Clinical Research Coordinator

## Clinical Research Coordinator AApply:
HUP:
Full time:
Posted Yesterday:
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** University Overview
** The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn’s distinctive interdisciplinary approach to scholarship and learning.

As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America’s Best Large Employers in 2023.Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities.

With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play.

The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
** Posted Job Title
** Clinical Research Coordinator A
** Job Profile Title
** Clinical Research Coordinator A
** Job Description Summary
** 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.
** Job Description
** 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, inform consent forms and questionnaires, and complete IRB…