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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
Key ResponsibilitiesIndependently supervises the conduct of assigned regulatory field studies and ensures trials are conducted according to ISO/GLP standards as well as follows CTNBio biosafety rules and stewardship standards.Develops relationship with Contract research Organization (CROs) and
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