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- Flag outdated or incorrect regulatory information.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 Evaluator - FDA Regulatory - Fully Remote (India)
🏢 Grayde.ai
📍 India