Our Clinical Site Managers will support your trial starting from the Services onset, through to Start Up, Clinical and Post Clinical Activities, and Project close out:

  • Key contact with the Sponsor and CRO Team,
  • Thorough project oversight, Driving resources and timelines,
  • Risk management and issue escalation,
  • Essential Document Management,
  • Regular team meetings,
  • Training oversight,
  • Quality oversight,
  • Coordination of internal & external resources including vendors