UnityClinical — Clinical Research Operations

UnityClinical helps Principal Investigators and administrators manage clinical research in one connected platform. It brings together all stakeholders—including IRB, Clinical Research Office, study teams, and other services—into a single system that supports the full study lifecycle. UnityClinical reduces operational friction and improves collaboration across research teams. Built with intelligent automation and scalable workflows, it helps organizations move faster while staying organized, accountable, and audit-ready.

Our platform targets a 100-day cycle from feasibility study completion to activation.

Industry KPIs at-a-glance

Phase III end-to-end

- yrs

NDA execution through close-out

Startup time increase (10yr)

+%

Tufts CSDD, 2024 SCOPE Summit

Trials missing enrollment

%

Tufts CSDD 2023 - Medidata

Phase III direct daily cost

$.K

2023 USD - Tufts CSDD Jun 2024

Activation

NCI gold standard

days

Median (AACI, 61 ctrs)

days

The Core Problem

Across clinical research, teams are slowed down every day by friction that has simply become "normal" — but shouldn't be.

Most organizations are dealing with:

Disconnected systems that don't communicate across PIs, IRB, and study teams
Constant coordination overhead between administrators, clinical offices, and investigators
No real-time visibility into where a study stands or what's blocking progress
Heavy manual effort in tracking, documentation, and reporting across multiple tools
Repeated handoffs, follow-ups, and delays at every stage of the study lifecycle

What looks like process is often just fragmentation — and it's slowing everything down.

If this is your problem, we have a solution: one connected platform that simplifies clinical research from start to finish.

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UnityClinical — Clinical Research Operations

Activation

The Core Problem

Platform in action