Job Description

Remote SAS Programmer (Regulatory Submissions)

Can You Turn Data Into Regulatory Success Stories?

Imagine a remote role where your SAS programming expertise doesn’t just generate numbers—it shapes regulatory submissions that change lives. That’s the core of this opportunity: you’ll transform clinical trial data into compelling regulatory narratives, ensuring new therapies reach the patients who need them. This is your chance to combine analytical skills with mission-driven work—all from wherever you thrive best.

The Impact You’ll Make

Your daily work has a global impact. Each dataset you manage, every table and listing you create, directly supports major pharmaceutical filings—helping teams secure FDA, EMA, and other global approvals. You’ll deliver submission-ready deliverables that withstand the toughest scrutiny, knowing your efforts move essential treatments forward. Your programming ensures data quality, regulatory compliance, and smooth review cycles, empowering the medical community with reliable results.

What You’ll Tackle

Craft Submission-Ready Datasets: Your code translates complex clinical data into clear, auditable output—SDTM and ADaM datasets that form the backbone of regulatory filings. Expect your solutions to be as rigorous as they are elegant.
Build Dynamic Tables & Listings: You’ll transform statistical analysis plans into actionable outputs—summary tables, patient profiles, and efficacy listings — designed for clarity, precision, and adherence to global review standards.
Ensure Regulatory Compliance: From CDISC standards to company SOPs, you’ll keep every deliverable audit-ready and fully aligned with FDA, EMA, and ICH guidelines.
Problem-Solve in Real Time: Encounter a data discrepancy or a shifting deadline? Your expertise turns challenges into opportunities—solving issues before they escalate and keeping the submission timeline on track.
Collaborate Remotely for Unified Results: Work closely with biostatisticians, clinical data managers, and regulatory leads to achieve unified results. Whether it’s Zoom, Slack, or shared cloud docs, your communication makes the technical accessible and the complex simple.

Our Remote Workflow & Collaboration Stack

You’ll enjoy a wholly digital environment designed for focused, deep work and seamless connection. Our tech stack includes:

SAS (Base, Macro, SQL), R, Python: For advanced clinical programming and data wrangling.
Jira, Confluence, Microsoft Teams: For project tracking, documentation, and real-time feedback.
SharePoint & Secure Cloud Storage: For document management and compliance.
Digital Whiteboards & Virtual Standups: To keep projects transparent, collaborative, and agile—even across time zones.

How You’ll Succeed

Data-Driven Storytelling: You see each dataset as a narrative opportunity—your programming clarifies findings for global regulators, researchers, and stakeholders.
Efficient, High-Quality Delivery: We move quickly, but you’ll always have the space to focus intensely and deliver thoughtful, high-quality work.
Simplify the Complex: You simplify complex ideas—whether it’s over Zoom or Slack, your insights help teams understand both the details and the big picture.
Embrace Remote Freedom: Flex your schedule for optimal productivity and well-being. You’ll partner with a global team, but you’ll set your own rhythm for focus and creativity.

The Experience You Bring

Demonstrated mastery in SAS programming for clinical trials—especially in producing SDTM, ADaM, and regulatory submission datasets.
Hands-on experience with regulatory submissions (NDA, BLA, MAA, or similar)—you know what high-stakes deadlines and precision work feels like.
Familiarity with global submission standards, including CDISC, ICH, and FDA/EMA eCTD requirements.
Proven ability to troubleshoot, optimize, and document programming workflows for audits and global review.
You simplify technical language and make collaboration second nature, even when everyone’s remote.

What’s in It for You?

Annual Salary: $101,959 (USD) — Competitive, transparent, and paid in recognition of the expertise you bring.
Remote-First Culture: Your home office, your favorite coffee shop, or anywhere with Wi-Fi. We empower you to choose your environment.
Professional Growth: Work on high-impact global submissions and sharpen your programming, compliance, and regulatory skills alongside the industry’s best.
Mission-Driven Team: Join a group that believes every line of code and every submission packet can impact real patient outcomes.

Ready to Code Regulatory Change?

If you’re energized by the idea that your programming could help launch life-changing therapies, we want to hear your story. Let’s build submission pathways that accelerate medical progress—together, from anywhere.

Remote opportunity with global reach — applications are welcome from candidates in any country.