About the Role
What if your deep expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about biomedical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows — 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 built for experienced clinical scientists who want to work at the cutting edge of AI without leaving their field behind.
- 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 and evaluation
- 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 feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
- Help set the standard for how clinical evidence is structured, assessed, and applied within frontier AI systems
Who You Are
- Senior-level clinical scientist with substantial experience designing trial protocols 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
- Rigorous and detail-oriented — you can spot a flawed endpoint or a data inconsistency that others would miss
- Comfortable working independently and asynchronously in a remote, task-based environment
Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Background in pharmacology, epidemiology, or medical writing
- Familiarity with AI tools or research platforms as an end user
Why Join Us
- Work directly on frontier AI systems that are reshaping clinical and biomedical research
- Fully remote and flexible — structure your hours around your life
- Freelance autonomy with the substance of genuinely meaningful, expert-level work
- Influence how AI understands, evaluates, and communicates real-world clinical evidence at scale
- Potential for ongoing work and contract extension as new projects launch