Research operations
Trial Matching Agent
Map synthetic patient signals to trial eligibility questions and produce reviewable matching rationale.
Human review
before patient outreach, enrollment workflow, or clinical-trial recommendation
research coordinator or qualified clinician reviewer
01no enrollment recommendation
02no treatment recommendation
03human research review required
Minimum context required before workflow execution.
- trial criteria
- diagnosis signals
- biomarker signals
- prior therapy history
Reviewable artifacts the agent can produce.
- candidate trial list
- eligibility rationale
- evidence-gap list
Connector targets this workflow may eventually depend on.
- research platforms
- FHIR
- clinical trial registries
Least-privilege capabilities allowed for this workflow.
- read synthetic clinical fixtures
- compare structured eligibility criteria
- draft research-review rationale
Events that must remain observable and reviewable.
- criteria evaluated
- evidence gap detected
- candidate match produced
- research review requested
No SCRIMED agent should operate beyond explicit scope, consent, permissions, and review policy.
Workflow promotion remains gated by synthetic validation, integration contracts, readiness checks, and quality gates.