About the Role
What if your expertise in clinical trial design and regulatory science could directly influence how AI reasons about medicine, evidence, and patient outcomes? We're looking for a Principal Clinical Scientist to bring senior-level clinical expertise into the heart of cutting-edge AI development — ensuring that the systems shaping the future of biomedical research are grounded in real-world scientific rigor.
This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work at the intersection of medicine and artificial intelligence.
- 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, regulatory-ready datasets for AI training and evaluation
- Interpret and audit clinical trial results, ensuring accuracy, consistency, and alignment with regulatory standards
- Evaluate AI-generated clinical analyses for scientific soundness and adherence to FDA, EMA, or equivalent regulatory expectations
- Provide expert, structured feedback that directly improves how AI models understand and reason about clinical trial data and outcomes
- Help bridge the gap between frontier AI systems and the rigorous standards of real-world clinical research
Who You Are
- Senior-level clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
- Deep expertise interpreting clinical data for major regulatory agencies — FDA, EMA, or equivalent
- Strong foundation in clinical research methodology, biostatistics, translational science, or a closely related discipline
- Naturally detail-oriented with a systematic, methodical approach to evaluating complex scientific information
- Comfortable working independently and asynchronously in a remote environment
Nice to Have
- Prior experience with data annotation, data quality assurance, or AI evaluation workflows
- Background in pharmacology, medical writing, or clinical affairs
- Familiarity with AI tools or content evaluation platforms
Why Join Us
- Work directly on frontier AI systems that are reshaping clinical and biomedical research
- Fully remote and flexible — work when and where it suits you
- Freelance autonomy with meaningful, high-impact task-based work
- Influence how AI understands, evaluates, and communicates real-world clinical evidence
- Collaborate with world-leading AI research teams and labs
- Potential for ongoing work and contract extension as new projects launch