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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
Responsibilities Partner with the project lead to understand customer requirements and translate them into well-defined technical solutions; develop, test, deploy, and support data analytics deliverables. Design and implement optimized database structures and write high-performance SQL (queries, views,
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