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
  • Study specific feasibility
  • Site regulatory support & TMF management
  • Investigator relationship management and maintenance
  • Ongoing site surveys to find rooms for improvements
  • We have created robust database of strong sites depending on therapeutic areas and also gathered past site performance data that enables us to predict realistic site activity and data quality for your trial.