Assoc Principal Statistical Programmer/Sr Stat Programmer

IQVIA · Telangana, India

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Role summary

IQVIA seeks an associate principal or senior statistical programmer with strong SAS expertise and CDISC standards knowledge to support clinical trial data analysis and reporting. The role involves implementing statistical procedures, managing complex datasets, and ensuring compliance with regulatory guidelines.

What they're looking for

Proficiency in SAS Base, SAS Graph, and SAS Macros
Expert knowledge of CDISC standards including SDTM and ADaM
Solid understanding of relational database components and theory
Familiarity with ICH guidelines E6, E3, E8, and E9
Strong hands-on experience with clinical trial data manipulation and analysis
Advanced application development capabilities

What you'll be doing

Execute advanced statistical procedures according to biostatistician specifications
Manage and transform clinical trial datasets using SAS programming
Develop analysis datasets and create tables, figures, and listings for clinical reports
Ensure data outputs comply with CDISC standards and regulatory requirements
Collaborate with biostatisticians and cross-functional teams on study deliverables

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Date posted16 days ago

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