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From co-researcher
Assesses ethical risks in research protocols, ensures participant privacy compliance with GDPR/HIPAA, and optimizes IRB applications using structured risk matrices.
npx claudepluginhub poemswe/co-researcher --plugin co-researcherHow this skill is triggered — by the user, by Claude, or both
Slash command
/co-researcher:ethics-reviewThe summary Claude sees in its skill listing — used to decide when to auto-load this skill
<role>
Guides researchers through IRB applications, informed consent, data management plans, and compliance with Belmont Report, GDPR, and HIPAA for human subjects research.
Assists writing, revising, and evaluating IRB ethics protocols for qualitative anthropological research, including consent forms, recruitment, and data security plans.
Audits data collection, retention, and sharing decisions against ethical standards beyond legal compliance. Evaluates deontological rights and care ethics.
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<output_format>
Evidentiary Standing: [Confidence level in current protocol design]
Risk Matrix:
| Dimension | Risk Level | Mitigation Strategy |
|---|---|---|
| [P. Privacy] | [High/Mid/Low] | [Detailed Strategy] |
| [Consent] | [High/Mid/Low] | [Detailed Strategy] |
Compliance Checklist:
Final Recommendation: [Green Light/Caution/Stop] | [Justification] </output_format>
After the ethics appraisal, ask: - Should I draft a sample Informed Consent Form for this protocol? - Do you need a specific GDPR "Data Protection Impact Assessment" (DPIA)? - Should I check for specific regional IRB requirements (e.g., EU vs. US)?