Isabelle van der Dussen de K.

Dedicated market access professional | Pharmacist with a mission to bring better health to patients

Boortmeerbeek, Flemish Region, Belgium

About

Market Access Manager with a demonstrated history of working in the pharmaceutical industry.

Experience

  • Global Patient Access Director at Sobi - Swedish Orphan Biovitrum AB (publ)
    Jun 2022 - Present · 4 yrs 2 mos

    As Global Patient Access Director at Sobi, I lead the development and execution of global access strategies to ensure timely, sustainable, and equitable access to innovative therapies in haematology and nephrology. This in close collaboration with the global crossfunctional team to address unmet patient needs, shape access environments, and support value demonstration across diverse healthcare systems. My role is pivotal in aligning global strategy with local implementation to maximize patient impact and drive long-term value.

  • Patient Access Manager at Sobi Benelux
    Nov 2019 - Jun 2022 · 2 yrs 8 mos

    As a patient access manager I am responsible for all market access activities on the Belgian and Luxembourg territory. Sobi is active in the area of ultra-rare hematologic and metabolic diseases. Together with internal and external partners, I seek to bring innovative solutions to the patients in a fast and sustainable manner.

  • Market Access Manager at Takeda
    2016 - 2019 · 3 yrs

    As a market access manager I supported the market access activities for the rare hemato-oncology/ solid-tumour portfolio of Takeda in Belgium and Luxemburg.

  • Bayer (4 yrs 1 mo)
    • Lead Regulatory Affairs Manager Consumer Care
      2015 - 2016 · 1 yr

    • Regulatory Affairs Manager
      2012 - 2015 · 3 yrs

  • Regulatory Affairs Manager at Boehringer Ingelheim
    2007 - 2012 · 5 yrs

    As a Regulatory Affairs Manager I am responsible for the preparation & implementation of complex regulatory strategies to obtain and maintain marketing authorizations for product(s), including the submission of clinical trial applications towards the competent authorities. I also act as a back-up for the Person responsible for Pharmacovigilance.