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Clinical Research Coordinator III / Sr
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Full-time
- The primary responsibility of the Clinical Research Coordinator III is to manage all aspects of conducting clinical trials, with minimal supervision.
- The Clinical Research Coordinator III is required to have an in-depth knowledge of protocol requirements and good clinical practices asset forth by federal regulations.
- As the primary resource for the protocol, the Clinical Research Coordinator III acts as a liaison between the patient, investigator, Institutional Review Board and sponsor.
- The Clinical Research Coordinator III screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing,coordinating, and implementing all assigned research projects.
- The Clinical Research Coordinator III is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
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