Principal Clinical Scientist

Alignerr; Charlotte (AR); Teletrabalho; USD 138 000 - 207 000; Tempo parcial

Resumo da oferta

Alignerr is seeking a Principal Clinical Scientist (AI Training) for a fully remote hourly contract. You will bring senior clinical trial design and regulatory expertise to AI training data and evaluation, ensuring regulator-ready datasets and robust scientific standards.

The role emphasizes independent, asynchronous work with flexible hours, collaborating with leading AI研究 teams and labs, and potential for ongoing engagements as new projects launch.

Qualificações

• Senior-level experience designing clinical trial protocols for regulatory submission.
• Deep expertise interpreting clinical data for agencies such as FDA/EMA or equivalents.
• Strong grounding in clinical research methodology and biostatistics.

Responsabilidades

• Design and review clinical trial protocols used for AI training data.
• Interpret and audit trial results to ensure regulatory alignment.
• Evaluate AI-generated clinical analyses for scientific rigor.
• Provide structured feedback to improve AI model reasoning on clinical data.

Conhecimentos

Clinical trial design

Regulatory interpretation

Biostatistics

Clear writing

Ferramentas

AI tools

Data annotation

Descrição da oferta de emprego

Principal Clinical Scientist (AI Training)

About The Role

What if your deep expertise in clinical trial design and regulatory science 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 frontier AI research — helping ensure that the clinical intelligence built into next-generation AI systems meets the standards expected in real regulatory submissions. This is a fully remote, flexible contract role designed for experienced clinical scientists who want to do meaningful work at the intersection of medicine and AI — on their own schedule.

• 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 alignment with regulatory expectations
• Evaluate AI-generated clinical analyses for scientific soundness and methodological rigor
• Provide expert, structured feedback that directly improves how AI models reason about clinical trial data, endpoints, and outcomes
• Work independently and asynchronously — fully on your own schedule

Who You Are

• Senior-level experience designing clinical trial protocols intended for regulatory submission
• Deep expertise interpreting clinical data for agencies such as the FDA, EMA, or equivalent international bodies
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Naturally detail-oriented with a systematic, evidence-driven approach to evaluation
• Clear and precise written communicator — able to articulate complex scientific reasoning in structured feedback

Nice to Have

• Prior experience with data annotation, data quality assurance, or evaluation systems
• Familiarity with AI tools or clinical informatics platforms
• Background in pharmacology, oncology, rare disease, or another specialist therapeutic area
• Experience contributing to regulatory dossiers, CTD submissions, or scientific advisory processes

Why Join Us

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