Jobs at Argenx

Leads US and global regulatory strategy for biopharmaceutical products across development, filing, approval, commercialization, and post-approval stages. Serves as primary FDA contact, oversees IND/BLA/NDA submissions, briefing packages, responses, labeling, and regulatory interactions. Partners cross-functionally with medical, legal, quality, pharmacovigilance, and distribution teams, monitors regulatory and competitive landscapes, and supports product launches. The role requires strategic leadership, deep FDA and orphan-drug expertise, strong communication, project management, and team development capabilities.

Leads US and global regulatory strategy across the pharmaceutical product lifecycle, serving as the primary FDA contact and overseeing IND, BLA, and NDA submissions. Reviews regulatory documents, manages FDA responses, supports labeling and clinical study strategy, monitors regulatory changes and competitive precedents, and partners cross-functionally on product approvals and commercialization. Requires strong leadership, communication, project management, and biopharmaceutical regulatory experience, particularly involving orphan drugs and FDA interactions.

Lead the global commercial strategy, development, and launch readiness for FB102, a pipeline immunology product with multiple potential indications. Coordinate cross-functional teams across commercial, clinical, regulatory, medical, market access, manufacturing, and regional organizations. Develop lifecycle and product strategies, align clinical and manufacturing plans, gather regional market insights, prepare launches, build commercial teams, and maximize asset value. The role requires extensive pharmaceutical marketing experience, strategic leadership, stakeholder influence, and approximately 30% travel.

Leads commercial analytics and AI-enabled insight generation for US biopharmaceutical commercialization, including product launches, in-market performance, pipeline planning, forecasting, ROI analysis, dashboards, and executive decision support. Manages analytics teams, vendors, budgets, and cross-functional partnerships while expanding trusted data, self-service analytics, and AI adoption across commercial operations.

Leads commercialization data strategy for a biopharmaceutical organization, including data acquisition, governance, architecture, quality, vendor management, data products, and AI readiness. Partners with Digital Technology, analytics, business, legal, finance, and compliance teams to establish scalable data capabilities supporting launch planning, field execution, market access, reporting, forecasting, and commercialization decisions. The role also drives data fluency, adoption, investment prioritization, and enterprise standards across global markets.

Lead the global IQVIA enterprise partnership for argenx, overseeing strategic direction, governance, executive alignment, integration, innovation, and value creation across clinical operations, data and technology, pharmacovigilance, quality, and selected commercial activities. The role aligns senior stakeholders, simplifies complex operating models, establishes decision rights, drives co-innovation, and converts partnership scale into measurable business and patient outcomes.

Leads argenx’s global Thermo Fisher Scientific partnership as enterprise owner, aligning clinical development, operations, quality, supply, data, and enabling functions. Builds alliance strategy, governance, decision pathways, innovation models, and value-creation opportunities across the partnership portfolio. Requires senior leadership experience in complex, global, regulated environments, ideally within biopharma or life sciences, with strong influence, integration, and stakeholder-management capabilities.

Leads innovative statistical modeling and simulation for clinical trials, including adaptive, Bayesian, external-control, and model-informed designs. Applies AI/ML to disease modeling and precision medicine, provides statistical consultation, supports regulatory interactions, and translates evidence into development recommendations. Mentors statisticians, leads training, and contributes to publications and external collaborations.

Leads US HCP marketing strategy and commercial execution for the CIDP indication, maximizing VYVGART Hytrulo growth and preparing the Empasiprubart launch. Develops multi-asset positioning, disease awareness, HCP engagement, field enablement, evidence-generation priorities, and customer journeys. Partners across Medical, Market Access, Digital, Field, Patient Experience, Legal, Regulatory, and Compliance. Provides strategic direction, analytics-based recommendations, cross-functional leadership, talent development, and compliant execution in rare disease and biologics markets.

Advises European, Australian, and Canadian commercial and medical teams on pharmaceutical ethics and compliance. Develops policies, procedures, guidance, and training; supports product launches, transparency reporting, audits, monitoring, investigations, and stakeholder interactions. Partners with Legal and Ethics & Compliance teams to address regulatory requirements, manage business risks, and strengthen the company’s ethical culture across the product lifecycle.

