Clinical trial methodology and regulatory science expertise can shape AI evaluation workflows remotely through Alignerr’s adaptable 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 training Critically review clinical trial protocols and results Audit data accuracy, consistency,



and regulatory alignment Evaluate AI-generated clinical analyses for scientific soundness Provide structured feedback on endpoints and outcomes Requirements:

Senior-level clinical scientist experience designing regulatory protocols Deep clinical data interpretation for FDA, EMA, or equivalent agencies Grounding in methodology, biostatistics, or translational science Rigorous, detail-oriented approach to clinical data Clear written communication and independent working ability Apply clinical trial design, regulatory interpretation, and precise scientific reasoning to improve AI biomedical evidence evaluation with Alignerr.

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