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Job Description
Coordinate and conduct multiple clinical research studies according to protocol, which includes subject recruitment, consenting, and administration of protocol required procedures such as questionnaires, vital sign measurements, biospecimen collection, follow up contacts, etc. Collaborate with investigators to develop new strategic research initiatives to grow the teams' portfolio. Serve as a liaison to study participants, investigators, study team, regulatory personnel, sponsors, and vendors as applicable, and serve as a mentor to coordinators from other COM-T departments. Manage IRB submissions, regulatory documentation, and contract submissions for assigned studies, which involves interfacing with numerous systems including, eIRB, OnCore, UAHS Research Intake Application, and others. Maintain regulatory and study documentation in accordance with policies and regulations of University of Arizona Institutional Review Board (IRB), National Institute of Health, and other relevant organizations. Independently and accurately collect and evaluate clinical data from subject interviews, medical record review, and study indicated procedures with data entry into appropriate data management systems. Support investigators with research case report form and survey creation, customized REDCap database builds/management, and development of standard operating procedures as needed. Complete basic lab processing as required by study protocols (ie. centrifuge, aliquot, and freeze samples), maintain detailed specimen records for sample storage and shipment to central labs. Appropriately ship samples as needed.