What if your deep expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about biomedical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows - ensuring the clinical data powering next-generation AI systems meets the standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to work at the cutting edge of AI without leaving their field behind.
Organization: Alignerr
Type: Hourly Contract
Location: Remote
Commitment: 10-40 hours/week
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 regulatory relevance
Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
Provide expert feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
Help set the standard for how clinical evidence is structured, assessed, and applied within frontier AI systems
Who You Are
Senior-level clinical scientist with substantial experience designing trial protocols for regulatory submission
Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
Strong grounding in clinical research methodology, biostatistics, or translational science
Rigorous and detail-oriented - you can spot a flawed endpoint or a data inconsistency that others would miss
Comfortable working independently and asynchronously in a remote, task-based environment
Nice to Have
Prior experience with data annotation, data quality review, or AI evaluation workflows
Background in pharmacology, epidemiology, or medical writing
Familiarity with AI tools or research platforms as an end user
Why Join Us
Work directly on frontier AI systems that are reshaping clinical and biomedical research
Fully remote and flexible - structure your hours around your life
Freelance autonomy with the substance of genuinely meaningful, expert-level work
Influence how AI understands, evaluates, and communicates real-world clinical evidence at scale
Potential for ongoing work and contract extension as new projects launch
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