Dominic Tong

Dominic Tong, Ph.D.

Principal Bioengineer Data Scientist | Pharmacometrics, Machine Learning & AI

I'm a pharmacometrician and data scientist. I build hybrid machine learning and population PK/⁠PD models for precision dosing, used in 1,000+ U.S. hospitals, and now bring agentic AI to model-informed drug development.

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Professional Experience

  1. 2020 – present

    Principal Bioengineer Data ScientistFeb. 2025 – present

    InsightRX — San Francisco, CA / remote

    I lead pharmacometric and machine learning model development for a precision-dosing platform deployed across 1,000+ U.S. hospitals; five of my population PK models are live in the platform.

    • Shaped an AI-native agentic workflow that runs clinical pharmacology analyses for pharma drug development (InsightRX Astra) as its domain expert: ran user testing, recommended UI and workflow fixes, and presented product demos to 5 pharma clients and 45 participants in an ACoP workshop
    • Designed the GxP validation package for this agentic AI platform: human testing plus programmatic validation of nondeterministic outputs, intended to run each release
    • Led scientific direction and a large-scale quasi-experimental study across 90,295 patients in 19 hospital systems, demonstrating that pharmacokinetic model selection meaningfully improves vancomycin AUC target attainment and reduces AKI rates in precision dosing contexts
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    • Developed the first population PK model to pool multiple aminoglycosides across the human lifespan, using real-world data from 5,659 patients across 130+ sites; now deployed in the platform
    • Identified and corrected a systematic serum creatinine rounding bias in elderly patients that degraded renal function estimation and vancomycin/⁠aminoglycoside dosing accuracy; the corrected model is now deployed in routine clinical care
    • Developed and validated a novel vancomycin population PK model for critically ill patients on continuous renal replacement therapy using real-world data from 2,409 patients across 91 sites, outperforming five published models in predictive accuracy; now deployed in the platform
    • Led ML development on a cross-institutional collaboration with Memorial Sloan Kettering — feature engineering, algorithm selection, and evaluation — producing a hybrid PK/⁠PD-ML model that improved grade 3–4 neutropenia prediction precision from 47% to 61% across 9,121 patients
    • Directed simulation-based analysis identifying precision dosing failures in a pharma client's conditioning regimen; presented recommendations directly to clinical decision-makers, resulting in a redesigned trial dosing strategy
    • Built the analytics ETL pipeline behind real-time monitoring software supporting pharma drug development decisions, and presented the platform at ACoP
    • Mentored a summer intern, now a senior engineer in medical devices
    • Prototyped an LLM agent-based tool (GPT-4o) to assist pharmacometricians in NONMEM model development, then partnered with Pfizer to evaluate a more advanced version of this tool for pharmacometric model development against a manual workflow
    • Led a tri-institutional collaboration with Lucile Packard Children's Hospital (Stanford) and Children's Hospital of Philadelphia to develop a pediatric voriconazole population PK model and optimized sampling strategies for model-informed precision dosing

    Previously: Senior Bioengineer Data Scientist (2020–2025); Bioengineer Data Scientist (2020)

  2. 2019

    Health Data Science Fellow

    Insight Data Science — San Francisco, CA

    • Built a support vector machine classifier to predict the toxicity of 1,036 drugs in the FDA's Drug Induced Liver Injury data set using scikit-learn and pandas with 77% accuracy
  3. 2014 – 2019

    Doctoral Researcher

    University of California, San Francisco — San Francisco, CA

    • Developed a novel computational model that mimics complex diseases based on genetic data and evolutionary parameters to enable GWAS performance comparisons
    • Showed that sampling cases and controls from the extremes of a quantitative trait gives rare-variant association tests their highest statistical power
    • Discovered that methods for finding rare mutations causing disease are missing a vast amount of causal mutations when rare mutations explain most of the disease
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    • Demonstrated that using inexpensive genotyping arrays and imputation detects 90% of the associations identified by the much more expensive whole genome sequencing, potentially increasing sample size by 10-fold in any association study

Leadership & Service

  1. 2025 – present

    Chair-electOct. 2026 – present

    ISoP/ACCP Clinical Pharmacometrics Special Interest Group

    • A joint special interest group of the International Society of Pharmacometrics (ISoP) and the American College of Clinical Pharmacology (ACCP), the field's principal professional societies, focused on advancing pharmacometrics in patient care
    • Promote application of pharmacometrics to direct patient care and foster an international group of scientists and clinicians across therapeutic areas

    Previously: Vice-Chair (2026); Scientific Secretary (2025)

  2. 2025 – present

    Abstract Committee Member, Clinical PMX SIG Representative

    American Conference on Pharmacometrics (ACoP) Abstract Committee

    • Serve as the Clinical Pharmacometrics SIG's representative to the ACoP abstract review committee, evaluating submitted abstracts for scientific merit and selecting recipients of the conference's trainee awards
    • ACoP is the premier annual scientific meeting in the field

Publications

Presentations

Peer Review

Invited manuscript reviewer for thirteen international peer-reviewed journals across pharmacometrics, antimicrobials, and clinical medicine. Seventeen reviews completed, 2025–2026:

Education

  1. 2019

    Ph.D. in Bioengineering

    University of California, Berkeley – UC San Francisco

    My thesis simulated genetic association studies across study designs and disease architectures to find which designs can detect rare disease variants: the same simulate-then-infer approach I now use in pharmacometrics.

    • Thesis: Population genetic simulation study of power in association testing across genetic architectures and study designs (advisor: Ryan D. Hernandez)
  2. 2014

    Bachelor of Applied Science in Engineering Physics (Electrical option)

    University of British Columbia

    • Combines electrical engineering, applied physics, and emphasis on innovation

Awards

2025

Top Poster Ribbon

American Society for Clinical Pharmacology and Therapeutics (ASCPT) Annual Meeting

  • Agentic AI platform for PK/⁠PD analysis, developed with Pfizer
2015

Postgraduate Scholarship – Doctoral (PGS D)

Natural Sciences and Engineering Research Council of Canada (NSERC)

  • National award for academic performance, research potential, and excellence in natural sciences and engineering

Skills and Expertise

Pharmacometrics

population PK/PD modelingmodel-informed precision dosingsimulation-based trial design

Machine Learning & AI

hybrid ML/PK/PD modelingagentic AI for MIDDAI validation (GxP)deep learning

Software

NONMEMR (tidyverseShiny)Python (pandasscikit-learnXGBoost)Dockergit