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Part Time- Urology Clinical Research Coordinator-Research Professional 1
Study Start-Up - 25% of timeParticipate in site qualification visits, site initiation visits, and protocol training sessions with industry sponsors Support investigators and clinical research staff in preparing and completing various regulatory and Institutional Review Board (IRB) applications in coordination with sponsoring companies Assist in maintenance of study regulatory binders Study Participant Recruitment and Management - 65% of time Support participant recruitment effortsScreen, consent, and enroll appropriate participants with regards to established protocolsCoordinate participant study visits with guidance from clinical research staffSchedule appropriate clinic appointments, procedures, testing,
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