Medical Affairs Lead Pharmacovigilance Jobs in New Jersey

... guidance impacting global regulatory procedures Lead on identified process improvement initiatives, ... initiatives, as required Procedural Documents Lead the development and implementation of ... Practices (WPs) within Global Regulatory..

... with internal multidisciplinary stakeholders (Regulatory Affairs, Regulatory Operations, Worldwide Patient Safety, ... to support aRMM/REMS regulatory submissions Lead live meetings to adjudicate multiple ... in Pharmaceutical Industry (REMS Operations,..

... multidisciplinary RMP/REMS stakeholders (Submission teams, Lead Safety Physicians, Regulatory Affairs, Biostats, Regulatory Operations, Global Risk ... status reports for different audiences Lead status meetings to ensure transparency ... Industry..

... with internal multidisciplinary stakeholders (Regulatory Affairs, Regulatory Operations, Worldwide Patient Safety, ... to support aRMM/REMS regulatory submissions Lead live meetings to adjudicate multiple ... in Pharmaceutical Industry (REMS Operations,..

... results. Purpose/Objective: Support a strong pharmacovigilance quality system by contributing toward ... training materials Support and eventually lead investigations into quality issues within ... Stakeholders/Contacts: Cross-functional groups within Global..

... Manager, Document Management SUPERVISOR GRM Lead, Publishing and Support DEPARTMENT Center ... Pharmaceutical experience in REMS Operations, Medical Communications/Medical Affairs, Regulatory, or Safety/Pharmacovigilance. REMS and Risk Management Plan .....

... results. Summary The Clinical Trial Lead works with stakeholders across the ... commercial objectives. The Clinical Trial Lead reviews and interprets clinical data, ... clinical overviews. In collaboration with..