Clinical Research Coordinator II

📋 Description

• Coordinate daily activities for clinical studies per protocol, GCP, SOPs, and regulations
• Set up and conduct study compliant with protocol, SOPs, and GCPs
• Prepare and maintain study docs including protocol amendments and CRFs
• Perform station/instrumentation duties and collect clinical data
• Ensure clinic setup 30 minutes before study start
• Report to clinic on-time for all studies

🎯 Requirements

• Bachelor’s degree – preferably in science or equivalent
• Understands basics of clinical research and ability to learn
• 2+ years relevant work experience
• CCRC/CCRA certification a strong plus

🎁 Benefits

• Equal Opportunity Employer
• On-line application assistance for disabilities