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University of Kentucky
Lexington, Kentucky, United States
 
(on-site)
Posted
22 hours ago
University of Kentucky 
Lexington, Kentucky, United States
 
(on-site)
Salary
$52,021.00 - $85,800.00
Salary - Type
Yearly Salary
Job Function
Other
 Clinical Trial Compliance Administrator 
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
 Clinical Trial Compliance Administrator 
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Description
University of Kentucky
Equal Employment Opportunity/M/F/disability/protected veteran status.
Posting Details
 Posting Details 
| Job Title | Clinical Trial Compliance Administrator | 
|---|---|
| Requisition Number | RE52097 | 
| Working Title | |
| Department Name | 40133:Clinical Research Support Office | 
| Work Location | Lexington, KY | 
| Grade Level | 46 | 
| Salary Range | $52,021-85,800/year | 
| Type of Position | Staff | 
| Position Time Status | Full-Time | 
| Required Education | PhD | 
| Click here for more information about equivalencies: | https://hr.uky.edu/employment/working-uk/equivalencies | 
| Required Related Experience | 1 yr | 
| 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 | 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. About the Role: This position is eligible to be fully remote. The position serves as an education and compliance expert regarding federal regulations governing ClinicalTrials.gov. ClinicalTrials.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 ClinicalTrials.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. Click here for more information about equivalencies: http://www.uky.edu/hr/employment/working-uk/equivalencies Why Clinical Research Professionals Choose University of Kentucky 
 Want to learn more about the Department? 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: https://research.uky.edu/clinical-research-support-office. 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 total compensation at UK. These benefits include our 200 percent match on eligible retirement contributions; competitive health, dental, and vision coverage; tuition benefits for classes at UK, and much more. To learn more about these benefits, please visit: https://hr.uky.edu/employment/our-benefits. Ready to Make a Difference in Clinical Research Administration? Are you ready to take the next step in advancing clinical research and innovation? Join us in UK's Clinical Research Support Office as the next dedicated Clinical Trial Compliance Administrator and play a pivotal role in supporting groundbreaking projects that shape the future. Driving Clinical Research Excellence Apply Today! | 
| Skills / Knowledge / Abilities | Significant Clinical Research background in health related, research, or clinical field required. Ability to communicate for effective relationships; ability to establish working relationships across a variety of departments, centers, and administrative offices; current and relevant experience with analysis and reporting of data, preferably related to clinical trials; knowledge of University policies and procedures and federal regulations | 
| Does this position have supervisory responsibilities? | No | 
| Preferred Education/Experience | |
| Deadline to Apply | 11/10/2025 | 
| Our University Community | We value the well-being of each of our employees and are dedicated to creating a healthy place for everyone to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors, the University of Kentucky is a Tobacco & Drug Free campus. The University follows both the federal and state Constitutions as well as all applicable federal and state laws on nondiscrimination. The University provides equal opportunities for qualified persons in all aspects of institutional operations and does not discriminate on the basis of race, color, national origin, ethnic origin, religion, creed, age, physical or mental disability, veteran status, uniformed service, political belief, sex, sexual orientation, gender identity, gender expression, pregnancy, marital status, genetic information or social or economic status. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen. | 
Posting Specific Questions
Required fields are indicated with an asterisk (*).
-  * Describe your previous work experience with the clincaltrials.gov website (PRS system). (Open Ended Question) 
-  * Describe your experience reading, interpreting, or administering clinical trial protocols. (Open Ended Question) 
-  * Please describe your experience with regulatory compliance. (Open Ended Question) 
Applicant Documents
Required Documents
- Resume
- Cover Letter
PI279206076
Job ID: 80911426
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