Дополнительные сведения:
• Total years of professional experience: 15 years (10 years of academic experience in the field of molecular biology, 5 years of biostatistical experience in CRO and pharma)
• Key responsibilities in statistics: full aspects of statistical analyses (consultation on optimal study design and choice of primary and secondary endpoints, developments the statistical part of study protocol, CRF and database development, perform sample-size calculations, generation randomization lists, development statistical analyses plans, statistical analyses and writing statistical reports)
• Main statistical methodologies: parametric and nonparametric statistical methods, ANOVA, GLM, logistic and Poisson regression, contingency tables, intra- and interclass correlations, survival analyses, PK modelling, Bayesian statistics
• Main therapeutic areas: oncology (10 projects), rare and ultra-rare diseases (8 projects), observational studies (7 projects), registers of disease (5 projects), vaccines (4 projects), diagnostic tests (4 projects), topic creams and cosmetic products (3 projects), post-operational rehabilitation (2 projects), ophthalmology (1 project), erective dysfunction (1 project).
• Main study phases: phase III (10 projects), observational studies (8 projects), phase I (6 projects), phase IV (6 projects), epidemiological studies (5 projects), seamless phase II/III (4 projects), phase II (3 projects)
• Main statistical software: Stata, R, SAS, PASS, Minitab, WinBUGS, JAGS
• Key responsibilities in programming: full-service statistical programming, including datasets manipulations
• International experience developed in: France (1.5 year, English)
• Supervision experience: academic experience of supervision for three years
• Project management experience: not applicable (I have been working within teams where a Project Manager was responsible for every single project)