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job description role location: plymouth meeting, pa 19462summary:iqvia is developing our next-generation global data lake and Analytics platform to support Analytics and insights against hundreds of terabytes and petabytes of Health Care data, and .....
the position the positionwe are seeking a highly motivated senior Scientific Researcher to join the department of antibody Engineering. the successful candidate will work in the development of new Antibodies for therapeutic and Research Applications .....
key responsibilities include: deliver Sales performance, brand kpis, financial targets, Marketing objectives, etc. in order to meet or exceed on those objectives. create pre-call plan using smart objectives and execute post-call evaluation in order .....
description\: through integrative Leadership provide Clinical Development and Biomarker strategies to achieve proof of    clinical principle (pocp) as a Member of the early Clinical Development (ecd) team drive and support .....
job description purpose: the product and platform architecture team drives the future of the enterprise through development and advocacy of standards, principles, and solution architectures supportive of the iqvia Business Strategy.  working .....
responsibilities territory: north texas, oklahoma and arkansas. candidates must live in the territory. ideal location is dallas/fort worth.the mission of sanofi’s Medical Science Liaison (msl) team and the Medical Science Liaison is to be the .....
principal Scientist / Associate Director, Toxicology   omeros is seeking a principal Scientist / Associate Director, Toxicology who has experience designing, Planning and executing nonclinical development plans for both Small molecules and .....
description\:   the cardiovascular business specialist is responsible for developing and implementing a plan for maximizing net Sales of bipi and co-promoted cardiovascular products that aligns with direction from bipi commercial Leadership and .....
responsibilities 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 .....
summarythe clinical safety/Regulatory Affairs Associate performs safety reporting and trial submissions to Ethics committees and regulatory authorities according to the relevant legislation and guidelines for Clinical trials with Medical Devices .....
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