Remote Senior Clinical Scientist – AI Training & Regulatory Data

Alignerr Corp.; Oxford; Remote; GBP 83,000 - 165,000; Part time

Benefits offered by this job

Fully remote

Flexible hours

Contract extension potential

Job summary

Alignerr is seeking a Principal Clinical Scientist to shape AI training with rigorous clinical trials and regulator-ready data. This fully remote hourly contract role demands senior expertise in designing trial protocols and interpreting data for FDA/ EMA submissions, ensuring AI models meet high scientific standards.

You’ll work asynchronously across disciplines, providing expert feedback to improve how AI reasons about clinical evidence while maintaining regulatory discipline and scientific

Qualifications

• Senior-level experience designing clinical trial protocols for regulatory submission.
• Experience interpreting clinical data for agencies such as the FDA/EMA or equivalent.
• Strong grounding in biostatistics or translational science.
• Rigorous mindset with AI-generated outputs; high standards for evidence.
• Clear, precise written communication; ability to provide actionable feedback.
• Self-directed and reliable when working independently.

Responsibilities

• Design and review clinical trial protocols used to generate regulator-ready datasets for AI training.
• Interpret and audit clinical trial results to ensure accuracy and regulatory relevance.
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory alignment.
• Identify gaps and weaknesses in how AI reasons about clinical data and outcomes.
• Provide structured feedback to improve AI understanding of clinical evidence.
• Work independently and asynchronously on your own schedule.

Skills

Clinical trial design

Regulatory submissions

Data interpretation

Biostatistics

Regulatory science

Scientific communication

Independent work

Job description

Alignerr is seeking a Principal Clinical Scientist to shape AI training with rigorous clinical trials and regulator-ready data. This fully remote hourly contract role demands senior expertise in designing trial protocols and interpreting data for FDA/ EMA submissions, ensuring AI models meet high scientific standards.

You’ll work asynchronously across disciplines, providing expert feedback to improve how AI reasons about clinical evidence while maintaining regulatory discipline and scientific