Clinical Research Coordinator

IMH

Clinical Research Coordinator managing clinical research studies at Intermountain Health. Collaborating with investigators and educating study teams on protocols and timelines.

Posted 7/18/2026full-timeProvo • Utah • 🇺🇸 United StatesMid-LevelSenior💰 $25 - $40 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical research studies, ensuring compliance with GCP guidelines, and effectively coordinating with clinical teams. Proficient in educating and mentoring Clinical Research Coordinators while utilizing database applications and laboratory protocols.

Highest-signal resume keywords

Clinical Research CoordinationGCP ComplianceMentorship and TrainingDatabase Application ProficiencyClinical Area Expertise

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchLaboratory ProtocolsDocumentation TechniquesPatient Information ManagementStudy Protocols

Soft Skills

CommunicationCollaborationProblem-Solving

Tools & Technologies

Microsoft ApplicationsDatabase Applications

Industry Keywords

Clinical Research StudiesHealthcareResearch SettingGCP GuidelinesCardiologyPulmonaryOncologyWomen and Newborn

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Assists in managing clinical research studies of Intermountain Healthcare.
Responsible for the efficient coordination of clinical studies by working closely with clinical investigators, physicians, department managers and others.
Support various research studies across the Intermountain system, working on complex or large projects with limited supervision, demonstrating high competency in clinical research.
Provide support and mentorship to Clinical Research Coordinators I, reinforcing training and knowledge of study protocols and procedures.
Educate and disseminate information about research projects, communicating with study teams and physicians about protocols and timelines.
Ensure compliance with best practices for transmitting patient information as required by study approvals and protocols, supporting study team and investigator adherence to GCP guidelines.

Requirements

What you’ll need

Experience in a role requiring the ability to demonstrate proficiency with Microsoft and database applications.
Experience using laboratory protocol, systems, and documentation techniques.
Demonstrated experience in a healthcare, academics or research related setting or research related setting working with patients.
Bachelor's Degree or higher from an accredited institution (preferred).
Prior experience in a clinical research setting (preferred).
Expertise or prior experience in the clinical area applicable to this research role (ie cardiology, pulmonary, oncology, women and newborn, etc.).

Benefits

Comp & perks

We care about your well-being – mind, body, and spirit – which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.