This job at argenx is not available

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

Click here to see more jobs at argenx .

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

or go to our job search page.

Similar jobs selected for you

  • Top Job

    Business Development in-Licensing Manager

    MPP - Medicines Patent Pool
    Geneva, Switzerland

    You will directly assist the Business Development Director in meeting the strategic, scientific, therapeutic, and commercial needs of MPP. The role contributes to shaping MPP business development strategy through the in...

    Clinical Research Hybrid Regulatory Affairs Sales, Marketing and Communications
    Posted 4 days ago    Deadline 20 February
  • Top Job

    Global Regulatory CMC Lead

    Sobi
    Basel, Switzerland

    The Global Regulatory CMC Lead develops and executes global regulatory CMC strategy for assigned Sobi assets in development, prepares CMC sections of IND/IMPD, MAA, NDA/BLA as well as assesses global filing strategy for post approval changes.

    Clinical Research Hybrid Regulatory Affairs
    Posted 8 days ago   
  • Planning, preparation, submission and support of regulatory applications in EU for designated projects/products in different therapeutic areas, including new Marketing Authorization applications, line extensions, variations, clinical trial applications,

    Clinical Research Regulatory Affairs
    Posted 15 days ago   
  • Associate Director, Precision Medicine Digital Health

    BMS - Bristol-Myers Squibb
    Warsaw, Poland

    Leads global regulatory strategies to support the development and approval of biomarkers, companion diagnostic tests, digital health solutions, and other devices associated with pharmaceutical products across therapeutic areas. This role involves

    Clinical Research Medical Devices Regulatory Affairs
    Posted 21 days ago   
  • Director, Regulatory Affairs

    ICON
    Multiple Locations, Multiple Countries

    Act as a regulatory subject matter expert for ICON. Support initiatives to ensure ICON maintains awareness of new regulatory requirements and opportunities and can deliver services accordingly. Actively contribute to maintaining company awareness of new

    Clinical Research Regulatory Affairs Remote
    Posted 25 days ago   

EuroPharmaJobs Logo

© EuroJobsites 2026