About This Role
This Principal Clinical Scientist role focuses on bringing senior-level rigor to AI-driven research workflows, ensuring that clinical data used for next-generation AI systems meets the standards expected in real-world regulatory submissions. It involves shaping how AI understands, evaluates, and reasons about medical evidence, leveraging years of clinical trial expertise.
Responsibilities
- Design and review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI training
- Interpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory standards
- Evaluate AI-generated clinical analyses for scientific soundness and compliance with FDA, EMA, or equivalent agency expectations
- Provide expert, structured feedback that directly improves how AI models reason about clinical trial data, outcomes, and evidence
- Work independently and asynchronously on your own schedule
Requirements
- Senior-level experience designing clinical trial protocols intended for regulatory submission
- Deep expertise interpreting clinical data for regulatory agencies such as the FDA, EMA, or equivalent
- Strong background in clinical research methodology, biostatistics, or translational science
- Naturally rigorous and detail-oriented, holding AI outputs to the same standards applied to a real submission
- Clear and confident communicator who can translate complex clinical concepts into actionable feedback
Nice to have:
- Prior experience with data annotation, data quality review, or AI evaluation systems
- Background in pharmacovigilance, medical affairs, or clinical operations
- Familiarity with AI tools or content evaluation workflows
- Experience working across multiple therapeutic areas or regulatory jurisdictions
Benefits
- Work directly on frontier AI systems that are reshaping clinical and biomedical research
- Influence how AI understands, evaluates, and applies real-world clinical evidence
- Fully remote and flexible work, when and where it suits you
- Freelance autonomy with the structure of meaningful, expert-level work
- Collaborate with world-leading AI research teams and labs on high-impact projects
- Potential for ongoing work and contract extension as new projects launch
Important Details
- Schedule: 10–40 hours per week
- Contract: hourly
About the Company
Alignerr is a company that offers hourly contracts for clinical scientists.