Biostatistics Consulting for Clinical Research Teams
Supporting academic medical centers, funded clinical investigators, research hospitals, and pharma / biotech teams with rigorous statistical analysis — from study design and pre-registered SAPs through publication-ready reporting.
- Pre-specified SAP — agreed before analysis begins
- R or Python — rigorous, validated methodology
- Publication-ready tables, figures, and methods report
- Full documentation: methods, data dictionary, audit trail
- NDA before any data or materials are shared
All projects begin with a scoping call. No data transfer before NDA is in place.
Study Designs Supported
Interventional trials, observational epidemiology, evidence synthesis, and real-world data — from first-in-human to population registries.
Randomized Controlled Trials
Phase I–III; parallel, crossover, factorial, superiority / non-inferiority
Observational Cohort Studies
Prospective and retrospective; time-to-event and longitudinal outcomes
Case-Control Studies
Matched and unmatched; rare outcome focus; conditional logistic regression
Cross-Sectional Studies
Prevalence estimation, burden of disease, registry surveys
Registry & Database Studies
EHR, claims data, disease registries, national administrative databases
Systematic Review & Meta-Analysis
Fixed and random-effects models, heterogeneity assessment, PRISMA reporting
Adaptive & Platform Trials
Interim analyses, response-adaptive randomization, seamless designs
Real-World Evidence Studies
Comparative effectiveness, propensity score methods, target trial emulation
Grant Proposal Biostatistics
Power analysis, sample size justification, and SAP sections for NIH/MRC/NIHR
Statistical Services for Healthcare Research
Precise, confidential, and timely biostatistics support — from clinical trial design to peer-review response.
Advanced Statistical Analysis
Regression modeling, survival analysis, Bayesian methods, longitudinal models, meta-analysis, and machine learning — applied to complex medical data.
Explore statistical analysisManuscript Writing Support
Statistical input for Methods, Results, and Discussion sections. Guideline-compliant reporting for medical journal submission.
Explore manuscript supportData Cleaning & Interpretation
Dataset preparation, missing data handling, quality control documentation, and statistical interpretation with clinical context.
Explore data cleaningStudy Design Consultation
Sample size calculation, power analysis, randomization strategy, endpoint selection, and Statistical Analysis Plan development.
Explore study designResults Validation & Reporting
Independent verification of statistical findings and publication-ready reports meeting journal and regulatory requirements.
Explore results validationGrant Proposal Support
Statistical methodology sections, power analyses, and sample size justifications for NIH, MRC, NIHR, and similar funding bodies.
Explore grant supportAnalytical Methods & Reporting Standards
All work follows pre-specified plans, reproducible workflows, and the reporting standards required by leading medical journals and regulatory agencies.
Software
Reproducibility
- ·Reproducible analysis following pre-specified SAP
- ·Documented data pipeline and cleaning log
- ·Deliverables include methods documentation and session metadata
How an Engagement Works
Every project follows a structured, documented process — from initial scoping through final delivery — with confidentiality and reproducibility built in at every stage.
Request Consultation01Project Scoping
No data shared yetSubmit project details. We confirm study type, objectives, data status, and timeline. No files are transferred at this stage.
02Confidentiality Agreement
NDA firstNDA executed before any data or materials are shared. All content is handled under confidentiality for the lifetime of the engagement.
03Statistical Analysis Plan
Pre-specifiedPre-specified SAP drafted collaboratively and approved before analysis begins. Defines endpoints, methods, populations, and missing data handling.
04Analysis and Documentation
ReproducibleAnalysis executed in a reproducible environment following the pre-specified SAP. Outputs logged with software versions.
05Reporting and Delivery
Full packagePublication-ready report with tables, figures, and methodology narrative. Full package: analysis code, data dictionary, and audit trail.
Research Support Across Clinical Specialties
Completed engagements across study types and institution types. Details presented in de-identified form.
Risk Factors for Eosinophilic Esophagitis
Gastroenterology · Academic Medical Center — United States
Methods applied
- ·Multivariable logistic regression
- ·Risk factor identification and effect estimation
- ·Dataset handling and quality control
Key risk factor associations identified. Report described by the research team as clear, concise, and publication-ready.
Keratoconus Prevalence and Associated Factors
Ophthalmology · Academic Medical Center — Saudi Arabia
Methods applied
- ·Descriptive statistics and prevalence estimation
- ·Multivariable analysis of associated factors
- ·Dataset management and validation across collection protocols
Dataset adeptly managed; analyses described by the research team as robust, with professional and timely delivery.
A Statistical Consultancy for Medical Research
StatMedAnalysis provides expert biostatistics consulting and statistical support to healthcare researchers and institutions globally. We work across the full research lifecycle — from protocol design through regulatory submission and publication.
Our focus is collaborative, rigorous work that meets the standards expected by leading medical journals, funding agencies, and regulatory bodies.
Engagements completed for researchers at academic medical centers in the United States, Europe, Middle East, and Asia.
Statistical work delivered across gastroenterology, ophthalmology, and related clinical research specialties.
Analytical deliverables aligned with CONSORT, STROBE, and observational study reporting standards.
Statistical Precision
Every analysis follows a pre-specified plan. Methods are chosen to match the study design, not the desired result.
Data Confidentiality
NDA executed before data transfer. Strict access controls, secure handling, and research-data retention governed by each project agreement.
Scientific Rigor
Rigorous, reproducible workflows with full audit trails — suitable for regulatory submission and peer review.
Timely Delivery
Realistic timelines set at scoping. Milestone communication throughout. Expedited options for urgent deadlines.
Frequently Asked Questions
Common questions about our statistical consulting services for medical research.
What types of advanced statistical analysis do you offer?
We provide a wide array of advanced analyses, including Bayesian statistics, various regression models (linear, logistic, Cox), survival analysis, longitudinal data analysis, meta-analysis, and machine learning techniques tailored for medical data.
How do you ensure data confidentiality?
Data confidentiality is paramount. We adhere to strict protocols, including secure data transfer and storage, access controls, and non-disclosure agreements. All client data is treated with the highest level of security and ethical consideration, compliant with international standards.
Can you assist with manuscript sections beyond Methods and Results?
Yes, while we specialize in the Method and Results sections, we can also provide expert input on the Discussion section, helping you interpret statistical findings in the context of your research question and existing literature.
What is your process for study design consultation?
Our study design consultation involves understanding your research objectives, helping select appropriate methodologies, determining optimal sample sizes (power analysis), defining variables, and creating a robust statistical analysis plan to ensure your study is well-powered and scientifically sound.
What is the typical turnaround time for projects?
Timely delivery is one of our core values. Turnaround times vary based on project complexity. We provide estimated timelines upfront and work diligently to meet them. For urgent projects, we can discuss expedited service options.
How are quotes for services determined?
Quotes are tailored to each project's specific needs, considering the scope of work, complexity of analysis, dataset size, and required deliverables. We offer transparent pricing and will discuss this in detail during your initial consultation. You can request a quote via our contact form.
Request a Statistical Analysis Quote
Describe your research project and we'll acknowledge your inquiry within 24 hours and follow up with a scoped proposal within 3 business days. Prefer email? support@statmedanalysis.com
Contact Information
Engagement Process
- 1.Submit project details via the form
- 2.Acknowledgment within 24 hrs · Proposal within 3 business days
- 3.Review and approve the Statistical Analysis Plan
- 4.Receive analysis, report, and reproducible documentation
All engagements are covered by a non-disclosure agreement. Data is handled securely and returned with full audit documentation.
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