A BDN client is looking for a Senior Drug Safety Scientist who will be responsible for pharmacovigilance activities involving the company’s products and/or studies. The successful candidate will manage individual adverse events (AE) cases, including review, processing, and evaluation of safety reports for both marketed and investigational medicinal products. These responsibilities are performed under the direction of the Head, Global Pharmacovigilance. Responsibilities for this role include participating in the proper and timely collection and reporting of AE information from all sources as well as supporting the medical review of AEs/ADRs for both marketed and pre-marketed products and medical device reports, interfacing with reporters as needed. A minimum of 3 years of experience in the pharmaceutical industry or CRO within drug safety, pharmacovigilance, and risk assessment or relevant experience is desired. A Health Science Degree: RN (BSN or MSN), NP, RPH, PharmD, PA, or MD is preferred for this role.