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Principal/senior principal biostatistician

Basel
Novartis
EUR 115’000 pro Jahr
Inserat online seit: 20 Juli
Beschreibung

Join to apply for the Principal/Senior principal Biostatistician role at Novartis

Join to apply for the Principal/Senior principal Biostatistician role at Novartis

Summary

We are in search of a Principal/Senior Principal Biostatistician to join a passionate team in late development. Come to an industry leader where you will lead implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study or project level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners in the early development analytics team.

Summary

We are in search of a Principal/Senior Principal Biostatistician to join a passionate team in late development. Come to an industry leader where you will lead implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study or project level and you will be responsible for all statistical work, scientific and operational, in collaboration with the clinical trial teams and other quantitative partners in the early development analytics team.

About The Role

Your Key Responsibilities:


* Responsible for all statistical tasks on the assigned trials.
* Protocol development in alignment with the development plan, developing statistical analysis plan, reporting activities.
* Contribute to planning and execution of statistical analyses and statistical consultation within your cross-functional teams.
* Initiate, drive and implement novel methods and innovative trial designs in alignment with the Lead Statistician.
* Collaborate with clinical, regulatory and other strategic functions to drive quantitative decision making in assigned indications/program with oversight.
* Collaborate cross-functionally (e.g. data management, programming, medical writing) to ensure timeliness and quality of statistical deliverables.
* Contribute to external engagement with consultants, advisory boards, health authorities, congresses, and scientific meetings

Role Requirements

Essential Requirements:

* PhD with 3+ years’ experience preferred OR MS with 7+ years’ experience
* Fluent English (oral and written)
* 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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

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


Seniority level

* Seniority level

Mid-Senior level


Employment type

* Employment type

Full-time


Job function

* Job function

Education and Training
* Industries

Pharmaceutical Manufacturing

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