About the Role
What if your decades of clinical trial expertise could directly influence how AI reasons about medical evidence, regulatory submissions, and patient outcomes? 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 that matter in the real world.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work on their own terms.
- 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 standards
- Provide expert, structured feedback that directly improves how AI models reason about clinical trial data and outcomes
- Work independently and asynchronously — fully on your own schedule
Who You Are
- Senior-level clinical scientist with hands-on 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, translational science, or related disciplines
- Sharp eye for scientific accuracy, regulatory alignment, and data quality
- Self-directed and comfortable delivering high-quality work independently
Nice to Have
- Prior experience with data annotation, data quality assurance, or AI evaluation workflows
- Background in pharmacovigilance, outcomes research, or clinical evidence synthesis
- Familiarity with AI tools or clinical informatics platforms
Why Join Us
- Work directly on frontier AI systems shaping the future of clinical and biomedical research
- Fully remote and flexible — contribute on a schedule that fits your life
- Freelance autonomy: set your own pace, work from anywhere, collaborate globally
- Make a tangible impact on how AI understands and evaluates real-world clinical evidence
- Potential for ongoing work and contract extension as new projects launch