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:
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Recruitment/screening
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Regulatory management (local and central IRBs)
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Participant interactions
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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.