Jobs at Argenx

Lead global FP&A reporting strategy and governance, standardize and automate reporting and KPI frameworks, partner with Digital/Systems to deliver scalable BI solutions, drive insight-led analysis, and coordinate cross-functional reporting initiatives to ensure a single source of truth and reduce duplication.

Lead and execute CMC activities for antibody drug products including process development, scale-up, site transfers, validation, stability and regulatory CMC documentation. Oversee external vendors, track project critical path, develop SOPs, support supply strategies and liaise with QA to ensure GMP/ICH-compliant progress of clinical and commercial initiatives.

Lead global FP&A operations, owning consolidated P&L, reporting strategy, enterprise planning cycles, FP&A systems, projects, governance, and building a scalable, high-performing FP&A operations team to enable executive decision-making and automation across regions.

Lead bioanalytical strategy and execution for large-molecule clinical programs (PK/PD and immunogenicity). Serve as BA SME in late-stage development, support regulatory submissions, manage outsourced labs, ensure GCP/GCLP compliance and inspection readiness, coach team members, and drive cross-functional stakeholder alignment.

Own the technology vision and unified backlog for the US HCP experience. Prioritize and govern multi-team delivery, define KPIs, measure business value, align US and global strategy, mentor teams, and communicate roadmaps and outcomes to senior Commercialization leadership. Up to 20% travel.

Lead US rheumatology insights strategy: design and execute qualitative and quantitative research, synthesize multi-source data, advise cross-functional leadership, manage vendors and budget, and translate insights into go-to-market recommendations to support market development and launches.

Coordinate and drive planning, tracking, and cross-functional alignment for preclinical product development projects. Maintain integrated timelines, lead meetings, capture decisions and action items, manage trackers and portfolio dashboards, improve processes and templates, document knowledge, and enable the PPD team to ensure milestones, risks, and readiness are visible and acted upon.

Lead commercial drug product (parenteral) supply activities with external vendors and internal stakeholders. Manage GMP manufacturing operations, deviations, change controls, continuous process verification, product quality review, CMC technical reviews, and lifecycle/continuous improvement to ensure on-time global supply. Support audits, registration documentation, specs, and risk mitigation across CMOs and supply chain.

Lead regional pharmacovigilance activities for the US (EST timezone), ensuring local regulatory compliance, harmonizing processes with global PV, supporting audits/inspections, managing safety data intake and PSMF data collection, driving PV agreements, cross-functional collaboration, and improving regional PV efficiency through digital automation and process improvements.

Lead clinical operations for a therapeutic indication or asset lifecycle, providing strategic and operational input from FIH through registration and post-approval. Manage budgets, timelines, resources and CRO relationships; drive risk management, trial design input, regulatory interactions, cross-functional execution, audit readiness, and team leadership including coaching of CTLs/CTMs.

Lead identification, evaluation, and management of high-impact external partners for Digital Technology. Define engagement models, integrate partner capabilities, govern partner selection and performance, collaborate with domain leaders, and report insights to senior leadership to accelerate DT innovation and impact.

Lead global commercial strategy and pre-launch activities for rheumatology indications. Build integrated brand strategy, drive insight-driven messaging and launch campaigns, coordinate cross-functional Indication Commercialization Team, partner with clinical, market access and regional teams, manage budget, monitor market trends, and engage KOLs and partners to maximize product launch and lifecycle value.

Lead North America total rewards and recognition strategy for US and Canada. Build compensation, benefits, equity, mobility and recognition programs; partner with HRBPs and business leaders; co‑lead global initiatives; manage vendors and a small team; ensure compliant mobility/immigration programs and flawless compensation cycle execution.

Partner with CMC and Asset Development to translate R&D strategy into budgets, forecasts, models, and KPI dashboards. Own R&D budgeting, forecasting, accruals and vendor spend management, provide variance analysis and decision-focused recommendations, support programme reviews and drive automation/AI adoption.

Lead biomarker biostatistics strategy across the drug development lifecycle. Design and execute fit-for-purpose statistical approaches for biomarker analyses, integrate biomarker and clinical data, support regulatory and program decisions, mentor colleagues, and promote reproducible, robust analyses to enable biomarker qualification and clinical use.

Territory Business Manager responsible for driving demand generation and sales for neurology franchise within an assigned geography. Develop territory plans, engage HCPs and specialty pharmacy/infusion providers, collaborate with cross-functional teams, meet sales objectives, use market tools and CRM, and adhere to compliance and approved messaging.

Field-based Key Account Manager responsible for territory planning and execution to support launch and adoption of innovative immunology therapies. Build scientific relationships with KOLs and institutions, provide clinical insights, support cross-functional initiatives, ensure compliance, maintain CRM data, and drive stakeholder engagement to shape local treatment landscape.

Field-based Key Account Manager responsible for executing territory and account plans, building trust-based relationships with healthcare stakeholders and KOLs, delivering scientific exchange, mapping accounts, providing field insights, coordinating cross-functional initiatives, maintaining CRM data, and ensuring compliant stakeholder engagement to support launch and integration of argenx therapies.

Provide commercial and regulatory legal advice for argenx Germany, supporting product launches and commercialization. Partner with global/regional teams on promotion, market access, contracting, competition law, compliance, permits, and external counsel management. Develop trainings, monitor legal developments, and contribute to cross-functional legal and compliance projects.

Lead HCP marketing strategy and execution for the VYVGART Hytrulo myositis launch. Develop disease-state education, branded and unbranded campaigns across personal and non-personal channels, manage media strategy, advisory boards, market research, KPIs, agency partners, conference presence, KOL engagement, and cross-functional promotional review to ensure compliant, on-time delivery.