Medical Advisor, Medical Affairs and Evidence Generation

il y a 2 semaines


Brussels, Belgique argenx SE Temps plein

Medical Advisor, Medical Affairs and Evidence Generation (MAEG), Partner Markets

Apply locations: Gent, Belgium; Switzerland - Remote

Time type: Full time

Posted on: Posted 14 Days Ago

Join argenx
At argenx, we build our culture from the collective power of the team and the knowledge that together, we are better. If you are entrepreneurial, curious, and committed to making a difference for patients and thrive on creating solutions for rare autoimmune diseases, then argenx is for you.
Next to a competitive salary with extensive benefits, we offer you the chance to grow and be a part of a team driven by purpose, creativity, innovation, and science.

Company Overview
argenx is a fast-growing global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Thanks to colleagues based in Europe, the United States, and Japan, we translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines.

For the expansion of our Emerging & Partner Markets team, argenx is looking for a Medical Advisor, Medical Affairs and Evidence Generation (MAEG), Partner Markets, based in Europe (Switzerland and Belgium preferred).

PURPOSE OF THE FUNCTION

The argenx Medical Advisor MAEG is an office-based medical and scientific expert on argenx’s scientific data, products, and trials. The Medical Advisor reports to the Director MAEG, Partner Markets.

The Medical Advisor, MAEG is responsible for engaging medical stakeholders in healthcare settings across Partner Markets territory and with other relevant decision makers, patient groups, policymakers, and government payors.

The Medical Advisor, MAEG designs and delivers innovative & collaborative medical affairs projects, has a significant role in developing and driving the Medical Affairs Plan, operates as a medical reviewer (and final signatory where qualified), and partners with other functions (e.g., commercial) to shape strategies to improve patient outcomes, and supports related internal training initiatives.

ROLES AND RESPONSIBILITIES
  • Coordinate and supervise the regional Medical Affairs plan that meets business priorities for the therapeutic areas, including tactical deliverables such as scientific exchange, real-world evidence, post-licensure research, publication plans, investigator-sponsored studies, and other knowledge transfer activities.
  • Build and maintain a network of key scientific leaders in areas of relevance to the current and anticipated needs.
  • Develop and foster relationships with external and internal stakeholders to ensure that robust local insights from healthcare practitioners and patients enable the generation of data needed to understand and value our innovative medicines properly.
  • Ensure the delivery of effective medical education campaigns, scientific advisory boards, KOL engagements, webinars, and presentations to develop an effective scientific engagement strategy for Partner Markets.
  • Attend appropriate local, national, and international meetings and congresses to gather intelligence, develop productive collaborations, engage in scientific exchange, and ensure insights are shared within argenx.
  • Collaborate with Market Access and Commercial departments through Medical Affairs insights and scientific contributions.
  • Compliant management of compassionate use requests, pre-licensure patient access programs, patient access/support programs, and similar activities.
  • Support the Medical Affairs Lead in carrying out the day-to-day operational activities of the Medical Department.
  • Review and sign off on promotional and non-promotional material to ensure compliance with the Codes of Practice.
  • Understand concepts of pharmacovigilance (PV).
  • Work to ensure compliance in all argenx/Partner Markets procedures.
SKILLS AND COMPETENCIES
  • Ability to quickly understand complex disease areas, treatments, and clinical development plans.
  • Exceptional collaboration track record with internal stakeholders.
  • Strong track record of developing and delivering strategic and compliant medical plans.
  • Strong influencing skills to engage effectively with stakeholders and within the company.
  • Digitally savvy, with practical experience in engaging with external stakeholders using real-world and digital/virtual techniques.
  • Positive mindset with an emphasis on meaningful quantitative and qualitative value and impact measures.
  • Proven capability in problem framing, empirical analysis, assessment, and articulation of clear recommendations.
  • Comfortable giving and receiving feedback in a diverse environment.
  • Ability to work collaboratively and effectively within cross-functional teams and networks.
  • Demonstrated communication skills in a multi-cultural and multi-lingual global environment.
  • Agile, adaptable, and resilient in a dynamic, complex, fast-moving, and frequently changing business environment.
  • Demonstrable experience with project management, proactive planning, priority setting, and securing alignment.
  • Drives toward outcomes.
  • Ambitious, inquisitive, and eager to continuously learn and self-improve.
  • Passionate about leading and contributing to our culture, driven by our corporate values of co-creation, innovation, empowerment, excellence, and humility.
EDUCATION AND EXPERIENCE
  • Master’s degree, Ph.D., or equivalent in a relevant scientific discipline. MD or PharmD is an advantage.
  • Demonstrated 5-7+ years’ experience in the biotech or pharmaceutical industry in Medical Affairs with a proven successful track record; Multi-country experience is required; previous experience with external collaboration Partners/Companies is an advantage.
  • Scientific and/or clinical experience in neurology and/or rare diseases is strongly preferred.
  • Experience working across multiple therapeutic areas/products.
  • Fluency in English; additional language a plus, preferably Arabic.
OTHER
  • Ability to travel as required (up to 30%).
About Us

argenx is a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and cancer. Partnering with leading academic researchers through its Immunology Innovation Program (IIP), argenx aims to translate immunology breakthroughs into a world-class portfolio of novel antibody-based medicines. argenx is evaluating efgartigimod in multiple serious autoimmune diseases. argenx is also advancing several earlier stage experimental medicines within its therapeutic franchises. argenx has offices in Belgium, the United States, Japan, and Switzerland.

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