Clinical Research Coordinator, On-Site
About the role
Join Avacare, a dynamic Site Management Organization (SMO), where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.
Responsibilities
- Manage 2–6 trials of varying complexity
- Perform clinical procedures
- Lead study coordination from start to finish
- Work closely with investigators, sponsors, and monitors
- Mentor junior staff and contribute to internal training
- Experience across multiple therapeutic areas
- Manage complex protocols
- Take ownership of key trial activities
- From patient recruitment and informed consent to regulatory documentation and site audits
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
- Clinical Skills: 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
- 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
Benefits
Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.
Pay
The potential base pay range for this role, when annualized, is $37,800.00 - $94,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).
Schedule
Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.