Remote SAS Programmer (SDTM/ADaM)

Step Into Purpose—Shape the Future of Clinical Data

Does your code make sense of the world’s most complex data? Are you energized by transforming clinical trial information into actionable insights that improve patient outcomes? Here’s where your programming fluency turns medical data into progress. As a Remote SAS Programmer with SDTM and ADaM expertise, you’ll empower teams worldwide to drive drug development and regulatory approvals faster, smarter, and with total confidence. With your knowledge of SDTM, ADaM, and CDISC standards, you’ll shape data workflows that power breakthrough clinical research—annual salary: $82,234.

Why This Role Matters

Every new therapy begins with a story hidden in data. Your programs set the stage for regulatory submissions, define data standards, and ensure that the science behind every trial is both robust and reproducible. Instead of just writing code, you’ll build the very pipelines that help doctors and scientists unlock new treatments. Here, your work touches lives—far beyond the screen.

What You’ll Achieve

• Drive Data Transformation: Your SDTM and ADaM expertise will shape data from raw collection to regulatory-ready formats—fueling submissions, publications, and life-changing research.
• Bridge Science and Software: By partnering with clinical teams, data managers, and biostatisticians, you’ll transform protocol ideas into clean, validated datasets. Your work translates the language of research into regulatory and patient-friendly deliverables.
• Champion Data Integrity: Design and execute rigorous data checks that safeguard quality at every step. Every dataset you touch is reliable, auditable, and future-proof.
• Simplify Complexity: You break down technical concepts—whether on Zoom or Slack—so colleagues can move forward with clarity and confidence. Your influence helps teams align, communicate, and move decisively.
• Contribute to Global Impact: Your programming delivers timely and precise data for clinical decisions that impact thousands of patients worldwide. It’s real work with a real-world footprint.

How You’ll Make a Difference

• Lead SDTM mapping from diverse source data, ensuring compliance with evolving CDISC guidelines.
• Develop, document, and optimize ADaM datasets for statistical analysis and regulatory submission.
• Collaborate daily with statisticians, medical writers, and global project leads—your code fuels unified solutions.
• Innovate SAS programming practices that save time and reduce manual review cycles across remote teams.
• Identify and resolve data issues with urgency and creativity, maintaining a focus on study timelines and scientific rigor at all times.
• Bring continuous improvement to data review, metadata management, and automation.

Tools & Technology

You’ll craft code in the latest versions of Base SAS, SAS/STAT, and SAS Macro. Remote collaboration is second nature—whether you’re syncing with global teams via Microsoft Teams or sharing documentation in Confluence and Jira. You’ll keep your skills sharp by leveraging version control, code reviews, and automation to build scalable workflows.

What You Bring

• Deep, hands-on experience with SDTM and ADaM standards in a clinical research setting
• Comfort navigating CDISC requirements and a knack for interpreting evolving regulatory guidance.
• A record of producing datasets, TLFs, and documentation that pass audits with flying colors
• The ability to turn protocol and SAP requirements into actionable programming solutions—no guesswork
• Clear, persuasive communication: you make complexity approachable, whether it’s through clean code or cross-team discussions
• Curiosity and adaptability—you thrive on feedback, rapid iteration, and the satisfaction of progress
• Experience working across time zones and remote cultures, flexing your schedule to support shared project goals.

The Environment You’ll Thrive In

We move quickly, but you’ll always have space to focus intensely. You’ll partner with data management, biostatistics, and medical writing teams—not just to deliver but to shape how clinical programming adds value across every phase of a trial. Every conversation, code review, and shared solution presents an opportunity to learn and lead.

The Outcomes You’ll Drive

Your deliverables don’t sit on a shelf—they drive regulatory approvals, publication milestones, and, most importantly, fundamental advances in patient care. The programs you build unlock actionable insights for trial sponsors, investigators, and regulatory bodies worldwide. You’re not just meeting requirements; you’re setting new standards for data clarity and integrity in the industry.

Ready to Create Something Meaningful?

If you’re excited to see your work ripple through the world of clinical research—and you thrive in a remote environment built on trust, learning, and impact—we’re ready to meet you. Let’s turn clinical data into cures together.