Clinical Research Coordinator

Intermountain Health
Hybrid

About The Position

Bring your clinical research expertise—especially in Cardiology, Pulmonary, Oncology, Women & Newborn, or related specialties—to the forefront of patient-centered innovation. As a Clinical Research Coordinator, you’ll be on the front lines of discovery, partnering closely with patients, providers, and investigators to advance impactful clinical studies. If you thrive in a fast-paced, mission-driven environment and are motivated by work that truly makes a difference, this role offers the opportunity to contribute to research that shapes the future of patient care.

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.

Nice To Haves

  • Bachelor's Degree or higher from an accredited institution.
  • Prior experience in a clinical research setting.
  • Expertise or prior experience in the clinical area applicable to this research role (ie cardiology, pulmonary, oncology, women and newborn, etc.
  • Previous experience running an Investigational drug study is preferred.

Responsibilities

  • Collect, process, maintain, and ship study samples, ensuring proper stewardship of lab kits and shippers.
  • Safely operate laboratory equipment when applicable.
  • Understand assigned protocols and effectively communicate project details to patients, caregivers, and principal investigators.
  • Screen participants for eligibility, obtain patient consent, and develop recruitment strategies.
  • Monitor participant progression and manage patient visits to ensure protocol compliance.
  • Coordinate clinical patient information and assist physicians or residents with gathering clinical data.
  • Comply with training on clinical research coordination, FDA Good Clinical Practices (GCP), and standard operating procedures.
  • Safely operate laboratory equipment and maintain research records in compliance with policies and regulations.
  • Perform other duties as assigned, such as data entry, expense tracking, patient chart reviews, and source document creation, with moderate supervision.

Benefits

  • Comprehensive 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.
  • PEAK program supports caregivers in the pursuit of their education goals and career aspirations by providing up-front tuition coverage paid directly to the academic institution.
  • The program offers 100+ learning options to choose from, including undergraduate studies, high school diplomas, and professional skills and certificates.
  • Caregivers are eligible to participate in PEAK on day 1 of employment.
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