You will be part of a large organisation with strategic partnership in the pharmaceutical industry allowing you to grow and develop a long term career in the business.
As an experienced Biostatistician you will be expected to cover the following responsibilities:
- Performing advanced scientific statistical analyses
- Statistical part of the protocol development and statistical support for clinical studies (i.e.: statistical review, sample size, statistical analysis…)
- Writing of the statistical analysis plan
- Representing Biostatistics as a member of clinical trial teams, providing input and technical guidance to elicit meaningful and/or productive outcomes.
- Presentation of statistical results
- Collaborating with statistical programming and other functions to ensure timely delivery of TFLs with good quality.
- Implementing design and analysis methods at the study level and participates in Statistical Review Forum (SRF) discussions of studies assigned to others.
Requirements:
- MSc or PhD statistics, biostatistics, or related field
- Demonstrated experience as a Statistician within a pharmaceutical, biotech or CRO environment
- Experience developed across Phase I to III studies
- Good experience with SAS and R statistical software
- Fluent in English (spoken and written)
- Ability to work in team and independently
- Demonstrated understanding of advanced statistical methods used in drug development
- Ability to show critical thinking with logical problem-solving
- Excellent written and verbal communication skills
- Excels in a team environment
Please contact me at yanick.millet@seclifesciences.com for more information.
