Clinical Trial Compliance Administrator
Lexington, Fayette County, Kentucky, 40598, USA
Listed on 2026-09-27
-
Research/Development
Clinical Research -
Healthcare
Clinical Research
for more information about equivalencies:
Required License/Registration/Certification
None
Physical Requirements
sitting for long periods of time; repetitive motion related to computer use
Shift
Fully remote
Monday-Friday, 8:00 am-5:00 pm EST
Job Summary
Internal Employee Being Considered Shape the Future of Clinical Research Administration at the University of Kentucky Wildcat Wisdom, Kentucky Innovation – Supporting Discoveries, Transforming Outcomes! Why Join Us?The University of Kentucky’s Clinical Research Support Office ( CRSO ) is seeking a dedicated and skilled Clinical Trial Compliance Administrator
. This vital role supports and enables groundbreaking clinical research across the University.
This position is eligible to be fully remote.
The position serves as an education and compliance expert regarding federal regulations governing Clinical Trials.gov. Clinical Trials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. Clinical research trials must be registered and reported in the publicly accessible database as required by Food and Drug Administration, National Institutes of Health, International Committee of Medical Journal Editors, and the Centers for Medicare and Medicaid Services.
This position will administer the University of Kentucky’s Clinical Trials.gov program, including registration and reporting. The position is responsible for writing, implementing, and maintaining Standard Operating Procedures and University policies, developing training programs for investigators, providing one‑on‑one assistance for investigator‑initiated trials, preparing reports to ensure compliance and to keep institutional leadership updated, and coordinating the program with other compliance offices including Office of Sponsored Projects Administration, Office of Research Integrity, and Office of Corporate Compliance.
The University of Kentucky uses equivalencies in determining if a potential applicant meets the minimum education and experience. Related experience can be substituted for education. for more information about equivalencies: (Use the "Apply for this Job" box below)./equivalencies
- Top 10% of Academic Medical Centers Nationwide:
Recognized as a leader in research excellence and innovation. - Forbes’ Best Large Employers:
Ranked among the Top 100 Employers Nationwide in 2024 and named one of Kentucky’s Best Employers on Forbes’ America’s Best-In-State Employers list. - 1 of 34 Universities Nationwide:
Holds the prestigious trifecta of research designations in cancer, aging, and translational science. - Flexible Remote Work Options:
Enjoy the convenience of fully remote or hybrid roles while supporting groundbreaking research. - Professional Development Opportunities:
Engage in interdisciplinary collaborations, virtual conferences, and training programs to advance your career.
The Clinical Research Support Office ( CRSO ) provides support to investigators and study teams conducting clinical research, including clinical trials. Services provided by the CRSO include maintaining a clinical trial management system ( CTMS ), conducting coverage analysis, developing study budgets, negotiating payment terms with sponsors, and regulatory services. More information can be found at: .
Interested in what UK Benefits have to offer?The University of Kentucky is proud to offer a benefits package that helps us recruit and retain the very best faculty and staff. In addition to your take‑home pay, your benefits package is a major component of your…
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