Principal Clinical Scientist

Alignerr

Greater London

Remote

GBP 83.000 - 131.000

Teilzeit

vor 28 Stunden
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Benefits dieser Stelle

Fully remote
Flexible schedule
Contract extension

Zusammenfassung

Alignerr is recruiting a Principal Clinical Scientist (AI Training) for a fully remote hourly contract. You will lead the design and review of clinical trial protocols to create regulator-ready datasets for AI training and evaluation, ensuring alignment with FDA/EMA expectations.

You will interpret trial results, audit data quality, and provide expert feedback that shapes AI model reasoning on clinical endpoints and outcomes, with autonomy in a flexible remote setting.

Qualifikationen

  • Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission.
  • Expert in interpreting clinical data for agencies such as FDA/EMA.
  • Strong grounding in biostatistics or translational science.
  • Detail-oriented and able to work independently in a remote environment.

Aufgaben

  • Design and review clinical trial protocols used to generate regulator-ready datasets for AI training.
  • Interpret and audit clinical trial results for accuracy, consistency and regulatory relevance.
  • Evaluate AI-generated clinical analyses for scientific soundness and regulatory alignment.
  • Provide expert feedback shaping how AI models reason about trial data, endpoints and outcomes.
  • Help establish scientific standards frontier AI systems use to understand real-world evidence.

Kenntnisse

Clinical trial design
Regulatory submissions
Biostatistics
Data interpretation
Remote work

Tools

Data annotation
Data quality review
AI tools
Clinical informatics

Jobbeschreibung

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
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
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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