Leads the technology vision, roadmap, and portfolio supporting clinical development, trials, data platforms, and Development operations. Partners with R&D and Development leadership, ensures GxP compliance and data integrity, drives digital innovation, manages global programs and vendors, and builds a high-performing international team. The role also shapes governance, operating models, value tracking, stakeholder alignment, and technology strategy across a complex, regulated biopharmaceutical environment.

Leads strategic planning, execution, and performance for argenx’s South Central market covering Oklahoma and Texas. Integrates multiple therapeutic areas, coordinates cross-functional field teams, develops market opportunities, strengthens provider and payer relationships, and drives patient access, revenue growth, launches, and compliance. The role analyzes market and competitive trends, aligns local execution with national strategy, and leads through influence across commercial, medical, market access, and patient support functions. Travel may reach 80%.

Leads the portfolio marketing operating model across Neurology and Rheumatology, prioritizing resources across brands, launches, and lifecycle needs. Translates therapeutic and indication strategies into integrated marketing activation, omnichannel engagement, congress execution, performance optimization, and measurable outcomes. Partners with senior cross-functional stakeholders, agencies, and vendors while building scalable capabilities, AI-enabled practices, agile ways of working, and a high-performing marketing team.

Leads strategic direction, business planning, cross-functional alignment, customer engagement, and execution for the Great Lakes biotech market across Illinois, Indiana, Michigan, and Wisconsin. Integrates multiple therapeutic areas, drives revenue and patient access, analyzes market and competitor dynamics, coordinates field teams, develops partnerships, and ensures compliant execution. Requires extensive rare disease commercial leadership, biologics and payer expertise, strong healthcare ecosystem knowledge, and up to 80% travel.

Leads strategic direction, business planning, cross-functional execution, customer engagement, and performance for the Northeast market across multiple therapeutic areas. Integrates Neuro and Rheumatology strategies, drives revenue and patient access, develops market opportunities, analyzes trends and competitors, coordinates field teams, and ensures compliant launch and commercial execution. Builds relationships with providers, payers, and healthcare leaders while influencing teams without direct authority.

Leads strategic direction, business planning, customer engagement, cross-functional coordination, and execution for the South Atlantic market across multiple therapeutic areas. The role drives revenue growth, patient access, launches, resource optimization, and stakeholder alignment across Georgia, North Carolina, South Carolina, and Virginia. It requires extensive biotech or pharmaceutical leadership experience, rare disease sales success, healthcare ecosystem expertise, and collaboration with Market Access, Medical Affairs, and patient support teams. Travel may reach 80%.

Leads strategic direction, business planning, cross-functional alignment, customer engagement, and execution for the Southeast market across multiple therapeutic areas. The role integrates Neuro and Rheumatology priorities, drives revenue and patient impact, identifies growth opportunities, coordinates field teams through influence, and ensures compliant execution. It requires deep pharmaceutical commercial expertise, rare disease sales experience, healthcare ecosystem knowledge, and strong analytical, leadership, and relationship-building skills.

Lead HCP commercial strategy for emerging biotech pipeline assets, future indications, partnerships, and strategic opportunities. Develop customer ecosystem and KOL strategies, assess commercial readiness, guide launch and transition planning, and integrate scientific, market, and customer insights into investment decisions. Partner across Medical Affairs, Clinical Development, Business Development, Market Access, Insights, and commercial teams. Lead and develop teams while building capabilities in early commercialization, pipeline prioritization, ecosystem development, and launch readiness.

Leads strategic planning, cross-functional execution, customer engagement, therapeutic-area integration, and commercial performance for the NYC Metro and Tri-state market. Drives revenue growth, patient access, launches, partnerships, and provider and payer engagement while coordinating field teams through influence rather than direct authority. Analyzes market and competitor dynamics, ensures compliance, and translates insights into actionable strategies across multiple autoimmune disease indications.

Leads enterprise HCP customer engagement and experience strategy across therapeutic communities, brands, and lifecycle stages. Oversees TLL and KOL engagement, journey design, omnichannel planning, customer insights, experience standards, and cross-functional orchestration across Commercial, Medical Affairs, Clinical Development, Field, Digital, and other functions. Builds organizational capability, develops leaders, aligns priorities, and ensures compliant, consistent customer experiences in complex biotech markets.