Associate Director, Global Real-World Evidence, Oncology

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We are searching for the best talent for Associate Director Global Real-World Evidence Oncology to be in Raritan NJ

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

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Learn more at this position the Associate Director GlobalReal-WorldEvidenceOncologywill supportthedevelopment and execution ofglobal RWE strategies and high-priority evidence-generationprogramsacrossthe oncology portfolio.Reporting directly to the Senior Director Global Real-World Evidence Oncology this individual will workunder the strategic guidance of the Global RWE Disease Leadstohelp translate asset-and disease-area evidence priorities into timely high-quality RWE studies and deliverables that support market shaping medical adoption access and evidence-based decision-making. The AssociateDirectorwillpartner closely withRWE ResearchersProgrammers in the GRWE Analytic Hub cross-functional collaborators regional and local evidence-generation teams and external vendors to ensure scientific rigor operational excellence and effective dissemination ofRWE.This individual will alsosupport theDisease Leadsinstakeholder management acrossIEGPlong-rangeWorldwideRWERoadmap development RWE Working Groups and project execution forums.

You will be responsible for:

• Support the Global RWE Disease Lead in developing and maintaining Integrated Evidence Generation Plans and long-rangeWorldwideRWERoadmaps for assigned disease areas and assets ensuring alignment with Global Core Asset Strategy evidence gaps regional priorities and key stakeholder needs.

• Drive high-quality execution of priority RWE studies and evidence-generation projects under the strategic guidance of the Disease Lead ensuring timely delivery scientific rigor operational excellence and appropriate interpretation and dissemination of study outputsto maximize the impact of RWE.

• Collaborate closely with RWE Researchers Programmers in the GRWE Analytic Hub cross-functional partners regional and local evidence-generation teams and external vendors to translate study concepts into protocols analyses deliverables publications and other evidence-dissemination materials.

• Support the Disease Lead in global and regional stakeholder management across cross-functional workstreams RWE Working Groups Evidence Labs and project executionforums.

• Serve as a methodology subject matter expert in assigned cross-functional workstreams providing scientific input on real-world data sources observational study designs analytic approaches fit-for-purpose evidence methods and best practices to strengthen scientific excellence.

• Analyze interpret and synthesize real-world data literature competitive evidence and stakeholder insights to inform evidence-gap assessments strategic trade-off discussions urgent business requests and cross-functional decision-making.

• Contribute toGRWE operationalgovernance standardsprocessesand operating models bysupportingprioritization resource planning deliverable trackingreview processesvendor oversightandconsistency across disease- and asset-level RWE activities.

• Ensure assigned RWE activities are conducted in compliance with applicable regulatory legal privacy publication and commercial requirements while upholding high standards for scientific integrity responsible communication and evidence dissemination.

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