Principal Clinical Scientist

What You'll Do

• Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training
• Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
• Provide expert feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
• Help establish standards for how frontier AI systems understand and evaluate real-world clinical evidence

Who You Are

• Senior-level experience designing clinical trial protocols for regulatory submission
• Strong expertise interpreting clinical data for regulatory agencies such as the FDA, EMA, or equivalent
• Background in clinical research methodology, biostatistics, or translational science
• Naturally detail-oriented with a rigorous, systematic approach to evaluating data quality
• Able to communicate complex clinical concepts clearly in written 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 pharmacovigilance, medical affairs, or health outcomes research
• Experience working across multiple therapeutic areas or global regulatory frameworks