Full-Time

Associate Director, Patient Services

Updated on 9/12/2026

argenx

argenx

1,001-5,000 employees

Biotech immunology company developing therapeutic antibodies

Compensation Overview

CA$159k - CA$209k/yr

Remote in Canada

Remote

Remote within Canada, with approximately 20% travel.

Bachelor's

Category
Project & Program Management (1)
Required Skills
Data Visualization
Electronic Health Records (EHR)
Data Analysis

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Requirements
  • Bachelor's Degree.
  • Preferred 7–10 years of relevant biopharmaceutical, specialty pharmaceutical, healthcare, patient services, market access, reimbursement, or related industry experience.
  • Preferred 5+ years of Patient Support Program, patient services, marketing, market access, reimbursement, or patient access experience, including responsibility for program operations, vendor management, and cross-functional collaboration.
  • Demonstrated experience leading complex patient support initiatives and driving operational excellence across the patient journey.
  • Understanding of the Canadian pharmaceutical environment, customers, and internal operations.
  • Experience managing patient-related projects and programs or related experience.
  • Bilingual French and English is an asset.
  • Ability to work with minimum supervision and demonstrate a proactive approach.
  • Ability to travel approximately 20% while working remotely from Canada.
Responsibilities
  • Contribute to the development of patient program strategy supporting patient access to Vyvgart in Neurology.
  • Lead execution of strategic imperatives through annual operating plans and tactical initiatives aligned with the Vyvgart patient journey through the MyPATH patient support program.
  • Provide daily program oversight and serve as the key point of contact for patient support program providers and program vendor management staff.
  • Lead the planning and execution of vendor-led projects and strategic initiatives, ensuring timely delivery and measurable outcomes.
  • Identify and propose innovative or digital initiatives to improve program efficiency and patient experience.
  • Attend relevant industry forums and share insights on evolving patient support, reimbursement, and market access trends.
  • Partner with Marketing to develop program tools and initiatives communicating MyPATH services to patients and healthcare professionals.
  • Develop and maintain strategic partnerships across Sales, Marketing, Market Access, Medical Affairs, Patient Support Program Operations, Regulatory, Finance, Legal, and Compliance.
  • Build productive relationships with external stakeholders, including advertising agencies, patient support program vendors, and electronic medical record support partners.
  • Support patient support program education and provide guidance to internal stakeholders on patient services strategy and operations.
  • Support the Director of Patient Services in planning and executing patient support program vendor collaboration meetings.
  • Use patient support program data to drive strategic decision-making, optimize operational performance, identify insights, and improve patient outcomes.
  • Enhance vendor data reporting through dashboards, analytics, and performance reporting.
  • Lead and manage patient support program contracts, including master services agreements and statements of work, from development through purchase order issuance and execution.
  • Partner with the Director of Finance to manage budgets, invoicing, and financial reporting, monitor variances, and escalate significant risks.
  • Create and manage purchase orders for programs and vendors and identify opportunities to improve operational efficiency through process and digital innovation.
  • Support internal and external audit activities and ensure audit readiness.
  • Develop and maintain patient support program governance and operating guidance documents.
  • Drive operational efficiency and cost optimization through continuous improvement of patient support program processes, standard operating procedures, and vendor management practices.
  • Ensure compliance with company policies, procedures, and applicable regulatory requirements.
  • Deliver tactical plans on time and within budget to maximize patient value and achieve business objectives.
  • Execute digital strategy initiatives and business transformation programs that enhance patient and stakeholder experiences.
  • Establish and maintain strategic relationships with Commercial and Key Account Management teams.
  • Manage agency partners and vendors with accountability and a focus on performance.
  • Partner with the Director of Patient Services to achieve departmental and organizational objectives.
  • Develop and maintain cross-functional partnerships across Sales, Marketing, Market Access, Medical Affairs, Finance, Legal, and Compliance.
Desired Qualifications
  • Preferred 7–10 years of relevant biopharmaceutical, specialty pharmaceutical, healthcare, patient services, market access, reimbursement, or related industry experience.
  • Preferred 5+ years of Patient Support Program, patient services, marketing, market access, reimbursement, or patient access experience, including responsibility for program operations, vendor management, and cross-functional collaboration.
  • Bilingual French and English.

argenx develops antibody therapies to treat autoimmune diseases and cancer by translating scientific discoveries in immunology into therapeutic antibodies. Its work centers on R&D and then licensing and collaborations for commercialization, with cusatuzumab being developed with Janssen R&D to target hematological cancers such as leukemia. The company funds and accelerates discovery mainly through partnerships and licenses, bringing products to market via partner-based commercialization rather than building its own sales force. Its goal is to advance antibody-based treatments for serious autoimmune diseases and cancer by turning scientific insights into clinically useful therapies through industry and academic collaborations.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Ghent, Belgium

Founded

2008

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 revenue rose 60% year over year to $1.54 billion.
  • August 17, 2026 ALKIVIA Phase 3 showed positive autoimmune myositis results, expanding the franchise.
  • BenchSci signed a two-year enterprise deal with argenx, signaling continued R&D investment and adoption.

