RWE Associate Director
4 weeks ago
The RWE Associate Director will support the development and execution of Real World Evidence (RWE) strategies for molecules within a disease area, with a focus on non-interventional studies.
Key Responsibilities- Support the development and implementation of RWE strategies across multiple molecules, collaborating with internal partners to ensure the value of our medicines is supported by evidence globally and locally.
- Collaborate with cross-functional RWE teams to deliver scientifically valid and robust evidence to support product development and drive global and local value demonstration.
- Lead non-interventional studies and other RWD projects, staying current with emerging analytical methodologies, tools, and applications to ensure innovative approaches.
- Apply rigor in study design and analytical methods, designing fit-for-purpose analysis plans and implementing effective communication strategies to maximize impact and interpretability.
- Drive RWE innovations and effective communication to internal stakeholders, regulatory bodies, health technology assessment bodies, and scientific communities.
- Lead functional, cross-functional, enterprise-wide, or external RWE communities, networks, collaborations, initiatives, or goals on knowledge sharing, methodologies, innovations, technology, IT infrastructure, policy shaping, processes, etc.
- Master's degree in a field such as epidemiology, public health, biostatistics, statistics, bioinformatics, economics, or similar.
- Previous experience in conducting research in the pharma industry, contract research organization, healthcare provider / HTA, or academic institute, or experience in a closely related discipline within the pharma industry.
- Deep understanding and experience of Real World Data/Real World Evidence or related disciplines to generate scientifically rigorous and value evidence from secondary data sources.
- Experience/knowledge in causal inference methods including propensity score matching, inverse probability of treatment weights.
- Strong experience and excellent knowledge of observational and/or epidemiological research and statistical methods.
- Demonstrated track record of leading and executing research projects with no or minimal supervision using real world data from claims, electronic health records, registries, biobanks, and/or digital applications.
- Proven ability to interpret, discuss, and represent data relating to the assigned area.
- Demonstrated ability to publish study results in peer-review journals and conferences.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Why NovartisHelping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
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