The Clinical Research Coordinator I at Cedars-Sinai's Heart Institute is responsible for managing clinical research studies, including participant screening, data collection, and documentation. This role involves compliance with regulatory standards and supporting research focused on improving kidney transplant outcomes through various interventions. Strong organizational skills and attention to detail are essential for ensuring accurate records and effective communication within the research team.
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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, study coordinator, data collection, health care, kidney transplant, protocol compliance, research participant, FDA regulations, IRB, medical research
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