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Switzerland - Allschwil: Biostatistics

Date: 16-Oct-2012
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Biostatistics in Biotech

* Prepares analysis plans and reporting specifications * Develops, modifies, and/or implements appropriate statistical techniques for the analysis of data from clinical studies * Works with programmers, writers, and clinicians to coordinate data summarization and analysis activities * Produces and reviews tables, listings, figures, and SAS® datasets to support the analysis of clinical trials data

* Perform statistical programming to check and process data, generate tables, figures, and data listings * Perform independent QC programming for tables, listings and figures * Perform statistical programming and QC for analysis datasets

* Prepares and reviews integrated statistical and clinical reports including summary statistics, graphics, tabulations, and raw data listings * Builds and maintains strategic relations with customer groups * Consults with other statisticians on statistical methodology, study design, and data analysis * Other project related activities and duties as assigned

* MS (or PhD) degree in Statistics or Biostatistics with a minimum of two years’ experience in a CRO or pharmaceutical industry. * Strong experience using statistical programming systems (SAS® required) * Demonstrated expertise in multiple statistical areas * Excellent knowledge of drug development process and regulatory requirements, including ICH/GCP guidelines * Excellent organizational skills with ability to prioritize and work in a high volume and strict deadline environment * Ability to work independently and as a team member * Positive attitude, professional and excellent communication skills both written and speaking * Substantial pharmaceutical industry related environment is required

* Fluent in spoken and written English

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