Precision Medicine Data Lead (AI Training) About the Role What if your expertise in genomic and clinical data could directly shape how AI understands and advances personalized medicine for millions of patients worldwide?
Principal Clinical Scientist
Job description
Principal Clinical Scientist (AI Training)
About the Role
What if your career designing rigorous clinical trials and interpreting regulatory-grade data could directly shape how AI understands biomedical science? We're looking for a Principal Clinical Scientist to bring senior-level clinical expertise into the development of cutting-edge AI systems — ensuring these models reason about clinical evidence the way the world's top regulatory scientists do.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work at the frontier of AI and biomedical research.
- 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
- 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 shapes how AI models reason about clinical trial data, outcomes, and evidence
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level experience designing clinical trial protocols intended for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
- Strong command of clinical research methodology, biostatistics, or translational science
- Rigorous, detail-oriented thinker who can translate complex clinical concepts into clear, structured feedback
- Self-motivated and reliable when working independently without supervision
Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Background in regulatory affairs, medical writing, or clinical operations
- Familiarity with AI tools or machine learning applications in healthcare or life sciences
- Experience contributing to multi-site or global clinical trials
Why Join Us
- Work directly on frontier AI systems making an impact in clinical and biomedical research
- 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, evaluates, and reasons about real-world clinical evidence
- Collaborate with world-leading AI research teams and labs
- Potential for ongoing work and contract extension as new projects launch
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