Ethics and Data Protection 13
Consent, data protection assessments, ethics review and doing no harm.
Consent, data protection assessments, ethics review and doing no harm.
Review an M&E plan or data collection tool for potential harm, ethical risks, safeguarding gaps, and unintended negative consequences for participants and communities.
Create a data management plan covering collection protocols, storage, cleaning, analysis workflows, archiving, ethical safeguards, and data sharing agreements.
Create an ethics review or Institutional Review Board submission package with protocol summary, risk assessment, informed consent forms, and data protection measures.
Create an informed consent form template for M&E data collection that meets ethical standards, is written in plain language, and covers voluntary participation, confidentiality, risks, and data use.
Create a Data Protection Impact Assessment (DPIA) for an M&E data system covering data flows, privacy risks, legal basis, and mitigation measures aligned with GDPR and humanitarian data protection standards.
Review an M&E data collection plan for ethical compliance against UNEG ethical guidelines, covering informed consent, do no harm, confidentiality, and vulnerable population protections.
Review the ethical standards in a methodology, evaluation design, or research protocol.
Review evaluator self-reflection on bias, perspective, and positionality in qualitative methods.
Review the protections for vulnerable populations in an evaluation or research design.
Review data storage and privacy practices in a methodology or data management plan.
Draft a do-no-harm risk identification and mitigation protocol for an evaluation or research activity.
Draft an informed consent form or script with information completeness, comprehension aids, voluntariness, confidentiality, and special-population accommodations.
Draft safeguarding procedures including training, reporting channels, escalation chain, response protocols, and audit trail.