• Job Description

  Req#: REF8940D

  Company Description

  At SGS, you can choose!

  First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors’, people who can connect our diversity to our services. To each other. And this way, enrich our business.

  SGS is the world’s leading inspection, verification, testing and certification company. We’re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to almost 100 000 colleagues worldwide, with more than 1650 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.

  SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. SGS Life Sciences has also expertise in the quality control of pharmaceuticals.

  In the spirit of continued growth and to help improve our business, we have a challenge
  for a SAS PROGRAMMER for our Secure Data Office team!

  Job Description

  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:

  • Program and validate NCA and NONMEM datasets
  • Create and review of specifications for the generation of NCA and NONMEM datasets which will serve as input files for Pharmacokinetic (PK)/ Pharmacodynamic (PD) analysis
  • Program and validate randomisation lists and medication kit lists
  • Create and review specifications and requirements for randomisation documents
  • Develop and validate SAS macros
  • Communicate with all external and internal stakeholders that need to deliver or receive data
  • Manage your own projects in terms of communication, timelines, documentation, and reporting

  Do you already understand part of what we just described? Do read on!

  Qualifications

  · You have a master's degree in 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!

  Additional Information

  What we have to offer:

  Were you already considering a switch in your career?
  Maybe this could be your next step!
  
  At SGS you can count on an interesting position where you can take responsibility.
  Come enjoy our fun team of colleagues and on top of that, we will reward you with an interesting salary package (incl. retirement plan, meal vouchers, …)

  Do you want to be part of this?

  We are looking forward to hearing from you!
  
  Send us your story and your resume via the apply button and maybe you will soon join us for work and coffee breaks.
  
  Still have questions?

  Heidi Aerts can give you more details about the job. Send her an e-mail at heidi.aerts@sgs.com

• About the company

  SGS is the world’s leading inspection, verification, testing and certification company. Our value to society is enabling a better, safer and more interconnected world.

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