Senior Statistician I - Barcelona, España - AstraZeneca

AstraZeneca

Empresa verificada

Barcelona, España

hace 2 semanas

Publicado por:

Isabel García

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Descripción

Job Description / Capsule

The Senior Statistician I has necessary academic qualifications, and sufficient experience working as a statistician in the pharmaceutical industry, to work independently on standard activities.

More complex studies, and analytical work, will be guided by a more experienced statistician. Common activities include study-level support, including set-up, conduct, analysis and reporting. Technical statistical projects can also be addressed.

Typical Accountabilities

Demonstrate independence in providing statistical support for standard design and interpretation of study data
Under guidance of a more experienced statistician will undertake design and analysis of complex studies, and provide statistical support for broader programmes, which may include preclinical studies, complex regulatory submissions or commercialisation activities and/or high level internal governance committee interactions
Under guidance of a more experienced statistician, analyse internal and external information to inform design decisions and the development of decision criteria
Develop a Statistical Analysis Plan for study and/or project delivery
Produce analysis, supporting graphics and analysis tables for standard studies, such as in preclinical or clinical study reports, Global Medical Affairs studies or publications
Able to interpret, summarise and communicate results of standard studies
Contribute to the improvement of methodology and provide practical solutions for problems
Contribute to the development of best practice to improve quality, efficiency and effectiveness
Accountable for the quality of their statistical work; provide disciplinespecific understanding, insight and constructive challenge and selfaware of own development needs

Education, Qualifications, Skills and Experience

Essential

MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognised equivalent to stats MSc
Competent statistical programmer (SAS and R)
Knowledge of key technical and regulatory requirements
Experience of design, analysis and reporting of preclinical or clinical studies in more than one setting
Communication skills
Collaboration and team working skills

Desirable