Clinical Research Coordinator - Trauma & Acute Care Surgery - Atrium Health
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About The Position
The position involves managing protocols to ensure the safety of patients and the quality of clinical trial data. The individual will prepare and submit Institutional Review Board (IRB) paperwork and maintain all related regulatory document submissions. They will communicate and coordinate study activities with the Primary Investigator and any Sub-Investigators of clinical studies. The role requires determining protocol-related needs to conduct trials, ordering supplies and equipment, recruiting and screening potential patients, and obtaining informed consent. Additionally, the individual will assist in providing patient education regarding the benefits and risks of participating in clinical drug trials, design organizational tools for accurate data collection, conduct in-service programs, manage research funds, schedule patient visits, and coordinate drug shipments and accountability with the pharmacy. The position also involves reviewing trends, problems encountered, patient adverse events, and patient progress, as well as drawing blood or collecting other samples as needed.
