Associate Director Biostatistics Real World Data

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Summary

Our Scientists are responsible for providing robust statistical support for the design and analysis of real-world evidence studies, including patient preference studies. This involves developing methodologies and utilizing your statistical and programming expertise. There may also be opportunities to contribute to the regulatory aspects of such studies.

About The Role

Our Development Team is driven by our purpose: to reimagine medicine to improve and extend lives. We are enhancing our processes, investing in new technologies, and building specialized capabilities to accelerate bringing medicines to patients. We seek talented individuals like you to join us and help create a brighter future for patients and their families.

This role offers a hybrid working model, requiring 3 days per week in our London office.

Key Responsibilities

• Design, analyze, and manage non-interventional studies (NIS), including Patient Preference Studies (PPS), collaborating with stakeholders to deliver critical analyses.
• Represent the real-world data (RWD) statistical expertise within Global Medical Affairs and Patient Engagement.
• Contribute to regulatory documents as needed for such studies.
• Develop study protocols, analysis plans, and reports.
• Conduct data analysis, develop statistical models, and perform programming (preferably in R and/or SAS).
• Support and train team members on RWD study methods and principles.
• Manage vendors related to statistical deliverables.
• Represent Novartis at meetings related to NIS (including PPS).
• Develop internal processes for NIS design, reporting, and execution.
• Stay updated on the latest methods and identify opportunities for methodological innovation.

Required Experience

• MSc in Statistics or related field with at least 5 years of relevant experience, or PhD with at least 3 years of experience in RWD analysis methodology.
• Advanced knowledge of statistical applications and innovative approaches.
• Proficiency in R (advanced skills required); knowledge of SAS, STATA, or similar is a plus.
• Ability to manage multiple projects with scientific rigor.
• Strong curiosity, independence, and self-motivation.
• Proactive, responsive, and capable of managing shifting priorities.
• Excellent relationship management skills with internal and external stakeholders.
• Fluent in English with strong communication and presentation skills, able to articulate complex concepts clearly.

Why Join Novartis

Helping people with disease and their families requires more than science; it requires a passionate community. Join us to collaborate, support, and innovate to change lives. Learn more about our culture and values: Novartis Culture.

Our Commitment to Diversity & Inclusion

We are dedicated to creating an inclusive, diverse work environment that reflects the communities we serve.

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Benefits & Rewards

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Additional Details

• Seniority Level: Mid-Senior level
• Employment Type: Full-time
• Job Function: Research, Analysis, IT
• Industry: Pharmaceutical Manufacturing