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., setup.sas, formats.sas, 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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Thank you,
Developer FYI Center
http://dev.fyicenter.com/