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 (FDA, EMA, or equivalent)
• Evaluate AI-generated clinical analyses for scientific soundness and methodological integrity
• Provide expert, structured feedback that directly improves how AI models reason about clinical trial data, outcomes, and evidence
• Help establish and uphold the quality standards that govern clinical data used in AI-driven research workflows

Who You Are

• Senior-level experience designing clinical trial protocols for regulatory submission
• Strong expertise interpreting clinical data for major regulatory agencies such as the FDA, EMA, or equivalent bodies
• Sharp analytical mind with a rigorous, detail-oriented approach to evaluating data quality and scientific validity
• Able to communicate complex clinical concepts clearly and precisely in written feedback
• Self-directed and comfortable working independently in an asynchronous environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or AI evaluation systems
• Familiarity with AI tools or clinical informatics platforms
• Background in oncology, rare disease, or other complex therapeutic areas
• Experience working across multi-site or international clinical research settings