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You’re looking for Life Sciences jobs . On BrightOwl, we centralise vacancies from biotech, pharma and life sciences companies in general. Register for free, build your profile so that companies can contact you for new openings.

25766 jobs

 do you want to watch Clinical Development change, or do you want to be the one to shape it? because we’re hoping you’re here for the latter. who are we?we are pra. we are 15,000+ employees strong, operating in more .....
supports and leads the Clinical data review activities that contribute to delivery of an analyzable database.2 years of Clinical data experiencebachelor’s degreetbdpra is an eeo/aa employer and is committed to providing opportunities to .....
the Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure Clinical trials are conducted, recorded, and reported in accordance with the science)" rel="nofollow">Protocol, standard operating procedures .....
the Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure Clinical trials are conducted, recorded, and reported in accordance with the science)" rel="nofollow">Protocol, standard operating procedures .....
do you want to watch Clinical Development change, or do you want to be the one to shape it? because we’re hoping you’re here for the latter. who are we?we are pra. we are 15,000+ employees strong, operating in more than 85 .....
who are we?we are pra. we are 15,000+ employees strong, operating in more than 85 countries. we are committed to saving lives and we are constantly striving to be the best at what we do. our impact is real and we see it every single day. we .....
do you want to be responsible for the development and Analysis of contractual relationships including Investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to Clinical trials?  who .....
provides scientific, pharmacoepidemiology, and Biomedical Leadership (direction and technical expertise) for Planning of Internal medicine or device studies, benefit-risk investigations, Risk Management programs and Health economical assessments. .....
a Clinical data standards Consultant is responsible for supporting the operational staff in the use of CDISC standards, sponsor specific standards, or pra standards. they will develop tools to increase the efficiency, timeliness and quality of .....
as a vendor business Operations Associate, you will be responsible for the management and tracking of vendor invoices from initial receipt until paid by Accounting.desired skills and qualifications:bachelor’s degreeexperience in CRO or .....
25766 jobs