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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. Serves
Location : Kruševac, Serbia Main responsibilities : - Work with vednors and cusomers to reconsile balances - Work in E invoice portal - Shopping Card coding on simpler typology or clusters with no check for VAT
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