Clinical Research Coordinator III

University of Kentucky; Lexington (VA); On-site; USD 58,000 - 96,000; Full time

Job summary

University of Kentucky is seeking a Clinical Research Coordinator III in the Otolaryngology department to coordinate patient research visits across multiple studies. You will obtain patient consents, ensure that protocols are followed, and maintain high patient safety standards in accordance with GCP guidelines.

Responsibilities include identifying potential study patients, organizing study files, and documenting activities with accuracy.

Qualifications

• Advanced leadership skills and empathy.
• Extensive knowledge and experience with study-related activities.
• Excellent verbal and written communication skills.

Responsibilities

• Coordinate patient research visits across multiple studies.
• Obtain informed consent and ensure patient safety considerations.
• Ensure study protocols are followed and documentation is accurate per GCP.
• Assist investigators in identifying potential study patients.

Skills

Leadership

Empathy

Education

BS

Job description

Posting Details

Job Title Clinical Research Coordinator III

Requisition Number RE55909

Department Name 7H860:Otolaryngology

Work Location Lexington, KY

Grade Level 47

Salary Range $58,302-96,179/year

Type of Position Staff

Position Time Status Full-Time

Required Education BS

Click here for more information about equivalencies: https://hr.uky.edu/employment/working-uk/equivalencies

Required Related Experience 5 yrs

Required License/Registration/Certification None

Physical Requirements Sitting or standing for long periods of time, lifting, pushing, or pulling of objects up to 25 lbs., repetitive motion.

Shift Monday – Friday 8:00AM – 5:00PM

Job Summary The Clinical Research Coordinator III in the Department of Otolaryngology will be responsible for coordinating patient research visits on multiple studies, obtaining patient consents, ensuring that research protocols are followed and patient safety considerations are of the highest standards. This position will also be responsible for helping investigators to identify potential study patients as well as ensure that all study files and documentation is accurate and follows GCP guidelines. Internal Employee Being Considered ( IEBC ).

Skills / Knowledge / Abilities Advanced leadership skills and empathy. Extensive knowledge and experience with the implementation of study-related activities. Excellent verbal and written communication skills. High-level organizational skills. Able to problem-solve independently and collaboratively.

Does this position have supervisory responsibilities? No

Preferred Education/Experience 5 years research and/or patient coordination, data collection or data management, and/or clinical trial regulatory supervision or management

Deadline to Apply 10/06/2026

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.

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