This job at Sanofi is not available

We're sorry, the job you are looking for at Sanofi on EuroPharmaJobs has expired.

Click here to see more jobs at Sanofi .

We still have many live jobs. Click below for similar jobs in:

or go to our job search page.

Similar jobs selected for you

  • Responsible for leading non‑clinical and early clinical pharmacology strategy across drug development programs. Provides expertise in PK/PD, modeling & simulation, and Model‑Informed Drug Development (MIDD) to support dose selection, study design, and

    Clinical Research Data, Programming and Statistics Hybrid Pre-clinical Research and Development
    Posted 3 days ago   
  • The successful candidate will serve as Lumis' medical device regulatory subject matter expert, leading project delivery, supporting business growth, enhancing industry visibility, and further developing the Lumis brand as a recognized provider of medical

    Clinical Research Hybrid Medical Devices Regulatory Affairs
    Posted 14 days ago   
  • Manager, Medical Affairs

    Gilead
    Amsterdam, Netherlands

    The role is responsible for ensuring Gilead’s medical affairs activities comply with pharmaceutical regulations and laws and providing expertise on drug safety and medical topics. Provides medical expert advice to ensure accuracy of data to support

    Clinical Research Hybrid Medical
    Posted 39 days ago   
  • Teva
    Sofia, Bulgaria
    Hybrid Manufacturing and Logistics Quality Assurance
    Posted 7 days ago   
  • Norgine
    Hengoed, UK or Dreux, France, Multiple Countries
    Hybrid Quality Assurance
    Posted 7 days ago   

EuroPharmaJobs Logo

© EuroJobsites 2026