Principal Statistical Programmer (SAS) – Oncology

📍 Remote (Europe)

💰 up to $60/hour

🕒 Full-time

About the Role

We are looking for a Principal Statistical Programmer with solid experience in clinical trials and oncology to join a global healthcare and pharmaceutical environment.

This is a senior-level role combining hands-on SAS programming with technical leadership, supporting international studies and working closely with global teams.

Key Responsibilities

• Lead statistical programming activities for clinical trials and research projects
• Provide technical guidance to study teams
• Mentor or support a small team (2–4 programmers)
• Develop and validate SAS analysis datasets
• Create and validate Tables, Listings, and Figures (TLFs) for:
• Clinical Study Reports (CSRs)
• Safety and efficacy reports
• Perform data migration to CDISC standards (SDTM / ADaM)
• Ensure data quality and accuracy of outputs
• Collaborate with international teams (including US stakeholders)
• Follow SOPs and regulatory compliance standards
• Support hiring and team growth when needed
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Required Qualifications

• Bachelor’s or Master’s degree in:
• Statistics
• Computer Science
• Life Sciences or related field
• 5+ years of SAS programming experience in clinical trials
• Strong knowledge of:
• CDISC standards (SDTM and ADaM)
• Clinical trial processes
• Regulatory requirements (FDA, EMA, etc.)
• Mandatory experience in Oncology studies
• Ability to work independently in a remote setup
• Strong English communication skills

Preferred Experience

• Experience leading studies or mentoring teams
• Exposure to Phase I–III clinical trials
• Experience with regulatory submissions

What We Offer

• 100% remote role across Europe
• Competitive hourly rate ($60/hour USD)
• International exposure working with global teams
• Opportunity to contribute to impactful clinical research
• Stable and collaborative work environment