Clinical Research Coordinator, On-Site, Bountiful, Utah

About the role

Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.

Qualifications

- Clinical Skills: Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens. - Site Operations Knowledge: Solid understanding of site operations and the drug development process. - Experience: - CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants. - CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants. - Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management. - Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.