RWE Strategy Lead, Developed Brands

Make your mark for patients

We are looking for a RWE Strategy Lead Developed Brands Immunology who iscollaborative solutions-oriented and passionate about leveraging real world data to improve the patient experienceto join our HTA and Payer Team. This role can be based in Europe either at our headquarters in Brussels Belgium or at one of our primary hubs in Monheim Germany or Slough United Kingdom. The position is also available in multiple locations across the United States.

This hybrid rolerequires a minimum of 40% on-site presence and 5-10% domestic and international travel.

About the Role
You will lead the development and execution of global real-world evidence (RWE) strategies that support the value safety effectiveness and patient impact of UCBs therapies. You will identify critical evidence needs for existing product lifecycle and translate them into further integrated RWE epidemiology outcomes research and data strategies that inform regulatory market access reimbursement and business decisions while supporting and expanding our patient access reach.

This strategic leadership role requires a deep understanding of evidence generation healthcare data and the evolving external landscape. You will drive the use of innovative study designs registries real-world data sources and emerging technologies to address key evidence gaps and ensure decision-makers have the insights needed to improve outcomes for patients. Success in this role requires scientific expertise strategic thinking and the ability to influence complex evidence agendas while balancing diverse stakeholder needs and long-term business priorities.

Who youll work with

Internally you will work with colleagues across Real World Evidence Medical Affairs Clinical Development Pharmacovigilance HEOR Market Access Safety Epidemiology Patient Impact and Data & Analytics functions to shape evidence strategies identify evidence gaps and generate insights that support and defend reimbursement and business decisions.

Externally you will work with academic researchers healthcare data providers registry organizations contract research organizations (CROs) scientific experts and industry stakeholders to advance evidence-generation initiatives access relevant data sources and ensure the delivery of high-quality decision-grade evidence.

What youll do

• Develop and co lead integrated real-world evidence (RWE) epidemiology outcomes research and data strategies that support UCBs assets across the product lifecycle.
• Identify evidence gaps and define research plans that address regulatory market access reimbursement safety and patient-centered evidence needs.
• Shape evidence-generation strategies using real-world data registries external control arms innovative study designs and other fit-for-purpose methodologies.
• Anticipate evolving scientific regulatory and business challenges and translate them into actionable evidence solutions and investments.
• Oversee the execution of RWE studies and programs ensuring delivery on time within budget and in accordance with quality and governance standards.
• Drive alignment across complex evidence-generation activities balancing the needs of multiple stakeholders while maximizing impact and efficiency.
• Provide strategic guidance on topics including disease burden natural history comparative effectiveness long-term outcomes drug utilization safety commitments and health technology assessment requirements.
• Leverage emerging technologies including AI-enabled approaches to enhance data strategy evidence generation and decision-making.
• Mentor and develop RWE talent while contributing to the continued growth of evidence-generation capabilities across the broader organization.
• Represent UCB externally through engagement with scientific experts research partners and industry initiatives to advance the use and impact of real-world evidence.

Interested For this role were looking for the following education experience and skills
Minimum Experience/

Skills Required:

• Masters degree PhD MD or equivalent advanced degree in Epidemiology Public Health Health Economics & Outcomes Research (HEOR) Biostatistics Life Sciences or a related discipline.
• 8 years of experience within the pharmaceutical biotechnology healthcare or academic sectors with demonstrated involvement in evidence generation clinical development market access regulatory and/or payer-related initiatives. Experience with Big Data and AI is an advantage
• Strong understanding of real-world evidence (RWE) epidemiology outcomes research and healthcare data sources.
• Experience developing evidence strategies that support regulatory reimbursement clinical and business decision-making.
• Demonstrated ability to lead complex initiatives and influence stakeholders in a matrix environment.

Preferred Qualifications

• Formal training in epidemiological research methods outcomes research health economics or related quantitative disciplines.
• Experience developing and executing integrated RWE strategies for or with pharmaceutical…