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.

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