Clinical Research Coordinator A/B (Department of Translational Medicine and Human Genetic)

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Posted Job Title

Clinical Research Coordinator A/B (Department of Translational Medicine and Human Genetic)

Job Profile Title

Clinical Research Coordinator A

Job Description Summary

The Clinical Research Coordinator A/B position will assist in the management of multiple clinical trials and responsibilities in specific research area.  The Clinical Research Coordinator A/B will participate in all phases of subject recruitment, enrollment, and completion of clinical trials in the field of lipoprotein metabolism, atherosclerosis, and cardiovascular disease. Assist with Institutional Review Board (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations. Works closely with the Principal Investigator, manager, and study team to identify problems and develop solutions. Implement approved changes to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects.

Job Description

The Clinical Research Coordinator A/B will coordinate Phase I-IV clinical trials or other clinical studies in the field of lipid metabolism, atherosclerosis, and cardiovascular disease. Recruit, consent and screen patients according to protocol. Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to protocol requirements. Organize and maintain all documentation required by the Investigator, sponsor or CRO, including source documentation, case report forms, and research charts. Collect, review and report study data. Complete case report forms and resolve data queries. Process and ship study specimens including blood and urine. Participate in initiation, monitoring, audit, and close-out visits as well as actively participate in team meetings. Participate in the development of complex documents such as protocols, informed consent forms a