Jobs at Argenx

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.

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 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.

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.

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 ongoing safety surveillance and signal detection for investigational and marketed products. Analyze aggregated safety data, leverage analytics/AI outputs, support benefit-risk assessments, draft periodic safety reports, and collaborate cross-functionally to maintain compliance with global pharmacovigilance requirements.

Lead configuration, maintenance, and operation of safety databases (Argus) and related systems to ensure compliant case processing, reporting, and analytics. Support system validation, generate and QC aggregate reports and line listings, collaborate with PV/clinical/regulatory teams and vendors, contribute to SOPs and audit readiness, and continuously improve safety data workflows and integrations.

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.

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.