Medical, Regulatory & PV Specialist Category :Reg Affairs & Safety Pharmacovigilance Location :Podgorica, Podgorica, RS The Position - As a Medical, Regulatory and Pharmacovigilance Specialist at Novo Nordisk, you will secure timely safety reporting in compliance with relevant
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What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.