Clinical Research Coordinator - Rehab Services

Intermountain Health

22h • $25 - $39 • Hybrid

About The Position

This position assists in managing clinical research studies of Intermountain Healthcare and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, physicians, department managers and others. Essential Functions 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.

Requirements

• Organizational Skills
• Communication Skills
• Team Oriented
• Compassionate
• High Reading Comprehension
• Administrative Skills
• Self-starter
• Critical Thinking Skills
• 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.
• Prior experience running trials and dealing with federally funded studies.

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

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level