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Join a growing international CRO and take the next step in your Clinical Research career. We are looking for a Freelance Clinical Research Associate (CRA) in Brazil to support an exciting Infectious Disease clinical trial. Our client
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.
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