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This role is open to candidates based in Brazil only. About SigmaMD SigmaMD is changing the way people manage their health. We build the platform where modern clinics run their entire business on — clinician apps,
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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