Clinical Trial Workspace
A protocol-driven workspace that turns dense study documents into executable visits, forms, subject workflows, and continuous integrity checks.
- My role
- Product architecture, protocol ingestion, workflow design
- System
- React, TypeScript, structured AI output, versioned templates, audit trails
Protocol model
A trial protocol describes visits, procedures, eligibility, timing windows, medications, safety rules, and exceptions across hundreds of pages.
The workspace converts those instructions into a structured study model that drives visit schedules, eCRFs, subject tasks, and data checks throughout execution.
Study setup
The Schedule of Assessments connects every procedure and form to its visit window, creating one operational map for study setup and execution.
Subject execution
At subject level, the same protocol structure becomes a live view of completed, pending, and outstanding work across visits, forms, medical history, adverse events, medications, and source documents.
Cross-form checks
The integrity layer compares related data across forms. In this example it identifies a medication start date that precedes the associated adverse event, and separately flags draft forms requiring completion.