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. Clinical Research Coordinator A will be responsible for the screening, recruitment and enrollment of study participants and the administration of study measures during study visits; will conduct in-home and on-site study visits; assist in data entry, coding of interviews, and preparation of data summaries and reports; participate in weekly study progress meetings with the PI and research team. Clinical Research Coordinator A will be responsible for the screening, recruitment and enrollment of study participants and the administration of study measures during study visits; will conduct in-home and on-site study visits; assist in data entry, coding of interviews, and preparation of data summaries and reports; participate in weekly study progress meetings with the PI and research team. CRC A will coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines, assure compliance with the protocol and regulatory requirements including collecting, recording, and maintaining data and source documentations. Promote good clinical practice in the conduct of clinical investigations, including possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Position is contingent on funding.
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Job Type
Full-time
Career Level
Entry Level