Clinical Research Coordinator, On-Site, Bountiful, Utah

Responsibilities

• Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish
• Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training

Benefits

• Incentive plans, bonuses, and/or other forms of compensation may be offered
• A range of health and welfare and/or other benefits
• Glassdoor
• 3.9
• IQVIA provides analytics, compliance, and management solutions to the life sciences industry.
• Durham, North Carolina, USA
• https://www.iqvia.com
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Education and Training
• Engineering and Development
• Management and Executive
• Sales
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• Marketing
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• Creatives and Design
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• Trends of Total Sponsorships
• *2026
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Qualifications

• Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
• Solid understanding of site operations and the drug development process
• 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
• Strong written and verbal communication skills, with attention to detail and time management
• Comfortable using CTMS, eCRFs, and Microsoft Office tools
• CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.

Required skills

• Clinical Trial Management System (CTMS), Clinical specimen processing, Clinical trial management, Drug development process, ECG, Electronic Case Report Forms (eCRFs), Microsoft Office, Phlebotomy, Site operations

Experience

• 1-3 years