Clinical Research Data Coordinator I — Hybrid Role

University of Kentucky; Lexington (VA); Hybrid; USD 48,000 - 80,000; Full time

Job summary

The University of Kentucky’s Markey Cancer Center seeks a Clinical Research Coordinator I – DATA to join a trials team in Lexington. You will enter and manage clinical and demographic data for trials, supporting monitoring visits and audits while ensuring FDA and IRB compliance.

After training and a 90-day orientation, a hybrid work arrangement is offered. Applicants should have a BS and at least 1 year of related experience.

Qualifications

• Enter and manage clinical and demographic data for clinical trials.
• Abstract data for study sponsors including past medical history, treatment details, adverse events and outcomes.
• Assist in designing a system to organize and control workflow for clinical studies and protocols.
• Prepare for monitoring visits and audits; ensure compliance with FDA and IRB requirements.

Responsibilities

• Enter and manage clinical trial data for studies.
• Assist in designing workflow for trial conduct.
• Prepare for monitoring visits and audits; ensure regulatory compliance.

Skills

Attention to detail

Organizational skills

Interpersonal skills

Microsoft Office

Written communication

Verbal communication

Time management

Initiative

Collaboration

Technical skills

Education

Bachelor's degree

Tools

Microsoft Office suite

Job description

The University of Kentucky’s Markey Cancer Center seeks a Clinical Research Coordinator I – DATA to join a trials team in Lexington. You will enter and manage clinical and demographic data for trials, supporting monitoring visits and audits while ensuring FDA and IRB compliance.

After training and a 90-day orientation, a hybrid work arrangement is offered. Applicants should have a BS and at least 1 year of related experience.