Principal Clinical Scientist

Alignerr; Montreal; Remote; CAD 103,000 - 248,000; Full time

Benefits offered by this job

Remote work

Flexible schedule

Freelance contract with project-based续

Job summary

Alignerr is seeking a Principal Clinical Scientist (AI Training) to bring senior clinical trial expertise to the development of regulator-ready AI training data. This fully remote hourly contract role emphasizes independent, rigorous work on clinical evidence and regulatory alignment.

You will design and review trial protocols, interpret results for FDA/EMA-style regulators, and provide expert feedback shaping how AI models reason about endpoints and outcomes.

Qualifications

• Must have hands-on experience designing trial protocols for regulatory submission.
• Strong ability to interpret clinical data for regulatory agencies (FDA/EMA or equivalent).
• Proficient in biostatistics and translational science methodologies.

Responsibilities

• Design and critically review clinical trial protocols used to generate 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 regulatory alignment.
• Provide expert feedback that shapes how AI models reason about trial data, endpoints, and outcomes.
• Help establish quality standards for clinical evidence used in AI research workflows.

Skills

Clinical trial design

Regulatory submission experience

Biostatistics

Regulatory compliance

Independent remote work

Education

Master's or PhD in clinical science/biostatistics

Regulatory affairs certification

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