About Grayde
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Flag outdated or incorrect regulatory information.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, Medical Device Regulatory

Work Location: Remote

📌 AI Trainer (India)
🏢 Grayde.ai
📍 India