Principal Clinical Scientist

Alignerr Corp.; Montreal; Remote; CAD 83,000 - 165,000; Part time

Job summary

Alignerr Corp. is seeking a Principal Clinical Scientist (AI Training) for a remote hourly contract. You will apply senior clinical trial expertise to ensure AI systems reason about medical evidence and regulatory data with scientific rigor.

Role emphasizes designing protocols, auditing trial results, and aligning AI analyses with FDA/EMA expectations while enabling flexible scheduling across 10–40 hours per week.

Qualifications

• Experience designing trial protocols for regulatory submission.
• Ability to interpret clinical data for FDA/EMA/regulators.
• Strong background in clinical research methodology or biostatistics.

Responsibilities

• Design and review clinical trial protocols for regulator-ready AI datasets.
• Audit clinical trial results for accuracy and regulatory relevance.
• Evaluate AI-generated analyses for scientific soundness for regulators.
• Provide expert feedback shaping how AI models reason with trial data.
• Help establish quality standards for clinical evidence in AI research.

Skills

Trial protocol design

Regulatory submission experience

Biostatistics

Regulatory knowledge FDA/EMA

Remote work discipline

Tools

AI tools familiarity

Job description

Principal Clinical Scientist (AI Training)

What if your decades of clinical trial expertise could directly influence how AI reasons about medical evidence, regulatory data, and patient outcomes? We're looking for a Principal Clinical Scientist to bring senior-level rigor to the frontier of AI development — ensuring the clinical knowledge embedded in next-generation AI systems meets the highest standards of scientific and regulatory integrity.

About The Role

This is a fully remote, flexible contract role designed for experienced clinical scientists who want to do meaningful work on their own schedule. No AI background required — your deep domain expertise is what matters.

• Organization: Alignerr
• Type: Hourly Contract
• Location: Remote
• Commitment: 10–40 hours/week

What You'll Do

• Design and critically review clinical trial protocols used to generate high-quality, regulator-ready AI training datasets
• Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance
• Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
• Provide expert feedback that directly shapes how AI models reason about clinical trial data, endpoints, and outcomes
• Help establish quality standards for clinical evidence used in cutting-edge AI research workflows

Who You Are

• Senior-level clinical scientist with hands-on experience designing trial protocols for regulatory submission
• Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Naturally rigorous and detail-oriented — you hold clinical evidence to the highest standards
• Comfortable working independently and asynchronously in a remote environment

Nice to Have

• Prior experience with data annotation, data quality review, or evaluation frameworks
• Background in clinical pharmacology, oncology, rare disease, or other specialized therapeutic areas
• Familiarity with AI tools or emerging applications of machine learning in clinical research

Why Join Us

• Work directly on frontier AI systems shaping the future of clinical and biomedical research
• Influence how AI understands, evaluates, and communicates real-world clinical evidence
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, expert-level work
• Collaborate with world-leading AI research teams and labs
• Potential for ongoing work and contract extension as new projects launch