Principal Clinical Scientist

Alignerr Corp.; França; Teletrabalho; EUR 165 000 - 248 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Fully remote

Flexible schedule

Contract-based work

Resumo da oferta

Alignerr is seeking a Principal Clinical Scientist to infuse senior clinical trial expertise into the development of AI systems for biomedical research. This fully remote hourly contract role emphasizes regulatory science and rigorous data interpretation.

The position requires deep clinical research experience and regulatory proficiency, with flexible hours between 10 and 40 per week. Join a team shaping how AI reasons about real-world clinical evidence.

Qualificações

• Experience designing clinical trial protocols for regulatory submission.
• Strong understanding of regulatory expectations from FDA/EMA or equivalents.
• Solid background in biostatistics and clinical research methodology.

Responsabilidades

• Design and review protocols to generate regulator-ready training data for AI systems.
• Interpret and audit trial results to ensure regulatory relevance and accuracy.
• Evaluate AI-generated analyses for scientific soundness and regulatory alignment.
• Provide expert feedback that shapes how AI models reason about trial data.
• Flag methodological gaps or regulatory misalignments in AI outputs.
• Work independently and asynchronously to meet project needs.

Conhecimentos

Clinical trial design

Regulatory submissions

Biostatistics

Regulatory compliance

FDA/EMA knowledge

Effective communication

Descrição da oferta de emprego

Principal Clinical Scientist (AI Training)

About The Role

What if your years of clinical trial expertise could directly influence how AI reasons about medical evidence, patient outcomes, and regulatory science? We're looking for a Principal Clinical Scientist to bring senior-level clinical knowledge into the development of cutting-edge AI systems — helping ensure the models shaping the future of biomedical research actually get the science right.

This is a fully remote, flexible contract role built for experienced clinical scientists who want to do meaningful work on their own terms. No AI background needed — just deep expertise in clinical research and regulatory standards.

• 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 training datasets for AI systems
• 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, study design, and real-world outcomes
• Flag methodological gaps, statistical inconsistencies, or regulatory misalignments in AI outputs
• Work independently and asynchronously — on your schedule, at your pace

Who You Are

• Senior clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
• Deep expertise interpreting clinical data for major regulatory agencies (FDA, EMA, or equivalent)
• Strong command of clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented, and confident making complex scientific judgments
• Clear and precise written communicator who can document feedback systematically

Nice to Have

• Prior experience with data annotation, data quality review, or AI evaluation workflows
• Background in pharmacology, epidemiology, medical affairs, or health outcomes research
• Experience authoring or reviewing regulatory submissions (INDs, NDAs, CTDs, or similar)
• Familiarity with AI tools or clinical decision support systems as an end user

Why Join Us

• Work directly on frontier AI systems making an impact on clinical and biomedical research
• Fully remote and flexible — work when and where it suits you
• Freelance autonomy with the structure of meaningful, expert-level task-based work
• Influence how AI understands, evaluates, and communicates real-world clinical evidence
• Collaborate with world-leading AI research teams and labs
• Potential for ongoing work and contract extension as new projects launch