Clinical Research Coordinator A

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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 The Clinical Research Coordinator A will assist in the management of multiple clinical trials and responsibilities in specific research areas. Coordinate the screening of patients and subject enrollment for one or more federally-funded studies in a fast-paced inpatient hospital setting; screen/enroll eligible subjects 5 days/week, in-person; obtain informed consent from study subjects or their proxies (in-person or by phone); human specimen collection (anatomical and environmental swabs) with hospital subjects; specimen collection from healthcare workers and other hospital staff; coordinate specimen tracking and drop off with research laboratory staff; coordinate study operations with staff; ensure protocol compliance; data abstraction from medical records; data entry, maintain patient and data tracking system; participate in the development of study materials and procedures; participate in weekly research team meetings. This position involves working in the hospital and spending the majority of the workday on the hospital units. This position also involves collection and coordination of biological samples with transport to the microbiology laboratory as well as coordination of study activities with data management. Collection and coordination of biological samples require extreme flexibility within the daily work schedule. This position reports directly to the study's project manager. This position may require flexibility to work occasional nights/weekends. Job Description Job Responsibilities Determination of subject eligibility upon detailed review of medical chart via EPIC; assembling study enrollment packets. Approach all eligible subjects every weekday and obtain informed consent. Collection of multiple sets of human or environmental specimens on two hospital units (nose, throat, groin swabs and hand cultures) Medical Chart Abstraction (using multiple hospital databases) - Data to be collected will include: patient demographics, clinical and laboratory data, vital signs, medications. Data Entry into study database / database management Coordination of biological specimen collection and transport that involves labeling & organizing specimens; Attend web-based or in-person meeting to discuss data Other duties and responsibilities as assigned The appointment will run through December 31, 2026. Continuation beyond this date may be possible if additional funding becomes available.

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