Clinical Trials Coordinator – CNS & Behavioral Health - Chicago, IL
$60,000–$65,000 year
On-siteChicago, Illinois, United States
Job Summary
Oversee daily clinical trial activities, ensuring protocol compliance and study success while coordinating participant scheduling, study procedures, assessments, and follow-up visits. Perform phlebotomy and assist with collection and processing of study specimens, serving as the key liaison between study participants, investigators, sponsors, CROs, and monitoring teams. Maintain source documentation, case report forms, and study records with rigorous attention to quality and accuracy, and support site readiness for audits, monitoring visits, and regulatory reviews. Assist with safety reporting, adverse event documentation, and participant retention efforts. Work in a predictable schedule with no evenings, weekends, or on-call responsibilities.
Required Qualifications
- 2+ years of experience coordinating clinical research studies
- Phlebotomy proficiency
- Bachelor's degree
Desired Qualifications
- Prior experience in CNS, mental health, psychiatry, psychology, neuroscience, or behavioral health research
- Strong organizational skills with the ability to manage multiple active studies at once
- CCRC certification
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