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| | Clinical SAS Programmer (KS) | KS |
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| | Sr. Clinical SAS Programmer (KS) | KS |
| | Sr. Clinical SAS Programmer (MA) | MA |
| | Sr. Clinical SAS Programmer (Telecommute) | US |
| | Sr. Clinical SAS Programmer (TX) | TX |
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| | Sr. Statistician (WA) | WA |
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Clinical SAS Programmer (KS) |
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Category : 1 - SAS Location/City : KS |
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| Opportunity for a Sr. SAS Programmer with 3+ years clinical / pharmaceutical / CRO industry experience to provide technical expertise within a leading CRO. In this role, you will • Program, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients and (iii) the programming of database quality control checks.
• Program and plan the integration of databases from multiple studies or sources.
• Develop, plan, and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.
• Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.
• Fulfill project responsibilities at the level of lead for single complex studies or group of studies.
• Manage project budget and resource requirements
• Provide training and guidance to junior level staff. | | | Qualifications | • 3+ years relevant experience; or equivalent combination of education, training and experience
• Knowledge of statistics and/or clinical drug development process
• Knowledge of electronic submissions
• Advanced knowledge of statistical computing applications such as Base SAS, SAS/STAT and SAS Macro Language
• Good organizational, interpersonal, leadership, communication skills and multi-tasking abilities. | |
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