Principal Clinical Scientist

What You'll Do

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

Who You Are

• Senior-level experience designing clinical trial protocols intended for regulatory submission
• Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent international bodies
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Naturally detail-oriented with a systematic, evidence-driven approach to evaluation
• Clear and precise written communicator — able to articulate complex scientific reasoning in structured feedback

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Familiarity with AI tools or clinical informatics platforms
• Background in pharmacology, oncology, rare disease, or another specialist therapeutic area
• Experience contributing to regulatory dossiers, CTD submissions, or scientific advisory processes