I will design your medical research protocol, study synopsis, and biostatistics

A successful clinical study or dissertation requires an airtight protocol. Flawed methodology, incorrect sample size calculations, or ambiguous statistical plans lead directly to institutional review board (IRB) objections and journal desk rejections. As a medical doctor and clinical research consultant specializing in study design, synopsis development, and biostatistical methodology, I help researchers, clinicians, and postgraduate trainees construct rigorous, publication-grade proposals aligned with international reporting guidelines like STROBE, CONSORT, and PRISMA.

I provide end-to-end methodological support for observational and interventional studies, including exact formula-based sample size calculations (WHO, Cochran) with attrition buffers, operational definitions, and clinical scoring integration (Phoenix, SOFA, APACHE). I also develop complete biostatistical pipelines for SPSS and R covering hypothesis testing and multivariable regression modeling, alongside standardized clinical proformas (CRFs), consent forms, and EndNote reference formatting. All services are delivered as advisory consulting and substantive editing in full compliance with academic integrity policies.