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
The Mid-Level Pharmacovigilance Analyst will manage the preparation and submission of RPBR/PBRER and PGR/RMP reports, ensuring compliance with regulatory requirements and supporting process improvements. Key Responsibilities Prepare and review RPBR/PBRER and PGR/RMP reports independently. Coordinate with
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