Jobs at Argenx

Lead and optimize governance for the Senior Leadership Team, Operations Committee, and Portfolio Committee: prioritize agendas, build forum structure and charters, ensure high-impact prework, facilitate meetings to clear decisions and owners, publish and track actions, embed agile and AI-enabled ways of working, and develop capability across the organization.

Lead global market access strategy for Myasthenia Gravis and related FcRn pipeline assets. Define pricing, HTA/P&R positioning, evidence and HEOR plans, payer engagement, contracting and launch readiness. Align access strategy with development and commercial teams, manage external partners, and support lifecycle management and indication expansion.

Lead clinical development strategy and execution for assigned therapeutic indications, co-chair Clinical Development Team, oversee trial design, budgets, timelines, CRO/vendor management, risk mitigation, and regulatory interactions. May line-manage CTMs/CTAs, act as CTM for select trials, ensure ICH-GCP compliance, audit readiness, and cross-functional alignment across the program lifecycle.

Provide regional, patient-centered education and coordination for gMG patients using argenx therapies; communicate insurance and financial assistance, troubleshoot reimbursement, collaborate with internal teams, ensure policy compliance, and travel regionally to support patient programs.

Lead UK & Ireland pricing, reimbursement, market access and policy strategy for rare disease launches. Build payer relationships, negotiate HTA outcomes, coordinate HEOR/evidence generation, develop access tools, and influence global and local cross-functional teams to secure reimbursement and optimise launch pathways.

Lead and deliver the Rewards & Recognition strategy across Developed Markets (excl. US, Canada, Japan). Own compensation cycles, benefits, equity program decisions, recognition mechanisms, and global mobility. Co-architect global R&R initiatives, partner with HRBPs and business leaders, build vendor relationships, and grow a high-impact R&R team to drive talent attraction, retention, and pay transparency.

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.

Provide regional, patient-centered education and support for individuals with generalized Myasthenia Gravis. Coordinate treatment logistics, insurance and reimbursement troubleshooting, financial assistance guidance, and collaborate with internal access teams while ensuring regulatory and company policy compliance. Requires travel to support patient programs and flexible scheduling.

Lead strategy and execution for an enterprise AI platform and MLOps/LLMOps frameworks. Define multi-year platform roadmap, manage teams, vendors, and budget, drive deployment and lifecycle management of LLMs and enterprise AI tools, ensure security/compliance and ethical AI practices, and partner with data science and business units to operationalize AI at scale.

Provide high-level administrative support to senior leaders: manage calendars, schedule meetings and travel, draft communications, prepare agendas and minutes, handle expense reports and vendor/contract tasks, liaise with global admin teams, and maintain confidentiality while juggling competing priorities.

Lead and build a global GxP partner ecosystem (CDMOs, CROs) across TechOps/CMC, Development, and Preclinical. Define external manufacturing and clinical sourcing strategy, enable cross-functional empowered sourcing, deploy modern sourcing tools/AI, and develop a senior team to accelerate pipeline resilience, capacity, and speed to clinic/commercialization.

Provide legal and regulatory counsel for clinical development, advising on EU Clinical Trials Regulation, ICH GCP, pharmacovigilance, and GxP matters; support clinical operations and safety teams; draft and negotiate clinical trial, CRO, vendor, and pharmacovigilance agreements; guide regulatory interactions, inspections and audits; develop policies, SOPs and training; and monitor EU regulatory and caselaw developments to translate into practical business advice.

Serve as the strategic digital technology partner for Research (Discovery, Pre-Clinical, Translational). Define and govern a multi-year digital roadmap, translate scientific needs into integrated technology solutions, ensure GxP-compliant data integrity and quality, manage stakeholder relationships, drive portfolio prioritization, and lead value realization and continuous improvement across research initiatives.

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 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 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.

Own the technology vision and value delivery for US Market Access. Translate business strategy into a prioritized product backlog, guide delivery teams, steward end-to-end user experience for reimbursement, payer engagement and contract management, define and monitor KPIs, measure value, and integrate technology components to enable payer negotiations and streamline patient access.

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.

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 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.