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/B (GYN Oncology)(Center for Research on Reproduction and Women's Heallth)
Job Profile Title

Clinical Research Coordinator A
Job Description Summary

Reporting to the Project Manager and Director of Clinical Research Operations, Clinical Research Coordinators in the Division of GYN Oncology support multiple externally funded investigator initiated, industry funded, and cooperative group clinical trials.
Job Description

Job Responsibilities

Clinical Research Coordinator A

Subject screening, subject enrollment, scheduling.
Collect, process, store, and ship biological samples.
Collect and filing of study documents.
Collect and enter clinical data utilizing a variety of electronic systems..
Document study activities with accuracy.
Assist with Institutional Review Board (IRB) filings and inquiries.
Assist in preparation of manuscripts, grant proposals, and research related presentations.
The Clinical Research Coordinator B will perform the same duties as above with less supervision. May be assigned to more complex trials.
Ensure proper reporting of serious and non-serious adverse events to the Sponsor and all applicable institutional or study related committees and personnel .
*Position is contingent upon funding*

Qualifications

CRC-A Bachelor’s degree and 1-2 years of experience or equivalent combination of education and experience is required.

CRC-B Bachelor’s degree and 2-3 years of experience or equivalent combination of education and experience is required