Clinical Research Coordinator Ii
Chicago, Illinois, United States
Conduct study start-up activities and prepare and maintain all regulatory documents required by sponsor and/or regulatory agenciesPrepare protocols, informed consent documents, modifications, and renewals for review by the IRB and sponsorIdentify and recruit eligible study subjects; conduct informed consent/assent processesArrange and conduct clinical research visitsConduct and participate in site qualifications, study initiation, and monitoring visitsAttend investigator meetingsAbstract data from medical records and enter medical information/data onto protocol-specific case report forms, study flow sheets, and other required study forms; prepare abstracted/coded data for processing/analysisCreate and update case report forms and source document templatesCoordinate reimbursement of subjectsMaintain inventory of supplies and equipmentPrepare lab kits and requisitions prior to visitsCollect specimens from subjects, process specimens, and work with research laboratory to ensure samples are processed and sent out correctlyRecord data on source documents, CRFs, and electronic web-based systemsMonitor adverse events and report them as requiredFunction as a patient liaison for study questions and billing issuesPromote ethical conduct of research by actively participating in research related educational meetings and conferencesPerform job functions adhering to service principals with customer service focus of innovation, serviceexcellence, and teamwork to provide the highest quality care and service to patientsAdhere to research protocol in compliance with applicable institutional, local, and federal regulationsMaintain all study documents, including regulatory binders and source documents
