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description\:   the Director has responsibility for the Pharmacovigilance Risk Management activities of core strategic * marketed and/or investigational compounds on global level. in additional to reporting to us Line Management, this position .....
correct title: senior manager, trial safety science core work hours - 8 hour day as long as core hours of 9am-4pm are covered. extension of the contract will be contingent upon performance. work site: summit, nj. general responsibilities: • .....
responsibilities job summary: the oversight Clinical Project Leader (ocpl) is responsible for the functional oversight of field-based cras in a given region. the ocpl ensures that adequate resources are available to support the Clinical Trial .....
at astrazeneca we win through science, it’s at the heart of our every success. that science is only possible when we all work together - we’ll always make sure you’re clear about how your role is connected to our wider mission to really show .....
env000602 merck & co., inc. kenilworth, n.j., u.s.a. known as merck in the united states and canada, is a Global Health care Leader with a diversified portfolio of prescription medicines, Vaccines and Animal Health products. the difference .....
the position we are seeking an experienced Veterinary/anatomic pathologist to join the genentech development Sciences safety assessment department. the successful candidate will provide Expert Pathology support, scientific Leadership and play an .....
rb            a fantastic opportunity is available for an information Coordinator to join our consumer safety team on a 12month ftc in hull.    responsible for   ensuring supporting documents are in place .....
job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
the position a study Director (e4) provides operational management and reporting for Toxicology non-glp nonclinical safety studies of drug candidates and marketed products in the department of safety assessment (sa). this person is responsible for .....
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