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
Come to one of the biggest IT Services companies in the world! Here you can transform your career! Why to join TCS? Here at TCS we believe that people make the difference, thats why we live
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