Clinical research operations · by Layrek
A clear window into every trial.
Built by a working research site for research sites, TrialWindow brings your studies, volunteers, visits and team together in one secure workspace — schedules, tasks, source documents, signatures and reports in the same place, so you spend less time chasing details and more time on your volunteers.
Every study, volunteer and visit in one clear view — where the trial stands, who is overdue, and what happens next, without opening five different programs.
Shared calendars, task lists and automatic follow-ups keep your coordinators, recruiters and PI in step — so nothing slips between visits, labs and vendors.
Electronic signatures, locked records and a complete audit trail — every record stays inspection-ready without the paperwork headache.
TrialWindow replaces the scattered spreadsheets, binders and inboxes most sites juggle — and keeps the records behind them inspection-ready.
Build each study's visit schedule, see it on the calendar, and generate every volunteer's visits automatically.
Assign tasks across the team, track pre-screening outcomes, and see overdue work at a glance — per person or per study.
File source documents and vendor reports in a guided binder, with protected health information kept safely separated.
Scan paper source documents into the visit record, certify them as true copies, and keep the originals traceable in the volunteer's file.
PI approvals, signed vendor reports and electronic signatures that lock the record the moment it's signed.
A simple portal for your volunteers — schedules, reminders and communications, without exposing study data.
Delegations, 1572s, IRB documents, deviations, drug accountability and staff training — logged, dated and exportable.
Layrek
Transforming patient volunteers into heroes.
TrialWindow is part of the Layrek family of clinical research tools — built in Tulsa, Oklahoma, by people who run trials every day.
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