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 discussing clinical research studies; monitoring study participants and ensuring proper follow-up visits are scheduled and conducted; overseeing and preparing for external quality assurance and control review; collaborating with sponsoring agencies and serving as liaison with an inter-disciplinary research team; designing database components and reporting tools; completing data entry and monitoring data quality with assurance and quality control; developing detailed reports for data related to strategic decision-making, research, publications, or presentations; analyzing, querying, interpreting and summarizing data for principal investigators (PI); preparing proposals requesting further clinical research; executing and overseeing technical processes to collect and extract data; making recommendations to PI based upon data analysis; maintaining patient inventory in Oncore; assisting the PI in writing manuscripts and in preparation of grant submission; creating and maintaining tools and workflows for research with clinic and faculty; educating hospital staff and non-Hematology physicians on study protocols and purpose; working with the PI in developing plans to meet requirements of new clinical research studies and research requests; responsible for review of institutional review board (IRB) submissions; participating in ensuring protocol compliance with all federal, local and institutional 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 a clinical research capacity conducting clinical research studies required; prior clinical research database management desired; computer literacy with basic database tools and methods required.
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