IIT Protocol Development Project Coordinator

Requisition Number RE53017

Working Title IITs Senior Project Manager

Department Name 7H024:

MCC - CLINICAL RESEARCH ORG

Work Location Lexington, KY.

Grade Level 46

Salary Range $52,/year

Type of Position Staff

Position Time Status Full-Time

Required Education MS

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

Shift Monday-Friday 8:00am-4:30pm (40 hrs. minimum)

Job Summary

The Markey Cancer Center is seeking an experienced and driven IIT Protocol Development Project Coordinator (Senior Project Manager) to play a pivotal role in advancing investigator-initiated interventional cancer clinical trials. This is an exciting opportunity for professionals with backgrounds in clinical trials, oncology research, project management, or clinical research operations who want to make a meaningful impact in cancer research. In this highly collaborative role, you will independently lead and coordinate the full life cycle of institutional interventional clinical trial protocols—from concept development through study close-out—working closely with physician investigators, research staff, and the IIT Protocol Development and Support Unit team.

You will serve as a central facilitator, guiding protocol and document development, managing amendments, supporting accruals, and ensuring studies meet institutional, regulatory, and federal standards. This role is ideal for someone who thrives in a fast‑paced, mission‑driven environment, enjoys managing multiple complex projects simultaneously, and excels at bringing teams together to move research forward efficiently and compliantly. You will be a trusted partner to investigators and research teams, helping transform innovative ideas into active, high‑quality clinical trials.

This position has the potential to be a hybrid work arrangement.

IMPORTANT :
Resumes and CVs cannot be substituted for a completed application. Incomplete applications could disqualify you from being considered for this position. To be considered you must fully complete the online application ensuring that the information on your resume is entered on the application, ... You will also be required to upload a cover letter, resume and as Optional Request 1, CV.

To view our exceptional benefits, please visit https://(Use the "Apply for this Job" box below)..

Excellent skills in oral & written communication (particularly treatment study protocol writing). Microsoft Office suite, OnCore and Forte EDC CTMS experience preferred.

Does this position have supervisory responsibilities? No

Preferred Education/Experience Master’s Degree; SOCRA CCRP or ACRP certification is preferred. Experience in clinical trials protocol writing is preferred as is cancer clinical research.

Final date to receive applications 02/22/2026

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.

Required fields are indicated with an asterisk (*).

• * Please choose your full-time employment experience in clinical trials.
  • None
  • More than 0, up through 1 year
  • More than 1 year, up through 2 years
  • More than 2 years
• * Please choose your full-time employment experience in cancer research.
  • None
  • More than 0, up through 1 year
  • More than 1 year, up through 2 years
  • More than 2 years
• * Please choose your employment experience in project management.
  • None
  • More than 0, up through 1 year
  • More than 1 year, up through 2 years
  • More than 2 years (25 points)
• * Describe a project where you were responsible for target deadlines and how you prioritized tasks, and your interactions with stakeholders.

  (Open Ended Question)