Grayde.ai is a specialised healthcare and life science AI data and evaluation company. We work with the best clinicians and life science researchers to make medical AI models better.
Overview
Evaluate AI-generated responses to FDA regulatory questions for accuracy and compliance with US regulatory requirements.
About this job
We’re seeking specialists to evaluate AI-generated answers about FDA submission pathways, requirements, and correspondence. You will judge whether responses correctly reflect current FDA regulations and guidance documents. Your evaluations help ensure AI-generated FDA guidance is accurate and current.
What you'll do
- Evaluate AI-generated answers on FDA submission pathways.
- Check accuracy of cited FDA regulations and guidance documents.
- Assess responses to hypothetical FDA correspondence scenarios.
- Flag outdated or incorrect regulatory information.
- Compare responses against current CFR and FDA guidance.
- Score responses using a structured regulatory-accuracy rubric.
- Provide written rationale for each evaluation.
Who can apply
Anyone with FDA submission experience
Field of study: Drug Regulatory Affairs, Health Policy, Regulatory Affairs
Pay: ₹800.00 - ₹2,000.00 per hour
Work Location: Remote
📌 AI Evaluator (India)
🏢 Grayde.ai
📍 India
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