Biostatistician Technical Expert – Cmc Statistics

Sanofi

Barcelona, Spain
Hybrid
Statistical support for cmc activities
Experimental designs and data analysis
Statistical reports and presentations
As part of the development of Sanofi’s pharmaceutical products, the R&D Data Sciences department and more specifically the Statistics department for the Chemical Manufacturing Control (CMC) (CMC Statistics), is responsible for contributing to statistical support, modelling, digitalization, decision-making and filing of new product registration files

Job Summary

  • As part of the development of Sanofi’s pharmaceutical products, the R&D Data Sciences department and more specifically the Statistics department for the Chemical Manufacturing Control (CMC) (CMC Statistics), is responsible for contributing to statistical support, modelling, digitalization, decision-making and filing of new product registration files.
  • As a Biostatistician Technical Expert – CMC Statistics within our Data Sciences/CMC Statistics, you’ll be supporting the CMC activities for process, analytical methods and formulation development, for several CMC sites in the world.
  • We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives.

Matching Summary

As part of the development of Sanofi’s pharmaceutical products, the R&D Data Sciences department and more specifically the Statistics department for the Chemical Manufacturing Control (CMC) (CMC Statistics), is responsible for contributing to statistical support, modelling, digitalization, decision-making and filing of new product registration files.

Skills & Requirements

Must-have

  • statistical support for CMC activities
  • experimental designs and data analysis
  • statistical reports and presentations
  • statistical modeling and simulation
  • R and SAS programming

Nice-to-have

  • promote statistical thinking and culture
  • develop state-of-the-art methodologies
  • harmonization of practices
  • cross-functional team collaboration

Key Requirements

  • PhD/MS with 5+ years (PhD) or 8+ years (MS) pharmaceutical experience in CMC
  • Good knowledge of pharmaceutical development process
  • Good expertise in non-clinical statistics applied to CMC
  • Good expertise of industrial statistics and DoE
  • Experience in reporting and communicating plans and results

Work Rights

Not specified

Tailored Resume

Cover Letter