Metrics and Analytics Coordinator, Lombardi Comprehensive Cancer Center - Georgetown University Medical Center
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The CRMO Metrics and Analytics Coordinator will have the opportunity to work under the general direction of the CRMO Administrative Director to ensure LCCC's compliance with the data management and reporting requirements of the National Cancer Institute (NCI) Cancer Center Support Grant (CCSG). Specifically, this coordinator is responsible for maintaining quality oversight of data in Medstar's OnCore Clinical Trials Management System (CTMS) and data reported from LCCC's consortium partner, John Theurer Cancer Center (JTCC), according to NCI Cancer Center Support Grant (CCSG) requirements. As needed, this coordinator will engage with study teams and investigators to verify and reconcile data, inform and instruct study teams and PIs on reporting requirements, and monitor and report on data quality to leadership.
The CRMO Metrics and Analytics Coordinator works with staff at affiliate sites participating in LCCC's consortium sites to confirm that study and patient level data is entered into OnCore and reported appropriately. This coordinator will also support LCCC's Cancer Center Support Grant (CCSG) by analyzing key performance metrics, providing analysis to leadership via business intelligence, and assisting in preparation of CCSG data as needed for grant reporting and competitive renewal requirements.
Works under direct supervision of the CRMO Administrative Director to ensure high-quality, timely, and accurate data reporting. This person also works with LCCC and JTCC investigators, study staff, CRMO CTRP Coordinator, CRMO OnCore Coordinator, Lombardi Cancer Center administrative staff and other personnel involved in and/or assisting with clinical research at Lombardi Cancer Center. This position may also interact with pharmaceutical sponsors, national and international cancer research Cooperative Groups, and representatives from other institutions and organizations. This position may also interact with NCI's Clinical Trials Reporting Office (CTRO) within the Coordinating Center for Clinical Trials (CCCT) to reconcile LCCC's NCI CCSG data reporting with NCI Clinical Trials Reporting Program (CTRP).
Bachelor's degree and 5 years work experience in the healthcare or clinical trial industry; or equivalent combination of education and experience.
Demonstrated knowledge regarding requirements for research involving human subjects and/or clinical background and experience.
Ability to communicate with clinical teams to explain requirements and vision; resolve questions and QA issues.
Strong written and oral communication skills, attention to detail, customer service orientation and proven ability to perform work accurately and efficiently.
Outstanding work ethic and excellent attendance record.
Demonstrated ability to work independently and with a team. Excellent organizational and analytic skills, with the proven ability to multi-task, trouble shoot and prioritize work.
Demonstrated proficiency with Microsoft Office, including Outlook, Word and Excel skills.
Ability to learn new programs and electronic information systems.
Desired: Demonstrated proficiency with OnCore CTMS, secondarily of other Clinical Trials Management Systems.
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