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Clinical Research Services

What we do

The Clinical Trials Unit support includes (but is not limited to):

Methodologic Support:

  • Innovative Trial Design
  • Statistical Analysis Plan
  • Health Economic Evaluation
  • Data Management
  • Evidence Synthesis
  • Child Health Research Standards (Design, Conduct, Reporting)

Regulatory Support:

  • Health Canada Regulatory Submission
  • Auditing and Monitoring
  • Contracts and Agreements 
  • Industry Liaison
  • Research Ethics Board Application

Trial Conduct:

  • Feasibility Assessment
  • Liaison with Other Departments (Pharmacy, Clinical Research Unit, Biobank, IP&C)
  • Budget Development
  • Good Clinical Practice and Applicable Regulations
  • Standard Operating Procedures/Tools/Templates
  • Education and Training Support

Do you want to consult with the CTU?  

Download the CTU intake form

Contact us:

Please email us at ask.crs@sickkids.ca or visit the contact us page.