Job Title

Principal Clinical Scientist (AI Training) About The Role What if your decades of clinical trial expertise could directly shape how AI understands and evaluates biomedical evidence for millions of researchers, clinicians, and patients worldwide? We''re looking for a Principal Clinical Scientist to bring seniorlevel authority in clinical trial design and regulatorygrade data interpretation into cuttingedge AI research workflows. Your expertise will help ensure that the AI systems influencing the future of clinical and biomedical science are built on rigorous, accurate, and regulationready foundations. This is a fully remote, flexible contract role. No prior AI experience needed just deep command of clinical trial methodology and regulatory science. Organization: Alignerr Type: Hourly Contract Location: Remote Commitment: 1040 hours/week What Youll Do Design and critically review clinical trial protocols that generate highquality, regulatorready datasets for AI training and evaluation Interpret and audit clinical trial results to verify accuracy, consistency, and alignment with regulatory standards Evaluate AIgenerated clinical analyses for scientific soundness and regulatory appropriateness Provide expert, structured feedback to improve how AI models reason about clinical trial data, endpoints, and outcomes Work independently and asynchronously fully on your own schedule Who You Are Seniorlevel clinical scientist with handson experience designing clinical trial protocols for regulatory submission Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent regulatory bodies Strong grounding in clinical research methodology, biostatistics, or translational science Naturally rigorous and detailoriented you hold clinical data to the highest standards Clear and precise written communicator who can document scientific reasoning effectively Comfortable working independently across varied clinical topics and therapeutic areas Nice to Have Prior experience with data annotation, data quality assurance, or evaluation frameworks Familiarity with AI tools or model evaluation workflows as an end user Background spanning multiple therapeutic areas or regulatory jurisdictions Experience in medical writing, evidence synthesis, or systematic review Why Join Us Work directly on frontier AI systems shaping the future of clinical and biomedical research Fully remote and flexible work when and where it suits you Freelance autonomy with the structure of meaningful, highimpact scientific work Influence how AI understands, evaluates, and reasons about realworld clinical evidence at scale Collaborate with leading AI research teams and labs on genuinely novel challenges Potential for ongoing work and contract extension as new projects launch #J-18808-Ljbffr