Principal Clinical Scientist - AI Training (Remote) in Edinburgh

Principal Clinical Scientist - AI Training (Remote) in Edinburgh

Edinburgh Full-Time 10 - 40 Β£ / hour (est.) No working from home possible
Alignerr

At a Glance

  • Tasks: Shape AI development by designing trial protocols and interpreting clinical data.
  • Company: Alignerr, a leader in AI-driven clinical solutions.
  • Benefits: Flexible remote work, competitive hourly pay, and the chance to influence AI in healthcare.
  • Other info: Part-time hours with a focus on innovation and excellence.
  • Why this job: Make a real impact on AI's role in clinical research and regulatory standards.
  • Qualifications: Senior-level clinical expertise and experience in AI applications.

The predicted salary is between 10 - 40 Β£ per hour.

Alignerr is seeking a Principal Clinical Scientist to bring senior-level clinical rigor into AI development. This fully remote contract role involves shaping how AI reasons about clinical data for regulators and researchers.

You will design trial protocols, interpret results, and audit AI analyses to FDA/EMA expectations, delivering expert feedback and setting the standard for trustworthy clinical reasoning in AI systems.

10–40 hours/week, hourly contract.

Principal Clinical Scientist - AI Training (Remote) in Edinburgh employer: Alignerr

Alignerr is an exceptional employer that champions innovation in healthcare through AI, offering a dynamic remote work environment that fosters collaboration and creativity. Employees benefit from a culture of continuous learning and professional development, with ample opportunities to grow within the organisation while contributing to groundbreaking projects that have a real impact on clinical research. Join us to be part of a forward-thinking team dedicated to transforming healthcare for the better.

Alignerr

Contact Details:

Alignerr Recruitment Team

We think you need these skills to ace Principal Clinical Scientist - AI Training (Remote) in Edinburgh

Clinical Rigor
AI Development
Trial Protocol Design
Data Interpretation
Audit Skills
Regulatory Knowledge (FDA/EMA)
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