A Senior SAS Programmer is responsible to provide high level skills of clinical programming support of clinical projects and regulatory submissions.
The Senior SAS Programmer is playing a lead role generating and validating study and/or analysis datasets, tables, listings and figures. The Senior SAS programmer participates in the development of global data standards, SDTM, ADaM and Teva's database structure . The Senior SAS programmer is responsible for providing professional expertise and leadership through leading departmental tasks and taking initiatives in improving clinical programming processes with focus on SAS Programming.
Temp position replacement for Maternity Leave for up to a year
Education Required: Bachelor's or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
Experience Required: Up to 5 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
Experience in SDTM and ADaM as applicable, acquainted with CDISC guidelines and requirements.