Description
Join Avacare, a dynamic Site Management Organization (SMO), as a Clinical Research Coordinator (CRC) in Tempe, AZ. You'll gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.
As a CRC, you'll wear multiple hats, gaining experience across various therapeutic areas, managing complex protocols, and taking ownership of key trial activities, including patient recruitment, informed consent, regulatory documentation, and site audits.
What You'll Gain:
- Broadened Skill Set: Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
- Professional Growth: 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.
- Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.
Qualifications:
- Clinical Skills: 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.
Experience:
- CRC I: Minimum of 1-3 years in a 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.
- Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management.
- Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.
The potential base pay range for this role is $37,800.00 - $94,500.00 per year.