Principal Clinical Scientist for AI Training (Remote)

Alignerr Corp.; Auckland; Remote; NZD 295,000 - 491,000; Part time

Job summary

Alignerr is seeking a Principal Clinical Scientist to guide AI training with senior clinical expertise. You will design and review regulatory-grade trial protocols for AI data powering next-generation systems, ensuring rigor and regulatory alignment across projects.

You will interpret clinical results, audit analyses for regulatory relevance, and provide structured feedback to influence how AI models reason about real-world evidence, working remotely in a flexible, contract role.

Qualifications

• Senior-level clinical professional with hands-on experience designing trial protocols for regulatory submission.
• Deep expertise interpreting clinical data for major regulatory agencies such as FDA/EMA or equivalent.
• Strong grounding in clinical research methodology, biostatistics, translational science, or closely related discipline.
• Rigorous, detail-oriented, and comfortable working independently in a flexible, asynchronous environment.
• Clear and precise communicator — able to document findings and feedback in structured formats.

Responsibilities

• 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 standards (FDA, EMA, or equivalent).
• Evaluate AI-generated clinical analyses for scientific soundness and regulatory relevance.
• Provide structured expert feedback that directly shapes how AI models reason about clinical trial data, outcomes, and evidence.
• Help bridge the gap between frontier AI systems and the real-world standards of clinical research.

Skills

Clinical trial design

Regulatory submissions

Biostatistics

Translational science

Independent work in async environment

Clear communication

Job description

Alignerr is seeking a Principal Clinical Scientist to guide AI training with senior clinical expertise. You will design and review regulatory-grade trial protocols for AI data powering next-generation systems, ensuring rigor and regulatory alignment across projects.

You will interpret clinical results, audit analyses for regulatory relevance, and provide structured feedback to influence how AI models reason about real-world evidence, working remotely in a flexible, contract role.