Clinical Study Coordination

We have a long history of coordinating clinical trials. Our experienced staff excels at patient recruitment and has a proven track record of patient retention in long term studies. Each of our team members has GCP (good clinical practice) guidelines training and certification.


Services Include:

  • IRB (institutional review board) approvals
  • Regulatory document management
  • Patient recruitment
  • Patient consent
  • Source document completion
  • CRF (case report form) completion both paper and online
  • Study drug handling
  • IVRS (interactive voice response system) randomization and drug management
  • Adverse Event and Serious Adverse Event reporting
  • Blood collection and handling
  • -20 C freezer storage with backup generator
  • Staff dangerous goods certified for dry ice shipments
  • Data query resolution
  • Record storage

EDUCATIONAL PROGRAMS:


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RESEARCH OPPORTUNITIES:


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SANSAR

CCRN is partnering with SANSAR to provide community initiatives, implement research projects and support clinical services. Click below for more information

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