CLINICAL RESEARCH COORD A
Duties: Participate in all phases of subject recruitment, enrollment, and completion of clinical trials in the field of lipoprotein metabolism, atherosclerosis, and cardiovascular disease.
Assist in the coordination of Phase I-IV clinical trials in the field of lipid metabolism, atherosclerosis, and cardiovascular disease, including 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, includes 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; Participate in study team meetings, and ongoing protocol training; Show vigilance in patient safety, protocol compliance and data quality; Adhere to all University of Pennsylvania, FDA and GCP guidelines.
Qualifications: A Bachelor's Degree and 1 to 3 years of experience or equivalent combination of education and experience required. Position requires a highly motivated, articulate individual with excellent oral and written communication skills. The candidate should possess the ability to work independently and also as a part of a team. Strong planning, organizational and prioritizing capabilities along with problem solving skills desired. Must be able to work flexible hours.
Reference Number: 40-25021
Salary Grade: 025
Employment Type: Exempt
Org: DM-Translational Medicine and Human Genetics
Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
Job Family: I-Technical/Professional Research