Clinical Research Study Coordinator Services

The CRU employs research study coordinators across all clinical disciplines. Our staff can assist investigators with Institutional Review Board (IRB) submissions and follow-up; participant screening and enrollment; all study procedures and documentation; adverse event reporting; blood draws, infusions, and ECGs; continuing reviews and modifications to approved research and study closure.

The CRU offers comprehensive study coordination services for studies across all clinical disciplines, including:

  • IRB submissions, including pre-review of regulatory documents and follow-up (Clinical Investigator Resource Core)
  • Participant screening and enrollment
  • All study procedures and documentation
  • Adverse event reporting
  • Blood draws, infusions, and ECGs
  • Continuing reviews and modifications to approved research and study closure
  • Specimen packaging and shipping services
  • Pharmacokinetic and pharmacodynamic studies
  • Electrocardiograms
  • Administration of research questionnaires
  • Data acquisition
  • Specimen storage