Clinical Research Coordinator A

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

Coordinate the day-to-day management of clinical research trials, MRI imaging, and lab studies, including IRB, and NIH regulatory documentation. Follow study protocols and SOPs to recruit potential research participants, study eligibility, obtain informed consent, administer study assessments, and conduct research interviews visits. Meet regularly with the Principal Investigator and study team to identify problems and develop solutions. Implement changes to procedures as needed and monitor results.

Job Description

Job Responsibilities

• Coordinate day-to-day management of clinical research studies
• Maintain study regulatory documents
• Follow research protocols to recruit participants
• Data entry and management of study data
• Meet regularly with PI and study staff
• Manage clincard subject payments and perform additional duties as assigned

Qualifications

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

Position is contingent upon continued funding.

Job Location - City, State