Associate Director, Global Integrated Evidence Operations

Summary:The Global Integrated Evidence Operations, Associate Director roleoversees and coordinatestheoperational processes, digital system support, and governanceforGlobal Integrated Evidence & Innovation(GIE&I), which includesresponsibility foroperating models, system readiness,andprocess adherenceforintegrated evidence planning (IEP)and generationprogramsacross the enterpriseIn addition, the role will play a crucial role in enhancing the efficiency and effectiveness of general department operations to supporttimelyand transparent delivery of high impact evidence.Responsibilities:Support the creation and management ofIEPprogramwith a focus on operational efficiency by building out andmaintainingdigital planning platform/repositoryTrack and reportIEP programupdatesto leadership Overseethe digitalIEPplanning platform/repository andmonitordata qualityEnsure operational excellence through the continued development and implementation of standardized processes, tools, and governance forIEPand generationContribute to the development of operational KPIs and dashboards tomonitorperformance and drive continuous improvement forIEPplanning and generation Lead enterprise training,change management, and capability building forsystems, process, and governanceSupportevidence planning governance to ensure alignment with asset vision and strategic objectivesSupportevidence generation governance to oversee the execution of evidence generation activities.Contribute strategic thinking and thought partnership forevidenceoperations,systemsand governance Recommend process improvements and efficiencies toleadershipDevelop andmaintainrelationships with colleagues involved in theIEP, evidencegenerationand governance processes.Requirements:Bachelor's degree in drug development or business management.5years of experience in life sciences or project management supporting research needs.Proventrack recordin program management with matrixed teams in health or life sciences.Strategic mindset with the ability to prioritize tasks andfocuswork accordingly.Capability to synthesizelarge amountsof data into meaningful content.Strong written, verbal, and presentation skills for diverse stakeholders.Excellent project, time management, and organizational skills.Ability to thrive under pressure, meet deadlines, and lead parallel projects.Competence in drug development lifecycle and scientific understanding of assets.Preferred:Formal training or certification in project management methodologies (PMP, Six Sigma, Agile).Experience in developing IEPs or managing complex processes across cross-functional stakeholders.Experience in leading or working closely with leadership governanceSuccessful execution and management of multiple projects supporting life sciences research.Technical experience in drugdevelopment/commercialization.Knowledge of drug development lifecycle functions such as Discovery, Clinical Trials, and Regulatory.Experience with digital technology to support management of planning and research