Job Description

Senior Medical Writer 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. Key Accountabilities / Responsibilities Author and project manage SME contribution to develop content for regulatory submissions that is well‑organized, consistent, accurate, and compliant with argenx Medical Writing standards, including style guide, lexicon, templates, and libraries. Author content for phase 1‑4 protocols, master ICFs, IBs, and CSRs. Responsible for inspection‑readiness of medical writing activities. Supports the lead writer and project teams to ensure project deadlines are met. Executes corporate objectives, goals, measures, and strategies. Capable of working on multiple deliverables simultaneously. Desired Skills and Experience Bachelor’s degree in a scientific or clinical discipline or related field is required; Ph.D. preferred. Minimum of 3 years of related, sponsor‑level pharma or biotech clinical/regulatory medical writing experience required; CRO experience considered. Native/bilingual or fluent American English proficiency. Solution‑focused experience with Veeva Vault. Experience with implementing lean writing techniques. Basic understanding of scientific methodology as applied to drug development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission. Familiarity with pharmacovigilance guidelines and developing aggregate reports. Ability to work precisely according to procedures and regulations. Ability to prioritize and multi‑task successfully in a fast‑paced environment. Ability to work autonomously, as well as in a team. Excellent written and verbal communication skills. Excellent time management skills and a proven ability to work on multiple projects at any given time. Proficient in MS Office. Salary and Benefits The annual base salary hiring range for this position is $128,000.00 – $176,000.00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job‑related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks. This job is eligible to participate in our short‑term and long‑term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines. Equal Opportunity 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. #J-18808-Ljbffr

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