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University of Kentucky
Lexington, Kentucky, United States
(on-site)
Posted
11 hours ago
University of Kentucky
Lexington, Kentucky, United States
(on-site)
Job Function
Other
Clinical Research Coordinator II
The insights provided are generated by AI and may contain inaccuracies. Please independently verify any critical information before relying on it.
Clinical Research Coordinator II
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 Research Coordinator II |
|---|---|
| Requisition Number | RE53827 |
| Working Title | |
| Department Name | 7H854:OPHTHALMOLOGY & VISUAL SCIENCE |
| Work Location | Lexington, KY |
| Grade Level | 46 |
| Salary Range | $25.01-41.25/hour |
| 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 | 3 yrs |
| Required License/Registration/Certification | None |
| Physical Requirements | Sitting or standing for long periods of time; lifting, pushing or pulling of objects up to 50 lbs. |
| Shift | Monday through Friday; 8:00AM 5:00PM. |
| Job Summary | The Clinical Research Coordinator II in the UK Department of Ophthalmology 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. IEBC (Internal Employee Being Considered). |
| Skills / Knowledge / Abilities | Attention to detail and organizational skills. Ability to operate various office machines including computers, printers, and various software packages. Interpersonal skills. Knowledge of Microsoft Office products. Written and verbal communication skills. Initiative, collaboration, advanced time management skills. Technical skills applicable to essential functions and initiative. |
| Does this position have supervisory responsibilities? | No |
| Preferred Education/Experience | Bachelor's degree and at least 3 years of related experience. Clinical research certification (CCRC, CCRA, CCRP, etc.) preferred. |
| Deadline to Apply | 04/05/2026 |
| 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. |
Posting Specific Questions
Required fields are indicated with an asterisk (*).
- * How many years of paid work experience do you have in coordinating clinical research studies?
- 0 - 3 years
- 3 - 5 years
- 5- 10 years
- * What is the largest number of studies you have been the coordinator for at the same time?
(Open Ended Question)
- * Describe a time when attention to detail was critical. What did you do to ensure details were correct?
(Open Ended Question)
Applicant Documents
Required Documents
- Resume
PI283445086
Job ID: 83287550
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