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ARION
For sponsors

Run your own studies without a CRO in the loop

Study design, multi-center oversight and native analytics for sponsor teams running trials directly.

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How it works

Access scoped to your organization, not your headcount

Thirteen roles ship configured out of the box — study managers, monitors, data managers — so a sponsor team can run oversight without a configuration project first.

Role-based access, by capability areaA matrix of six representative roles (of thirteen total) against five capability areas, showing which roles can access study design, patient data, queries and SDV, reports and export, and PI signature. Site PI and Site coordinator are marked as center-scoped -- limited to their single assigned center.Study designPatient dataQueries & SDVReports/exportPI signaturePlatform adminStudy builderData managerCRA / monitorSite PISite coordinatorcenter-scoped6 of 13 seeded roles shown, each org- and center-scoped identically in the API and the UI.

The same permission map runs multi-center oversight for one study or twenty.

AI-assisted study build

Upload a protocol and get a first-draft eCRF structure back in minutes — start review sooner instead of starting from a blank builder.

Native analytics, no handoff

Descriptive statistics, comparison tests, survival analysis and ML run directly on live study data — no biostatistics export step to schedule.

Multi-center oversight in one view

The patient matrix, query workspace and SDV workspace all filter by center, so a sponsor team sees the whole study without losing site-level detail.

See it on your protocol

Bring a protocol or an existing study and we'll show you what this looks like in Arion.

Request a demo