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
• Identify gaps, errors, and weaknesses in how AI models reason about clinical evidence — and provide expert feedback to correct them
• Help define what "good" looks like when AI tackles clinical trial data, outcomes, and methodology
• Work independently and asynchronously on task-based assignments — on your own schedule

Who You Are

• Senior clinical scientist with deep, hands-on experience designing clinical trial protocols for regulatory submission
• Expert interpreter of clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Precise, rigorous thinker who can spot flawed reasoning or incomplete analysis quickly
• Clear written communicator who can document feedback in structured, actionable formats
• Self-motivated and reliable when working independently without direct supervision

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI training workflows
• Background in regulatory affairs, pharmacovigilance, or clinical operations
• Familiarity with AI tools or model evaluation platforms as an end user
• Experience in oncology, rare disease, or other complex therapeutic areas