Clinical Research Coordinator

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.

• 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.).

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.

• Microsoft Applications
• Database Applications