... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project ... Oncology or equivalent) with sound clinical oncology experience and (ideally) some ... of Basic Science and or Clinical Research Sound medical and scientific ...
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... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project ... Oncology or equivalent) with sound clinical oncology experience and (ideally) some ... of Basic Science and or Clinical Research Sound medical and scientific ...
de.talent.com
... house team as a Freelance Clinical Research Associate for 0.5 ... general support to the Clinical Research Division on quality control of clinical data. Promptly address the Projects ... agreed for each single clinical trial. Develops training material and ...
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... and contribute to impactful clinical programs during an exciting growth ... you will be the clinical and scientific expert for trial ... quality, and compliance of clinical studies. This role is essential ... years of experience in clinical research, with a focus on ...
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... planning, coordinating, and conducting clinical research studies for in vitro ... regulatory submissions. Define the clinical utility of investigational products. Gather ... Requirements: Basic understanding of clinical research regulations and guidelines. Good ...
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... German team and engage in clinical trial management on a day- ... Work closely with the Project Clinical Trial Manager for timely delivery ... -specific status reports within the Clinical Trial Management System (CTMS); Interact ...
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... guidelines Coordinate timely shipment of clinical supplies and study drug to ... , Lead CRA, Project Manager and Clinical Operations Manager accordingly Assist with ... , including conducting monitoring visits for clinical trials, from either a pharmaceutical ...
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... to shape the future of clinical development. At ICON, it’s our ... . We want to be the Clinical Research Organisation that delivers excellence ... Study Monitoring Plan. • To contact Clinical sites for specific requests (e. ...
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... safety strategies for molecules in clinical development and post-marketing phases ... Team (SMT) meetings Participate in clinical study team meetings for assigned ... governing pharmacovigilance activities for both clinical trial and post-marketing environments ...
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... embed yourself in the wider clinical operations teams and work on ... regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference ...
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