How a Study Comes to Life

Watch a study advance Build → UAT → Live: the roles that enter at each stage, the operations they perform, and what is honestly not built yet. Play it, or read the role × environment matrix.

Environments and versioning →

Driven by real source: rbac-data.ts (generated from the role catalog) · reference/statuses · tasks/sign-off-and-go-live

Watch a study come to life. It advances Build → UAT → Live; roles enter as they’re needed, and every operation is marked built, partial, or not built yet — honestly.

Cast — 1 of 15 roles active

OAOrganization AdminPMProject ManagerEDeCRF DesignerDMData ManagerCRAClinical Research AssociateSTMSite MonitorMOMedical OfficerCDCClinical Data CoordinatorSMSponsor ManagerSSMSponsor Supply ManagerRMRegulatory ManagerAUDAuditorPIPrincipal InvestigatorCRCClinical Research CoordinatorPHPharmacy

BuildSetup · design

UATValidation · test data

LiveProduction

What a real trial still needs — not built yet

These clinical capabilities would live in the Live environment but aren’t built. Shown here so the picture is honest, not aspirational.

Safety submissionNot built yet

MOSM

Generating and sending expedited reports (E2B), a gateway, and automatic reconciliation with the safety database.

What is not built yet

Drug supply and accountabilityNot built yet

SSMPH

Inventory, dispensing, resupply, kits, depots and shipments.

What is not built yet

Randomization and blindingNot built yet

SMPICRC

Allocation of participants to treatment, and hiding the arm from the people who must not see it.

What is not built yet

Medical coding (MedDRA, WHODrug)Not built yet

Coding of adverse events, history and medications to standard dictionaries.

What is not built yet

Central monitoring and monitoring reportsNot built yet

CRASTM

Key risk indicators, central statistical monitoring and monitoring-visit reports.

What is not built yet