Principal Clinical Scientist

Alignerr Corp.; Christchurch; À distance; GBP 110 000 - 165 000; Plein temps

Résumé du poste

Alignerr is seeking a Principal Clinical Scientist (AI Training) to bring senior-level clinical trial expertise to AI-driven research workflows, ensuring regulatory-ready data for next‑generation AI systems.

This fully remote hourly contract offers flexible hours and the opportunity to influence how clinical evidence informs AI reasoning, regulatory expectations, and patient outcomes.

Qualifications

• Senior-level clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission.
• Deep expertise interpreting clinical data for regulatory agencies (FDA/EMA or equivalent).

Responsabilités

• Design and review clinical trial protocols used to generate high-quality, regulator-ready AI training datasets.
• 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 agency expectations.
• Provide expert feedback that shapes how AI models reason about clinical trial data, endpoints, and outcomes.
• Help establish quality standards for how clinical evidence is represented and evaluated within AI systems.

Description du poste

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, regulatory submissions, and patient outcomes? 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 exacting standards of real-world regulatory practice.

This is a fully remote, flexible contract role built for experienced clinical scientists who want to work at the frontier of biomedical AI without leaving their area of expertise.

• 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 AI training datasets
• 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 agency expectations
• Provide expert feedback that shapes how AI models reason about clinical trial data, endpoints, and outcomes
• Help establish quality standards for how clinical evidence is represented and evaluated within AI systems

Who You Are

• Senior-level clinical scientist with hands-on experience designing clinical trial protocols for regulatory submission
• Deep expertise interpreting clinical data for regulatory agencies (FDA, EMA, or equivalent)
• Strong grounding in clinical research methodology, biostatistics, or translational science
• Rigorous, detail-oriented thinker who can identify gaps between AI-generated outputs and real-world regulatory standards
• Comfortable working independently and asynchronously in a remote environment

Nice to Have

• Prior experience with data annotation, data quality evaluation, or AI training workflows
• Background in pharmacovigilance, medical affairs, or clinical data management
• Familiarity with ICH guidelines, GCP, or similar regulatory frameworks
• Experience reviewing or contributing to regulatory dossiers or clinical study reports

Why Join Us

• Work directly on frontier AI systems shaping the future of clinical and biomedical research
• Fully remote and flexible — structure your hours around your existing commitments
• Freelance autonomy with the substance of high-impact, intellectually demanding work
• Influence how AI understands, evaluates, and reasons about real-world clinical evidence
• Collaborate with leading AI research teams and labs at the cutting edge of the field
• Potential for ongoing work and contract extension as new projects launch