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Principal Clinical Scientist (AI Training) About The Role 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...
Principal Clinical Scientist (AI Training)

About The Role

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, flexible 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.

  • 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, 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 outcomes research
  • Familiarity with AI tools or clinical decision-support systems
  • Experience working across multiple therapeutic areas or trial phases

Why Join Us

  • Work directly on frontier AI systems shaping the future of clinical and biomedical research
  • Influence how AI understands, evaluates, and reasons about real-world clinical evidence
  • Fully remote and flexible — work when and where it suits you
  • Freelance autonomy with the structure of meaningful, expert-level work
  • Collaborate with leading AI research labs and teams pushing the boundaries of medical AI
  • Potential for ongoing work and contract extension as new projects launch

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