Senior Statistical Data Analyst
5 days ago
may work directly within a project and/or support statistical methodological advances.Accountabilities for Supporting Projects Directly:
Provide statistical expertise for sophisticated design and interpretation for preclinical or clinical programmes, high level internal governance committees, regulatory submissions and/or commercialisation.Analyse internal and external information, perform modelling and simulation to advise design decisions and the development of decision criteria.Develop a Statistical Analysis plan for complex studies and/or project deliveries.Act as a mentor/guide for less expert statisticians in the production of analysis, supporting graphics and analysis tables for study reports, Global Medical Affairs studies or publications.Able to analyse, interpret, summarise and communicate results of sophisticated studies.Contribute to the regulatory submissions including specification of overview documents and response to regulatory questions.Contribute to the development of standard methodologies to improve quality, efficiency and effectiveness.Accountable for the quality of their statistical work; provide discipline-specific understanding, insight and constructive challenge and take ownership of development needs, seek coaching or training opportunities.Draft statistical analysis plans for complex studies.Provide consultancy within area of expertise to fellow statisticians working within therapeutically aligned statistics groups, as well as medical scientists and other key roles across the business.Investigate and apply novel statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration.Identify new areas where we can make valuable contributions, developing collaborative relationships with the external scientific/academic community and maintaining academic links.Communicate research and results internally and externally through participation at conferences and journal publications.MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc.Knowledge of key technical and regulatory requirements.Experience of design, analysis and reporting of preclinical or clinical studies in more than one setting.Experience and knowledge of statistical methods and applications in study design, analysis and interpretation.View our YouTube channel.AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.-
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