Senior Clinical Scientist, AI Training (Remote)

Alignerr Corp.; United States; Remote; AUD 138,000 - 248,000; Part time

Job summary

Alignerr Corp. is seeking a Principal Clinical Scientist (AI Training) to bring senior clinical and regulatory expertise to cutting-edge AI development.

You will help ensure AI models handling clinical data meet real-world regulatory standards, working remotely on a flexible hourly contract. You will design and review protocols, interpret trial results for regulatory relevance, and provide structured feedback to improve AI reasoning about clinical evidence, all while maintaining strict

Qualifications

• Senior-level experience designing and reviewing clinical trial protocols for regulatory submission.
• Deep expertise interpreting clinical data for regulatory agencies (FDA/EMA or equivalents).
• Strong background in clinical research methodology and biostatistics.
• Rigorous, detail-oriented with ability to critique scientific content.
• Ability to provide structured written feedback on AI-derived clinical analyses.

Responsibilities

• Design and review clinical trial protocols used to generate high-quality, regulator-ready training datasets for AI systems.
• 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, structured feedback to help AI models reason accurately about trial data and evidence.
• Flag errors, inconsistencies, and methodological gaps in AI-generated clinical content.
• Work independently and asynchronously — fully on your own schedule.

Skills

Clinical trial design

Regulatory submissions

Regulatory science

Biostatistics

Critical thinking

Job description

Alignerr Corp. is seeking a Principal Clinical Scientist (AI Training) to bring senior clinical and regulatory expertise to cutting-edge AI development.

You will help ensure AI models handling clinical data meet real-world regulatory standards, working remotely on a flexible hourly contract. You will design and review protocols, interpret trial results for regulatory relevance, and provide structured feedback to improve AI reasoning about clinical evidence, all while maintaining strict