Remote SAS Programmer (Oncology Studies)

Drive Oncology Research Forward from Anywhere

Imagine contributing your SAS expertise to cancer studies that accelerate lifesaving treatments. Here, you won’t just run scripts—you’ll power data-driven breakthroughs and empower clinical teams to make decisions that impact patients worldwide. If you thrive in remote environments, excel at transforming raw data into actionable insights, and want your work to shape the next chapter of oncology research, this is your space to shine. With an annual salary of $101,929, you’ll see the impact of your work every step of the way.

Key Contributions and Outcomes

You’ll be the architect of robust SAS solutions that translate complex oncology trial data into clear, regulatory-ready outputs. Your experience with SDTM and ADaM standards ensures that the integrity of every dataset withstands global scrutiny. Instead of simply preparing reports, you’ll design analytical workflows that inform new protocols and refine existing therapies. Working closely with clinical scientists, data managers, and medical writers, your insights will help drive the success of submissions and support critical decision points for oncology product pipelines.

How You’ll Partner and Lead

Every day, you’ll interact with stakeholders across the clinical research spectrum. Whether it’s on Zoom calls, troubleshooting analysis flags, or collaborating in Slack threads to resolve data anomalies, you simplify complex ideas, making clarity your superpower. You’ll mentor junior programmers, championing best practices and fostering a collaborative, high-trust environment that brings out the best work from everyone.

Advanced Tools and Technology

Your toolkit includes advanced SAS programming, CDISC standards (SDTM, ADaM), and remote collaboration tools like JIRA and Confluence. You’ll use data visualization platforms to share key findings, all while maintaining rigorous documentation that stands up to regulatory audits. Experience with oncology datasets, patient-level data, and statistical review tools provides a unique edge, enabling you to proactively surface data patterns, uncover insights, and ensure that every deliverable exceeds expectations.

The Remote Work Culture

Here, remote doesn’t mean disconnected. Our virtual stack—ranging from secure cloud environments to synchronous video standups—keeps collaboration seamless and accountability clear. We move quickly, but you’ll always have space to focus intensely and deliver quality results. Feedback is direct and constructive, and your input actively shapes our clinical programming playbook.

Your Profile and Impact

You’re passionate about using SAS programming to drive innovation in oncology research. You’ve contributed to the delivery of SDTM and ADaM datasets for regulatory submissions and are confident managing multiple timelines across international teams. Instead of just handling tasks, you identify process bottlenecks and propose solutions that save time and reduce errors.

Your communication style is pragmatic—you turn technical findings into actionable next steps for both technical and non-technical colleagues. Your curiosity fuels continuous learning, keeping you ahead of evolving regulatory and data standards in the oncology space.

What You’ll Achieve

• Transform oncology clinical data into high-integrity, submission-ready datasets that directly support FDA/EMA regulatory filings.
• Surface data issues early, guiding study teams to solutions that safeguard trial outcomes.
• Deliver clear, validated TLFs (Tables, Listings, Figures) that tell the whole story behind every study.
• Mentor and coach peers, raising the bar for quality across remote programming teams
• Recommend new automation approaches and data pipelines that accelerate delivery and reduce manual workload.
• Champion data privacy, compliance, and reproducibility throughout every phase of the study

Why This Role Matters

Oncology research is both challenging and rewarding. Your work here will touch thousands of patient lives by making cancer trials safer, faster, and more accurate. If you thrive when tackling the unique challenges of oncology programming—balancing innovation, compliance, and real-world impact—this is where you’ll do your best work.

Ready to Shape Oncology’s Future?

If you’re driven to deliver data that transforms the landscape of cancer research and want your career to be as purpose-driven as your code, let’s build something meaningful together. Join us in a position where your technical mastery sets new standards in oncology programming, making a meaningful difference that resonates throughout the cancer research community.