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 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 exact scientific reasoning to improve AI biomedical evidence evaluation with Alignerr.

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📌 Principal Clinical Scientist AI Training (British Columbia)
🏢 Alignerr
📍 British Columbia