Senior Medical Safety Evidence Lead

Argenx; Belgique; Remote; EUR 130,000 - 180,000; Full time

Job summary

argenx is seeking a Safety Evidence (Medical) Lead to translate safety data into strategic insights across the product lifecycle. Based in Belgium, Switzerland or the US (EST), you will identify evidence gaps, shape integrated plans, and lead late-stage safety studies while partnering with Medical Affairs, Regulatory and Clinical Development.

You will translate complex safety information into decision-ready narratives, support cross-functional teams, and engage with external experts to

Qualifications

• Medical degree preferred; PhD/PharmD considered with immunology expertise.
• Minimum 5 years leading scientific or clinical projects.
• Experience in Safety Evidence, late-stage development or related roles.

Responsibilities

• Identify opportunities for strategic differentiation by assessing safety profiles across products and competitors.
• Shape Integrated Evidence Generation Plans (IEGPs) ensuring safety evidence supports key questions.
• Provide medical interpretation of safety data across multiple sources for decision-making.
• Lead safety-focused studies, including real-world evidence, and communicate findings clearly.
• Serve as a medical thought partner to cross-functional teams and influence strategy.

Skills

Strategic thinking

Medical affairs

Data interpretation

Cross-functional collaboration

Scientific communication

Education

Medical degree preferred

Tools

Analytical dashboards

Job description

argenx is seeking a Safety Evidence (Medical) Lead to translate safety data into strategic insights across the product lifecycle. Based in Belgium, Switzerland or the US (EST), you will identify evidence gaps, shape integrated plans, and lead late-stage safety studies while partnering with Medical Affairs, Regulatory and Clinical Development.

You will translate complex safety information into decision-ready narratives, support cross-functional teams, and engage with external experts to