Clinical Research Coordinator to plan, coordinate and implement Hematology/Leukemia Tissue Bank patient clinical research projects within the Comprehensive Cancer Center (CCC). Responsibilities include assisting in the coordination and oversight of trials in the acute leukemia and other hematologic malignancy patient population; identifying and assessing eligibility of patients for clinical research study participation; obtaining informed consent both in person and remotely; educating patients and their family members on the diagnosis and clinical research studies; monitoring study participants and ensuring proper follow-up visits; overseeing and preparing for external quality assurance and control review; collaborating with sponsoring agencies and interdisciplinary research teams; designing database components and reporting tools; completing data entry and monitoring data quality; developing detailed reports for strategic decision-making, research, publications, or presentations; preparing proposals for further clinical research; executing and overseeing technical processes to collect and extract data; making recommendations to principal investigators based on data analysis; maintaining patient inventory in Oncore; assisting in manuscript writing and grant preparation; creating and maintaining research tools and workflows; educating hospital staff and non-Hematology physicians on study protocols; working with principal investigators to meet requirements of new clinical research studies; reviewing institutional review board submissions; ensuring protocol compliance with regulations; assisting with research sample collection including blood draws. Minimum education required is a Bachelor's Degree in biological sciences, health sciences or related field or equivalent combination of education and experience. One year experience in clinical research capacity required; prior clinical research database management desired; computer literacy with basic database tools and methods required.
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