Job Description Summary Evidence Manager Location : Taipei #LI-Hybrid Are you passionate about using evidence, data, and innovation to shape better healthcare decisions? Join Novartis Taiwan and play a key role in translating global evidence strategies into meaningful local impact for patients, healthcare professionals, and the broader healthcare ecosystem. This is an opportunity to shape evidence generation in Taiwan, collaborate with local and global teams, and help bring meaningful insights into healthcare decision-making. If you are motivated by scientific excellence, cross-functional collaboration, and the opportunity to make a real impact, we would love to hear from you. Job Description Main accountabilities Lead the adaptation of Global Integrated Evidence Plans (IEPs) to the Taiwan market, ensuring alignment with local regulatory, access, reimbursement, and clinical practice needs. Identify and prioritize local evidence gaps based on stakeholder insights, product strategy, and evolving healthcare priorities. Translate evidence strategy into actionable Local Evidence Plans (LEPs), partnering closely with cross-functional teams to drive high-quality execution. Lead local clinical studies and real-world evidence activities across the full lifecycle, from study design and execution through analysis, interpretation, and communication of results. Build and strengthen collaborations with medical experts, investigators, academic institutions, data partners, and other external stakeholders. Integrate external insights into evidence strategy, study design, and evidence generation priorities. Drive adoption of advanced RWD methodologies, novel study designs, and data-driven approaches. Ensure strong alignment with Global Medical Affairs evidence generation strategies, processes, governance, and compliance expectations. Requirements Advanced degree in Life Sciences, Epidemiology, Biostatistics, or a related field. Minimum 3 years of RWE experience using healthcare databases or EMR, gained in industry, consulting, or CRO settings. Strong expertise in study design, protocol writing, statistical methodology, and evidence generation execution. Experience with analytical tools such as SAS, R, S-Plus, or other business or research analytics software. Understanding of multivariable models, including Cox, Poisson, binomial and multinomial logistic models, ANOVA, MANOVA, and multivariate approaches such as cluster, discriminant, and factor analysis. Relevant medical or clinical background, with strong communication and interpersonal skills. Fluent English and Mandarin communication skills, both written and spoken. Skills Desired Clinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Medical Information, Patient Care, Stakeholder Engagement Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. Novartis is not responsible for any claims, losses, damages, or expenses resulting from scams. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

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