Clinical Research Coordinator 1

We are seeking a full-time Clinical Research Coordinator to support, facilitate, and coordinate daily clinical trial activities and play a critical role in the conduct of the study.

Requirements

• Administratively and clinically manage industry-sponsored clinical trials
• Lead patient recruitment activities
• Schedule patient research visits and procedures
• Conduct patient visits
• Dispense study medication
• Collect vital signs and perform ECGs
• Perform blood draws
• Process and ship specimens
• Ensure study information is entered into the CTMS system
• Maintain documentation study files
• Adhere to Research SOPs, Good Clinical Practices, and study protocols
• Maintain ongoing communication with stakeholders
• Ensure safety data is reviewed by the PI
• Maintain inventory of study equipment and supplies
• Assist with routine data verification and quality control
• Schedule and prepare for monitor visits
• Assist with protecting the rights and welfare of human research participants