Clinical Research Coordinator - On-Site

This on-site clinical research coordinator role in Bountiful, Utah involves managing multiple trials of varying complexity, performing clinical procedures, and overseeing study activities. Key Responsibilities Include Managing 2-6 concurrent trials across different therapeutic areasPatient recruitment, obtaining informed consent, and handling regulatory documentationPerforming clinical procedures such as vital signs, phlebotomy, and ECGsCoordinating study activities from initiation to completion and during site auditsMentoring junior staff and supporting internal training initiatives Qualifications And Skills Required 1-3 years of clinical research experience at an investigative site (CRC I level) or more for CRC IIProficiency in vital signs, phlebotomy, ECGs, and specimen processingExcellent written and verbal communication with strong attention to detailUnderstanding of site operations and drug development processesCompetency with CTMS, eCRF systems, and Microsoft Office The role offers a base annual compensation ranging from $36,600 to $91,300.