Job Summary: The Clinical Research Coordinator (CRC) for the WMC Cancer Center's Cancer Clinical Trials Office (CCTO) will manage clinical research studies by coordinating and participating in the collection, compilation, documentation and analysis of clinical research data. The CRC also directly interacts with study participants to monitor progress, including documenting and reporting adverse events. The CRC will be responsible for maintaining source documents and submitting case report forms as required for clinical trials and assist clinical staff with sample collection, processing, handling, and shipping as outlined in the protocol. The CRC specialist will report directly to the Medical Director of the CCTO. Responsibilities:
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