CLINICAL RESEARCH & CROs
Faster enrollment, cleaner data, audit-ready trial ops
Clinical research operations are riddled with manual handoffs and disconnected systems. We automate the pieces that do not need a human - so coordinators can focus on the pieces that do.
THE PATTERN WE SEE
Every CRO we audit shows the same shape: the people closest to the trial spend the most time on tasks the system should handle.
Pain · 1
Pre-screen → enrollment leaks at every handoff
Recruiters bring in 100 candidates. Pre-screen drops 40. Coordinator handoff drops another 25. Final enrollment: 22. Most leak is fixable.ters every field into the EMR. Average: 18 minutes per new patient.
Pain · 2
Sponsor reporting eats Friday afternoons
Weekly status reports are stitched manually from CTMS, EDC, and email. PMs spend 3-4 hours per study every week assembling them.
Pain · 3
EDC reconciliation discovers errors weeks late
Source-to-EDC discrepancies surface during monitoring visits, not in real time. Late corrections cascade into protocol deviation flags.
WHAT NAITUR BUILDS
REPRESENTATIVE CASE
A US-based mid-market CRO running 14 active oncology and rare-disease studies. Coordinator load on reporting + reconciliation was averaging 12 hours per week per study.
We deployed pre-screen funnel automation + sponsor report assembly across all studies in 28 days. New coordinator load: under 3 hours per study per week. Zero protocol amendments required.
Audit posture: Every Naitur automation in clinical environments preserves complete audit trails - who saw what, when, and what the system did automatically. 21 CFR Part 11 alignment built in.