
1001 - 5000 employees
Founded 2008
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
argenx is a biotechnology company committed to improving the lives of patients through immunology innovation. The company focuses on developing novel antibody-based therapies to treat severe autoimmune diseases. Using a collaborative approach with pioneering scientists and academic partners, argenx accelerates the discovery of therapeutic antibodies that target specific disease pathways. The company's proprietary products, such as efgartigimod, are aimed at treating diseases where IgG antibodies are pathogenic. Argenx emphasizes innovation, science of collaboration, and patient-centric approaches in its mission to deliver life-changing medical solutions.
🔥 16 hours ago
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
Founded 2008
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
argenx is a biotechnology company committed to improving the lives of patients through immunology innovation. The company focuses on developing novel antibody-based therapies to treat severe autoimmune diseases. Using a collaborative approach with pioneering scientists and academic partners, argenx accelerates the discovery of therapeutic antibodies that target specific disease pathways. The company's proprietary products, such as efgartigimod, are aimed at treating diseases where IgG antibodies are pathogenic. Argenx emphasizes innovation, science of collaboration, and patient-centric approaches in its mission to deliver life-changing medical solutions.
• Advise business functions on compliance and evolve the regional Global Ethics & Compliance program • Serve as advisor to regional and local commercial and medical teams across the product portfolio • Review and advise on interactions with patients, patient organisations, healthcare professionals, institutions, payors, regulatory agencies and other external stakeholders • Draft and implement policies, procedures and guidance with Legal and Ethics & Compliance colleagues • Support transparency reporting requirements and reporting obligations • Conduct or assist with compliance-related investigations and misconduct allegations • Prepare and deliver Ethics & Compliance training and education, including to field-based employees • Foster argenx’s strong ethical culture • Lead and contribute to compliance projects, issues and priorities across the Global Legal and Compliance function • Perform other duties as assigned
• 4-7 years of regional biopharmaceutical industry experience in a relevant compliance function • Extensive experience within a commercial stage pharmaceutical or biotech company • Regional experience launching new products and/or new indications • Experience with healthcare compliance systems, training employees, engagement of healthcare professionals and transparency • Strong understanding of European corporate commercial healthcare law and regulation related to pharmaceutical product development and commercialisation • Expertise in relevant industry codes and guidelines • Legal degree preferred; other relevant accreditations or degrees considered • Fluent in English • Travel 25-30% • Regional experience in specialty markets, particularly rare diseases, preferred
• Eligibility to participate in short-term and long-term incentives program • Inclusive environment and equal opportunity employment
Apply Now🕒 September 2
EU Regulatory Lead guiding EMA submissions, lifecycle strategy, and commercialization for argenx’s pharmaceutical clients. Advising global teams and authorities across product development.
🕒 September 1
Regulatory Affairs Scientist supporting pharmaceutical regulatory strategies and submissions for global clinical programs. Collaborating with Regulatory Leads and experts on Health Authority interactions, risk assessment and compliance.
🕒 August 31
Regulatory Liaison coordinating EU CTR submissions and compliance for ICON’s embedded biotech clinical-trial team. Serving as the regulatory interface among trial teams, partners, and scientists.
🕒 August 20
Regulatory Affairs Specialist supporting clinical-trial regulatory submissions at Worldwide Clinical Trials. Maintaining country-specific documentation and advising teams on EU-CTR and ICH GCP compliance.
🗣️🇳🇱 Dutch Required
🕒 August 13
Regulatory Affairs Specialist managing CMC compliance for Thermo Fisher Scientific’s life-science products. Coordinating submissions, change controls, deviations, commitments, and product quality across global teams.