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Job description
Principal Clinical Scientist (AI Training)
About the Role
What if your years of clinical trial expertise could directly influence how AI reasons about medical evidence, regulatory submissions, and patient outcomes? We're looking for a Principal Clinical Scientist to bring senior-level rigour into the development of cutting-edge AI systems - ensuring these models understand clinical data the way the world's top regulatory scientists do.
This is a fully remote, flexible contract role designed for experienced clinical scientists who want to make a meaningful impact beyond traditional research settings. Your domain expertise will directly shape how frontier AI handles real-world clinical evidence.
Organization
: Alignerr
Type
: Hourly Contract
Location
: Remote
Commitment
: 10-40 hours/week
What You'll Do Design and review clinical trial protocols that generate high-quality, regulator-ready datasets for AI training
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, structured feedback that helps AI models reason more accurately about clinical trial data and outcomes
Work independently and asynchronously - entirely 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 regulatory agencies (FDA, EMA, or equivalent)
Strong foundation in clinical research methodology, biostatistics, or translational science
Naturally rigorous and detail-oriented - you hold data to the highest standard
Clear and precise written communicator who can translate complex scientific concepts into structured feedback
Nice to Have Prior experience with data annotation, data quality assurance, or evaluation systems
Familiarity with AI tools or machine learning workflows in a clinical or biomedical context
Background in pharmacovigilance, outcomes research, or evidence-based medicine
Experience working across multiple therapeutic areas or regulatory jurisdictions
Why Join Us Work directly on frontier AI systems that are reshaping clinical and biomedical research
Fully remote and flexible - work when and where it suits you
Freelance autonomy with the structure and purpose of meaningful, expert-level work
Influence how AI understands, evaluates, and communicates 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
Worksite address
miami, FL, 33222, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.