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with over 45 beds, our early phase Clinical unit, located in northwick park Hospital in london harrow is staffed around the clock by our highly trained and certified team. it features state of the art monitoring technologies and offers our .....
with over 45 beds, our early phase Clinical unit, located in northwick park Hospital in london harrow is staffed around the clock by our highly trained and certified team. it features state of the art monitoring technologies and offers our .....
we are currently Recruiting for an experienced proposal specialists to join a dedicated global team in a very fast paced environment. as a proposal specialist, you will develop compelling proposals and associated Budgets, with strategic input from .....
<職務内容>医薬品開発に関する治験関連文書を法規制に順守し、適正にファイリング保管するインベントリークオリティチェックのスペシャリスト業務です。 .....
responsibilities key accountabilities:as a Statistical programmer you will support various SAS® programming activities related to the Analysis and reporting of Clinical study data; you will use programming techniques to produce Analysis datasets, .....
central files and edc management create central files for new studies and maintain central files for ongoing studies according to parexel SOP’s or contractual obligation to sponsor.track and scan paper case report forms, as required.support edc .....
responsibilities lead production and Quality Control of Randomization, Analysis plans, Statistical reports, Statistical sections of integrated Clinical reports and other process supporting documents.provide a supporting role as a non-voting .....
the purpose of parexel’s Internal Audit and controls group is to provide objective and professional evaluations of parexel and their Operations and internal controls, and assist management in achieving goals and objectives. the senior manager .....
essential functionthe Research associate (ra) is responsible for completion of the required procedures in carrying out a Clinical Trial study science)" rel="nofollow">Protocol within an outpatient and/or inpatient environment, upholding Good Clinical Practice (gcp) and .....
responsibilities understanding of current global regulatory submission standardsoverall understanding of regulatory cmc, labeling, Clinical etc. within post-approval activitiesstrong Project Management skillsfamiliarity with departmental standard .....
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