PCRO Services

Study start up:

  • Meet with Investigators
  • Review Protocol
  • Assess feasibility and patient population available for trial


  • Initial IRB Submission including consent forms and other required documents
  • Continuing Review, Modifications
  • IRB Document Maintenance


  • Negotiate budget and start up costs
  • Detailed financial reports
  • Financial tracking and billing
  • PPQ, Billing Schedule, Research Rates, Industrial Account set up

Study coordination:

  • All aspects of Study Coordination
  • Pharmacy Interface
  • CRF Completion
  • Monitor Visits
  • Study Audits
  • Study close out and archive

Fees for PCRO services are built into our Clinical Trial budgets.The negotiated start up fee will cover all start up activities.All other activities are charged at an hourly rate. 

Please contact , PCRO Administrator, for details.

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