Statistical consulting
for research that counts.
I’m currently supporting researchers across my academic and industry network and opening capacity for a small number of external partners. The focus: clear statistical reasoning, reproducible delivery, and honest conversations about what’s possible with the data on hand.
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?+
Yes. I’m comfortable translating between clinical intent and statistical method, and I explain every recommendation in plain language for teams and reviewers.
Can you support an ongoing trial that’s already running?+
Yes. I can review what’s already 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 so expectations stay aligned.
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 depending on complexity and reviewer requirements.
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 →