Then join one of the most reputable and highest ranking research-based pharmaceutical corporations in the world, working in their Clinical Biostatistics Team and be responsible to support the preparation, conduct and reporting of phase 3 trials in the respiratory area.

You will work closely with the Project Statistician and Additional interfaces are to the other members of the trial team (Trial Manager, Data Manager and SAS Programmer) and the project team (Project Data Manager, the Project Statistical Programmer


Accountabilities/Responsibilities:

The candidate will act as a fully responsible trial statistician and will support the Project Statistician.

In the early study conduct phase, main tasks are the definition and review of data quality checks and the review of statistical issues during study conduct. Thereafter, the preparation of specifications for analysis and reporting have to be created. A prototype Trial Statistical Analysis Plan for the entire phase 3 program of the compound has to be written and corresponding SAS programs and outputs have to be discussed and QC'd.
Statistical standards for the projects have to be reviewed.

Depending on the scope of work the candidate may also work as a fully responsible trial statistician for phase 2/3 trials in the diabetes area.

Essential Skills & Capabilities:

MSc or PhD in statistics or math.
At least 2 years experience working on phase 2/3 studies in a Pharma company / CRO.
Excellent general biostatistics knowledge.
Good communication skills.


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