Clinical Research Coordinator BC (Transplant)
University of PennsylvaniaAbout the role
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 BC (Transplant)Job Profile Title
Clinical Research Coordinator BJob Description Summary
The Clinical Research Coordinator B (CRC-B) will provide support of regulatory and operational aspects of clinical trials in abdominal solid organ transplantation. The CRC-B will be responsible for the entire life-cycle of clinical trials (start-up, protocol implementation, and closure, including activities such as, staff education, subject screening and consenting in clinics, obtaining research samples, and coordinating subject visits. This individual will also be responsible for providing regulatory support, data entry into electronic data capture systems (e-CRFs), appropriate reporting of AEs and SAEs to the sponsor and IRB per protocols, and will ensure all data entry requests and subsequent queries, including monitor findings, are addressed in a timely manner. The CRC-B will participate in study meetings, and site visits (eg SIVs, monitoring, and audits). The CRC-B will also be responsible for 24/7 on call activity in rotation with other clinical research coordinators. Additionally, the CRC-B will conduct phone interviews and verbally consent if indicated for studies/repositories.The Clinical Research Coordinator C (CRC-C) will have the responsibilities described above working with minimal to no daily supervision. The CRC-C will also be a resource for best practices of managing major clinical trials. The Clinical Research Coordinator C may also be responsible for collaborating with faculty in the development of investigator initiated protocols, analysis of clinical data to determine response and clinical outcomes, and contribute to preparation of some study manuscripts and grant applications.
Position is contingent on continued funding.
Qualifications:
CRC B: Bachelor's Degree with 2 to 4 years of experience or equivalent combination of education and experience is required
CRC C: Bachelor's Degree with 4 to 6 years of experience or equivalent combination of education and experience is required.
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