... . Works with Project Manager (PM); Clinical Team Leader (CTL), SSU (Study ... knowledge of medical terminology and clinical monitoring process. Ability to travel ... Training Budget for furthering professional development Flexible Working hours (within reason) ...
de.talent.com
... . Works with Project Manager (PM); Clinical Team Leader (CTL), SSU (Study ... knowledge of medical terminology and clinical monitoring process. Ability to travel ... Training Budget for furthering professional development Flexible Working hours (within reason) ...
de.talent.com
... business unit. As a Business Development Manager at ProBioGen, you will ... a plusProven experience in business development, preferably in a CDMO or ... : Deep understanding of manufacturing for clinical studiesStrong understanding of the biopharmaceutical ...
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... implemented in the combination product development programs. Liaise with clinical department for design of human ...
www.finest-jobs.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, ...
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, ...
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, ...
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, ...
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, ...
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, ...
de.talent.com