Principal Clinical Scientist

Principal Clinical Scientist (AI Training) About The Role What if your hard-won expertise in clinical trial design and regulatory science could directly shape how AI reasons about medical evidence — influencing the next generation of biomedical AI systems used by researchers and clinicians worldwide? We're looking for a Principal Clinical Scientist to bring senior-level clinical and regulatory knowledge into cutting-edge AI development. You'll work with Alignerr — a team that partners with the world's leading AI research labs — to ensure that AI models handling clinical data meet the rigorous standards of real-world regulatory science. This is a fully remote, flexible contract role. No AI background needed — just deep clinical expertise and a sharp eye for scientific quality. 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 training datasets for AI systems Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations from agencies such as the FDA, EMA, or equivalent Provide expert, structured feedback that helps AI models reason more accurately about clinical trial data, outcomes, and evidence Flag errors, inconsistencies, and methodological gaps in AI-generated clinical content Work independently and asynchronously — fully on your own schedule Who You Are Senior‑level experience designing and reviewing clinical trial protocols for regulatory submission Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent) Strong background in clinical research methodology, biostatistics, or translational science Naturally rigorous and detail‑oriented — you hold clinical content to the highest standards Comfortable evaluating scientific reasoning and providing clear, structured written feedback No prior AI or tech experience required Nice to Have Experience with data annotation, data quality review, or evaluation systems Background in pharmacology, medical affairs, or clinical operations Familiarity with AI tools or scientific content evaluation workflows Experience spanning multiple therapeutic areas or regulatory jurisdictions Why Join Us Work directly on frontier AI systems that are shaping the future of clinical and biomedical research Influence how AI understands, evaluates, and reasons about real‑world clinical evidence Fully remote and flexible — work when and where it suits you Freelance autonomy with the structure of meaningful, high‑stakes expert work Collaborate with leading AI research teams on problems that matter Potential for ongoing work and contract extension as new projects launch #J-18808-Ljbffr