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IQVIA

Senior Stat Programmer

IQVIA

Senior Stat Programmer leading SAS-based clinical-trial programming at IQVIA. Owning statistical outputs, quality compliance, complex projects, and junior programmer mentorship.

Posted 9/4/2026full-timeNorth Sydney • 🇦🇺 AustraliaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical programming for clinical trials, with advanced skills in SAS and R, and a strong understanding of CDISC standards. Capable of leading programming teams, mentoring junior staff, and ensuring compliance with regulatory standards.

Highest-signal resume keywords
Advanced SAS ProgrammingStatistical Programming in Clinical TrialsCDISC Standards (SDTM and ADaM)Leadership and MentoringRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
SAS ProgrammingR ProgrammingDatabase IntegrationStatistical OutputsMacros DevelopmentProcess ImprovementsProgramming SpecificationsDocumentationStatistical PrinciplesClinical Data Analysis
Soft Skills
Excellent CommunicationLeadership AbilitiesMultitaskingProblem SolvingCollaboration
Tools & Technologies
SAS GraphSAS MacroADNCA
Industry Keywords
Clinical TrialsRegulatory StandardsQuality BenchmarksTechnical ExpertiseProject Challenges

About the role

Key responsibilities & impact
  • Plan, coordinate, and oversee programming activities for complex clinical studies
  • Serve as Programming Team Lead for assigned projects
  • Own the programming lifecycle from database integration to statistical outputs
  • Design and implement advanced macros, tools, and process improvements
  • Collaborate with statisticians, data managers, and clients
  • Provide technical expertise and innovative solutions to complex project challenges
  • Mentor junior programmers
  • Ensure deliverables meet regulatory standards and internal quality benchmarks
  • Develop and maintain programming specifications, documentation, and other study-related deliverables

Requirements

What you’ll need
  • 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
  • Unable to require sponsorship to work in Australia

Benefits

Comp & perks
  • 🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account IQVIA Website LinkedIn All Job Openings 10,000+ employees 💼 Consulting 🏭 Manufacturing 📣 Marketing 💰 $1G Post-IPO Debt on 2023-05 Consulting
  • Manufacturing
  • Marketing IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients. Senior Stat Programmer 🔥 28 minutes ago 🏢 North Sydney – Onsite ⏰ Full Time 🟠 Senior 🖥 Software Engineer 👻 Ghost score 10% Apply Now Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
  • Plan, coordinate, and oversee programming activities for complex clinical studies
  • Serve as Programming Team Lead for assigned projects
  • Own the programming lifecycle from database integration to statistical outputs
  • Design and implement advanced macros, tools, and process improvements
  • Collaborate with statisticians, data managers, and clients
  • Provide technical expertise and innovative solutions to complex project challenges
  • Mentor junior programmers
  • Ensure deliverables meet regulatory standards and internal quality benchmarks
  • Develop and maintain programming specifications, documentation, and other study-related deliverables 🎯 Requirements
  • 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
  • Unable to require sponsorship to work in Australia Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score View More Software Engineer Jobs 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Remote jobs Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources About us Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Is Remote Rocketship legit? Privacy policy Terms of service Job board SEO course Remote Job Search MasterClass Resume Review AI Apply Copilot OpenClaw job finder API docs Find jobs using your resume Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs