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6.0 - 10.0 years
6 - 12 Lacs
kolkata, west bengal, india
On-site
We are looking for a skilled and dedicated Safety & Pharmacovigilance Specialist to join our team. This role is responsible for the collection, processing, and reporting of adverse event data, ensuring compliance with global regulations and company standards. The ideal candidate will have hands-on experience in pharmacovigilance and a strong understanding of safety reporting requirements to contribute to patient safety. Roles & Responsibilities Case Processing: Perform end-to-end management of Individual Case Safety Reports (ICSRs) , including data entry, coding of adverse events using MedDRA , and drug coding using WHO-DD . Ensure timely and accurate processing of adverse event reports from...
Posted 4 months ago
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