SAS Programmer (Clinical Trials) in Mechelen
StepStone
Antwerpen, 1000, Belgium
5 dagen geleden
source : StudentJob

Are you an experienced SAS programmer or are you interested to become one?

You are welcome!

As a SAS Programmer within Secure Data Office, you will be responsible for the creation of unblinded datasets and related documentation in support of clinical trials.

Your day-to-day activities will include :

  • Programming and validating NCA and NONMEM datasets
  • Creating and reviewing of specifications for the generation of NCA and NONMEM datasets which will serve as input files for Pharmacokinetic ( PK ) / Pharmacodynamic ( PD ) analysis
  • Programing and validating randomisation lists and medication kit lists
  • Creating and reviewing specifications and requirements for randomisation documents
  • Developing and validating SAS macros
  • Communicating with all external and internal stakeholders that need to deliver or receive data
  • Managing your own projects in terms of communication, timelines, documentation, and reporting
  • Do you already understand part of what we just described? Do read on!

  • You have a bachelor’s or master’s degree in sciences (e.g., Computer Sciences, Life Sciences, Statistics )
  • You have good knowledge of SAS or are keen to learn (we do consider entry level and have an in-house training program)
  • Your knowledge of English is as close to mother tongue’ as possible, this in written language as well as spoken
  • You are eager to learn and have an analytical mindset
  • You are quality minded and have an eye for detail
  • You have good communications skills, you are flexible and pro-active
  • Of course you are also well-organized, able to manage multiple priorities simultaneously and stress resistant!

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