Principal Clinical Scientist

* 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 alignment with regulatory standards * Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance * Provide expert feedback that directly improves how AI models reason about clinical data, trial outcomes, and evidence quality * Work independently and asynchronously — fully on your own schedule

Who You Are

* Senior-level experience designing clinical trial protocols for regulatory submission (FDA, EMA, or equivalent) * Deep expertise interpreting clinical data in the context of regulatory review and submission * Strong background in clinical research methodology, biostatistics, or translational science * Naturally rigorous and detail-oriented — you hold scientific work to a high standard * Able to communicate complex clinical concepts clearly in written feedback * Comfortable working independently in a remote, task-based environment

Nice to Have

* Prior experience with data annotation, data quality evaluation, or AI training workflows * Background in pharmacovigilance, medical affairs, or clinical operations * Familiarity with AI tools or research platforms as an end user * Experience across multiple therapeutic areas or trial phases

Why Join Us

* Work directly on frontier AI systems impacting clinical and biomedical research worldwide * Fully remote and flexible — work when and where it suits you * Freelance autonomy with the structure of meaningful, expert-level work * Influence how AI understands and evaluates real-world clinical evidence at a foundational level * Potential for ongoing work and contract extension as new projects launch