Jobs and Careers
Perelman Center for Adv Medicine, United States, United Statesfull_timeVerifiedPosted 21 May 2026
💰 $47,313/yr

About 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 A

Job Profile Title

Clinical Research Coordinator A

Job Description Summary

The Clinical Research Coordinator will report to the UPENN Coordinating Center’s Project Manager for the RadComp trial, a national multi‑site randomized clinical study (www.radcomp.org). Responsibilities include supporting the RadComp Call Center through participant follow‑up (phone calls, data collection, data entry) and reviewing and extracting EHR source data from external facilities for roughly 1,200
participants.
The position is contingent on continued funding and becomes hybrid‑eligible after the introductory period and six months of service.
Standard hours may be 9–5, 10–6, with some evening and weekend work provided advanced notice and only due to a participant requesting
a call outside of normal business hours.

Job Description

Job Responsibilities

  • Conduct participant follow up visits including, but not limited to: tracking participants through timepoints, documenting all attempts, scheduling and completing calls within protocol specified windows, responding to and resolving participant queries, collecting and entering and/or updating data in the appropriate systems, ensuring timely and accurate data collection and entry.

  • Review, extract and code data from EHR source documentation from external sites for approximately 1200 participants; collect, record, and track adverse events of interest from EHR, ensure all necessary documents are received, communicate with and inform EHR Coordinator and PM of any issues.

  • Assist with updating study documents and maintaining regulatory binder as required by the sponsor, regulatory bodies and funder, including, but not limited to: reviewing and updating master tracker, requesting and collecting essential documents from participating sites, organizing files, updating MOPs and SOPs to align with current practices.

  • Participate in the auditing and monitoring process, as required.

Standard hours may be 9–5, 10–6, with some evening and weekend work provided advanced notice and only due to a participant requesting a call outside of normal business hours.

Qualifications

  • Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.

The position is contingent on continued funding and becomes hybrid‑eligible after the introductory period and six months of service.

Job Location - City, State

Ph

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