argenx
argenx

501-1000 employees

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pharmaceutical-manufacturing
biotechnology-research
biopharmaceutical
immuno-oncology
antibody-engineering
medical-equipment-manufacturing
acute-myeloid-leukemia
autoimmune-diseases
immunology
immunotherapy
myasthenia-gravis
oncology
rare-diseases
About argenx

argenx is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Partnering with leading academic researchers through its Immunology Innovation Program (IIP), argenx is translating immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. argenx’s first experimental medicine, efgartigimod, is being evaluated in multiple autoimmune diseases, including myasthenia gravis (MG), pemphigus vulgaris (PV), immune thrombocytopenia (ITP), and chronic inflammatory demyelinating polyneuropathy (CIDP).argenx is located in Ghent, Belgium, Boston, Massachusetts and Tokyo, Japan.

5 months ago

Global Indication Lead, Medical Affairs & Evidence Generation

Full-time
Lead
Global Indication Lead, Medical Affairs & Evidence Generation
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Description
  • Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART®, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.
  • We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business.
  • We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.
  • The Integrated Medical Affairs and Evidence Generation group delivers ambitious, patient-focused cross-regional and cross-indication medical strategies, driving data generation and dissemination, to maximize patient benefit from argenx products.
  • The Global Indication Lead will provide expert medical leadership to guide development, launch planning, life cycle management and support for approved products, as relevant for the indications stage of development.
  • Working in collaboration with cross-functional colleagues, and as a key member of the Indication Development Team the Global Indication Lead will input to development and delivery of the target product profile, clinical development plans and pre-launch strategy, and brand plans ensuring regional Medical Affairs teams insights and requirements inform all stages of development.
  • Key Accountabilities/Responsibilities: Provide expert medical input to guide clinical development, comprehensive evidence generation, launch planning and brand plan execution in relevant indications Develop and execute ambitious short-term and long-term medical strategies, as key elements of the integrated data generation plan and brand plan Accountable for the alignment of all global medical affairs activities in partnership with other cross-functional members of the Indication Development Team Develop close partnerships with regional and country medical affairs leads/teams, and the regional indication strategy teams and ensure all activities maximise cross-regional impact whilst enabling regional team empowerment and supporting local delivery Build and maintain close partnership with external experts, in collaboration with regional/country Medical Affairs teams, to bring insight to all activities Initiate and support high impact medical activities, such as advisory boards, congress symposia and medical research projects Drive the identification and development of productive collaborations including with healthcare organisations and experts, other important customers and stakeholders and professional organizations Support strategy development for investigator sponsored studies and assessment of proposals Partner with scientific communications to support development of publication and medical education strategies Develop and continuously maintain the highest scientific and medical expertise with relevant diseases and products and be acknowledged internally and externally as an expert Systematically capture, distil and proactively communicate insights and activities within argenx Ensure all medical affairs activities maintain the highest standards, comply with applicable pharmaceutical regulations, as well as argenx policies and procedures Skills and Competencies: Able to quickly understand complex disease areas, treatments and development and brand strategies Proven track record of building productive collaborations with external medical experts and networks and to gain actionable insights Understands how to build internal cross-functional and cross-regional collaborations, ensuring broad input to decision making Embraces innovation and shared goals Has excellent communication skills: verbal, written and when giving presentations Has strong influencing skills to be able to engage effectively with internal and external stakeholders Able to thrive as part of a team and when working independently Proven track record of delivering results that meet or exceed targeted objectives Fluency in English, in addition to the local language(s), both oral and written.
  • For US applicants: Salary range is $296,000 - $444,000 USD.
  • The role involves developing and executing medical strategies, collaborating with external experts, and supporting clinical development and medical activities.
  • The position emphasizes scientific expertise, cross-functional collaboration, and compliance with regulations.

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Requirements
  • Scientific, healthcare or medical degree (BSc, MS, PhD, PharmD, RN, MBBS, MB.ChB or equivalent).
  • Substantial medical affairs experience, throughout the product lifecycle.
  • A strong understanding of the drug development process and launch planning.
  • Relevant drug development, therapeutic area expertise and existing external expert network is an advantage.
  • Robust knowledge of regulations and practices related to industry interactions with healthcare professionals.
  • Experience partnering with regional/country and global functions and leadership.
  • Fluency in English, both oral and written.

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Benefits
  • Comprehensive benefits package including retirement savings plans.
  • Health benefits.
  • Participation in short-term and long-term incentive programs.
  • Additional benefits subject to plan terms.