Principal Clinical Scientist

What You'll Do

• Design and review clinical trial protocols used to generate high-quality, regulator-ready training datasets for AI systems
• Interpret and audit clinical trial results to ensure accuracy, consistency, and alignment with regulatory standards
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
• Provide expert, structured feedback that improves how AI models reason about clinical trial data, endpoints, and outcomes
• Serve as a domain authority at the intersection of clinical science and frontier AI development

Who You Are

• Senior-level clinical scientist with hands-on experience designing trial 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 clearly articulate why something meets — or falls short of — regulatory expectations
• Self-directed and comfortable working independently in an asynchronous, remote environment

Nice to Have

• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in clinical data management or medical writing for regulatory submissions
• Familiarity with AI tools or interest in how machine learning is applied in biomedical contexts