Clinical Research Coordinator A
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 AJob Profile Title
Clinical Research Coordinator AJob Description Summary
The Clinical Research Coordinator will work on an Adolescent Teen Driving Health Program at the School of Nursing and work directly with Principle Investigator and when available, Project Manager, Research Assistants and temporary workers.Job Description
Job Responsibilities
Conducting recruitment and screening activities.
Collecting data; entering detailed data into a database program.
Filing, preparing data packets for research subjects.
Assisting in subject follow-up via phone and mail.
Scheduling research subject visits, and administrative support such as administering surveys, scheduling meetings, and creating mailing lists.
They will also be responsible for delivery guided health coaching intervention materials.
Assist in onboarding and training new study staff members and aid in completing progress and data safety monitoring plan and reports.
Maintaining study charts, data management and analysis, preparation and maintenance of regulatory (IRB) paperwork, and grant and presentation/publication preparation as necessary.
- Other duties and responsibilities as assigned
Qualifications
- Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
Job
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