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, structured feedback to improve how AI models reason about clinical trial data and real-world outcomes
• Help define the standards by which AI systems engage with clinical evidence — shaping the field from the ground up

Who You Are

• Senior clinical scientist with hands-on experience designing trial protocols for regulatory submission
• Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
• Strong foundation in clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented thinker who holds AI outputs to the same standards as a regulatory dossier
• Self-directed and comfortable working independently in an async, remote environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Background in pharmacovigilance, post-market surveillance, or real-world evidence
• Familiarity with AI tools or clinical data platforms
• Experience in translational research or early-phase drug development