Clinical Research Coordination
CTSI’s Clinical Research Coordination (CRC) staff are trained in GCP, HIPAA, and Human Research Protections (HRPP/IRB), and can provide comprehensive protocol implementation and study subject-related services; including: informed consent, subject eligibility, study visits and procedures, participant recruitment, required documentation, electronic data entry, and AE and SAE reporting. CTSI CRCs are for hire to assist researchers on a case-by-case basis, with support tailored to specific needs of the study. Rates for services can be hourly for shorter term needs or FTE for study management. Areas of support include:
Regulatory management (local and central IRBs)
Phlebotomy support, sample collection and handling
If you would like to learn more about using any of our services, please contact us to discuss your needs.