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Urology Clinical Research Coordinator Research Professional 2
Study Start-Up - 40% of timeParticipate in site qualification visits and protocol training sessions with industry sponsors Prepare and complete Institutional Review Board (IRB) applications in coordination with sponsoring companies and investigatorsFacilitate appropriate ancillary review processesServe as liaison between investigators, sponsors, and regulatory committeesEnsure regulatory compliance throughout the duration of the studyMaintain study regulatory binders Negotiate budgets with sponsoring companies under guidance of Clinical Trials ManagerCreate protocol calendars in OnCore Study Participant Recruitment and Management - 50% of timeInitiate and run participant recruitment efforts
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