Senior Clinical Scientist: AI Training & Regulatory

Alignerr Corp.; Spain; Remote; EUR 152,000 - 262,000; Full time

Benefits offered by this job

Fully remote

Freelance autonomy

Job summary

Alignerr is seeking a Principal Clinical Scientist (AI Training) to bring senior-level rigor to AI-driven clinical research workflows. You will design and review protocols, audit results, and ensure regulatory relevance for FDA/EMA standards.

This fully remote hourly contract role offers flexible scheduling and ongoing collaboration with AI research teams. The ideal candidate has deep regulatory expertise and a proven track record in clinical trial design, biostatistics, and translational

Qualifications

• Senior-level clinical scientist with hands-on experience designing and reviewing clinical trial protocols for regulatory submission.
• Deep expertise interpreting clinical data for agencies such as FDA/EMA or equivalents.
• Strong command of clinical research methodology and biostatistics.

Responsibilities

• Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets for AI training and evaluation.
• Interpret and audit clinical trial results, ensuring accuracy and regulatory relevance.
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory alignment.
• Identify gaps and weaknesses in how AI models reason about clinical outcomes and trial methodology.
• Provide structured expert feedback that improves how frontier AI systems understand real-world clinical evidence.
• Work independently and asynchronously—fully on your own schedule.

Skills

Clinical trial design

Regulatory submissions

Biostatistics

Regulatory affairs knowledge

Education

PhD in clinical sciences or MD/PhD

Tools

Data annotation tools

Job description

Alignerr is seeking a Principal Clinical Scientist (AI Training) to bring senior-level rigor to AI-driven clinical research workflows. You will design and review protocols, audit results, and ensure regulatory relevance for FDA/EMA standards.

This fully remote hourly contract role offers flexible scheduling and ongoing collaboration with AI research teams. The ideal candidate has deep regulatory expertise and a proven track record in clinical trial design, biostatistics, and translational