AI Evaluator - FDA Regulatory Responses - Fully Remote

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• Flag outdated or incorrect regulatory information.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.

Required skills

Regulatory affairs

FDA submissions

Who can apply

Field of study: Drug Regulatory Affairs, Health Policy, Regulatory Affairs