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

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