Your Key Responsibilities:
- Responsible for all statistical tasks on the assigned trials.
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Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
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Contribute to planning and execution of exploratory analyses and statistical consultation within your cross-functional teams.
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Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
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Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
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Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
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Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings
Role Requirements:
Essential Requirements:
- PhD experience preferred OR MS with extensive experience
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Fluent English (oral and written)
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Strong communication and presentation skills
Why Novartis: Helping 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? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
