About this role
We are looking for a meticulous individual with attention to detail to assume the position of Pharmacovigilance Associate (PV). The key functions include managing the collection, processing and reporting of Adverse Reactions (ARs) and Product Quality Complaints (PQPs) in accordance with corporate and national pharmacovigilance requirements (BioScript/NavieGo/CRC). In addition to these core functions, the ideal candidate would also assist with quality assurance related tasks such as; but not limited to audit preparation, CAPA investigations, change management and program compliance.