{
  "id": "workflow:clinical-trial-protocol",
  "_kind": "Workflow",
  "_file": "workflows/workflows/workflows-expanded-3.yaml",
  "_cluster": "workflows",
  "attributes": {
    "displayName": "Clinical Trial Protocol Design",
    "workflowKind": "operational",
    "triggerType": "event-driven",
    "typicalCadence": "per-trial",
    "complexity": "cross-team",
    "description": "End-to-end clinical trial protocol development — study design,\nendpoint definition, sample size calculation, site selection, and\nregulatory submission preparation. Includes protocol amendments,\nsafety monitoring board coordination, and interim analysis planning.\n"
  },
  "outgoingEdges": [
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "role:clinical-data-scientist",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "role:epidemiologist",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "role:research-scientist",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "domain:clinical-trials",
      "kind": "applies_to_domain",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "domain:pharmaceuticals",
      "kind": "applies_to_domain",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "responsibility:patient-safety-compliance",
      "kind": "triggers_responsibility",
      "attributes": {}
    },
    {
      "from": "workflow:clinical-trial-protocol",
      "to": "responsibility:clinical-data-integrity",
      "kind": "triggers_responsibility",
      "attributes": {}
    }
  ],
  "incomingEdges": []
}