Advancing today’s discoveries to improve health for all.

Study Monitoring

Study Monitoring

The CTSI can provide assistance with clinical research monitoring on investigator-initiated trials. 

This is a service under the CTSI Trial-CORE. These services are available to staff at both Ohio State and Nationwide Children's Hospital. At Nationwide Children's Hospital the CRC provides study monitoring services.

  • Templates and Guidance- If you have a research team we can provide Study Monitoring templates, monitoring plans and guidance on how to ensure you have a strong data quality assessment.
  • Staffing of Study Monitoring- An independent experienced staff member can be budgeted to provide regulatory oversight and source data verification paying special attention to the following items:
    • Adverse Events
    • Protocol Deviations
    • Protocol specified Outcome Measures
    • Regulatory Document Review
    • Training Documentation
    • Consent Process Documentations
    • Inclusion/Exclusion Criteria Review

Contact Us

To learn more or to request a consultation, contact Amy Bartlett.

Amy Bartlett, BA, CCRC

Associate Director of Clinical Research Development

CLINICAL SERVICES CORE

Phone

Amy Bartlett