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Clinical Trial Manager
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- The Clinical Trial Manager Responsible for ensuring studies are being conducted in adherence with the protocol, ICH Good Clinical Practice Guidelines (GCP), FDA regulations, applicable Standard Operating Procedures (SOPs), policies and any other applicable regulations.
- Participate in the mentorship of project specific CRA education, training, and performance assessment for more junior clinical research staff.
- Assures studies are conducted in adherence to the protocol, GCP, Investigator integrity, and compliance with all study regulations.
- Clinical Trials: Provide clinical monitoring expertise, support, and leadership for more junior clinical research staff.
- Communicate new developments in clinical research to CRA’s.
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