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about you do you bring experience working in Drug Safety? do you bring know-how in the area of Regulatory Affairs? are you committed to learning and developing your skills, further? our team in buenos aires is growing and in this newly created .....
Drug Safety Associate, aggregate reporting, r&d Pharmacovigilance – malvern, pa about endo international plcendo international plc (nasdaq: endp) is a highly focused generics and specialty branded Pharmaceutical company delivering quality .....
imove, the sanofi vie program, is available to citizens of the european economic area (eu + norway, liechtenstein and iceland) aged between 18 and 28.please note that since this program is primarily an international development program, candidates .....
requisition id: cli007988 perform registry and case assignment tasks as needed. perform Data entry/review of all adverse experience information received and processed within safety database within the established timeframes. through daily case .....
    position summary this position has primary responsibility for ensuring that there is appropriate local pv system oversight, including any elements of the pv system that are contracted to a third party. this includes responsibility for ensuring .....
the global safety Therapeutic Areas serve as the safety experts for all amgen products globally and are accountable for the safety Strategy and major safety deliverables for each amgen product. leaders in the therapeutic area safety teams are .....
requisition id: env000616are you ready to invent, impact, inspire? msd is a Global Health care Leader with a diversified portfolio of prescription medicines, Vaccines and Animal Health products. the difference between potential and achievement lies .....
purpose of job apply subject matter knowledge and demonstrate technical/business insight. work within a unit and/or across functional areas with limited supervision. long description major tasksbe a safety Leader and influencer.report regularly to .....
the Drug Safety specialist will provide technical and process-related support to Drug Safety management (Clinical Trial and post-marketed) and medical monitoring activities, ensuring Compliance with relevant regulations and standard operating .....
% of time job function and description 20% Product management/oversight. may act as a line manager or mentor to pv scientists, or as a manager for a product or group of products. oversees and assumes responsibility for assigned therapeutic products .....
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