Job description Posted 26 March 2019

Description

The Data Standards Analyst provides support for the development and maintenance of GSK SDTM mappings, including Controlled Terminology (CT) mappings. These mappings provides instruction for transforming GSK legacy (IDSL) standards to CDISC SDTM standards. An eye for detail, ability to work to timelines and quality standards is critical. The role requires expert organisational skills. Experience with Data Standards Management is preferred. This role will not perform any programming to map studies from legacy GSK data standards to SDTM, since the study transformations are performed by external suppliers.

Responsibilities of this Role

• Create and QC mappings of GSK legacy data and terminology to SDTM domains and Controlled Terminology

• Support SDTM variable and controlled terminology mapping-related questions

• Support questions and requests for lab, biomarker, and PK data

Requirements for this Role

• The Data Standards Analyst must be a subject matter expert in SDTM including Controlled Terminology.

• The Data Standards Analyst must be attentive to detail, with a focus on quality and accuracy.

• Experience in standards management is preferred.

• The ideal candidate will preferably have expertise in Lab, Biomarker, and PK data with a background in medicine or science (e.g. a degree in a field such as Nursing, Biology, Biochemistry, Microbiology, Chemistry, etc.).

Additional information about the process

All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.