Job Description

• Must have expertise of SAS\xc2\xae Base, and good knowledge of SAS\xc2\xae graph and SAS\xc2\xae Macros.
• Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician.
• Must have excellent knowledge of CDISC standards (SDTM and ADaM)
• Thorough understanding of relational database components and theory.
• Excellent application development skills.
• Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
• Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes
• Perform all responsibilities associated with the Senior Programmer role.
• Assist all the Sr. Programmers and Programmers in their day to day activities.
• Act as escalation point for Sr. Programmer and Programmer.
• Regularly communicates with the sponsor on the progress of programming aspects of the project and proactively anticipates issues and works with the sponsor on resolution of the problems.
• Provide input and/or write the programming specifications
• Serve as subject matter expert on all aspects of SAS programming
• Understand pharmaceutical industry standards and trends and proactively plan, develop, and implement
• Develop consistent practices of clinical and statistical review of output and mentor programming staff
• Check for consistency across therapeutic areas Identify, plan, and oversee the implementation and success measures of all process improvement initiatives
• Maintain expertise in the use of the SAS\xc2\xae Macros and determine macro development priorities
• Other responsibilities as defined on ad-hoc basis by senior management.

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