Clinical trial methodology and regulatory science expertise can shape AI evaluation workflows remotely through Alignerr’s flexible contract work. Bring senior authority to biomedical evidence.As a Principal Clinical Scientist, you will support AI training and evaluation with clinical trial design expertise. The work involves regulatory-grade data interpretation, clinical research methodology, and biostatistics. No prior AI experience is needed for this fully remote contract.Key Responsibilities:

Design protocols generating regulator-ready datasets for AI trainingCritically review clinical trial protocols and resultsAudit data accuracy, consistency,



and regulatory alignmentEvaluate AI-generated clinical analyses for scientific soundnessProvide structured feedback on endpoints and outcomesRequirements:

Senior-level clinical scientist experience designing regulatory protocolsDeep clinical data interpretation for FDA, EMA, or equivalent agenciesGrounding in methodology, biostatistics, or translational scienceRigorous, detail-oriented approach to clinical dataClear written communication and independent working abilityApply clinical trial design, regulatory interpretation, and exact scientific reasoning to improve AI biomedical evidence evaluation with Alignerr.

📌 Principal Clinical Scientist Ai Training (Winnipeg)
🏢 Alignerr
📍 Winnipeg