Statistical Programmer

Warman O'Brien
Swadlincote, United Kingdom
6 days ago

Role details

Contract type
Temporary to permanent
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English

Job location

Swadlincote, 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.

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