The Cancer Clinical Trials CRC I under direct supervision supports the research team in overall conduct of clinical trials using Good Clinical Practice. Mentored by an experienced Clinical Research Coordinator II or Sr. Clinical Research Coordinator, the CRC I is responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. This individual obtains informed consent for non-interventional studies, participates and supports investigators in the informed consent process for interventional trials, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor. Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees