Senior Biostatistician

**Date de parution**:7 févr. 2023**Ville**:Suresnes / Saclay**Pays/Région**:FR**Type de contrat**:CDI**N° offre**:2197Senior BioStatistician
- We are looking for a Senior Biostatistician to join our Global Biometrics Department / Biostatistics
- You join an international and committed team, in charge of methodological and statistical approaches serving our clinical studies and supporting related development plans.
- You drive the projects and 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.- Roles and Responsibilities- Propose the implementation of methodological and statistical approaches (preparation of the protocol, conduct and preparation of statistical analysis, in particular Statistical Analysis Plan, validity and robustness of results, and clinical report), while ensuring their consistency on the whole project.
- Develop simulation programs to assess trial operating characteristics
- Promote and develop innovative approaches in terms of statistical methodology to support clinical development plans, study designs, and statistical analyses
- Contribute to productive collaborations with other stakeholders, promoting teamwork, quality, operational efficiency and innovation
- Statistical support to regulatory filing documents, as well as to the responses to the agencies, in collaboration with the development and regulatory teams, and, potential external experts.
- Lead or participate in working groups on methodological and statistical issues, as well as in transversal and multidisciplinary projects
- Contribute to the internal and external visibility of the department and promote the development of internal scientific knowledge.

Qualifications/Requirements- Engineer, Master or Doctoral course in BioStatistics (MSc, or Ph.D) or similar field
- Minimum 5 years experience
- Strong experience and in-depth knowledge of innovative statistical concepts and methods
- Mastery of reference regulatory guidelines (e.g. ICH, FDA and EMEA)
- SAS and R expertise appreciated
- 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
- This is a full-time, permanent position located at our headquarter in Suresnes and will be located from Spring 2023 onwards at our new international R&D headquarters in Saclay.