Overview
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