Senior Statistician I
hace 2 días
**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 discipline-specific understanding, insight and constructive challenge and self-aware 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**
- Collaboration required
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