Senior Stat Programmer

IQVIA · New South Wales, Australia +1 more

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Role summary

IQVIA seeks a Senior Stat Programmer to lead complex clinical trial programming projects in Australia. The role involves overseeing the programming lifecycle, mentoring junior staff, and delivering high-quality statistical outputs that meet regulatory standards.

What they're looking for

Bachelor's degree in Computer Science or related field; Master's preferred
3–5 years statistical programming experience in clinical trials
Advanced SAS skills including Base SAS, SAS Graph, and SAS Macro
Strong knowledge of CDISC standards (SDTM and ADaM)
Understanding of clinical data, statistical principles, and regulatory requirements
R programming and ADNCA experience considered advantageous
Leadership, communication, and independent problem-solving abilities

What you'll be doing

Lead and coordinate programming activities for complex clinical studies as Programming Team Lead
Own the programming lifecycle from database integration through statistical outputs
Design and implement advanced macros, tools, and process improvements
Collaborate with statisticians, data managers, and clients on project delivery
Mentor junior programmers and develop programming specifications and documentation

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Date posted15 days ago

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