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Senior Stat Programmer

IQVIA ArgentinaSydney, Sydney🇦🇺AustraliaPosted 6 Sept 2026

Why This Role Stands Out

This hybrid Senior Stat Programmer role at IQVIA Argentina offers exciting opportunities to lead complex clinical trial projects, innovate with advanced programming techniques, and mentor a growing team, making it ideal for a seasoned professional with strong SAS and CDISC expertise. You'll develop your skills while contributing to high-impact work within a reputable global organization, enjoying the flexibility of a hybrid work environment. Apply today to advance your career in a dynamic and collaborative setting!

Quick Overview

Seniority
Mid Senior
Employment type
Full Time
Work mode
Hybrid
Location
Sydney, Sydney, Australia
Clinical ResearchClinical TrialsComplianceR

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.

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

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.

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