Clinical Research Coordinator: Study Operations & Compliance Lead

Intermountain Healthcare Inc.; Murray (UT); On-site; USD 35,000 - 55,000; Full time

Job summary

Intermountain Healthcare Inc. in Murray, Utah seeks an on-site Subject Matter Expert in clinical research to coordinate and manage studies across the Intermountain system.

You will work with investigators, physicians, regulatory coordinators, sponsors, and study teams to ensure compliant, high-quality participant care throughout the research process. Responsibilities include supporting research across complex projects, mentoring coordinators, educating teams on protocols and timelines, ensuring

Qualifications

• Experience with Microsoft and database applications.
• Experience using laboratory protocols, systems and documentation.
• Healthcare, academic or research setting with patient interactions.
• Ability to work in a collaborative, regulated environment.

Responsibilities

• Coordinate and manage clinical studies across the Intermountain system.
• Educate and mentor Clinical Research Coordinators on protocols.
• Ensure GCP compliance, safety oversight and data integrity.
• Support recruitment strategies and participant retention.
• Train staff on SOPs and regulatory requirements.

Skills

Research protocols

Independent worker

Critical thinking

Detail-oriented

Verbal communication

Written communication

Education

Bachelor's degree in clinical or life sciences

Job description

Intermountain Healthcare Inc. in Murray, Utah seeks an on-site Subject Matter Expert in clinical research to coordinate and manage studies across the Intermountain system.

You will work with investigators, physicians, regulatory coordinators, sponsors, and study teams to ensure compliant, high-quality participant care throughout the research process. Responsibilities include supporting research across complex projects, mentoring coordinators, educating teams on protocols and timelines, ensuring