Clinical Operations /
In-House Clinical
Site Management

Clients of Technical Resources International, Inc. (TRI) benefit from our full site support and monitoring services from study start-up to close-out. TRI’s in-house CRAs provide site management and logistics support to allow the field CRAs to focus on the critical aspects of the monitoring visit. Every member of TRI’s in-house clinical operations team works with clients to maximize project performance, clinical excellence, data integrity, and product safety.

Our In-House CRAs:

  • Draft the study protocol and evaluate protocol compliance
  • Review project materials (e.g. MOPs, SOPs)
  • Correct procedures and track corrections
  • Monitor regulatory documents
  • Review Adverse Events (AEs) reporting
  • Coordinate Institutional Review Boards (IRBs) and site communications
  • Draft Case Report Forms (CRFs)
  • Monitor compliance with Electronic Data Capture (EDC)
  • Monitor data using Source Documentation Verification (SDV)
  • Review data through our Clinical Trial Management System (CTMS)
  • Prepare monitoring reports

Key Services

  • In-House Site Management
    • Remote monitoring of regulatory files
    • Site queries resolution

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