Location: Netherlands (Full Remote)
My client is an innovative independent institution specialising in early stage clinical drug research. They are currently seeking several SAS Programmers to help support and grow their Data Programming team.
This is a great team to be a part of which has a solid collaborative and supportive culture.
The Data Programming team is involved in every study from the beginning to the end. During the study and once it is completed the major tasks for the clinical programmers are to create transfer files for the client and deliver safety tables, figures and listings (TFLs). We also have SDTM programmers in house that can deliver a complete SDTM package if requested by the client. The team works closely with all departments, in particular the clinical scientists, statisticians, and data managers.
Your initial focus when starting will be the development and validation of macros that can be used to create safety, PD and PK TLFs in RTF format based on ADaM datasets. Once this project is completed, you will not only be responsible for maintaining existing macros and creating new macros, but you will also be involved in generating safety reporting, processing electronic data files and setting up transfer files as per DTA/DTS.
Ideally someone with a minimum of 5 years of experience in SAS programming within the pharmaceutical industry/CRO.
Please send your CV