The Clinical Research Coordinator I supports cancer research by independently coordinating clinical studies, screening patients, and ensuring compliance with regulatory standards such as FDA and IRB. Responsibilities include data collection, documentation, scheduling patient visits, responding to sponsor queries, and participating in auditing activities. The role requires strong computer literacy, attention to detail, and the ability to work collaboratively within a dynamic medical research team in a hybrid work environment based in Los Angeles.
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
This exciting opportunity at a top medical center involves cutting-edge cancer research and requires strong skills in data entry, planning and scheduling, and computer literacy to support a dynamic and collaborative team.
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents study information at regular research staff meetings. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).Primary Duties and Responsibilities
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.
Requirements:
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Req ID : 8674clinical research, data management, cancer research, patient screening, protocol compliance, FDA regulations, IRB submissions, data entry, case report forms, clinical trials
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