Statistical consulting
for research that counts.
From first-in-human trials to population-scale studies, I work alongside your team to design, analyze, and interpret research with rigor that holds up to scrutiny — and software that makes it repeatable.
Who I work with
From bedside to boardroom
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
What I cover
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
- Machine learning 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 commitment
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 — pay for what you use
FAQ
Questions clinicians ask
Do you work with physician investigators who aren't statisticians?+
That's most of my clients. I translate between the clinical question and the statistical method — and deliver results in language your team and reviewers can act on.
Can you support an ongoing trial that's already running?+
Yes. Mid-study support is common — interim analyses, protocol amendments, DSMB memos, or just a second opinion on the analysis plan.
Will you co-author on manuscripts or grants?+
On a case-by-case basis, yes. If I'm doing substantive statistical work, co-authorship is appropriate and I'm open to it.
How quickly can you turn around a power calculation or SAP?+
A focused power calculation is usually 1–3 days. A full SAP is typically 1–2 weeks depending on study complexity.
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. I'll come back with a concrete path within 48 hours.
Start a conversation →