Statistical Programmer I / II

• Lead statistical programming activities across multiple studies
• Develop and review SDTM and ADaM datasets in line with CDISC standards
• Produce and validate TLFs for clinical study reports and regulatory submissions
• Provide technical oversight and mentorship to programming teams
• Contribute to standards, automation, and programming efficiency initiatives
• Support development and review of SAPs and specifications
• Collaborate closely with biostatistics and data management teams, Job Title: Director Study Management (Director Statistics) Duration of Contract: 12 Months IR35 Status: Outside About the Role AZ are seeking an experienced and visionary Statistics Director to join our Team and lead strategic statistical innovation across AZ's oncology...

• Extensive experience in SAS programming within clinical trials
• Strong oncology experience preferred
• Expert knowledge of CDISC (SDTM / ADaM)
• Proficiency in SAS, SQL, and advanced reporting (STAT / Graph)
• Experience acting as technical lead or study lead programmer
• Background in CRO or pharmaceutical settings
• Ability to work autonomously and manage competing priorities
• Join a high-performing team working on innovative clinical research with real impact for patients.

Contract Opportunity - SAS Statistical Programmer (12 Months, Extendable) Location: UK or Europe (Remote/Flexible) Industry: CRO / Pharma Start Date: Feb/March 2026 Contract Length: 12 Months (Strong potential for extension) Rate: Competitive hourly rate (IR35 would...

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