What if your decades of clinical trial expertise could directly shape how AI understands and evaluates biomedical evidence for millions of researchers, clinicians, and patients worldwide?
We're looking for a Principal Clinical Scientist to bring senior-level authority in clinical trial design and regulatory-grade data interpretation into cutting-edge AI research workflows. Your expertise will help ensure that the AI systems influencing the future of clinical and biomedical science are built on rigorous, accurate, and regulation-ready foundations.
This is a fully remote, flexible contract role. No prior AI experience needed - just deep command of clinical trial methodology and regulatory science.
- Design and critically review clinical trial protocols that generate high-quality, regulator-ready datasets for AI training and evaluation
- Interpret and audit clinical trial results to verify accuracy, consistency, and alignment with regulatory standards
- Evaluate AI-generated clinical analyses for scientific soundness and regulatory appropriateness
- Provide expert, structured feedback to improve how AI models reason about clinical trial data, endpoints, and outcomes
- Work independently and asynchronously - fully on your own schedule
Who You Are
- Senior-level clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
- 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 clinical data to the highest standards
- Transparent and precise written communicator who can document scientific reasoning effectively
- Comfortable working independently across varied clinical topics and therapeutic areas
Nice to Have
- Prior experience with data annotation, data quality assurance, or evaluation frameworks
- Familiarity with AI tools or model evaluation workflows as an end user
- Background spanning multiple therapeutic areas or regulatory jurisdictions
- Experience in medical writing, evidence synthesis, or systematic review
Why Join Us
- Work directly on frontier AI systems shaping the future of clinical and biomedical research
- Fully remote and flexible - work when and where it suits you
- Freelance autonomy with the structure of meaningful, high-impact scientific work
- Influence how AI understands, evaluates, and reasons about real-world clinical evidence at scale
- Collaborate with leading AI research teams and labs on genuinely novel challenges
- Potential for ongoing work and contract extension as new projects launch
📌 Principal Clinical Scientist (Vancouver)
🏢 Alignerr
📍 Vancouver
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