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Data Management Analyst Senior

Remote / Online - Candidates ideally in
Louisville, Jefferson County, Kentucky, 40201, USA
Listing for: University of Kentucky
Remote/Work from Home position
Listed on 2026-10-21
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 44000 USD Yearly USD 44000.00 YEAR
Job Description & How to Apply Below

Posting Details

Job Title

Data Management Analyst Senior

Requisition Number

RE56138

Working Title

Clinical Research Associate Senior

Department Name

40133:

Clinical Research Support Office

Work Location

Lexington, KY

Grade Level

44

Salary Range

$44,/year

Type of Position

Staff

Position Time Status

Full-Time

Required Education

BA

for more information about equivalencies:

(Use the "Apply for this Job" box below)./equivalencies

Required Related Experience

3 yrs

Required License/Registration/Certification

None

Physical Requirements

Ability to sit for long periods of time utilizing mouse, keyboard, computer and telephone. Ability to lift, push, or pull objects up to 50 lbs.

Shift

Monday — Friday, 8:00am to 5:00pm with occasional early or late meetings required.

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 Data Management Analyst Senior (Clinical Research Associate Senior). This vital role supports and enables groundbreaking clinical research across the University.

About the Role:

eligible to be fully remote.

Responsibilities include, but are not limited to …

  • assisting all clinical research teams with the CRSO services including the development of the electronic schedule of events and initial data entry content
  • reviewing and interpreting complex clinical research protocols and determines the level of data entry in the CTMS (clinical trial management system)
  • producing clinical research calendars, to drive participant tracking, compliant billing, and financial practices in the CTMS and the proper billing charge in Epic
  • supporting the CRSO by being the first contact with all new studies requiring CRSO services, serving as a subject matter expert for the content of each study entered into the CTMS including the minimum data requirements based on the study type, and assisting with the tracking of Epic reports related to new patients, new studies, first tier dashboard and others

Collaboration with clinical research team members and other UK internal partners, in addition to possessing the ability to prioritize and manage project workload, is important to this position.

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:  .

Why Clinical Research Professionals Choose University of Kentucky
  • 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.
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…

Position Requirements
10+ Years work experience
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