Clinical Research Coordinators are available through the CCRM Clinical Research Center to assist with the day-to-day conduct of a study and ensure that research is conducted in compliance with the study protocol as well as federal, state and institutional guidelines and regulations.

Clinical Research Coordinator can assist with:

• Recruitment and screening 
• Consenting
• Coordination of participant tests, procedures and research visits 
• Data collection
• Administering questionnaires
• Drug dispensation 
• Maintenance of study documentation 

Learn more:

Holly Bookless, BSN, RN, NE-BC

Nurse Manager, Clinical Research Center

614-293-8749