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About

About

Paul Steven

Program Lead Biostatistician · 13+ years across oncology, biomarker development and companion diagnostics.

I specialise in adaptive trial design for biomarker-driven oncology, with a focus on complex and non-standard study endpoints across clinical, translational, and device applications. I bring a strong biological and assay-level understanding — including mechanistic pathways, molecular diagnostics and translational biomarkers — to ensure statistical approaches are aligned with underlying science and program decision-making.

I actively contribute to scientific knowledge-sharing through publications, presentations, and analytical tools.

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What I Work On

  • Bayesian Adaptive Trial Design — dose escalation (BOIN), dose expansion (MATS), biomarker-driven trials (basket, adaptive enrichment)
  • Translational & Non-Traditional Endpoints — PD, ctDNA, MRD, analytical device output across a range of indications
  • Assay Development & Validation — statistical leadership for IVD and companion diagnostic programs
  • Simulation Frameworks — dose-response, biomarker thresholds, and design operating characteristics
  • Core Therapy Areas and Software - Oncology, Infectious Disease, Rare (including Opthalmology), IVDs. SAS, PASS, R (shiny), nQuery.

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