Senior RWE statistician

As a senior RWE statistician, you join an international and committed team, in charge of methodological and statistical approaches serving our real-world data studies and supporting related development plans. You drive the RWD studies you are assigned, ensuring state-of-the-art methodologies and deliverables, in compliance with regulatory guidelines as well as all Servier policies and procedures. Missions & activities: Collaborates in the preparation of the RWD study protocol: methodological choices, statistical estimation of the number of patients and statistical analysis strategy. Develop, implement or advise on appropriate new statistical methodologies and keep abreast of current issues and developments in statistical innovation with RWE applications. Ensures RWE data statistical analysis: Contributes to statistical methodology definition for study designs Writes the Statistical Analysis Plan (SAP), the table/listings/graph document (TLG), Perform data analyses for real-world datasets Ensures validation of the results produced and their validity and robustness, Participates in internal communication of results, Review the study report and ensures proper statistical interpretation of the results Collaborates with multi-disciplinary project teams to establish project goals and timelines. Establishes effective communication with various internal stakeholders to understand and support the strategy for when and how to use RWD. Contributes to productive collaborations with other stakeholders, promoting teamwork, quality, operational efficiency and innovation Lead or participates in working groups on methodological and statistical issues, as well as in transversal and multidisciplinary projects Contributes to the internal and external visibility of the department and promote the development of internal scientific knowledge. Master or Doctoral degree or equivalents in Biostatistics, Statistics or closely related fields. 5 years’ experience as statistician for real-world data studies Strong knowledge of real-world study methodologies Experience leading secondary data analysis, including medical claims, electronic medical records, chart reviews, and registries. Mastery of regulatory guidelines (FDA, EMEA, ICH) R expertise Ability to effectively communicate with others on the project team and in the department; strong interpersonal communication skills Detail oriented, well organized with the ability to work on several projects simultaneously Excellent team player, collaborative and maintains a positive, results‑orientated work environment English fluency is required Positions offered is based at our new international R&D headquarters, at the heart of the Paris Saclay cluster. #J-18808-Ljbffr