Principal Clinical Scientist

What You'll Do

• Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training and evaluation
• 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 to improve how AI models reason about clinical trial data, outcomes, and evidence hierarchies
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Senior-level clinical scientist with hands-on experience designing trial protocols for regulatory submission
• Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Naturally rigorous and detail-oriented — you hold data to the highest scientific standard
• Clear, structured written communicator who can translate complex findings into actionable feedback

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI output review
• Background in pharmacovigilance, medical writing, or health technology assessment
• Familiarity with AI tools or scientific evaluation workflows
• Experience working across multiple therapeutic areas or regulatory jurisdictions