About the Role
What if your decades of clinical trial expertise could directly shape how AI reasons about medical evidence, regulatory data, and patient outcomes? We're looking for a Principal Clinical Scientist to bring senior-level rigor to the AI systems that are rapidly transforming biomedical research.
At Alignerr, we partner with the world's leading AI research teams to build and train cutting-edge models. In this role, your expertise in regulatory-grade trial design and clinical data interpretation won't just inform internal processes — it will influence how next-generation AI understands and evaluates real-world clinical evidence.
This is a fully remote, flexible contract role designed for senior clinical scientists 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 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 structured expert feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
- Help establish quality benchmarks for clinical content used across frontier AI systems
Who You Are
- Senior-level professional with hands-on experience designing clinical trial protocols for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies
- Strong grounding in clinical research methodology, biostatistics, or translational science
- Meticulous, structured thinker who can communicate complex scientific judgments clearly and consistently
- Self-directed and comfortable working independently in an async, remote environment
Nice to Have
- Prior experience with data annotation, data quality assurance, or AI evaluation workflows
- Background in clinical pharmacology, outcomes research, or medical affairs
- Familiarity with AI tools or experience reviewing AI-generated scientific content
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
- Collaborate with world-class AI research teams on problems that matter
- Potential for ongoing work and contract extension as new projects launch