Statistical Programmer
Warman O'Brien
Brighton and Hove, United Kingdom
6 days ago
Role details
Contract type
Temporary to permanent Employment type
Full-time (> 32 hours) Working hours
Regular working hours Languages
EnglishJob location
Brighton and Hove, United Kingdom
Tech stack
SAS (Software)
SQL Databases
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
- Collaborate closely with biostatistics and data management teams
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
- Join a high-performing team working on innovative clinical research with real impact for patients.
