Pantheon Clinical Research
Clinical Research Coordinator
Pantheon Clinical Research, Bountiful, Utah, United States, 84010
Overview
We are hiring a Clinical Research Study Coordinator with at least 2 years of experience managing clinical trials. This is a contract-to-hire role: the first six months will be a performance-based contract with strong potential for permanent employment. Responsibilities Coordinate day-to-day operations of assigned clinical trials Screen, consent, and schedule participants Conduct study visits and procedures per protocol Ensure adherence to ICH-GCP, FDA regulations, and sponsor requirements Maintain accurate source documents and enter data into EDC systems Communicate with monitors, sponsors, CROs, and internal staff Track investigational product and lab kits Support regulatory documentation and audits Experience Minimum 2 years of clinical research coordination experience (required) Strong working knowledge of GCP, FDA, and IRB regulations Experience with CTMS and EDC systems (e.g., RealTime, Rave, Medrio) Bachelor's degree in a health or life sciences field preferred CCRC or CCRP certification is a plus Excellent organizational and communication skills Ability to work independently and manage multiple trials Salary $25 – $34.13/hour, depending on experience and qualifications. Salary reviewed for adjustment upon permanent hire. Job Types: Full-time, Contract Pay: $ $34.30 per hour Expected hours: 40 per week Benefits: Paid time off Work Location: In person
We are hiring a Clinical Research Study Coordinator with at least 2 years of experience managing clinical trials. This is a contract-to-hire role: the first six months will be a performance-based contract with strong potential for permanent employment. Responsibilities Coordinate day-to-day operations of assigned clinical trials Screen, consent, and schedule participants Conduct study visits and procedures per protocol Ensure adherence to ICH-GCP, FDA regulations, and sponsor requirements Maintain accurate source documents and enter data into EDC systems Communicate with monitors, sponsors, CROs, and internal staff Track investigational product and lab kits Support regulatory documentation and audits Experience Minimum 2 years of clinical research coordination experience (required) Strong working knowledge of GCP, FDA, and IRB regulations Experience with CTMS and EDC systems (e.g., RealTime, Rave, Medrio) Bachelor's degree in a health or life sciences field preferred CCRC or CCRP certification is a plus Excellent organizational and communication skills Ability to work independently and manage multiple trials Salary $25 – $34.13/hour, depending on experience and qualifications. Salary reviewed for adjustment upon permanent hire. Job Types: Full-time, Contract Pay: $ $34.30 per hour Expected hours: 40 per week Benefits: Paid time off Work Location: In person