Vendor Management & Governance

When engaging multiple providers in a study, all can be project-managed by one governance officer under one consolidated contract, if preferred.

Additional Services

  • Full and complete Medical Writing
  • Clinical Site Agreement negotiations and management
  • Patient Recruitment and Retention
  • Regulatory Strategy
  • Audit – GCP Preparedness
  • Printing and Fulfillment for Clinical Research
  • Responsible for the day-to-day execution of a clinical trial
  • Vendor management (EDC, IRT, Rating/assessments, ePRO/eCOA, Imaging, Central Safety and Specialty labs etc.)
  • CRO management
  • Site management
  • Budget management
  • Site feasibility
  • Clinical Development Planning