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!