Join our team as a Biostatistician and become a key contributor to the analysis and interpretation of critical data for the advancement of our projects. In this central role, you will directly contribute to the validity and relevance of our statistical studies, playing an essential part in strategic decision-making. Your Responsibilities: Analyze data and program data processing Draft statistical reports, including the Statistical Analysis Plan (SAP) Write study results Perform data randomization Program data according to Adam (CDISC) and FDA standards Your Qualifications: Academic background: Bachelor’s or Master’s degree from a university specializing in data or statistics, or engineering school with a data specialization Experience with SAS programming language Experience in the design and analysis of clinical trials or observational studies Attention to detail and ability to manage multiple projects Excellent written and verbal communication skills English fluent. French is a plus....