Pharmaceuticals RWE Lead
2 days ago
The RWE Associate Director will be responsible for supporting the development and execution of Real World Evidence strategies for our molecules within a disease area. This includes the execution of RWE activities with a particular focus on non-interventional studies (NIS).
Key Responsibilities:
1. Develop and implement RWE strategies that ensure the value of our medicines is supported by evidence globally and locally.
2. Collaborate with internal partners to deliver scientifically valid and robust evidence to support all stages of product development and drive global and local value demonstration.
3. Lead non-interventional studies and other RWD projects, adopting emergent analytical methodologies, tools, and applications to ensure fit-for-purpose and innovative approaches.
4. Apply rigor in study design and analytical methods, designing a fit-for-purpose analysis plan and implementing it to maximize impact and interpretability.
5. Drive RWE innovations and effective communication to internal stakeholders, regulatory bodies, health technology assessment (HTA) bodies, and scientific communities.
6. Participate in external meetings and forums as a thought leader and lead functional, cross-functional, enterprise-wide, or external RWE communities to enable broader and more effective use of data and analytics to reimagine cancer treatment.
Minimum Qualifications:
1. Master's degree in epidemiology, public health, biostatistics, statistics, bioinformatics, economics, or similar fields.
2. Previous experience in conducting research in the pharma industry, contract research organization, healthcare provider / HTA, or academic institute.
3. 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.
4. Experience/knowledge in causal inference methods including propensity score matching, inverse probability of treatment weights.
5. Strong experience and excellent knowledge of observational and/or epidemiological research and statistical methods.
6. 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.
7. Proven ability to interpret, discuss, and represent data relating to the assigned area.
8. Demonstrated ability to publish study results in peer-review journals and conferences.
9. Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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