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US-MA-Durham: Principal SAS Programmer

Date: _23-Jun-2011_
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Principal SAS Programmer

- The Principal SAS Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors.

- Provide oversight and guidance on multiple-trial programs, complex trials, and submission projects (including Integrated Summary of Safety or Efficacy). - Coordinate project start-up activities, including Unix/PMED project area set-up, creation of global programs (e.g.,,, etc.), tracking spreadsheets, and required documentation. - Assist in the production and QC of analysis plans, TLF mock-shell development, derived dataset specifications, programming specifications, and other process supporting documents. - Use efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings.

- Provide input into monthly PERFORM forecasts and monitor the completion of forecasted units. - Create standard macros and applications to improve the efficiency of the department.

Experience: - Proficiency in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java). - Bachelor's degree and / or other medical qualification or equivalent experience. - Relevant Clinical Trial industry experience - Project leadership experience required.

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