Lead Clinical Stat Programmer

IQVIA; Sydney; On-site; AUD 110,000 - 170,000; Full time

Job summary

IQVIA in Sydney, Australia seeks an experienced Statistical Programmer to lead complex clinical studies. You will manage the programming lifecycle from database integration to statistical outputs, mentoring junior programmers and delivering high-quality results.

You will design advanced macros and tools to improve efficiency, collaborate with statisticians and data managers, and ensure regulatory compliance across deliverables in line with CDISC SDTM/ADaM standards.

Qualifications

• Degree in CS or related field; Master’s preferred.
• 3–5 years of statistical programming in clinical trials.
• Expert in Base SAS, SAS Graph and SAS Macro.
• Experience with R and PK analyses is a plus.
• Strong knowledge of CDISC SDTM/ADaM and regulatory requirements.

Responsibilities

• Lead Complex Projects: oversee programming for complex studies.
• Innovate with Purpose: develop macros, tools, and process improvements.
• Collaborate Across Teams: work with statisticians, data managers, clients.
• Mentor & Guide: coach junior programmers.
• Drive Quality & Compliance: ensure deliverables meet standards and documentation.

Skills

Advanced SAS programming

R programming

CDISC SDTM/ADaM

Statistical programming in clinical

Leadership & mentoring

Education

Bachelor's degree in Computer Science or related field

Master’s degree (preferred)

Tools

Base SAS

SAS Graph

SAS Macro

R

ADNCA for PK analysis

Job description

IQVIA in Sydney, Australia seeks an experienced Statistical Programmer to lead complex clinical studies. You will manage the programming lifecycle from database integration to statistical outputs, mentoring junior programmers and delivering high-quality results.

You will design advanced macros and tools to improve efficiency, collaborate with statisticians and data managers, and ensure regulatory compliance across deliverables in line with CDISC SDTM/ADaM standards.