Senior Clinical Research Coordinator - REDCap & IRB

University of Kentucky; Lexington (KY); Hybrid; USD 60,000 - 85,000; Full time

Job summary

The University of Kentucky College of Health Sciences seeks a Research Associate Senior to coordinate clinical research across the College. You will recruit, screen, consent, and schedule visits to protect retention and data completeness, coordinating procedures within the CCTS.

The role includes building REDCap projects, assisting with IRB submissions and adverse event reporting, and advising on contracts, DUAs, and MTAs, connecting investigators with OVPR, OSPA, and the CCTS.

Qualifications

• Experience coordinating human subjects research in academic medical settings.
• Documented informed consent processes and participant follow-up.
• Current CITI training and Good Clinical Practice (GCP) or ability to complete before start date.
• Experience building and maintaining regulatory documents and IRB submissions.
• Proficiency with REDCap or equivalent electronic data capture platforms.

Responsibilities

• Coordinate studies across the College of Health Sciences and CCTS, including recruitment, screening, consent, and follow-up visits.
• Schedule and track study visits to protect retention and data completeness; coordinate participant procedures.
• Develop and manage REDCap projects; assist with IRB submissions and adverse event reporting; provide regulatory guidance.

Skills

Academic research coordination

Informed consent management

CITI/ GCP training

IRB submissions

REDCap

Education

CCRP or CCRC certification

Tools

REDCap

Job description

The University of Kentucky College of Health Sciences seeks a Research Associate Senior to coordinate clinical research across the College. You will recruit, screen, consent, and schedule visits to protect retention and data completeness, coordinating procedures within the CCTS.

The role includes building REDCap projects, assisting with IRB submissions and adverse event reporting, and advising on contracts, DUAs, and MTAs, connecting investigators with OVPR, OSPA, and the CCTS.