Senior Statistician I

The Senior Statistician I has the 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.

Accountabilities:
Demonstrate independence in providing statistical support for standard design and interpretation of study data
• Under the guidance of a more experienced statistician, undertake the design and analysis of complex studies, and provide statistical support for broader programs, which may include preclinical studies, complex regulatory submissions or commercialization activities, and/or high-level internal governance committee interactions
• Under the guidance of a more experienced statistician, analyze internal and external information to inform design decisions and the development of decision criteria
• Apply modeling and simulation to inform study design, assess robustness of results, etc.
• 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, summarize, and communicate results of standard studies
• Contribute to the improvement of methodology and provide practical solutions for problems
• Apply statistical methodology to improve the process and delivery activities
• Contribute to the development of best practices 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-

Essential Skills/Experience:
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
• Communication skills
• Collaboration and team working skills

Desirable Skills/Experience
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When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. Here all doors are open, and every voice is heard. From working side-by-side with academia to innovating with biotech, we are forever expanding our horizons. By sharing and increasing our knowledge we are empowered to be the best we can be and accelerate progress.

Ready to make a difference? Apply now!