What critics are saying

  • FDA issued two January 30, 2026 untitled letters for misleading VYVGART Hytrulo TV ads.
  • VYVGART still drives most revenue, so any launch stumble hits growth immediately.
  • FB102 needs celiac and alopecia data in 2026; failure weakens the $2.2 billion Forte bet.

What makes argenx unique

  • VYVGART became first approved gMG therapy across all serotypes on May 8, 2026.
  • argenx's SIMPLE Antibody platform and FcRn expertise create a durable discovery-to-commercialization moat.
  • August 27, 2026 Forte acquisition added FB102, deepening differentiated CD122 immunology coverage.

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Benefits

Hybrid Work Options

Growth & Insights and Company News

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The Montreal Gazette
Sep 2nd, 2026
BenchSci announces two-year enterprise agreement with argenx to advance ai-driven preclinical drug discovery.

BenchSci announces two-year enterprise agreement with argenx to advance ai-driven preclinical drug discovery. Scientist-led competitive selection deepens BenchSci's presence in European biopharma TORONTO - BenchSci, a leading provider of AI software for biopharma research and development, today announced a two-year enterprise agreement with argenx, a global immunology innovation company, to deploy EMET, BenchSci's agentic research environment for preclinical drug discovery, within the organization. Selected through a competitive evaluation...

Yahoo Finance
Sep 2nd, 2026
Argenx posts 18 consecutive quarters of sales growth, Q2 2026 revenue up 60% YoY

Argenx has achieved 18 consecutive quarters of revenue growth, with second-quarter 2026 sales rising 60% year-over-year and 17% sequentially. The biotech's Vyvgart and Vyvgart Hytrulo therapies continue gaining traction in treating severe autoimmune diseases. Earnings reached $472 million in Q2, nearly double the prior year, with expanding operating margins. The company holds approvals in generalised myasthenia gravis, immune thrombocytopenia, and chronic inflammatory demyelinating polyneuropathy. Argenx recently reported positive late-stage results for Vyvgart Hytrulo in autoimmune myositis, affecting around 100,000 Americans. Management sees this as a multibillion-dollar opportunity. The company expects Phase 3 results for empasiprubart in multifocal motor neuropathy during Q4 2026. CFO Karl Gubitz noted only 20% of gMG patients currently receive novel biologics, suggesting significant growth potential.

wallstreet:online AG
Aug 21st, 2026
Not Moderna: this biotech stock still has potential after an 11,000% rally!

Not Moderna: this biotech stock still has potential after an 11,000% rally! Since its IPO in 2014, the Argenx stock has risen by more than 11,150 percent. A study success is fueling new enthusiasm for Argenx. The background. Photo: Andrew Brookes - Westend61 Europe's largest listed pure-play biotech group currently knows only one direction: upwards. The Argenx stock has gained 21 percent since last Friday's closing price, marked a record high and is heading for its best week in more than three years. This puts it at the top of the winners in the Stoxx Europe 600, reports Bloomberg. The long-term record is even more spectacular: Since the Brussels listing in July 2014, the price has shot up by more than 11,150 percent. The market capitalization climbed to 55.4 billion euros - putting Argenx ahead of Moderna again. Trade your assessment of BioNTech SE ADR!

Yahoo Finance
Aug 18th, 2026
Argenx rises 11.5% after positive phase 3 trial for autoimmune myositis treatment

argenx reported positive Phase 3 results for its ALKIVIA trial evaluating VYVGART Hytrulo in adults with autoimmune myositis. The trial met its primary endpoint, with patients showing statistically significant improvements in Total Improvement Score over 52 weeks versus placebo. The study marks the first Phase 3 trial demonstrating benefit in immune-mediated necrotizing myopathy, a subtype with no approved targeted therapies. The safety profile remained consistent with prior studies. The company recently received US FDA priority review for VYVGART in seronegative generalized myasthenia gravis, with a decision expected on 10 May 2026. These label expansions could broaden VYVGART's reach across multiple autoimmune conditions. argenx's shares rose 11.5% following the announcement. The company's narrative projects $9.7 billion revenue and $3.5 billion earnings by 2029, requiring 22.3% yearly revenue growth.

Yahoo Finance
Aug 11th, 2026
argenx shares up 39% in a year, but analysts debate $775 fair value vs $867 close

argenx, a commercial-stage biopharma company specialising in autoimmune disease treatments, has attracted investor attention following recent share price movements. The stock closed at €767, up approximately 6% over the past week and 38.6% over the past year, bringing its market value to around €47.97 billion. The company generates revenue of €5.3 billion, primarily from its VYVGART franchise, with operations spanning the United States, Japan, China, and other markets. According to a widely followed valuation narrative, argenx appears 11.7% overvalued, with a fair value estimate of €686.43. The analysis credits the company's leadership in FcRn inhibitors and strong commercial growth, whilst noting typical biotech risks including single-asset dependence and pricing pressure. Revenue has doubled over two years, supporting the growth thesis.