Principal Biostatistician

The primary purpose of the
Principal Statistician
is to act independently as Study Statistician for complex work in an established area within clinical studies. This position may also act as Global Statistical Lead for an early or back up asset or as a Methodology expert validating the execution of complex techniques.
Responsibilities:
Accountable for leading Biostatistics and Programming activities for a program of studies of high complexity and/or of high value with high impact.
Lead or provide the statistical input into the design of the program, protocol input such as study design, sample size calculations and patient randomization schemes and statistical aspects of case report form design
Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
Writing of the statistical methods sections of integrated study reports. Reviews draft integrated study reports.
Lead or supports responses to regulatory questions on the design of the program
Ongoing coaching and mentorship of team members.
Key Requirements:
PhD or M.S in Biostatistics, Statistics or related scientific field
Significant experience in applying statistical methods in Pharma or CRO setting
Advanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical data
Good ability in SAS required, knowledge of R preferred.
Ability to understand, implement, and explain complex statistical methodology,
Significant advantage: #oncology or #rarediseases
Further information:
This is a permanent role and can be based in
UK, Netherlands or Belgium
Remote based with ability to travel to the company's HQ - costs of travelling covered
If this opportunity is of interest, please apply now with your CV at your earliest availability. If further info needed, please feel free to connect with Catalin Zaharia.