Evidence Manager

Major accountabilities:

1. Integrated Evidence Planning (IEP) – global to local adaptation

• Co-build and adapt Global Integrated Evidence Plans (IEPs) to local market context, including regulatory requirements, access and reimbursement needs, clinical practice environment
• Identify and prioritize country-specific evidence gaps based on stakeholder needs and product strategy
• Ensure alignment between global evidence strategy and local execution plans
• Continuously assess and refine evidence priorities based on emerging data and insights

2. Local Evidence Planning, Execution Oversight, and Leadership

• Lead and oversee end-to-end Local Evidence Plan (LEP) execution, translating strategy into actionable studies with cross-functional alignment
• Provide strategic oversight of evidence generation activities, ensuring consistency with LEP priorities
• Maintain and continuously refine the Taiwan LEP framework to ensure adaptability to evolving environmental and business needs
• Lead local clinical studies and RWE across the full lifecycle, including design, execution, analysis, and result interpretation

3. External Collaboration & Evidence Co-creation

• Establish and maintain collaborations with medical experts, investigators and academic institutions, external stakeholders
• Explore data partners to expand local real-world data source
• Ensure external insights are integrated into evidence strategy and study design
• Timely and accurate handling of internal and external statistical inquiries

4. Innovation & Advanced Evidence Generation

• Drive adoption of innovative evidence generation approaches, including advanced RWD methodologies and novel study designs
• Leverage AI and emerging data technologies, to enhance efficiency, quality, and impact of evidence generation
• Promote continuous improvement of data-driven and innovative evidence generation capabilities

5. Global Alignment & Governance

• Ensure strong alignment with Global Medical Affairs – Evidence Generation (GMA) strategies, processes, and governance
• Ensure all activities comply with Novartis SOPs, GCP and regulatory requirements
• Maintain inspection readiness and documentation integrity

Requirement

• Advanced degree in Life Sciences, Epidemiology, Biostatistics, or related field
• 3+ years of RWE experience using healthcare databases or EMR in industry, consulting, or CRO
• Strong communication and interpersonal skills
• Strong expertise in study design, protocol writing and methodology
• Demonstrated ability to work collaboratively with cross-functional teams.
• Ability to leverage AI and data-driven tools
• Knowledge / experience with SAS/ R/ S plus or any other business or research analytic software.
• Understanding of multivariable models (cox, poisson, binomial and multinomial logistic, ANOVA and MANOVA and multivariate approach. (cluster discriminant, factor analysis)
• Relevant medical/ clinical background
• Fluent in English & Mandarin (oral and written)