CRO Senior SAS Programmer

  • Location

    Norfolk, England

  • Sector:

    Life Sciences

  • Job type:


  • Salary:


  • Contact:

    Janne Bate

  • Contact email:

  • Job ref:


  • Published:

    over 1 year ago

  • Expiry date:


  • Start date:


Senior SAS Programmer.

Responsible for the leadership and delivery of statistical programming activities relating to clinical trials.

Acting as Lead Programmer across multiple studies
Creation of CDISC compliant SDTM and ADaM programs and supporting documentation
Senior role will include project leadership activities
Additional areas:

Development, maintenance and validation of SAS® programs for the production of analysis datasets and tables, figures and listings for inclusion in clinical study reports
Creation and review of shells for tables, figures and listings from a programming perspective
Development, maintenance and validation of SAS based utilities
Data capture design review and input into data standards
Contributing to SQN's development of new systems, processes and SOPs
Experience and skills required:

Expertise in CDSIC standards, including a thorough understanding of SDTM/ ADaM IG, creation of SDTM and ADaM mapping specifications, defines and reviewer's guides.
Experience in the conversion of data sets into SDTMs
Experience of running data integration projects
Strong analytical, programming and data interpretation skills
Minimum of 5-6 years SAS® programming experience ideally in the CRO environment
Good organisational skills with the ability to proactively prioritise projects and allocated activities
Experience of leading project teams, forecasting work and assessing progress
Budgeting and resourcing skills
Leadership and mentoring skills
Commercial awareness
Practical experience with SAS v 9 and macro development
Understanding of clinical development processes
Good communication skills and high level of English language

Home or office based