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The Clinical Research Coordinator II works independently providing study coordination including 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 information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. 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:#Jobs-Indeed
Full Time
$64k-84k (estimate)
05/06/2024
05/25/2024
cedars-sinai.com
Los Angeles, CA
<25
The following is the career advancement route for Clinical Research Coordinator II (Onsite) positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator II (Onsite), it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator II (Onsite). You can explore the career advancement for a Clinical Research Coordinator II (Onsite) below and select your interested title to get hiring information.