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FDA Regulatory Response Evaluation

Remote · Global Hourly Rolling start $10–$20/hr
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  • Flag outdated or incorrect regulatory information.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
FDA (US)Device — FDA 510(k) / PMARegulatory IntelligenceSaMD / AI RegulationRegulatory AffairsRegulatory Writing (CSR / Protocol)
Who can apply
  • Field of study: Drug Regulatory Affairs, Health Policy, Regulatory Affairs
About grayder

Life science AI is only as good as the experts who train it.

A vetted network of doctors, scientists, and regulatory specialists who train and evaluate the models behind drug discovery, clinical trials, medical devices, and healthcare. Remote, flexible, matched to your field.

What specialists do

  • Annotation — labelling clinical text, imaging and molecular data
  • Model evaluation — scoring outputs against expert standards
  • Rubric design and execution
  • Fine-tuning data — writing expert responses
  • Q&A sets, summaries and reports

Why specialists join

  • Work matched to your speciality
  • Remote and flexible — on your own schedule
  • Credentialed by your peers
  • Meaningful impact on healthcare AI
Join the network to apply
Doctors · Scientists · Regulatory & Writing · Allied Health
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