Reference number: 03-010
Education: Ph.D. in biostatistics or statistics with 9 years of relevant experience. Alternatively: Masters degree in biostatistics or statistics with 12 years of relevant experience. A minimum of 4-5 years managing staff in a contract research or pharmaceutical industry setting.
Experience: Familiarity with most complex statistical methods that apply to Phase II-III clinical trials. Current applied knowledge of SAS programming is essential. Must have excellent written and oral communication skills.
Responsibilities will include oversight of statistical input to clinical study design, analysis plans, statistical analyses, and reporting. You will ensure that appropriate analysis procedures are used, and that final reports effectively describe statistical methods and results of analyses. Additionally, you will be responsible for ensuring that the Biostatistics function is working as efficiently and effectively as possible with other departments. You will serve as a biostatistical resource for the department, ensuring scientific integrity in the application of statistical methodology to Phase I-IV clinical trials. You will provide statistical direction, technical oversight, and consultancy for major projects or on projects involving particularly complex statistical analyses. You may be asked to represent clients at FDA meetings, FDA advisory boards, or other scientific meetings as required.
How to Apply for a Position at Guilford
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Human Resources Manager
Guilford Pharmaceuticals Inc.
6611 Tributary Street
Baltimore, MD 21224