Clinical Research Coordinator II

What you’d do

Supports clinical research studies, keeping them compliant with protocols, Good Clinical Practice and regulations. Tracks study, IRB and recruitment details, coordinates data collection and analysis, and interacts with participants. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 3+ years clinical research experience
• Site and study management experience
• IRB and federal research regulation knowledge
• Bachelor's in clinical research, science or healthcare field preferred