Duke University School of Medicine · Computational Biology & Bioinformatics

Kaiyuan Wu

Clinical AI Safety & Governance Scientist

I work on the safety, validation, monitoring, and governance infrastructure that helps high-risk clinical AI move from research prototypes into reliable, auditable healthcare workflows.

vincent.wu [AT] duke.edu Durham, NC

Portrait of Kaiyuan Wu

About

I am a 2nd-year PhD student in Computational Biology and Bioinformatics (CBB) at Duke University School of Medicine and a concurrent MA student in Applied Ethics and Policy with a Tech Ethics & Policy concentration. My work is positioned at the intersection of clinical AI & (multi-)agentic framework, AI safety, monitoring, and governance.

The central question guiding my work is how clinical AI systems can become reliable enough to support care delivery, auditable enough to be governed, and interoperable enough to be translated across real healthcare environments.

Education

Duke University, School of Medicine

Durham, NC · Aug 2024 – Dec 2028

PhD, Computational Biology and Bioinformatics. Concurrent MS, Applied Science and Policy, Tech Ethics concentration. Cumulative GPA: 3.955.

Selected graduate coursework: Deep Learning; Computational Sequence Biology; Intelligent Agents; Clinical Bioethics and Policy; Communicating Science Policy; Digital Intelligence; Advanced Web Application Development.

Rice University

Houston, TX · Aug 2020 – May 2024

BS, Bioengineering. BA, Statistics.

Research Mission

My proposed research endeavor is to develop, validate, and translate safety and governance frameworks for high-risk clinical artificial intelligence systems in U.S. healthcare. The work focuses on agentic clinical decision support, FHIR-based care planning, multimodal clinical prediction, continuous monitoring, and risk-control mechanisms for real-world deployment.

The practical need is clear: as clinical AI increasingly moves into discharge planning, critical care support, imaging, disease trajectory prediction, and hospital workflow optimization, model performance alone is not enough. AI systems must be clinically aligned, monitored after deployment, resilient to failure modes, and governed in ways that protect patients while supporting clinicians.

The broader value of this mission is system-level. Safe clinical AI governance is not limited to one model, one hospital, or one employer. Methods for validation, monitoring, bias detection, risk control, and workflow integration can support and scale across hospitals, research institutions, public health settings, and healthcare technology platforms that need trustworthy AI infrastructure.

In this sense, my work supports the safe translation of clinical AI from research prototypes into governable, monitorable, and clinically reliable healthcare infrastructure.

Research Focus

These research areas are organized around a single objective: building the technical and governance layer between AI innovation and responsible clinical deployment.

Clinical AI safety and governance
Evaluation, monitoring, and governance frameworks for high-risk AI systems in clinical settings, including asymmetric risk evaluation, runtime safety surveillance, audit design, and post-deployment oversight.
Agentic clinical decision support
Multi-agent systems for discharge planning and critical care decision support, with emphasis on guideline recall, self-improvement, counterfactual simulation, clinician-in-the-loop design, and failure-aware planning.
Multimodal clinical prediction
Models that integrate EHR, imaging, text, waveforms, and multi-site clinical datasets for trajectory prediction, risk identification, and care-planning support.

Publications and Preprints

  1. Planner-Auditor Twin: Agentic Discharge Planning with FHIR-Based LLM Planning, Guideline Recall, Optional Caching and Self-Improvement.
    Wu K, Nagori A, Kamaleswaran R. arXiv preprint arXiv:2601.21113, 2026. Preprint
  2. CXR-TFT: Multi-modal Temporal Fusion Transformer for Predicting Chest X-Ray Trajectories.
    Arora M, Ali A, Wu K, Davis C, Shimazui T, Alwakeel M, Moas V, Yang P, et al. International Conference on Medical Image Computing and Computer-Assisted Intervention (MICCAI), 2025.
  3. The detection, function, and therapeutic potential of RNA 2’-O-methylation.
    Wu K, Li Y, Yi Y, Yu Y, Wang Y, Zhang L, Cao Q, Chen K. The Innovation Life, 3(1), 100112, 2024.
  4. The therapeutic potential of targeting the CHD protein family in cancer.
    Zhang M, Wu K, Zhang W, Lin X, Cao Q, Zhang L, Chen K. Pharmacology & Therapeutics, 256, 108610, 2024.
  5. Exploring hippocampus segmentation on unbalanced data set using U-Net-based models.
    Wu K. Applied and Computational Engineering, 6, 758–763, 2023.
  6. The effect of selective c-MET inhibitor on hepatocellular carcinoma in the MET-active, β-catenin-mutated mouse model.
    Zhan N, Michael AA, Wu K, Zeng G, Bell A, Tao J, Monga SP. Gene Expression, 18(2), 135, 2018.

Translation, Intellectual Property, and Governance

Intellectual property

Grant contributions

Governance and stakeholder engagement

Technical Skills

Contact

Email: vincent.wu [AT] duke.edu
Institution: Duke University School of Medicine, Durham, NC