Principal Clinical Scientist

What You'll Do

• Design and critically review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI training
• Interpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory expectations
• Evaluate AI-generated clinical analyses for scientific soundness and methodological integrity
• Provide structured expert feedback that directly improves how AI models reason about clinical evidence, outcomes, and trial data
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Senior-level experience designing clinical trial protocols intended for regulatory submission
• Strong expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent global bodies
• Naturally detail-oriented with a rigorous, systematic approach to evaluating scientific quality
• Clear and precise written communicator — able to document findings and feedback with authority
• No prior AI or tech experience required
• Nice to have: Prior involvement in data annotation, data quality assurance, or evaluation systems; Experience reviewing or contributing to clinical evidence packages for drug, device, or diagnostic submissions; Background spanning multiple therapeutic areas or trial phases; Familiarity with AI-generated content or model evaluation workflows