Remote Clinical SAS Programmer

Shape Breakthroughs in Global Healthcare—From Anywhere

Imagine powering the future of clinical research—not from a cubicle, but from wherever you thrive best. As a Remote Clinical SAS Programmer, you'll translate data into stories that accelerate life-changing therapies. Your work will drive smarter clinical trials, ensuring every dataset has a voice and every patient outcome is counted. With an annual salary of $86,000, you’ll find your impact goes far beyond code.

Why Your Skills Matter

Every line you program helps shape protocols that define the next generation of medicine. You’ll team up with clinical leads, statisticians, and project managers to deliver clean, validated datasets for regulatory submissions and medical breakthroughs. Here, precision isn’t just a checkbox—it’s the heartbeat of global health progress. Whether you’re debugging a complex macro or optimizing a data pipeline, your decisions will ripple across patient lives and research timelines.

What You’ll Tackle—And Why It Matters

• Develop, validate, and maintain SAS programs that transform raw clinical trial data into actionable results for submissions, publications, and internal strategy.
• Ensure compliance with CDISC, SDTM, and ADaM standards, transforming regulatory hurdles into seamless processes that expedite trial milestones.
• Partner with data managers, biostatisticians, and medical writers to define deliverables that inform pivotal decisions on drug safety and efficacy.
• Automate data cleaning and reporting workflows so project teams can focus on discovery, not busy work.
• Audit and quality-check datasets, tables, and listings—because accuracy here can mean lives changed everywhere.

Your Daily Rhythm

Your mornings might start with a team sync—one where you simplify intricate programming challenges for colleagues in different time zones. Throughout the day, you’ll split your focus between hands-on coding, reviewing data transformations, and collaborating in remote working sessions. Your ability to turn ambiguous requests into crisp, executable solutions will set you apart.

Tools & Environment—How You’ll Work

You’ll immerse yourself in an environment built for productivity, connection, and flexibility. Our toolkit includes:

• SAS Base, SAS Macro, and SAS/STAT for clinical data management and analysis
• Remote communication platforms like Slack and Zoom to bridge global teams
• Secure cloud environments for storing, processing, and transferring sensitive clinical data
• Collaboration with design, operations, and quality assurance teams to align on every project milestone

You move quickly but never rush. Here, you’ll always find the breathing space needed to go deep into complex statistical programming while still being supported by a network that values clarity and collaboration.

What Sets You Apart

• You thrive on clarity, translating regulatory requirements into elegant programming workflows.
• Your written documentation is so clear that it’s often used as the gold standard by new hires.
• You simplify complex ideas—whether it’s over Zoom or in your annotated code.
• You’re the go-to problem solver when others hit a programming roadblock.
• Your passion for lifelong learning means you’re always seeking new ways to automate and optimize.

Qualifications

• Bachelor’s or Master’s degree in Statistics, Computer Science, Life Sciences, or a related field
• Proven experience in clinical SAS programming for Phase I-IV studies
• Expertise with CDISC (SDTM, ADaM) implementation and validation
• Hands-on skills with remote collaboration tools and secure data transfer protocols
• Ability to navigate ambiguous requirements and prioritize for maximum project impact

Career Growth & Learning

You’ll be at the center of the clinical data revolution, exposed to cutting-edge research and the latest in statistical programming. The skills you build here will open doors across biotech, pharma, and CROs worldwide. We champion mentorship, continuous training, and a culture where curiosity is always welcome.

How Success Is Measured

• Quality of deliverables: Regulatory submissions approved with minimal queries
• Collaboration: Your insights help project teams make decisions that move trials forward
• Innovation: You introduce automation or new techniques that increase team productivity

Our Remote Work Philosophy

We’re serious about flexibility. Set your own hours, embrace focused, deep work, and take your office wherever you’re most productive. Your well-being fuels your best work, and we trust you to manage your time and output.

Ready to Make Your Mark?

If you’re excited to shape the future of clinical data from anywhere, let’s build something meaningful together. Every dataset you transform, every process you optimize—it all adds up to global impact. If you’re ready to make a difference from day one, we’re prepared to meet you.