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
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
Thorough understanding of relational database components and
Excellent application development skills.
Strong understanding of clinical trial data and extremely hands
on in data manipulations, analysis and reporting of analysis
Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and
clinical research processes.
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the application process should contact IQVIA's Talent Acquisition
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