Clinical Research Coordinator, On-Site, Scottsdale, AZ

Why Avacare? At Avacare, Clinical Research Coordinators (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. What You'll Gain: Manage 26 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. 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. 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. 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. Strong written and verbal communication skills, with attention to detail and time management. Comfortable using CTMS, eCRFs, and Microsoft Office tools. Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.

Created: 2026-03-10