Senior Statistical Programming

The scope is “providing SAS programming expertise in support of the DRM standards”. (note. DRM is based on SDTM) 
He/She will collaborate with the Clinical Data Standards Architects (CDSA) and will deliver
The requirements for functions (during the mapping) and post-steps (after mapping) in the context of DRM standards
Developing and documenting the SAS code implementing the DCRM mapping functions and post-steps……..
Test the code for correctness.
Support the formal User Acceptance Testing (performed by an independent CDSA).
Must have excellent knowledge of SAS® Base, and good knowledge of SAS® graph and SAS® Macros.
Capable of programming simple 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.

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