Real-World Evidence Strategy Lead, Respiratory (Hybrid)

UCB; Brussel; Hybrid; EUR 165,000 - 216,000; Full time

Job summary

UCB is seeking a Real-World Evidence Strategy Lead, Respiratory, to drive global evidence strategies across the lifecycle of respiratory assets. This hybrid, results-driven role collaborates across clinical development, regulatory, market access and safety to inform decisions that improve patient outcomes.

The candidate will translate research questions into evidence plans, lead studies with governance and budget oversight, and mentor a global team.

Qualifications

• Advanced degree in life sciences, medicine, epidemiology, statistics, or related discipline.
• At least eight years of pharmaceutical industry experience, ideally within respiratory medicine or immunology.
• Strong expertise in epidemiology, outcomes research, clinical development, regulation, and market access.
• Proven ability to lead cross-functional teams and mentor colleagues.

Responsibilities

• Develop integrated real-world evidence strategies supporting respiratory assets throughout their lifecycle.
• Translate stakeholder research questions into impactful data, registry, and evidence-generation plans.
• Lead real-world evidence studies, ensuring quality, governance, timelines, and budget adherence.
• Collaborate across functions to align evidence priorities and resolve competing stakeholder needs.
• Build relationships with external experts, research partners, and healthcare decision-makers.
• Mentor evidence-generation professionals and support capability development across the global function.

Skills

Advanced degree

8+ years exp

Respiratory/immunology

Epidemiology

Outcomes research

Regulatory/market access

Cross-functional leadership

Scientific writing

Quantitative analysis

Education

Advanced degree in life sciences

Epidemiology or statistics

Job description

UCB is seeking a Real-World Evidence Strategy Lead, Respiratory, to drive global evidence strategies across the lifecycle of respiratory assets. This hybrid, results-driven role collaborates across clinical development, regulatory, market access and safety to inform decisions that improve patient outcomes.

The candidate will translate research questions into evidence plans, lead studies with governance and budget oversight, and mentor a global team.