Safety Evidence Medical Lead

argenx US; Belgique; On-site; EUR 120,000 - 180,000; Full time

Job summary

argenx seeks an experienced Safety Evidence (Medical) Lead to translate safety data into strategic insights across the product lifecycle. You will blend medical science, data analytics and clinical strategy to differentiate argenx therapies and shape evidence generation plans.

Based in Belgium, Switzerland or the US (EST), you will partner with medical affairs, regulatory and clinical teams to drive late-stage safety studies, real-world evidence and scientifically compelling narratives for

Qualifications

• Requires strong medical/scientific background and experience with safety evidence generation.
• Ability to translate complex safety data into decision-relevant insights.
• Experience collaborating with medical affairs, regulatory, clinical development and statistical teams.

Responsibilities

• Strategically evaluate safety evidence to differentiate argenx products and competitors.
• Lead strategy and interpretation of safety-focused studies, including real-world data.
• Shape Integrated Evidence Generation Plans (IEGPs) and ensure safety evidence answers key questions.
• Provide medical leadership for safety endpoints in real-world studies and PAS.
• Translate evidence into clear narratives for internal and external stakeholders.

Skills

Strategic thinking

Medical science

Data analytics

Cross-functional leadership

Scientific communication

Influence skills

Job description

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.

To strengthen our Safety Evidence and Insights team, we are seeking an experienced pharmaceutical professional who can connect medical science, safety evidence and business strategy across the product lifecycle.

The Safety Evidence (Medical) Lead will generate and translate safety evidence into insights that differentiate argenx therapies, strengthen understanding of their benefit-risk profile, and inform evidence and product strategy . The role combines medical/scientific expertise, data analytics and strategic thinking, integrating evidence from internal safety data, real-world data, post-authorization studies, medical literature and other relevant sources.

This role does not simply generate safety evidence. It identifies where safety evidence can create meaningful scientific and strategic differentiation, then builds the evidence needed to realize that opportunity.

The successful candidate will operate as both a strategic thought partner and hands-on evidence leader , bringing deep understanding of drug development, safety science and the broader competitive environment.

We are looking for candidates based in Belgium, Switzerland or US (EST time zone.

Purpose of the Role

The Safety Evidence (Medical) Lead will:

• Identify opportunities for strategic differentiation by assessing the safety profiles of argenx products in the context of competitors and the evolving treatment landscape.
• Identify critical safety evidence gaps and translate them into evidence-generation priorities.
• Shape and contribute to Integrated Evidence Generation Plans (IEGPs) , ensuring safety evidence supports meaningful scientific and strategic questions.
• Provide medical interpretation and contextualization of safety evidence across multiple data sources, converting complex data into decision-relevant insights.
• Provide safety expertise to cross-functional teams.
• Lead late-stage safety-focused studies, including real-world studies.
• Translate evidence into clear scientific narratives for internal and external stakeholders.

Key Responsibilities:

Strategic Safety Intelligence & Differentiation

• Continuously evaluate emerging safety evidence for argenx products and relevant competitors to identify differentiating attributes, evidence gaps and emerging opportunities .
• Integrate safety, clinical, real-world and scientific evidence to develop a holistic understanding of product safety profiles.
• Translate complex evidence into actionable insights that inform evidence strategy and cross-functional decision-making .

Evidence Strategy & Generation

• Partner with RWE, Medical Affairs, GPS, Regulatory, HEOR, Clinical Development, Clinical Science and Biostatistics to shape evidence-generation priorities and IEGPs.
• Lead the strategy, design, interpretation and scientific communication of safety-focused studies, including PASS.
• Provide medical and safety leadership for the interpretation of safety endpoints and outcomes in real-world studies.
• Ensure evidence generation addresses questions that matter to patients, healthcare professionals and other relevant stakeholders.

Scientific Leadership & Influence

• Serve as a medical and scientific thought partner on safety evidence across functions.
• Develop compelling scientific narratives that contextualize safety findings and articulate their relevance for argenx therapies.
• Partner with Scientific Communications to integrate safety evidence into publication strategies.
• Engage external experts and KOLs to strengthen evidence strategies and scientific understanding.

Skills & Competencies:

• Strong strategic, medical and scientific judgment , with the ability to connect evidence to broader product and business questions.
• Ability to integrate complex safety information across multiple data sources and distinguish meaningful signals and insights from data noise.
• Strong understanding of drug development and evidence generation across the product lifecycle.
• Ability to influence and collaborate effectively in a complex, cross-functional environment.
• Strong scientific communication skills, with the ability to translate complex evidence into clear, decision-relevant narratives.
• Intellectual curiosity and a proactive, solution-oriented mindset.
• High digital and analytical literacy, including