Kentucky Licensed Research Coordinator

Job Summary

To ensure compliance with regulatory requirements for clinical research studies, the full-time remote Kentucky Licensed Research Coordinator will oversee the regulatory aspects of projects, communicate with study teams, and establish standard operating procedures while working closely with various committees and external review boards.

Key responsibilities

• Develop processes and procedures to streamline regulatory oversight in UofL Health facilities and clinics
• Review all IRB correspondence and submissions, documenting necessary action items in the ULHRO system
• Facilitate the Clinical Research Review Committee process to assess the feasibility of clinical research projects

Required qualifications

• Bachelor's degree in a relevant field
• Experience in clinical research and human subjects' protection regulations, including HIPAA authorizations and the IRB process
• Preferred 5 years of experience in research administration
• Preferred professional certification such as CCRP, CHRC, or ACRP-CP