We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, general company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Lead all biostatistics activities related to clinical trials as responsible project statistician
Communicate with project teams, clients and vendors on statistical questions
Develop statistical analysis plans
Develop and document analysis database structures (i.e. SAS analysis data set structures)
Develop SAS program requirements and specifications
SAS programming and program validation
Review and QC of statistical deliverables (tables, listings, figures, etc.)
Perform statistical analysis and report results
Liaise with DM on statistical questions related to data issues, including coordination of data transfers from DM to Statistics
Train statisticians and SAS programmers
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
Ability to apply a range of advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information
Ability to consult with clinical investigators, interpret research requirements, and determine statistical analysis strategies
Expert knowledge and understanding of the SAS programming
Ability to work in English
Please submit your CV in English.