Principal Clinical Scientist

Principal Clinical Scientist (AI Training)About The RoleWhat if your career-long expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to frontier AI research — ensuring the clinical data and analyses powering next-generation AI systems meet the same exacting standards expected in real-world regulatory submissions.This is a fully remote, flexible contract role built for experienced clinical scientists who want to contribute to something genuinely new. No AI background required — just deep command of clinical research and a sharp eye for scientific quality.Organization: AlignerrType: Hourly ContractLocation: RemoteCommitment: 10–40 hours/weekWhat You'll DoDesign and critically review clinical trial protocols used to generate high-quality, regulatory-grade datasets for AI trainingInterpret and audit clinical trial results for accuracy, consistency, and alignment with regulatory expectationsEvaluate AI-generated clinical analyses for scientific soundness and methodological integrityProvide structured expert feedback that directly improves how AI models reason about clinical evidence, outcomes, and trial dataWork independently and asynchronously — fully on your own scheduleWho You AreSenior-level experience designing clinical trial protocols intended for regulatory submissionDeep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent global bodiesStrong grounding in clinical research methodology, biostatistics, or translational scienceNaturally detail-oriented with a rigorous, systematic approach to evaluating scientific qualityClear and precise written communicator — able to document findings and feedback with authorityNo prior AI or tech experience requiredNice to HavePrior involvement in data annotation, data quality assurance, or evaluation systemsExperience reviewing or contributing to clinical evidence packages for drug, device, or diagnostic submissionsBackground spanning multiple therapeutic areas or trial phasesFamiliarity with AI-generated content or model evaluation workflowsWhy Join UsWork directly on frontier AI systems with real impact on clinical and biomedical researchFully remote and flexible — work when and where it suits youFreelance autonomy with the structure of meaningful, expert-level workInfluence how AI understands, evaluates, and communicates real-world clinical evidencePotential for ongoing work and contract extension as new projects launch