Principal Clinical Scientist

About This Role

The Principal Clinical Scientist will apply senior-level expertise in clinical trial design and regulatory data interpretation to AI-driven research workflows, ensuring clinical data meets regulatory standards for advanced AI systems.

Responsibilities

• Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets
• Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations
• Provide expert feedback to improve how AI models reason about clinical trial data and outcomes

Requirements

• Senior-level experience designing clinical trial protocols for regulatory submission
• Deep expertise interpreting clinical data for agencies such as FDA, EMA, or equivalent
• Strong background in clinical research methodology, biostatistics, or translational science

Qualifications

• Senior-level experience designing clinical trial protocols for regulatory submission

Nice to Have

• Prior experience with data annotation, data quality, or evaluation systems

Benefits