Clinical Research Coordinator

What you’d do

Coordinate and monitor oncology research projects including participant recruitment, compliance, and reporting. Work day shift full-time in Appleton, WI, ensuring regulatory compliance and supporting IRB activities. 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 regulatory compliance and IRB processes
• Ability to manage participant recruitment and monitoring
• Day shift availability
• Certification in Research Professional preferred