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 directly improves how AI models reason about clinical trial data, endpoints, and outcomes
• Help establish the bar for what good clinical reasoning looks like — at the frontier of AI development

Who You Are

• Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
• Strong expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent global bodies
• Foundation in clinical research methodology, biostatistics, translational science, or a closely related discipline
• Naturally rigorous — you hold AI-generated outputs to the same standards you'd apply in a real submission context
• Comfortable working independently in an asynchronous, remote environment

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI output assessment
• Background in drug development, medical devices, or diagnostics
• Familiarity with clinical data standards such as CDISC, ICH guidelines, or GCP frameworks