... Teams and you take clinical development responsibility for the projects assigned. ... English language The VP Clinical Development role additionally requires: MD (specialist in Oncology or equivalent) with sound clinical oncology experience and multiple years ...
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... take clinical development responsibility for the projects assigned. ... Director Clinical Development, you: You author Investigator`s Brochures, Asset Evidence Plans, Core Clinical Trial Protocols and Pediatric Development Plans together with your cross ...
de.talent.com
... the Clinical Research Division on quality control of clinical data. Promptly address the Projects Coordinators Project Managers Senior Project Managers about any issues that can ... in clinical development and functional solutions for pharmaceutical, ...
de.talent.com
... customers a wide range of clinical development, patient access, and technology solutions ... scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, ...
de.talent.com
... Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical ...
de.talent.com
... project procurement services and business development The Regional Procurement Manager provides active leadership to procurement ...
de.talent.com
... Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical ...
de.talent.com
... in the expanding clinical research industry. Your role: Schedule, ... audit findings. Assists the Clinical Trial Manager with clinical operations activities by overseeing resource ... as requested by the Clinical Trial Manager. May conduct on-site evaluation ...
de.talent.com
... Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical ...
de.talent.com
... and adverse event reporting within clinical trial settings. Solid knowledge of clinical trial design, regulatory standards, and drug development. Proficient in Microsoft Office (Excel, ...
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