Principal Clinical Scientist
Alignerr · Columbus, OH · Yesterday
RemoteRemoteAnalystContract
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 alignment with regulatory standards
- Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance
- Provide expert, structured feedback that shapes how AI models reason about clinical trial data, outcomes, and evidence
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level experience designing clinical trial protocols intended for regulatory submission
- Strong expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent bodies
- Rigorous, detail-oriented thinker who can translate complex clinical concepts into clear, structured feedback
- Self-motivated and reliable when working independently without supervision
Nice to Have
- Prior experience with data annotation, data quality review, or AI evaluation workflows
- Background in regulatory affairs, medical writing, or clinical operations
- Familiarity with AI tools or machine learning applications in healthcare or life sciences
- Experience contributing to multi-site or global clinical trials