What if your career-long expertise in clinical trial design and regulatory science could directly influence how AI reasons about medicine, data, and patient outcomes?
We're looking for a Principal Clinical Scientist to bring senior-level rigor to one of the most consequential challenges in AI development: ensuring that AI systems trained on clinical data actually understand it the way regulators, researchers, and clinicians do.
This is a fully remote, adaptable contract role built for experienced clinical scientists who want to work at the frontier of AI and biomedical research — on their own terms.
Design and critically review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training
Interpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory standards
Evaluate AI-generated clinical analyses for scientific soundness and compliance with FDA, EMA, or equivalent agency expectations
Provide expert, structured feedback that directly improves how AI models reason about clinical evidence, trial methodology, and outcomes
Flag gaps, inconsistencies, or methodological errors in AI-generated clinical content
Work independently and asynchronously — fully on your own schedule
Who You Are
Senior-level experience designing clinical trial protocols for regulatory submission — you've done this at a high level in the real world
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 AI-generated content to the same standards you'd apply to a real submission
Clear and precise written communicator who can articulate complex scientific reasoning in
📌 Principal Clinical Scientist (Ciudad de México)
🏢 Alignerr
📍 Ciudad de México
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