Cervey’s Clinical Trials Site Operations Management System (SOMS) is a unified clinical site operations platform designed to replace fragmented tools with one source of truth. Developed from a Private Investigator (PI) and coordinator’s perspective, our solution anticipates the needs of day-to-day site operations. Unlike traditional CTMS tools or loosely bundled SOMS platforms, Cervey embeds safeguards directly into workflows—so sites move faster without sacrificing accuracy, compliance, or revenue.
Cervey embeds hard stops and validation controls directly into workflows, preventing users from progressing when data falls outside defined limits. Errors are caught at the point of entry—reducing downstream queries, rework, and monitoring delays. The result is cleaner data, faster reviews, and meaningful time
savings for site teams.
Tie budgeting and financial management directly to visits and source documentation—so sites never lose track of invoiceable activity. By linking source to visit, to invoice, to forecast, Cervey helps sites maximize revenue, improve forecasting accuracy, and understand financial performance in real time.
Centralized dashboards provide easy visibility into operational progress, financial performance, and emerging risk across studies. Site leaders can quickly assess whether trials are on track, identify gaps early, and make informed decisions about staffing, enrollment, and resource allocation
Cervey’s intuitive patient scheduling dashboard helps sites coordinate visits efficiently while reducing manual follow-up for staff. By connecting schedules directly to visits and workflows, sites can maintain adherence and stay organized without adding operational complexity.
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