Works under general supervision to ensure the appropriate gathering, evaluation, and entry of clinical data. The specialist is responsible for the receipt, completeness, and accuracy of research and departmental data requirements. The role monitors data and reports submitted to regulatory agencies to ensure reporting requirements are met within established timeframes and that regulatory requirements are followed. The position coordinates clinical data collection for adult and pediatric programs, maintains related databases, and prepares analyses and reports for quality assurance, case review, and other program needs. Professional experience in oncology abstraction and data management is preferred.
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Job Type
Full-time