Statistical Programmer I / II
The International Society For Bayesian Analysis
Coventry, United Kingdom
2 days ago
Role details
Contract type
Temporary to permanent Employment type
Full-time (> 32 hours) Working hours
Regular working hours Languages
English Experience level
SeniorJob location
Remote
Coventry, United Kingdom
Tech stack
SAS (Software)
SQL Databases
Performance Monitor
Data Management
Job description
- 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
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Requirements
- 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
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Benefits & conditions
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...
About the company
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