SITE SETUP

We can be the ‘helping hand’ and assist investigators in the setup of the clinical research (virtual or physical/brick-and-mortar) site. We work with experienced study-coordinators, research nurses and trial managers who have a in depth understanding of all aspects involved in running clinical trials at site level.

We can assist in establishing all the processes needed to conduct the trial ranging from ethics submission, contracts, budgets, equipment, source documents, and vendor selection, to trial administration, PI oversight processes and training of site staff in used of eCRF, eConsent, GCP, etc.