Levallois-Perret
Biostatistician with over 5 years' experience, I have developed my skills and knowledge throughout my different experiences in phase I to III clinical trials as well as in non-interventional studies within an international environment.
Currently working as a core statistician, I am responsible and in charge of all the statistical aspect of a project: writing the statistical part of the protocol, sample size calculation, writing of the statistical analysis plan, coordination and verification of data analysis with respect to SDTM recommendations, participating to the data review meeting, producing the protocol deviation plan, quality control of the TFL, writing, reviewing and finalising of the clinical study report. I also take part in project management and supervision of the team and I am responsible for managing timelines and deliverables. I was the first point of contact for statistical aspects when projects are performed externally within CRO.
I am eager and willing to expand my skills and try out new challenges that may come in my way.
Feel free to connect with me on LinkedIn or send me an email if you would like to share incoming opportunities.
Mes compétences :
SDTM
ADAM
SAS programming
ANOVA and ANCOVA analysis
Linear and Logistic Regression
Mixed Model
CRF
Survival Analysis
Descriptive and Inferential analysis
GCP
Non-interventionnel studies
Clinical Research – Studies phases I, II, III and
