Principal Statistical Programmer

Senior Statistical Programmer

We are looking for a Senior Statistical Programmer to conduct programming activities for clinical trials, early phase projects, and publication activities — working directly with US pharma and biotech client teams. This is a high-impact, fully remote role for a senior professional who can hit the ground running.

Key Responsibilities:

• Lead at least one study team, providing technical and domain-related guidance
• Manage and mentor a team of 2–4 programmers as needed
• Prepare SAS analysis datasets, tables, listings, and figures (TFLs) per specifications
• Develop programs for graphs and tables required in CSRs, safety and efficacy reports
• Validate and transform datasets and TFLs per client specifications
• Support data migration from legacy datasets to CDISC or client-specific standards
• Coordinate with US client teams on specifications, data issues, timelines, and reviews
• Conduct all work in compliance with applicable SOPs and Quality Management Systems

Requirements:

Must-Haves

• BS or MS in Computer Science, Statistics, Biostatistics, or related health science field
• 5+ years of SAS programming experience with clinical trial data
• Oncology therapeutic area experience — mandatory
• Strong understanding of CDISC standards (SDTM, ADaM) and regulatory requirements
• Experience with CSRs, safety/efficacy reporting, and FDA submissions
• Ability to work independently with minimal oversight
• Strong written and verbal English — direct client interaction with US pharma teams required

Nice-to-Haves

• CRO or FSP environment experience
• R programming knowledge
• Prior experience working directly with US-based sponsors

What We Offer:

• Competitive USD hourly rate.
• 100% remote from Latin America
• Work on real commercial clinical trials for top US pharma and biotech companies
• Be part of the first wave of offshore biometrics talent for this client