Write-Protocol Skill

Draft the scientific core of an IRB/ethics protocol and leave institution-specific sections as [TODO] skeletons. Read both reference files before generating a protocol draft:

• ${CLAUDE_SKILL_DIR}/references/protocol_template.md -- the 10-section structure, per-section guidance, and the [TODO] blocks for Sections 5-9
• ${CLAUDE_SKILL_DIR}/references/ethics_checklist.md -- jurisdiction-specific ethical requirements

Inputs

Collect the required inputs before generating; ask for any that are missing.

• Required: research question / hypothesis (specific, testable); study type (retrospective cohort, prospective cohort, cross-sectional, RCT, diagnostic accuracy, case-control, case series); target population (who, where, when); primary outcome; secondary outcomes (if any).
• Optional: key references (DOIs or search terms); institution name (header and ethics guidance); regulatory context -- Korea (PIPA), US (HIPAA/Common Rule), EU (GDPR), other.