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