Clinical Research Coordinator II

University of Kentucky; Lexington (KY); Hybrid; USD 45,000 - 60,000; Full time

Job summary

The University of Kentucky is seeking a Clinical Research Coordinator II for the Markey Cancer Center Clinical Research Organization. The primary duties include data collection, reporting, and coordinating workflow for clinical studies, while ensuring adherence to GCP/SOP and protocol requirements.

This onsite role involves patient flow management, collaboration with health professionals, and ongoing documentation.

Qualifications

• Strong attention to detail and excellent organizational skills.
• Proficient in operating office machines including computers and printers.
• Robust interpersonal skills and strong written/verbal communication.
• Advanced knowledge of Microsoft Office products.
• Ability to take initiative and manage time effectively.

Responsibilities

• Obtain, abstract and collate data, reports and forms for studies.
• Maintain and submit reports and updated records as required by the study.
• Assist in designing systems to organize and plan workflow for clinical studies.
• Coordinate patient flow through clinical studies and monitor events.
• Ensure protocol compliance and communicate with PI and health professionals.

Skills

Attention to detail

Organizational skills

Office software

Interpersonal skills

Microsoft Office

Written & verbal communication

Initiative

Time management

Technical skills

Collaboration

Tools

Computers

Printers

Job description

Click here for more information about equivalencies:

Required License/Registration/Certification

None

Physical Requirements

Requires handling of light-weight objects up to 10 pounds,sitting for long periods of time, some standing or walking, repetitive motion

Shift

Monday-Friday 8:00am-4:30pm (40 hrs/wk).

Job Summary

The Markey Cancer Center Clinical Research Organization is seeking a Clinical Research Coordinator II. The primary responsibilities for this position include: obtain, abstract and collate data, reports, etc. related to studies; maintain and submit all reports, forms and updated records to groups required by study; assist in designing a system for organizing, planning and controlling workflow related to the conduct of clinical studies and protocols; coordinate flow of patient through clinical study or protocol, monitoring all events related to patient and communicating any pertinent information to PI and appropriate health professionals; learn basics of Good Clinical Practice ( GCP ) and standard operating procedures ( SOP ); monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence; assist investigators with identification and recruitment of patients; ensure that per-study and eligibility requirements of the protocol have been met for patients, maintain cooperative and professional relationships with all Clinical Research participants; collaborate and consult with other health professional in planning care for study participation and to ensure protocol compliance; and other duties as assigned.This position has a fully onsite work arrangement.

To view our exceptional benefits, please visit https://www.uky.edu/hr/benefits.

Strong attention to detail and excellent organizational skills. Proficient in operating various office machines including computers, printers, and various software packages. Robust interpersonal skills. Advanced knowledge of Microsoft Office products. Strong 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

Deadline to Apply

Deadline to Apply 10/01/2026

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

• * Do you have SoCRA or ACRP certification?
  • Yes
  • No
• * How many years experience do you have working in clinical research
  • None
  • More than 0, up through 1 year
  • More than 1 year, up through 3 years
  • More than 3 years, up through 5 years
  • More than 5 years
• * Describe your experience working with clinical research as a clinical CRC?

  (Open Ended Question)