For Investigators

If you are interested in conducting clinical research, your first step will be identifying the study you wish to participate in; then contacting the SIH Office of Clinical Research. We will then assist you through the entire process.

Clinical Research Services Include

Regulatory Compliance
  • Contracting
  • Budgeting
  • IRB application
  • Informed Consent Form development
Clinical Research Assistant
  • Assist in the informed consent process
  • Data collection and submission
  • Develop and maintain all research records
Infrastructure Development/Navigation
(Collaborate with hospital ancillary and corporate departments)
  • Computer system access
  • Processes needed to conduct clinical research
  • Billing compliance

Mandatory Training

Clinical Research Education Links