Jobtailor seeks a Pharmacovigilance Specialist to manage end-to-end case processing for clinical trials and post-marketing safety data, including intake, data entry, triage, MedDRA coding, seriousness evaluations, and safety queries.
You will coordinate case exchanges with partners, track compliance metrics, and prepare quality reviews for SUSARs, DSURs, and line listings. Fluency in English and 2+ years PV experience are required.
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