Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Clinical Data Standards Specialist - 1 Year Contract - Belgium
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Library, Client
Projektbeschreibung
Clinical Data Standards Specialist - 1 Year Contract - Belgium
My client are a Global Pharmaceutical company with a large site based in Belgium. They are looking to recruit a Clinical Data Standards Specialist for a year long contract.
The daily rate is negotiable depending on experience.
You tasks will be to create and maintain Platform Independent (PI) CDASH compliant layouts from input provided by Global and Therapeutic area.
You will create and maintain CDASH and SDTM compliant metadata using the Metadata Repositort tool to complement the CDASH/SDTM layouts at all metadata layers.
You must have previous experience as a Data Standards Librarian with knowledge of library theory within an EDC environment.
An advanced knowledge of CDASH and SDTM sumbission principles as well as hands on practical experience in applying these principles.
Experience within Pharmaceutical/CRO industry with sound knowledge of the DM process and knowledge of the role of other clinical research functions in the process.
If you are interested in this opportunity please apply and I will provide fast feedback.
You can email or call me.
My client are a Global Pharmaceutical company with a large site based in Belgium. They are looking to recruit a Clinical Data Standards Specialist for a year long contract.
The daily rate is negotiable depending on experience.
You tasks will be to create and maintain Platform Independent (PI) CDASH compliant layouts from input provided by Global and Therapeutic area.
You will create and maintain CDASH and SDTM compliant metadata using the Metadata Repositort tool to complement the CDASH/SDTM layouts at all metadata layers.
You must have previous experience as a Data Standards Librarian with knowledge of library theory within an EDC environment.
An advanced knowledge of CDASH and SDTM sumbission principles as well as hands on practical experience in applying these principles.
Experience within Pharmaceutical/CRO industry with sound knowledge of the DM process and knowledge of the role of other clinical research functions in the process.
If you are interested in this opportunity please apply and I will provide fast feedback.
You can email or call me.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung