Clinical Research Coordinator – On-Site (Salt Lake City, Utah)
Location: Salt Lake City, Utah
Employment Type: Full-Time | Office-Based
Requisition ID: R1510623
Experience Level: 1–3+ Years (Depending on CRC Level)
Position Overview
Avacare is seeking a skilled Clinical Research Coordinator (CRC) to support on-site clinical trial operations in Salt Lake City, Utah. This role is fully office-based and offers significant exposure to diverse therapeutic areas, complex clinical protocols, and end-to-end study coordination. Ideal for professionals looking to accelerate their clinical research career within a high-growth Site Management Organization (SMO).
At Avacare, CRCs manage broader responsibilities than in traditional research settings, providing a strong foundation for future advancement into clinical operations, monitoring, and site leadership roles.
Key Responsibilities
Coordinate 2–6 clinical trials varying in complexity, ensuring adherence to protocol and regulatory standards.
Conduct clinical procedures including vital signs, phlebotomy, ECGs, and lab specimen processing.
Lead participant recruitment, screening, informed consent, and visit scheduling.
Maintain accurate study documentation, regulatory files, and source records.
Serve as a primary point of contact for investigators, sponsors, monitors, and site staff.
Prepare for and support monitoring visits, audits, and inspections.
Mentor junior research staff and contribute to internal process improvement.
Utilize CTMS, eCRFs, and standard office software for data entry and tracking.
Required Qualifications
Clinical Expertise
Hands-on skills including blood draws, ECGs, vital signs collection, and lab sample handling.
Technical & Operational Knowledge
Understanding of clinical site operations, study workflows, and the drug development lifecycle.
Proficiency in CTMS platforms, eCRFs, and Microsoft Office tools.
Communication & Coordination
Strong written and verbal communication abilities.
High attention to detail, time management, and documentation accuracy.
Experience Requirements
CRC I: Minimum 1–3 years of experience working at a clinical investigative site with human research participants.
CRC II: Minimum 3+ years of experience specifically as a Clinical Research Coordinator at an investigative research site.
Why Work With Avacare?
Expanded Skill Development: Gain comprehensive exposure to site operations, clinical procedures, and multi-therapeutic trials.
Career Advancement: Opportunities to grow into senior CRC, clinical operations, or monitoring roles.
Collaborative Environment: Supportive team culture that values initiative and continuous learning.
Global Reach: Operate within a structured SMO while benefiting from the resources of a global CRO.
About IQVIA
IQVIA is a global leader in clinical research, healthcare analytics, and technology-enabled solutions. The organization supports the development and commercialization of innovative medical therapies that enhance patient outcomes worldwide.
Compensation
Annual Base Pay Range: $36,600.00 – $91,300.00
Actual compensation may vary based on experience, education, geographic location, and role-specific qualifications. Additional incentives and benefits may apply.
Apply Now to join Avacare and advance your clinical research career with a globally recognized organization.
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