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Sanofi Group Manager - Evidence Synthesis in Chilly-Mazarin, France

Job overview

  • Serve as project lead for designated therapeutic areas within Real World Evidence Generation to conduct direct (pairwise) meta-analysis / network meta-analysis / indirect treatment comparison in support of medical affairs, market access or reimbursement evidence needs.

  • Develop or review study protocols / statistical analysis plans; ensure the highest standards of excellence are applied to these studies from scientific perspective and in full compliance with Sanofi SOPs and requirements from health authorities.

  • Identify, select vendors and manage deliveries in collaboration with internal stakeholders.

  • Interpret, communicate the findings to internal audience and publish externally in scientific congress, peer-reviewed journals.

Responsibilities

  • Consult with Medical Affairs, Health Economics, Value & Access (HEVA), and Real World Evidence Investigators to ensure timely execution to meet evidence needs.

  • Design and conduct analysis for direct (pairwise) meta-analysis, network meta-analysis (NMA) or indirect treatment comparisons (ITC), ensure compliance with best scientific practices and create study reports.

  • Provide statistical expertise to effectively communicate the findings within cross-functional teams including Medical Affairs, HEVA, Clinical Development, Biostatistics, and local affiliates.

  • Manage external vendors for the delivery of study protocol, statistical outputs and study reports.

  • Develop or review statistical inputs and results in submitted materials to external stakeholders, including scientific congress, peer-reviewed journals, regulatory/HTA submissions, core value dossiers etc.

Requirements & Qualifications

  • MSc or PhD in Statistics, Biostatistics or related quantitative sciences.

  • Minimum 5 years working experience as a statistician supporting clinical trials, RWE or HEOR studies, medical affairs or clinical development.

  • Good knowledge of Systematic Literature Review methodology (mandatory).

  • Good knowledge of NMA/ITC (mandatory).

  • Good knowledge of R, Winbugs/OpenBUGS.

  • Previous experience with submissions to regulatory and/or core value dossier development.

  • Good knowledge of technical guidelines (e.g. NICE DSU).

  • Excellent communication skills in English, both written and oral.

  • Ability to communicate effectively the methods and results of complex analyses to a wide range of audience.

  • Ability to function autonomously and manage the delivery of projects with quality control.

  • Ability to work effectively in a team environment.

  • Excellent project management skills and ability to meet deadlines.

  • Flexibility to adapt to diverse clients and project needs.

  • Demonstrated records of publication activities.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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