About the jobAt Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice. Sr. Manager, Integrated Evidence Generation Your Tasks And Responsibilities Contribute to IEG strategy of Bayer assets overarching TA data strategy and plans through effective collaborations with relevant internal and global stakeholders, responsible for evidence generation needs leveraging Real World Data (RWD) and Real World Evidence (RWE), serving all asset teams (Med, Mkt, MACS, R&D etc.) within the defined disease area Evidence Generation Lead the development and execution of Bayer-sponsored RWD/RWE studies based on RWD/RWE expertise in partnership with TA medical affairs (MATA) and Globalfunctions (such as IEG and GHEOR) Ø Primary RWD/RWE (e.g., Non-interventional study) by request Ø Secondary RWD/RWE (e.g., Database study including PMS) Ø Patient-generated health data including patient reported outcome, disease burden and digital biomarkers Support the development of concept and protocol of secondary RWD/RWE studies and support primary data collection study protocol development Responsible RWE publication and contribute to data communication strategies Facilitate the collaborative research projects on secondary data generation with academia Methodology guidance: Support senior IEG leads to translates the strategic needs of business stakeholders into portfolio of analytics projects and manage strategic initiatives incorporating the most innovative methodological approach and appropriate data sources, tools, and platforms Obtain the up-to-date information and new technologies/methodologies related to RWD/RWE and feed back to internal stakeholders Stakeholder engagement: Support trainings in RWD/RWE related field for internal stakeholders based on professional knowledge Act as a point of contact with global IEG/BI and internal stakeholders in responsible TAs for RWD/RWE Keep communication with KOLs and tracking environment changes YOUR APPLICATIONIf your background and personal experience fit this profile, please send us your complete application at www.career.bayer.cn If you have any recommendations, please kindly send mail to ***@***.***L ocation: China : BeiJing : BeiJingDivision:PharmaceuticalsReference Code:836028

Who You Are Master's degree and above in Medicine, Pharmacy, life science disciplines or related field, preferably combined with a degree in epidemiology, data science, health economics or comparable public health science Appropriate experience with Regulatory Agency and KOL interactions Track records in leading/managing projects involving cross-functional teams and expertise Desirable Ph.D. in related field and/or qualified medical doctor Experience in one or more of the following areas, including but not limited to Market Access, Commercial, Epidemiology, R&D, Data Science, and/or Medical Affairs (ideally 3 or more years) Previous experience in oncology, C> Competencies: Excellent knowledge of regulations relevant for RWE/RWD and GEP standards. Proven evidence of effective delivery of high-quality documents for RWE projects in both local language and English. Applies in-depth medical knowledge and expertise in the design, initiation and conduct of clinical-epidemiological studies, evidence generation activities and medical benefit-risk assessments Effectively translating strategy into actionable projects and initiatives Through understanding of diverse stakeholders