Clinical Research Coordinator

What you’d do

Coordinate oncology research projects including planning, conducting, and evaluating protocols. Manage participant recruitment, scheduling, compliance, and adverse events. Support IRB activities and prepare related documents. Full-time day shift in Racine, WI. Found on the employer's careers page on Oct 22, 2026. Apply through the link.

You’ll need

• Experience in clinical research coordination
• Knowledge of oncology research protocols
• Ability to manage participant recruitment and compliance
• Experience with Institutional Review Board (IRB) processes
• Full-time day shift