Principal Clinical Scientist

Alignerr Corp.; Greater London; A distancia; GBP 14.000 - 55.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible schedule

Remote work

Contract extension potential

Descripción de la vacante

Alignerr is seeking a Principal Clinical Scientist (AI Training) to steer clinical trial design and data quality for AI training and evaluation. This fully remote, hourly contract role requires senior expertise in regulatory submissions and biostatistics to ensure regulator-ready datasets for AI systems.

You will interpret trial results, audit analyses for regulatory relevance, and provide expert feedback that shapes how AI models reason about clinical evidence at scale.

Formación

• Senior clinical scientist with hands-on experience designing trial protocols for regulatory submission.
• Expert interpreting clinical data for major regulatory agencies (FDA/EMA).
• Strong grounding in biostatistics or translational science.
• Detail-oriented, methodical, able to articulate data quality issues clearly.
• Comfortable working independently in a remote environment.

Responsabilidades

• Design and review clinical trial protocols to generate regulator-ready datasets for AI training and evaluation.
• Interpret and audit 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 interpret real-world evidence.

Conocimientos

Clinical trial design

Regulatory submissions

Biostatistics

Translational science

AI tools familiarity

Herramientas

AI tools familiarity

Descripción del empleo

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