ICTU Global has capabilities and proven experience in providing clinical trial delivery including: 

  • Conception/design of trial
  • Ethics applications and submissions
  • Sites selection and set-up.  This includes contract and financial negotiations  
  • Sites initiation visits/training – this covers study objectives and e-CRF training
  • Recording and maintaining study’s essential documentations and trial master files


  • Overseeing site’s investigator’s site files
  • Monitoring sites’ recruitment progress ensuring the performance is on par with study milestones
  • Point of contact for any sites’ recruitment, data queries
  • Overseeing study’s finances – i.e. payment of sites’ set up fees, recruitment fees 
  • Study close-out activities





For further information regarding our services and how we can collaborate, please contact our team