Principal Clinical Scientist
Alignerr
Principal Clinical Scientist (AI Training)
About The Role
What if your years of clinical trial expertise could directly shape how AI reasons about biomedical evidence — influencing the systems that will power the next generation of clinical research?
We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows. You'll work with cutting-edge AI systems developed alongside the world's leading research labs, ensuring that clinical data used to train and evaluate these models meets the exacting standards expected in real-world regulatory submissions.
This is a fully remote, flexible contract role — built for senior clinical professionals who want meaningful, high-impact work on their own schedule.
- 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 regulatory relevance
- Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent agency expectations
- Provide expert, structured feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
- Help define the gold standard for how clinical evidence is represented and understood within advanced AI systems
Who You Are
- Senior-level experience designing clinical trial protocols intended for regulatory submission
- Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
- Strong grounding in clinical research methodology, biostatistics, or translational science
- Meticulous, detail-oriented, and comfortable working independently in an asynchronous environment
- Clear and precise written communicator — you can explain complex clinical reasoning in structured, actionable terms
Nice to Have
- Prior experience with data annotation, data quality review, or evaluation systems
- Background in pharmacovigilance, medical writing, or clinical operations
- Familiarity with AI tools or data evaluation workflows
Why Join Us
- Work directly on frontier AI systems making a real impact on 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 and evaluates real-world clinical evidence at a foundational level
- Collaborate with a global network of domain experts and leading AI research teams
- Potential for ongoing work and contract extension as new projects launch
