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responsible for hiring and general supervision of all cmc Regulatory Affairs submissions (pre and post submission support staff, as applicable). oversee the interaction and Communication of direct reports, as applicable. align departmental personnel .....
your responsibilities: manage, coordinate and oversee the implementation and execution of companion Diagnostics (cdx ) programs with external collaborators within agreed timelines, budget and resources lead cross-functional project meetings with the .....
design. progress. together. curevac ag is a biopharmaceutical company researching, developing and producing novel drugs based on the natural Molecule messenger RNA (mrna). our focus is on innovative Cancer immunotherapies, prophylactic Vaccines and .....
gemeinsam. fortschritt. gestalten. die curevac ag ist ein biopharmazeutisches unternehmen, das neuartige medikamente auf basis des botenmoleküls messenger RNA (mrna) erforscht, entwickelt und produziert. unsere schwerpunkte liegen auf innovativen .....
based in amsterdam and lexington (usa), uniqure is a biotech company dedicated to bringing innovative therapies or unmet medical needs to patients. in doing so each function in uniqure is directly or indirectly responsible for the lives of patients. .....
uniqure is dedicated to bring innovative therapies or unmet medical needs to patients. in doing so each function in uniqure is directly or indirectly responsible for the lives of patients. this responsibility should be part of our day-to-day working .....
descriptionthe Clinical Trial Associate (cta) is part of the Clinical operations unit within tfs develop and will work, when delegated, as a Member of the study team with the responsibility to organize and maintain the study master file (smf) and .....
descriptiongeneral description the senior Clinical Research Associate (sr CRA) is part of site management within tfs develop and will function operationally as a Member of a project team and is responsible for the initiation, on-site and remote .....
descriptiongeneral description responsible for the development of Clinical trials’ strategies, working closely with therapeutic, regulatory and delivery teams. essential job functions work independently on the collection, Analysis and presentation .....
descriptionduties and responsibilities: setting up, documenting and communicating project specific medical monitoring requirements for assigned projects. developing and reviewing medical monitoring and other study related plans Training project team .....
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