Principal Clinical Scientist

Principal Clinical Scientist

What if your years of clinical trial expertise could directly influence how AI understands and reasons about medical evidence at a scale that impacts millions of patients worldwide?

We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows. You'll work alongside world-leading AI research teams to ensure that clinical data used to train and evaluate advanced AI systems meets the scientific and regulatory standards expected in real-world submissions.

This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work on their own terms.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 1040 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 regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
• Provide expert, structured feedback to improve how AI models reason about clinical trial data and real-world outcomes
• Help define the standards by which AI systems engage with clinical evidence shaping the field from the ground up

Who You Are

• Senior clinical scientist with hands-on experience designing trial protocols for regulatory submission
• Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
• Strong foundation in clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented thinker who holds AI outputs to the same standards as a regulatory dossier
• Self-directed and comfortable working independently in an async, remote environment

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Background in pharmacovigilance, post-market surveillance, or real-world evidence
• Familiarity with AI tools or clinical data platforms
• Experience in translational research or early-phase drug development

Why Join Us

• Work directly on frontier AI systems with real impact on clinical and biomedical research
• Fully remote and async work when and where it suits you, with no commute and no fixed schedule
• Freelance autonomy: choose your hours, control your workload, and collaborate globally
• Influence how AI understands, evaluates, and communicates real-world clinical evidence
• Contribute to work that sits at the intersection of regulatory science and cutting-edge AI
• Potential for ongoing collaboration and contract extension as new projects launch