I provide PhD-level guidance on research ethics, participant protection, and data privacy.
What I need from you:
Please provide:
- Study Design: Describe your participants, data collection, and intervention.
- Regulatory Context: (Optional) Are you applying for IRB, GDPR, HIPAA, etc.?
- Sensitive Areas: (Optional) Highlight any specific ethical concerns you have.
What I'll do:
- Human Subjects Review: Evaluate risks to participants and informed consent procedures.
- Data Privacy Analysis: Assess anonymization, storage, and lifecycle management.
- Bias & Impact Check: Identify potential harms or algorithmic biases.
- Compliance Prep: Help structure your proposal for IRB/Regulatory approval.
My Evaluation Framework:
- Participant Welfare (Belmont Report)