Principal Clinical Scientist

Principal Clinical Scientist (AI Training) About The Role What if your career-long expertise in clinical trial design and regulatory science could directly shape how AI understands and reasons about clinical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to frontier AI research — ensuring the models influencing biomedical science are grounded in real-world regulatory standards. This is a fully remote, flexible contract role built for experienced clinical scientists who want to contribute to something genuinely new. No AI background required — just deep command of clinical trial methodology and regulatory data interpretation. Organization: Alignerr Type: Hourly Contract Location: Remote Commitment: 10–40 hours/week What You'll Do Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training Interpret and audit clinical trial results for accuracy, consistency, and regulatory relevance Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations (FDA, EMA, or equivalent) Provide expert feedback that directly shapes how AI models reason about clinical trial data, outcomes, and methodology Help define standards for how cutting-edge AI systems engage with biomedical and clinical research evidence Who You Are Senior clinical scientist with hands-on experience designing protocols for regulatory submission Deep expertise interpreting clinical data for regulatory agencies such as FDA, EMA, or equivalent bodies Strong command of clinical research methodology, biostatistics, or translational science Naturally rigorous — you hold your work to the standard that real submissions demand Detail-oriented and able to clearly communicate complex scientific reasoning in writing Comfortable working independently and asynchronously Nice to Have Prior experience with data annotation, data quality review, or evaluation systems Background in pharmacology, epidemiology, or health technology assessment Familiarity with AI tools or data-driven research platforms Why Join Us Work directly on frontier AI systems with real impact on clinical and biomedical research Influence how AI understands, evaluates, and communicates real-world clinical evidence Fully remote and flexible — work on your own schedule, from anywhere Freelance autonomy with the substance 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

The Principal Clinical Scientist will design and review clinical trial protocols to generate high-quality datasets for AI training. They will also audit clinical trial results and evaluate AI-generated analyses to ensure alignment with regulatory standards.

Candidates must be senior clinical scientists with extensive experience in designing protocols for regulatory submissions and interpreting clinical data. Strong expertise in clinical research methodology, biostatistics, or translational science is required.

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical trial design
• Regulatory science
• Biomedical research
• Data interpretation
• Protocol design
• Biostatistics
• Translational science
• Regulatory submission
• Data annotation
• Data quality review
• Pharmacology
• Epidemiology
• Health technology assessment
• Scientific reasoning
• AI training

• Science & Research
• Healthcare
• Technology
• Data & Analytics

Expérience minimale

10+ ans

Postuler avant le

11 sept. 2026

Langue de l’offre

anglais

Heures de travail

40 heures par semaine

Exigences de lieu

Country, Edmonton, Alberta, Canada

Niveau d’expérience

Mid-Senior level