Clinical Research Coordinator B (Department of Gastroenterology)
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 B (Department of Gastroenterology)Job Profile Title
Clinical Research Coordinator BJob Description Summary
The Clinical Research Coordinator B will play a pivotal role in managing and coordinating all phases of clinical research studies within the Division of Gastroenterology Inflammatory Bowel Disease Research Group, focusing on investigator-initiated and industry-sponsored clinical trials. This position involves collaborating with faculty investigators to design and implement study protocols, ensuring the logistical feasibility of study procedures, and overseeing the preparation and submission of regulatory documents. Key responsibilities include screening and enrolling study participants, managing study visits and treatments, coordinating the administration of investigational products, and ensuring protocol adherence and patient safety. The coordinator will also collect, review, and accurately report study data, maintain comprehensive documentation per GCP standards, and facilitate timely communication with the Principal Investigator to address study-related issues. The ideal candidate will be proactive, detail-oriented, and committed to advancing clinical research through high-quality data management and regulatory compliance.Job Description
Job Responsibilities
This individual will work under general supervision
- The CRC will be responsible for the coordination of a variety of clinical research protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol training. The CRC may also be responsible for research lab specimen processing/handling. The CRC will demonstrate vigilance in patient safety, protocol compliance, and data quality. Additional details of these responsibilities are provided below:
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