Senior Stat Programmer

IQVIA LLC; Sydney; Hybrid; AUD 130,000 - 180,000; Full time

Job summary

IQVIA LLC is seeking an experienced Programming Team Lead to oversee complex clinical study programming from database integration to statistical outputs.

You will drive innovations in macros, tools and processes, collaborating with statisticians and data managers to deliver high-quality results while mentoring junior programmers and ensuring regulatory compliance.

Qualifications

• Degree in Computer Science or related field; Master’s preferred
• 3–5 years of statistical programming in clinical trials
• Advanced SAS programming: Base SAS, SAS Graph, SAS Macro
• CDISC SDTM/ADaM knowledge
• Regulatory understanding and data standards proficiency

Responsibilities

• Lead Complex Projects: Plan, coordinate, oversee programming activities from database integration to outputs.
• Innovate with Purpose: Design advanced macros, tools and process improvements to boost efficiency.
• Collaborate Across Teams: Work with statisticians, data managers and clients to deliver high‑quality results.
• Mentor junior programmers and guide the programming team growth.
• Drive Quality & Compliance: Ensure deliverables meet regulatory standards and maintain documentation.

Skills

Programming leadership

SAS programming

R programming

Statistical thinking

Regulatory knowledge

Education

Master’s degree in Computer Science or related field

Bachelor’s degree in Computer Science or related field

Tools

Base SAS

SAS Graph

SAS Macro

ADNCA for PK analysis

Job description

The interview process will consist of 3 rounds. We regret to inform that we are unable to consider candidates requiring sponsorship to work in Australia.

What You’ll Do

Lead Complex Projects: Plan, coordinate, and oversee programming activities for complex clinical studies, serving as Programming Team Lead for assigned projects. Own the programming lifecycle from database integration to statistical outputs.

Innovate with Purpose: Design and implement advanced macros, tools, and process improvements that elevate programming efficiency.

Collaborate Across Teams: Work closely with statisticians, data managers, and clients to deliver seamless, high-quality results. Provide technical expertise and innovative solutions to complex project challenges.

Mentor & Guide: Share your expertise with junior programmers and help shape the future of our programming team.

Drive Quality & Compliance: Ensure all deliverables meet regulatory standards and internal quality benchmarks. Develop and maintain programming specifications, documentation, and other study-related deliverables.

What You Bring

• A degree in Computer Science or a related field (Master’s preferred).
• 3 to 5 years of experience in statistical programming within clinical trials.
• Advanced SAS programming skills (Base SAS, SAS Graph, SAS Macro).
• Experience with R programming and ADNCA for PK analysis will be considered an asset.
• Strong understanding of clinical data, statistical principles, and regulatory requirements.
• Advanced knowledge of CDISC standards (SDTM and ADaM).
• Excellent communication, leadership, and multitasking abilities.
• Demonstrated ability to independently solve complex technical challenges, lead technical initiatives, and adapt to evolving tools, technologies, and industry standards.

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.