argenx is a global immunology company committed to improving the lives of people living with 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.
Open Positions
Sr Manager, Medical Review Operations
5+ years of experience in Medical Affairs operations, promotional/medical review operations, or a related regulated environment
Reporting & Insights Lead
5+ years of FP&A experience, strong analytical skills, and experience with BI tools
Associate Director, Medical Writing
5+ years of related, sponsor-level pharma or biotech clinical/regulatory medical writing experience, PhD preferred, Native/bilingual or fluent American English proficiency
Senior Scientist CMC
PhD in chemistry, pharmaceutical sciences, bioengineering, or other discipline within pharmaceutical / biotechnology sciences. Strong technical expertise in biological drug substance and drug product manufacturing, process characterisation and process validation. Good understanding of statistics
Medical Safety Lead
MD degree or equivalent, at least 10 years of experience in pharmaceutical/biotech industry, proven leadership and interpersonal skills, working knowledge of pharmacovigilance regulatory requirements, and fluency in English
Toxicologist late stage clinical development and established Assets
Ph.D degree or equivalent, degree in toxicology or equivalent, at least 5 years of industry experience, and strong literature mining and excellent authoring skills
Biostatistics Director - Indication Lead Myasthenia Gravis (MG)
Master's or Doctorate degree in Statistics or related field with at least 7 years of experience in biotech/pharma industry and expertise in drug development and biostatistics
Gross to Net Finance Lead
12+ years of relevant finance and pricing experience, Bachelor's degree in Finance / Accounting / Economics, CPA, Biopharma or healthcare industry experience required
Senior Medical Writer
Bachelor’s degree in a scientific or clinical discipline or related field, 3+ years of medical writing experience, native or fluent English proficiency
Director, Regulatory CMC Device Leader
Deep expertise in combination product regulations, extensive experience leading combination product strategies, and solid understanding of drug and device development processes
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