines. You will support signal detection and aggregate report writing, and maintain safety database quality and compliance. Required: hands-on experience with Case processing, MedDRA coding, Signal detection, PSUR writing, and working knowledge of Argus Safety, ARISg, MedDRA. Preferred: Drug Safety certifications. Success in this role is measured by case processing timeliness, reporting compliance rate, QC error rate.