Principal Clinical Scientist
Salt Lake City, UT
Contract
Remote
1 month ago
About the role
Principal Clinical Scientist (AI Training)
About The Role
What if your career-long expertise in clinical trial design and regulatory science could directly shape how AI understands and evaluates clinical evidence?
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 being developed by leading research labs — ensuring the clinical intelligence built into these models meets the standards expected in real-world regulatory environments.
This is a fully remote, flexible contract role. No AI background needed — just deep command of clinical research and regulatory science.
What You'll Do
Who You Are
Nice to Have
Why Join Us
About The Role
What if your career-long expertise in clinical trial design and regulatory science could directly shape how AI understands and evaluates clinical evidence?
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 being developed by leading research labs — ensuring the clinical intelligence built into these models meets the standards expected in real-world regulatory environments.
This is a fully remote, flexible contract role. No AI background needed — just deep command of clinical research and regulatory science.
- 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 regulatory expectations (FDA, EMA, or equivalent)
- Provide expert, structured feedback that improves how AI models reason about clinical trial data, endpoints, and outcomes
- Help define quality standards for clinical data used across frontier AI research projects
Who You Are
- Senior-level experience designing clinical trial protocols for regulatory submission
- Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
- Strong background in clinical research methodology, biostatistics, translational science, or a closely related field
- Naturally rigorous and detail-oriented — you hold data and analysis to a high standard
- Able to communicate expert clinical judgment clearly in written feedback
- Comfortable working independently in a self-directed, asynchronous environment
Nice to Have
- Prior experience with data annotation, data quality evaluation, or AI model evaluation workflows
- Background in pharmacology, clinical pharmacokinetics, or outcomes research
- Experience working across multiple therapeutic areas or regulatory jurisdictions
- Familiarity with AI tools or structured evaluation platforms
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
- Potential for ongoing work and contract extension as new projects launch
- Global collaboration with world-class AI researchers and scientists
Skills
Technology, Information and Internet