When it comes to successful project execution, collaboration with dependable sites are key for on-time enrollment, data collection and quality, and patient safety. Our dedicated Site Relations team is responsible for:

  • New site identification and feasibility
  • Site selection and qualification
  • Site regulatory support & TMF management
  • Essential document collection, review and processing
  • Investigator relationship management and maintenance
  • Ongoing site surveys to find areas of improvements
  • Assist with obtaining approval from local Ethics Committees and Institutional Review Boards
  • Communication with investigator sites
  • Mass mailings and newsletters

We have generated a robust database of high-performing, dependable sites based on therapeutic area, We have also gathered past site performance data that enables us to predict realistic site activity and data quality for your trial.