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the position the position / responsibilitieswe are seeking a highly motivated individual for a Scientific Researcher/senior Scientific Researcher position in Drug metabolism and Pharmacokinetics (dmpk) department at genentech. in the drug .....
the position purpose: the Clinical Trial Leader (ctl) will provide support and/or Leadership to one or more study management teams (smts) and/or study review teams (srts), and provide Strategic Planning and organization to ensure successful .....
descriptionthe ideal candidate will be the designated lead Medical Writer for one or more oncology programs, responsible for supporting the critical regulatory Medical writing needs, and offering direction to other staff/contractors regarding these .....
descriptionresponsible for establishing and managing a formal Quality Control process to ensure all program development activities follow established sdlc methodologies; that all iods activities and processes are performed in accordance to the .....
descriptionenter a brief description of the position, why it exists and how it contributes to the organization. the eisai nbg is currently looking to fill an senior manager, of data Operations opening at its north american headquarters in woodcliff .....
descriptionthe manager of dm is primarily responsible for the direct management of Clinical study activities as they relate to data collection and cleaning, from study start up through ongoing oversight to completion. the manager of dm develops .....
descriptionthis position serves a critical role within the Clinical Development in that he/she will be responsible for designing Clinical Trial, performing Data Analysis, supporting regulatory interactions, overseeing CRO activities, validating tlgs .....
job description launched in 2015, q2 solutions is a leading global Clinical trials Laboratory services organization. we help biopharmaceutical, Medical Device and Diagnostics customers improve human Health through Innovation that transforms science .....
descriptionsupports all phases of Clinical study activities (feasibility, start-up, maintenance, and close-out). assist with filing and archiving project Documentation in the etmf within 20 day timeframe. assist with creating, updating and .....
descriptionthis Associate Director position will spearhead the Statistical programming activities for multiple studies and will lead the programming submission related activities. additionally, this position will work with the head of programming to .....
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