Senior Clinical Scientist, AI Training - Remote

Alignerr Corp.; Greater London; Remote; GBP 14,000 - 55,000; Full time

Benefits offered by this job

Flexible schedule

Remote work

Contract extension potential

Job summary

Alignerr is seeking a Principal Clinical Scientist (AI Training) to steer clinical trial design and data quality for AI training and evaluation. This fully remote, hourly contract role requires senior expertise in regulatory submissions and biostatistics to ensure regulator-ready datasets for AI systems.

You will interpret trial results, audit analyses for regulatory relevance, and provide expert feedback that shapes how AI models reason about clinical evidence at scale.

Qualifications

• Senior clinical scientist with hands-on experience designing trial protocols for regulatory submission.
• Expert interpreting clinical data for major regulatory agencies (FDA/EMA).
• Strong grounding in biostatistics or translational science.
• Detail-oriented, methodical, able to articulate data quality issues clearly.
• Comfortable working independently in a remote environment.

Responsibilities

• Design and review clinical trial protocols to generate regulator-ready datasets for AI training and evaluation.
• Interpret and audit trial results for accuracy, consistency, and regulatory relevance.
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory alignment.
• Provide expert feedback shaping how AI models reason about trial data, endpoints and outcomes.
• Help establish scientific standards frontier AI systems use to interpret real-world evidence.

Skills

Clinical trial design

Regulatory submissions

Biostatistics

Translational science

AI tools familiarity

Tools

AI tools familiarity

Job description

Alignerr is seeking a Principal Clinical Scientist (AI Training) to steer clinical trial design and data quality for AI training and evaluation. This fully remote, hourly contract role requires senior expertise in regulatory submissions and biostatistics to ensure regulator-ready datasets for AI systems.

You will interpret trial results, audit analyses for regulatory relevance, and provide expert feedback that shapes how AI models reason about clinical evidence at scale.