All sites operate under the same contract, budget, IRB and set of SOPs. By removing negotiations and reducing variability across sites, we’re able to take sites from selection to activation ~2-3x faster than industry average.
Once activated, all sites are supported by a centrally-managed research coordinator team. This team develops focused expertise in your protocol and executes activities consistently across all trial sites. By matching sites’ geographic spread to the number of coordinators staffed, we are able to smooth patient visits and supporting activities across a team. This unlocks scheduling flexibility and de-risks dependencies on single individuals, an industry challenge driven by high coordinator turnover rates.