Participate in all phases of subject recruitment, enrollment, and completion of clinical trials in the field of lipoprotein metabolism, atherosclerosis, and cardiovascular disease. 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 and questionnaires, and complete IRB submissions. Show vigilance in patient safety and protocol compliance. Adhere to all University of Pennsylvania, FDA and GCP guidelines.
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Job Type
Full-time
Career Level
Entry Level