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Clinical Research Coordinator II (Hybrid)
Job DescriptionThe 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
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