Senior Biostatistician - Pharma (5-12 yrs)

To provide statistical expertise for complex design and interpretation for preclinical or clinical programmes, regulatory submissions, and/or commercialization. You will analyse internal and external information, perform modelling and simulation to inform design decisions, and develop a Statistical Analysis plan for complex studies. You will also contribute to regulatory submissions and identify opportunities for the application of modelling and simulation to improve study design.

- MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognized 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

- Excellent communication skills

- Strong collaboration and team working skills

- Ability to apply statistical expertise to problems, problem-solving and quality focus

- Experience collaborating with all levels of functions within Biometrics

- Experience working with Therapeutic Area scientists

- Experience collaborating with partners in other departments