Senior Principal Statistician

329345BR
Oct 07, 2021
Ireland

Job Description

100,000+ unique, curious, and empowered individuals inspired by our purpose.

The Senior Principal Biostatistician is responsible and accountable for all statistical work, scientific and operational, for one or more assigned studies in collaboration with the clinical trial team. Works independently at the trial level and may lead indication or project level statistical activities for a development project under limited supervision. Proposes and leads implementation of modern and innovative trial/experimental designs, statistical models, analysis and data exploration methodologies at the study or project level. Is also responsible for the training and mentoring of other statisticians, and supporting drug project operational excellence.

Your responsibilities:
Your responsibilities include, but are not limited to:
• Responsible and accountable for the statistical activities and support on statistical solutions for trials/publications and conferences and support the tasks independently seeking peer inputs/ reviews as required. Activities include protocol development in alignment with the development plan, providing inputs on statistical scientific and operational aspects of the planning, design and reporting of mid to high complexity trials/experiments, and production and delivery of statistical deliverables and exploratory analyses. Initiate, drive and implement novel methods and innovative trial designs in alignment with the Group Head, Biostatistics.
• Propose and lead statistical/numerical/analytic research by providing advice and solutions on computational aspects of the problem.
• Guides the trial statistician to ensure that documents, specifications, programs/macros are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for all studies.
• Maintain effective interfaces with internal and external customers with advice from Principal Biostatistician and the Principal Statistical Programmers, CRO and CPOs as required.
• Assume responsibility and accountability for reporting and analysis execution for multiple studies. Responsibilities include, leading statistical deliverable meetings with necessary clinical trial team members and third parties, and exploratory analyses for ad-hoc analyses. Expected to provide support for publications for individual clinical studies and scientific analytical solutions.
• Provide guidance to trial statisticians and ensure compliance with project/study standards and specifications following internal guidelines.
• Oversee Biostatistics resources and deliverables for assigned trials and therapeutic area level. Ensure timeliness and adequate quality of all Biostatistics deliverables for the assigned studies and/or non-clinical related activities.
• Explain statistical methodology and interpret analysis results. Provide statistical expertise to support all activities and documents, meetings with and responses to customers and JOC meeting activities, as required.
• Take lead role to collaborate with other line functions including the clinical trial team. Explain statistical concepts in a manner easily understood by non-statisticians, and provide adequate statistical justifications for actions/decisions/statements, when required.
• Support quality control and quality audit of deliverables.
• Provide input on process improvement initiatives and participate in non-clinical project activities with support from group head.
• Actively contribute to cross-functional organizational / process /scientific consulting improvement initiatives. Identify, evaluate and promote the use and the acceptance of innovative methods within the organization, through scientific collaborations, publications in scientific peer re-viewed journals and presentations and chairing sessions at professional meetings.
• Provide support, coaching and mentoring to new hires, senior and junior statisticians.
• Manage the outsourcing of statistical activities from Biometrics to an approved vendor in accordance with Scientific Services vendor management procedures.
• Assist the Group Head in the assessment of applicants for statistician roles within Biometrics.


Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
CTS
NBS CONEXTS
Ireland
Dublin
United Kingdom
Research & Development
Full Time
Regular
No
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329345BR

Senior Principal Statistician

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