Our company is a global leader in clinical research and development, providing cutting-edge solutions to the life sciences and healthcare industries.
As a Senior Statistical Programmer, you will play a key role in driving real-world impact by building robust programming solutions that transform complex data into life-changing insights.
This is an exciting opportunity for a data-driven problem solver with a passion for clinical research to take the lead in transforming complex data into actionable insights.
The ideal candidate will have a strong understanding of statistical principles, regulatory requirements, and clinical data, as well as advanced knowledge of CDISC standards.
You will work closely with statisticians, data managers, and clients to deliver seamless, high-quality results and collaborate across teams to drive quality and compliance.
As a mentor and guide, you will share your expertise with junior programmers and help shape the future of our programming team.
We offer flexible hours and remote-friendly culture with opportunities for training, mentorship, and career advancement. Our team values creativity, continuous improvement, and cutting-edge technology.
* Lead Complex Projects: Own the programming lifecycle for high-impact studies—from database integration to statistical output.
* 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.
* 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.
What You Bring
* A degree in Computer Science or a related field (Master's preferred).
* 3–5 years of experience in statistical programming within clinical trials.
* Advanced SAS programming skills (Base SAS, SAS Graph, SAS Macro).
* Experience with R programming will be considered an asset.
* Strong understanding of clinical data, statistical principles, and regulatory requirements.
* Advanced knowledge in CDISC standards (SDTM and ADaM).
* Excellent communication, leadership, and multitasking abilities.
* Ability to quickly understand and follow processes and tools.
Why You'll Love Working Here
* Impact: Your work supports the development of new therapies and improves patient outcomes worldwide.
* Innovation: Be part of a team that values creativity, continuous improvement, and cutting-edge technology.
* Flexibility: Enjoy a remote-friendly culture with flexible hours and global collaboration.
* Growth: Access to training, mentorship, and career advancement opportunities.
IQVIA Overview
IQVIA is a leading provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
Our mission is to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.