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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Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/