The Clinical Research Coordinator I at Cedars-Sinai's Heart Institute plays a crucial role in managing clinical research trials by screening participants for eligibility and facilitating informed consent processes. This position requires meticulous data collection and documentation to ensure compliance with federal regulations while also supporting research aimed at improving kidney transplant outcomes. The coordinator collaborates with physicians to monitor patient conditions and collect quality of life data, contributing to the advancement of medical research.
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The Clinical Research Coordinator I works independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This position presents this information at research staff meetings and ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
This position supports Kidney Transplant clinical research, which focuses on improving outcomes in transplant through development of interventions focused on quality of life, reducing surgery burden, improving early detection, and enhancing imaging techniques.
Primary Duties and Responsibilities:Acquires quality of life data
clinical research, research coordinator, FDA compliance, clinical trials, data collection, kidney transplant, medical research, patient care, quality of life, ACRP certification
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