Consulting

Statistical consulting for clinical researchers, medical teams, and data-driven organizations.

Who I work with

Physicians & clinicians

IND applications, clinical trial design, IRB methodology

Principal investigators

Grant stats sections, SAP writing, reproducible analysis

Pharma & biotech

Phase I-III support, regulatory documentation, adaptive designs

Academic medical centers

Departmental consulting, resident/fellow methods training

Health tech & startups

Evidence strategy, real-world data analysis, investor decks

Public health orgs

Epidemiological modeling, surveillance analysis, reporting

Services

Study Design & Analysis

  • Protocol development & power calculations
  • Randomization & stratification strategies
  • Interim monitoring & adaptive design
  • Final analysis & manuscript-ready output

Modeling & Inference

  • Bayesian hierarchical models
  • Survival & time-to-event analysis
  • Longitudinal mixed-effects models
  • ML with uncertainty quantification

Regulatory & Grant Support

  • SAP (Statistical Analysis Plan) writing
  • FDA/IRB methodology documentation
  • NIH/NSF grant statistical sections
  • Peer review & second opinions

Engagement models

All engagements begin with a free 30-minute scoping call.

Sprint Engagement

3-6 weeks

Best for: One-time analysis, SAP, or study design

  • Scoped deliverables with fixed timeline
  • Statistical plan or analysis code
  • Results interpretation + visualization
  • Final report / manuscript section

Fractional Lead

Quarterly

Best for: Ongoing studies or growing research teams

  • Weekly working sessions
  • Review & sign-off on analyses
  • Team mentorship & methodology guidance
  • Priority response + standing office hours

Advisory Retainer

Monthly

Best for: Second opinions, audits, roadmap support

  • Same-day turnaround on questions
  • Lightweight memos & reviews
  • Private channel access
  • No minimum hours

FAQ

Do you work with physician investigators who aren't statisticians?+

Yes. I translate between clinical intent and statistical method, and explain every recommendation in plain language.

Can you support an ongoing trial that's already running?+

Yes. I can review what's in motion, surface risks, and suggest pragmatic adjustments or documentation updates.

Will you co-author on manuscripts or grants?+

If the work warrants it, yes. Co-authorship and grant contributions are discussed up front.

How quickly can you turn around a power calculation or SAP?+

A focused power calculation typically takes a few days. A complete SAP varies from one to two weeks.

Do you sign NDAs or BAAs?+

Yes to NDAs. BAAs for HIPAA-covered data are available under the Advisory Retainer or Fractional Lead models.

Ready to scope a project?

Send a brief with your hypotheses, data, and timelines. Response within 48 hours.

Start a conversation