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Clinical Research Coordinator III
Clinical Research Coordinator III Responsibilities PRIMARY FUNCTION:  The Clinical Research Coordinator III works under limited supervision and runs portions of clinical trials, assists with orientation and training, obtains signature for informed consent, central lab management, data management, completes expectancy reports, monitors visit preparation, submits low institutional risk trials and tracks TJU IRB submission and approvals.                                          ESSENTIAL FUNCTIONS: Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Trains and supervises research staff on the proper procedures


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