Senior Clinical Scientist for AI Training - Remote

Alignerr Corp.; Auckland; À distance; NZD 165 000 - 262 000; Temps partiel

Résumé du poste

Alignerr is seeking a Principal Clinical Scientist to provide senior clinical expertise for AI development. You will design regulator-ready trial protocols, interpret results for regulatory alignment, and evaluate AI-derived analyses to ensure scientific soundness and regulatory relevance.

Remote, hourly contract role with flexible hours (10–40 hours/week). You will collaborate with world-leading AI research teams to shape how AI understands clinical evidence for regulatory submissions.

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 the FDA, EMA, or equivalent.
• Strong grounding in clinical research methodology, biostatistics, translational science, or a closely related discipline.

Responsabilités

• 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.

Connaissances

Clinical trial design

Regulatory submissions

Biostatistics

Translational science

Independent work

Formation

Clinical research degree

Outils

Data annotation tools

AI evaluation workflows

Description du poste

Alignerr is seeking a Principal Clinical Scientist to provide senior clinical expertise for AI development. You will design regulator-ready trial protocols, interpret results for regulatory alignment, and evaluate AI-derived analyses to ensure scientific soundness and regulatory relevance.

Remote, hourly contract role with flexible hours (10–40 hours/week). You will collaborate with world-leading AI research teams to shape how AI understands clinical evidence for regulatory submissions.