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Clinical Research Assistant
Overview This position is responsible for the coordination and management of local data collection and submission for clinical trials (data management) as well as study coordination for both observational and registry studies (study coordination). Responsibilities include data collection via chart extraction and subject source documents, the timely completion of study data capture, submission of de-identified clinical data in accordance with protocols, completion or facilitation of all sponsor produced queries and data reconciliation, performance of data cleaning and quality control, screening of patient medical charts for study recruitment, acting as primary liaison for coordinators during monitoring visits, and providing overall support for the clinical trials depart


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