Digital Technology Product Owner, Medical Affairs

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.

We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.

For the expansion of our international DT Commercial team, argenx is looking for Product Owner – DT Commercialization - DT Medical Affairs.

This role will own the technology vision and value delivery for our Medical Affairs and Evidence Generation capability within Digital Technology (DT) Commercial. It is accountable for translating the goals of our Medical Affairs and Evidence Generation teams into a clear product vision and a prioritized backlog for platforms that support scientific exchange. By acting as the primary liaison between medical experts and technical teams, ensuring all solutions meet key compliance standards, and enabling the use of technology to generate insights, this position is directly responsible for ensuring our digital ecosystem supports effective and compliant medical engagement.

Roles & Responsibilities

• Own the digital product vision and prioritize the backlog for key Medical Affairs and Evidence Generation platforms, including Medical CRM and scientific exchange tools.

• Act as the primary medical-to-tech liaison, translating complex scientific engagement and evidence generation needs into clear, actionable user stories.

• Ensure all digital solutions strictly adhere to non-promotional regulations and medical integrity standards, embedding compliance into the design process.

• Drive the development of tools and analytics to capture and analyze global medical insights, enabling data-driven strategic decision-making for Medical Affairs and Evidence Generation leadership.

• Act as the steward for the end-to-end user experience for Medical Affairs and Evidence Generation platforms, ensuring they are intuitive and effective for field medical teams and HCPs.

• Define and monitor Key Performance Indicators (KPIs) for success, continuously measuring the value and impact of the technology on scientific engagement objectives.

• Provide clear, day-to-day direction to various delivery teams on what to build next, ensuring alignment with Medical Affairs priorities.

• Serve as the primary point of contact for delivery teams, providing constant feedback and clarification on medical requirements to empower effective execution.

Skills and Competencies

• Deep knowledge of product management principles, particularly in defining a product vision and strategy that aligns with Medical Affairs and Evidence Generation goals.

• Skilled in translating complex scientific or medical business needs into clear requirements and user stories for technical teams.

• Ability to own and prioritize a product backlog based on scientific value and strategic importance within a regulated pharmaceutical environment.

• Expert knowledge of the legal and regulatory compliance framework governing non-promotional activities and scientific exchange in the pharmaceutical industry.

• Knowledge of the digital technologies that support Medical Affairs and Evidence Generation, such as Medical CRM and platforms for insight gathering and scientific content dissemination.

• Ability to work collaboratively and effectively together within cross-functional teams and networks.

• Demonstrated communication skills, within a multi-cultural and multi-lingual global environment.

• Is agile and demonstrates adaptability, comfort with ambiguity, trust-building, and resilience.

• Drives toward outcomes.

• Ambitious, inquisitive naturally, a quick study, with demonstrated eagerness to continuously learn, self-improve and develop. This includes being comfortable giving and receiving feedback in a diverse environment.

• Passionate and prepared to lead and contribute to our culture, which is driven by our corporate values of co-creation, innovation, empowerment, excellence, and humility.

Education, Experience & Qualifications

Bachelor’s or Master Degree preferred in Life Sciences, Pharmacy, Information Technology, Business Administration, or related fields.

• 5+ Years experience as a Product Owner, Product Manager, or Business Analyst with a focus on delivering solutions for Medical Affairs, Clinical, or R&D functions.

• 5+ Years experience in the pharmaceutical or life sciences industry, with a strong understanding of Medical Affairs and Evidence Generation business processes and compliance requirements.

• 5+ Years experience owning a product roadmap and using KPIs to measure and communicate the value of technology solutions to scientific or medical stakeholders.
• Up to 20% travel required

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For applicants in the United States: The annual base salary hiring range for this position is $156,000.00 - $214,500.00 USD. This range reflects our good faith estimate at the time of posting. Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity. This means actual pay may differ from the posted range when justified by these factors. Because market conditions evolve, pay ranges are reviewed regularly and may be adjusted to remain aligned with external benchmarks.

This job is eligible to participate in our short-term and long-term incentive programs, subject to the terms and conditions of those plans and applicable policies. It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.

At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.

Before you submit your application, CV or any other personal details to us, please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates (“argenx”) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at privacy@argenx.com.

If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response.

About Us

argenx is a global immunology company dedicated to improving the lives of people suffering from severe autoimmune diseases. Through our rich pipeline of first-in-class therapies, led by VYVGART®, we are accelerating progress toward our bold 2030 vision: to reach 50,000 patients and transform the landscape of autoimmune treatment. Our innovation mission combines with meaningful work and endless opportunities for growth to create once-in-a-career experiences. argonauts work in locations around the globe including Belgium, Boston, Japan and Amsterdam. There's more to discover at argenx, where our passion inspires bold possibility.

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