Principal Clinical Scientist

What You'll Do

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

Who You Are

• Senior-level clinical scientist with hands-on experience designing protocols for regulatory submission
• Strong expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
• Grounded in clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented thinker who can translate complex clinical nuance into clear, structured feedback
• Comfortable working independently in a remote, task-based environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or AI evaluation systems
• Familiarity with AI-generated content or machine learning workflows in a clinical or research context
• Background spanning multiple therapeutic areas or regulatory jurisdictions