Clinical Research Coordinator A/B - (Department of Obstetrics and Gynecology - REI Barnhart Lab)
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 A/B - (Department of Obstetrics and Gynecology - REI Barnhart Lab)Job Profile Title
Clinical Research Coordinator AJob Description Summary
The primary role of Clinical Research Coordinator is the organization, coordination and implementation of a research study. The research coordinator will be responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data entry, subject visits and follow-up, biospecimen collection and processing, and regulatory management.Job Description
Job Responsibilities
Clinical Research Coordinator A
- Coordination and implementation of a research studies.
- Prepare protocols, informed consents, data collection forms and advertisements for regulatory approval with manager assistance.
- Be actively involved in planning and implementation of patient recruitment into studies (involves deciding which strategies are best, reaching out to potential recruitment sites/referring physicians, dropping off/posting recruitment materials, etc.).
- Screen, recruit and retain potential study participants. Obtain informed consent at multiple study sites within the Penn Health System (includes approaching potential subjects in the office, or speaking to them by phone, reviewing their medical records and discussing with investigators, asking pre-screening eligibility questions, etc.).
- Collect and report timely, valid, accurate data--maintain clinical trial databases. Respond to data queries. Maintain subject files and regulatory files per GCP.
- Perform required research activities per protocol and in accordance with Good Clinical Practice.
- Collect and process biospecimens (includes performing venipuncture).
- Meet regularly with the study PI and study team to update everyone on.
- Interface with regulatory authorities and sponsors. Attend resear
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