Director Real World Evidence Scientist (Oncology) (all genders)

Real-world evidence is reshaping how medicines are developed, approved, and valued — and in this role, you will be at the forefront of that transformation. As a Director Real-World Evidence Scientist in Oncology, you will own and drive the end-to-end RWE strategy for one or more complex, high-priority oncology programs, operating as a recognized scientific authority across the organization and beyond.

You will define and lead the integration of RWE into clinical development and regulatory strategies, working directly with global program teams and cross-functional partners across clinical, regulatory, market access, and commercial functions. You will design, initiate, and oversee non-interventional studies — from protocol development through to study reporting — and ensure the selection of fit-for-purpose real-world data sources that address critical research questions. Your scientific judgment will directly inform decision-making at the most senior levels of the organization.

Beyond program delivery, you will represent the organization in interactions with health authorities, contribute to peer-reviewed publications, and present at international conferences — actively shaping the external scientific landscape. You will also champion methodological innovation, drive process improvements, and serve as a scientific mentor to colleagues within the function, contributing to a culture of rigor, collaboration, and continuous learning.

‍