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 regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
• 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 for regulatory submission
• Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
• Strong background in clinical research methodology, biostatistics, or translational science
• Naturally detail-oriented with a systematic, rigorous approach to scientific evaluation
• Clear and precise written communicator comfortable providing structured, actionable feedback

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Familiarity with AI tools or machine learning workflows in clinical or biomedical contexts
• Background in pharmacovigilance, medical affairs, or health technology assessment
• Experience working across multiple therapeutic areas or global regulatory jurisdictions