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Clinical Trial Compliance Administrator

Remote / Online - Candidates ideally in
Lexington, Fayette County, Kentucky, 40598, USA
Listing for: University of Kentucky
Full Time, Remote/Work from Home position
Listed on 2026-01-01
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 52000 USD Yearly USD 52000.00 YEAR
Job Description & How to Apply Below

University of Kentucky

Equal Employment Opportunity/M/F/disability/protected veteran status.

Job Details
  • Job Title:

    Clinical Trial Compliance Administrator
  • Location:

    Lexington, KY (Full remote)
  • Grade: 46
  • Salary Range: $52, per year
  • Type:
    Staff, Full-time
  • Schedule:

    Monday-Friday, 8:00 am-5:00 pm EST (Fully remote)
  • Required

    Education:

    PhD
  • Required Experience:

    1 year
Job Summary

Shape the Future of Clinical Research Administration at the University of Kentucky.

Wildcat Wisdom, Kentucky Innovation – Supporting Discoveries, Transforming Outcomes!

The University of Kentucky’s Clinical Research Support Office (CRSO) is seeking a dedicated and skilled Clinical Trial Compliance Administrator.

Fully remote position. The administrator will serve as an education and compliance expert regarding federal regulations governing Clinical Trials.gov. Responsibilities include administering the university’s Clinical Trials.gov program, registration and reporting, writing and maintaining SOPs and university policies, developing investigator training, providing one‑on‑one assistance for investigator‑initiated trials, preparing compliance reports, and coordinating with other compliance offices.

Responsibilities
  • Administer the University of Kentucky’s Clinical Trials.gov program, including study registration and results reporting.
  • Write, implement, and maintain Standard Operating Procedures and University policies related to Clinical Trials.gov.
  • Develop and deliver training programs for investigators on registry and reporting requirements.
  • Provide individual assistance to investigators for trial registration, reporting, and compliance.
  • Prepare and submit compliance reports to institutional leadership.
  • Collaborate and coordinate with Office of Sponsored Projects Administration, Office of Research Integrity, and Office of Corporate Compliance.
Qualifications
  • PhD required.
  • Minimum of one (1) year of experience in clinical research, regulatory compliance, or related field.
  • Significant background in health‑related research, clinical field, or analysis of trial data.
  • Strong communication skills and ability to establish working relationships across departments.
  • Knowledge of University policies, procedures, and federal regulations governing clinical trials.
  • No supervisory responsibilities.
Benefits
  • 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.
  • One of 34 Universities Nationwide holding the prestigious trifecta of cancer, aging, and translational science designations.
  • Flexible remote work options: fully remote or hybrid.
  • Professional development opportunities: interdisciplinary collaborations, virtual conferences, and training programs.
  • University benefits package: 200% retirement match, health, dental, vision, tuition benefits, and more.
University Community & EEO

The University of Kentucky is a tobacco and drug‑free campus. The University follows federal and state nondiscrimination laws and provides equal opportunities for all qualified persons. A background check and/or drug screen may be required.

Final date to receive applications

November 10, 2025

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