About The Position

Work as a senior programmer on clinical and non-clinical trials; producing complex datasets and outputs to excellent quality whilst adhering to deliverable timelines. Good knowledge of CDISC SDTM and ADaM implementation guidelines; producing, reviewing and updating complex data specifications; creating and debugging complex macros; understanding Statistical Analysis Plans (SAPs) and output shells for day to day programming activities. Excellent team work ethos, willingness to help others and learn new skills from working in a team environment. This role is full-time and fully-remote. The successful candidate may be based in the US, the UK, Spain, Germany and France. The sucessful candidates timezone must overlap with US working hours.

Requirements

  • MSc or higher in Statistics, Mathematics or related field
  • The ability to be able to write post-hoc analysis plans, allowing internal programmers to do the formal programming of the required outputs/analysis
  • Good SAS programming skills for SAS/BASE, SAS/STAT, SAS/GRAPH and ODS functionality (Further languages are advantageous)
  • CDISC knowledge (SDTM and ADaM)
  • Applicable leadership experience

Nice To Haves

  • The ability to work on complex efficacy is advantageous
  • PhD or higher in Statistics, Mathematics or a related field is advantageous

Responsibilities

  • Statistical expertise and scientific leadership
  • Leadership and people development
  • Compliance, quality and governance
  • Communication and influence

Benefits

  • Remote working
  • flexible working hours
  • Career development
  • mentorship
  • continuous learning
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