Clinical Statistical Programmer


– Technical

  • Co-ordinate the creation of analysis dataset specifications
  • Co-ordinate the programming of analysis datasets, using specific SAS macros.
  • Co-ordinate the production of tables, listings & figures
  • Quality Control of project deliverables
  • Set & maintain professional programming standards
  • Maintain & archive program documentation - both electronic & paper - in an appropriate manner
  • Maintain professional programming standards


  • BSc, MSc or equivalent by working experience
  • 2 to 5 years of relevant clinical trial SAS experience preferably in a similar role
  • Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS Studio, SAS macro language. SAS/GRAPH is a nice to have.
  • Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial.
  • Good knowledge of statistical approaches applied in cancer clinical trials with a focus on survival analysis techniques.
  • Capacity to work independently or under the guidance of a senior programmer.
  • Knowledge and practice of CDISC SDTM and ADaM data standards.
  • Ability to work complying to the company programming SOPs, data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
  • Ability to effectively manage time and prioritize project work
  • Good organization skills
  • Creative and innovative, able to adapt to dynamic environment
  • Good verbal and written English skills



Contact person