Onsite Clinical Research Coordinator & Study Lead

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

Job summary

Intermountain Health in Murray, Utah, is seeking a Subject Matter Expert in clinical research to coordinate and manage studies across the Intermountain system. The on-site role partners with investigators, physicians, leaders, and sponsors to ensure regulatory compliance and high-quality participant care through the research process.

Responsibilities include mentoring coordinators, educating teams on protocols and timelines, and ensuring GCP compliance, data integrity, and proper study

Qualifications

• Experience in a healthcare, academics or research related setting working with patients.
• Knowledge of GCP guidelines and FDA Good Clinical Practices (GCP) as applicable to clinical research.
• Experience with laboratory protocols, systems and documentation techniques.

Responsibilities

• Coordinate and manage clinical studies across Intermountain Healthcare with limited supervision.
• Mentor Clinical Research Coordinators I on study protocols and procedures.
• Educate study teams and physicians about protocols and timelines.

Skills

Research Protocols

Independent worker

Critical thinking

Detail-oriented

Personable

Highly organized

Documentation

Verbal and written communication

Patient information

Clinical Information systems

Education

Bachelor's Degree in clinical or life science

Job description

Intermountain Health in Murray, Utah, is seeking a Subject Matter Expert in clinical research to coordinate and manage studies across the Intermountain system. The on-site role partners with investigators, physicians, leaders, and sponsors to ensure regulatory compliance and high-quality participant care through the research process.

Responsibilities include mentoring coordinators, educating teams on protocols and timelines, and ensuring GCP compliance, data integrity, and proper study