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