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The Eye Institute of Utah | Salt Lake City, UT
The Eye Institute of Utah is seeking a full-time Clinical Research Coordinator (CRC) to support our growing ophthalmic clinical research program. The CRC works under the direction of the Principal Investigator (PI) and is responsible for coordinating daily clinical trial activities, ensuring regulatory compliance, and supporting study participants throughout the research process.
Ophthalmology experience is strongly preferred, with 2+ years of ophthalmic clinical experience ideal. Certification as a Certified Ophthalmic Assistant (COA) or higher is a plus.
Coordinate day-to-day activities of clinical research studies
Screen, recruit, and consent study participants according to protocol requirements
Schedule and manage study visits, testing, and procedures
Maintain regulatory documentation and study files in compliance with FDA, IRB, and sponsor requirements
Enter and manage study data in electronic data capture systems
Coordinate monitoring visits and communicate with sponsors and CROs
Ensure study documentation follows Good Clinical Practice (GCP) and ALCOA standards
2+ years ophthalmology experience preferred
COA or higher certification preferred
Strong organizational, documentation, and communication skills
Ability to manage multiple studies and timelines
Benefits
401(k) with employer matching
Dental insurance
Paid time off
Employee assistance program
Schedule: Full-time, Monday–Friday (Day shift)
Location: Salt Lake City, UT – In person
The Eye Institute of Utah complies with applicable federal civil rights laws and does not discriminate on the basis of race, color, national origin, age, disability, or sex.
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