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8.0 - 12.0 years

0 Lacs

ranchi, jharkhand

On-site

You should have 8-12 years of experience in Pharmacovigilance, with familiarity in Pharmacovigilance Risk Management Plan (RMP) processes and Pharmacovigilance Periodic Safety Reports (PSR) processes. You should also have experience in translating business requirements into technical specifications and have worked with Top-30 Pharma companies. Cross-functional experience in safety, pharmacovigilance, and regulatory affairs is desired. Experience with Veeva.RIM and Feith Orbit platform is a plus. Strong organizational and verbal/written communication skills are essential for this role. If you meet the above criteria, please share your updated resume with us at connect@datakaar.com.,

Posted 2 days ago

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