Description
Statistical Programmer
6 months, Brussels
For one of our clients in the Pharmaceutical sector we are looking for a Statistical Programmer. You coordinate statistical programming for the review, reporting and transfer of data.
Your responsibilities
- Co-ordinate the creation of analysis dataset specifications within standards
- Co-ordinate the programming of analysis datasets, using specific SAS macros.
- Co-ordinate the creation of the metadata files (define.XML) using specific SAS macros.
- Ensuring traceability between SDTM and ADaM data.
- Co-ordinate the production of tables, listings & figures
- Co-ordinate the restructuring, review and integration of external data
- Co-ordinate the generation of consistency check programs and QC listings
- Co-ordinate the transfer of data according to customer specific requirements
- Develop adequately documented programs for the generation of randomisation schema/program
- Set & maintain professional programming standards
- Maintain & archive program documentation - both electronic & paper - in an appropriate manner
- Maintain awareness of current features & new developments in SAS
- Maintain professional programming standards
- Attend customer meetings to discuss project requirements/progress
- Understand scope of work, budget and scope assumptions
- Identify out of scope work & provide revised costs with supporting documentation
- Ensure project milestones are met to agreed timelines
Your profile
- 3 to 10 years of relevant clinical trial SAS experience
- Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a plus
- Able to read, write and speak fluently in English.
Please submit your CV and I will contact you to discuss the opportunity further.