Clinical Research Coordinator, On-Site, Bountiful, Utah

Benefits

Qualifications

• •** Clinical
• •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
• •+ CRC I:
• •Strong written and verbal communication skills, with attention to detail and time management
• •Comfortable using CTMS, eCRFs, and Microsoft Office tools
• •4 more items(s)

Responsibilities

• •At Avacare, CRCs wear more hats than in traditional research settings
• •You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits
• •This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond.##
• •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
• •** Collaborative Culture:
• •Be part of a supportive team that values initiative, adaptability, and continuous learning
• •Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.##
• •Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants
• •Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
• •7 more items(s)