- Cytel (Washington, DC)
- …& R-Shiny. + At least 5 years of R/ SAS programming experience with clinical trial data . + General knowledge of regulatory requirements and drug development ... programmer will also be required to utilize the SAS software system; they should be proficient in ...support electronic regulatory submissions; providing systems and support for clinical data management staff, clinical … more
- Cytel (Washington, DC)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Cytel (Washington, DC)
- …Clinical Development, and other functional representatives to develop, maintain and document clinical data standards. This role also acts as a statistical ... + Provides technical and/or operational guidance in the application of industry clinical data standards within the statistical programming data … more
- Amgen (Washington, DC)
- …this vital role you will ensure all statistical aspects pertaining to clinical activities meet required standards and are statistically accurate. The Biostatistical ... Programming Senior Manager (Product Lead Programmer ) lead a group of Rare Disease and/or other...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
- Amgen (Washington, DC)
- …this vital role you will ensure all statistical aspects pertaining to clinical activities meet required standards and are statistically accurate. The Biostatistical ... Programming Senior Manager (Product Lead Programmer ) lead a group of Oncology and other therapeutic...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
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