Coordinating pre-study activities including site selection and pre-qualification Visits
Securing regulatory approvals (ethical committee and MOH approvals)
Translating and implementing patient recruitment programs and materials
Monitoring study sites and conducting close-out visits and compliance audits
Coordinating serious adverse event identification and reporting
Site contract administration
Getting all MOH Import Permits for Clinical trial materials (drugs as well as
medical devices)
Import of Clinical Trial Materials
Distribution of Clinical Trial Materials to the sites
