Scientific Writer Job at argenx SE in Town of Belgium

Scientific Writer page is loaded## Scientific Writerlocations: Gent, Belgiumtime type: Full timeposted on: Posted Yesterdayjob requisition id: REQ-3633*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.*To support the advancement of our antibody discovery and development efforts, argenx is seeking a highly motivated Scientific Writer to join the R&D team. The role contributes to the development of drug-development documents that support regulatory submissions or patent applications.**The position is based at our facility in Zwijnaarde, Belgium, and requires daily on-site presence.** Applications should include a CV, cover letter, and references.**Main roles and responsibilities**• Developing, reviewing, and coordinating documents related to drug development (e.g., patents, nonclinical/clinical reports for regulatory submissions). • Working closely within and across project teams to ensure documentation is high-quality, well-organized, consistent, and accurate. • Contributing to the establishment of R&D writing infrastructure, including workflows, trainings, and document templates.**Profile**• PhD with industry experience and knowledge in immunology, autoimmune diseases, or biological drug discovery. • Experience in an industrial environment or regular interaction with industry is considered a strong plus. • Strong English written and verbal communication skills. • Clear interest in scientific writing for biopharmaceutical products. • Solid understanding of drug development and regulatory guidelines. • Proficiency in MS Office. • Familiarity with Veeva Vault and PleaseReview is preferred. • Ability to proofread documents for compliance with internal and external guidelines. • Problem-solving mindset with a quality-focused approach.• Comfortable working independently and in project teams. • Strong time-management skills and ability to handle multiple projects simultaneously. • Capable of prioritizing and multitasking in a fast-paced environment.**Offer**• Opportunity to contribute directly to the development of new therapeutic antibodies. • A newly created role with room to shape future ways of working. • A human-sized, dynamic, and rapidly growing biotech environment with strong support for learning, development, and growth. • A competitive salary package with extensive benefits.#LI-onsite*At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.**Before you submit your application, CV or any other personal details to us, please review our* *to learn more about how argenx B.V. and its affiliates (“argenx”) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at* *privacy@argenx.com**.* #J-18808-Ljbffr