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Build and improve pipelines that parse clinical documents and transform them into validated executable modules. Collaborate with clinicians to develop benchmarks and deterministic validators to ensure the safety and correctness of clinical decision systems.
Join a healthtech team building a production compiler that turns clinical standards into structured, executable decision logic. This research-focused role combines rigorous experimentation with production engineering to improve the safety, traceability, and fidelity of clinical decision systems.
Build and improve pipelines that parse clinical documents and transform their content into validated executable modules.
Design and refine a target representation for clinical guideline logic, including rules, exclusions, precedence, and recommendations.
Compare open and closed models, fine-tuning approaches, and constrained decoding through carefully designed experiments.
Develop benchmarks, datasets, metrics, and adversarial cases to assess source fidelity, logical completeness, and recommendation correctness.
Collaborate with clinicians and technical colleagues to turn model failures into hypotheses, experiments, and system improvements.
Develop deterministic validators using static analysis, constraint solving, or formal methods to make ambiguity, contradiction, and gaps in source material explicit.
At least 3 years of research or industry experience, or final-year PhD or postdoctoral experience, with production engineering work beyond research roles.
Experience shipping ML or NLP systems to production and validating model outputs rather than assuming plausible outputs are correct.
Production-level experience with Python, PyTorch, and the Transformers ecosystem, plus experience with LLM evaluation, training, or prompt engineering.
A bachelor's degree or higher in computer science, machine learning, mathematics, or a related technical field.
Clear technical writing about failed experiments, uncertainty, and results, along with comfort working across disciplines in ambiguous settings.
Experience with compilers, program synthesis, formal methods, static analysis, intermediate representations, constraint solving, SAT/SMT, or domain-specific languages is valuable.
Healthcare, safety-critical, or regulated-domain experience is valuable, as is a PhD in a relevant technical field.
Authorization to work remotely in the United States or Canada, and willingness to attend in-person offsites several times per year.
Salary range: $250,000 to $400,000 USD annually. Visa sponsorship is not available.
Remote, with the primary location in Canada. Candidates must be authorized to work in the United States or Canada.
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