Remote Principal Clinical Scientist for AI-Regulated Trials

Alignerr Corp.

Manchester

Remote

GBP 83,000 - 165,000

Part time

4 hours ago
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Job summary

Alignerr is seeking a Principal Clinical Scientist (AI Training) for a fully remote hourly contract. You will design and review clinical trial protocols to generate regulatory-grade data for AI training, and audit results for accuracy and regulatory alignment.

You will interpret AI-generated analyses for regulatory expectations (FDA/EMA) and provide expert feedback to improve AI model reasoning on clinical data and endpoints. Flexible, high-stakes scientific work awaits.

Qualifications

  • Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission.
  • Deep familiarity with interpreting clinical data for regulatory agencies (FDA/EMA).
  • Solid grounding in clinical research methodology and biostatistics.
  • Meticulous, systematic approach ensuring data quality and regulatory alignment.

Responsibilities

  • Design and review clinical trial protocols used to generate regulatory-grade data for AI training.
  • Interpret and audit trial results to ensure accuracy and regulatory standards.
  • Evaluate AI-generated clinical analyses for scientific soundness and regulatory compliance.
  • Provide structured expert feedback to improve AI models' reasoning on trial data and endpoints.
  • Define the standard of scientific quality for clinical content used in frontier AI systems.

Skills

Trial design
Regulatory submissions
Biostatistics
Regulatory interpretation
Written evaluations

Tools

AI evaluation tools

Job description

Alignerr is seeking a Principal Clinical Scientist (AI Training) for a fully remote hourly contract. You will design and review clinical trial protocols to generate regulatory-grade data for AI training, and audit results for accuracy and regulatory alignment.

You will interpret AI-generated analyses for regulatory expectations (FDA/EMA) and provide expert feedback to improve AI model reasoning on clinical data and endpoints. Flexible, high-stakes scientific work awaits.

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