Beschrijving
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!
Extra informatie
- Status
- Inactief
- Opleidingsniveaus
- Master
- Plaats
- Mechelen
- Werkuren per week
- 8 - 40
- Dienstverbanden
- Tijdelijke fulltime baan
- Beroepsgroepen subcategorie
- Secretarieel
- Rijbewijs nodig?
- Nee
- Auto nodig?
- Nee
- Motivatiebrief verplicht?
- Nee
- Talen
- Nederlands
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