Clinical Research Coordinator

Jobtailor; Provo (UT); On-site; USD 60,000 - 90,000; Full time

Job summary

Intermountain Healthcare seeks a Clinical Research Support role to assist in managing studies and coordinating with investigators and clinicians. You will support multiple projects with limited supervision and mentor junior coordinators on protocols and procedures.

The position focuses on education, timelines, and adherence to GCP guidelines to protect patient information and study integrity.

Qualifications

• Proficiency with Microsoft Office and database applications.
• Experience with laboratory protocols, systems and documentation.
• Healthcare/academic/research setting experience, including patient interaction.
• Bachelor's Degree or higher from an accredited institution.
• Prior clinical research setting experience preferred.
• Experience in a clinical area relevant to the research (e.g., cardiology, oncology, etc.).

Responsibilities

• Assist in managing clinical research studies under supervision.
• Coordinate efficiently with clinical investigators, physicians, and managers.
• Support multiple studies across the Intermountain system on large projects.
• Provide mentorship to Clinical Research Coordinators I and reinforce training.
• Educate teams about study protocols and timelines.
• Ensure compliance with GCP guidelines for patient information handling.

Skills

Microsoft Office

Database applications

Healthcare experience

Clinical research

Education

Bachelor's Degree or higher

Tools

Laboratory protocols

Documentation techniques

Job description

Responsibilities

• 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

• 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.).

Core Competencies

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.

Tools & Technologies

• Microsoft Applications
• Database Applications