Study Coordination

Supporting Principal Investigators and Study Teams

The Clinical Trials Office Research Coordination Center (CTO RCC) is a multidisciplinary team of research coordinators, and regulatory specialists, supporting the design and conduct of clinical and translational research. Our team provides expert consultation and flexible, fee-for-service staffing solutions to propel projects forward.

Study Coordinator and female physician

Our study coordinators perform all Principle Investigator delegated protocol activities including:

  • Recruit and screen potential study participants
  • Obtain informed consent
  • Schedule and coordinate participant visits
  • Implement protocol-required assessments and procedures
  • Complete electronic case report forms
  • Collect samples and administer questionnaires
  • Track adverse events (AEs), serious adverse events (SAEs) and protocol deviations
  • Coordinate sponsor monitoring visits
  • Support investigators with REDCap Database study submissions