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Alignerr

Principal Clinical Scientist

London
$40 – $80/hr
Posted about 8 hours ago
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Principal Clinical Scientist (AI Training)

About The Role

What if your years of clinical trial expertise could directly influence how AI understands and evaluates real-world medical evidence? We're looking for a Principal Clinical Scientist to bring senior-level rigor to AI-driven research workflows — ensuring the clinical data that trains and evaluates next-generation AI systems meets the standards expected in real regulatory submissions.

This is a fully remote, flexible contract role built for experienced clinical scientists who want to work at the cutting edge of biomedical AI without leaving their domain behind.

Organization: Alignerr
Type: Hourly Contract
Location: Remote
Commitment: 10–40 hours/week

What You'll Do

  • 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 to ensure accuracy, consistency, and regulatory relevance
  • Evaluate AI-generated clinical analyses for scientific soundness and alignment with FDA, EMA, or equivalent regulatory expectations
  • Provide expert feedback that directly shapes how AI models reason about clinical trial data, endpoints, and outcomes
  • Help establish the scientific standards that frontier AI systems use to understand real-world clinical evidence

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Who You Are

  • Senior clinical scientist with deep, hands-on experience designing clinical trial protocols for regulatory submission
  • Expert in interpreting clinical data for major regulatory agencies — FDA, EMA, or equivalent
  • Strong grounding in clinical research methodology, biostatistics, or translational science
  • Detail-oriented and systematic — you hold data to a high standard and can articulate exactly why
  • Comfortable working independently in an asynchronous, remote environment

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Nice to Have

  • Prior experience with data annotation, data quality review, or evaluation systems
  • Familiarity with AI tools or clinical informatics platforms
  • Background in drug development, medical devices, or digital health research
  • Experience bridging clinical and technical teams across complex research workflows

Why Join Us

  • Work directly on frontier AI systems that are reshaping clinical and biomedical research
  • Influence how AI understands, evaluates, and communicates real-world clinical evidence at scale
  • Fully remote and flexible — work on your own schedule, from anywhere
  • Freelance autonomy with meaningful, expert-level work that matches your seniority
  • Collaborate with leading AI research labs and teams on genuinely novel problems
  • Potential for ongoing work and contract extension as projects evolve
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Skills

Clinical Trial Design
Regulatory Submission
Clinical Data Interpretation
Biostatistics
Translational Science
Data Quality Review
AI Tools
Clinical Informatics
Drug Development
Medical Devices
Digital Health Research
Research Methodology
Asynchronous Work
Expert Feedback
Scientific Standards
AI Evaluation

Location

London, England, United Kingdom

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