Aline-Marie Florence

Biostatistician and clinical research methodologist, I support pharma, biotech, medtech, and academic teams in the design, analysis, and valorization of their studies.

• Methodological design of studies (clinical trials, observational studies, RWE) + protocol writing

• Sample size calculations and choice of statistical methods

• Writing of statistical analysis plans (SAP)

• Statistical analyses under R

• Production of tables, listings, and figures (TLF)

• Interpretation of results and support for scientific or regulatory writing

Areas of expertise:

– Clinical trials (phases I–IV)

– Real-World Evidence (RWE) studies

– Epidemiology and public health

– Longitudinal analyses, mixed models, survival, regression

– Management and valorization of clinical data

My approach combines methodological rigor, understanding of regulatory issues, and pedagogy, in order to provide reliable, reproducible, and directly usable analyses for decision-making or submissions.

Available for ad hoc missions or support throughout the project.