What if your career-long expertise in clinical trial design and regulatory science could directly influence how AI understands and reasons about clinical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research — ensuring the clinical data powering next-generation AI systems meets the standards expected in real-world regulatory submissions.
This is a fully remote, adaptable contract role designed for experienced clinical scientists who want to work at the frontier of AI and biomedical research. No AI background required — just deep clinical expertise and a sharp eye for scientific quality.
• Design and review clinical trial protocols used to generate high-quality, regulatory-grade 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 that helps AI models reason more accurately about clinical trial data, outcomes, and methodology
• 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 within regulatory frameworks
• Strong foundation in clinical research methodology, biostatistics, or translational science
• Naturally detail-oriented with high standards for scientific accuracy and consistency
• Clear and effective written communicator able to document feedback in structured formats
Nice to Have
• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in pharmacology, epidemiology, or out
📌 Principal Clinical Scientist (Madrid)
🏢 Alignerr
📍 Madrid
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