Clinical Research Coordinator A/B
University of Pennsylvania Perelman School of MedicineAbout 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/BJob Profile Title
Clinical Research Coordinator AJob Description Summary
The Clinical Research Coordinator is responsible for oversight, execution, and regulatory compliance of human subject research carried out in the Stroke Division of the Neurology Department.Job Description
The CRC will be responsible for the execution of clinical trials, including patient recruitment, data collection and management, and potentially some regulatory responsibilities. The coordinator must be detail oriented and have prior experience with IRB guidelines and policies and human subject research practices and appropriate professional skills in the execution of research protocols. The Clinical Research Coordinator will receive training in multiple research instruments, such as transcranial doppler ultrasound, optical blood flow monitor, and blood pressure monitors. This position will require significant bedside interaction with patients. The coordinator must be able to function autonomously and effectively manage study protocols.
In addition to the duties above, CRC Bs will manage IRB submissions and potentially help orient/train other CRCs.
Position is contingent on continued funding.
Qualifications
- CRC-A: Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
- CRC-B: Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
Job Location - City, State
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