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Clinical Research Coordinator
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- In this role you will ensure IRB approved protocols are implemented and followed; execute the
- The Clinical Research Coordinator must also be able to perform clinical
- Writes patient information sheet for clinical studies for submission to IRB, as well as
- complete the necessary documents for IRB admission in a timely fashion.
- Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as
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