Pharmacovigilance Specialist  

Who we are looking forMain Responsibilitieswill be responsible for conducting comprehensive reviews of adverse event reports for investigational and post-marketed products, ensuring compliance with regulatory guidelines and completeness of documentation.Assist in developing Safety forms, standard operating procedures, and process guidelines,Assist in signal detection activities and provide line listings for review,Collaborate with cross-functional teams e.g. Clinical Operations, Medical Affairs,Provide advice to Affiliates in managing local Non-interventional studies and other organized data collection...