Job Description

Provides input for Budget Planning Likely to oversee contingent workers and/or vendors; Likely to provide training to others Primarily works at the project level Delivers assignments with quality and within timelines Contributes strategy under moderate supervision Provides strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets Has good knowledge and understanding of the statistical models in efficacy data analysis Responsible for the standardization of Clinical Programming deliverables within a project Extends existing or develops new clinical programming methods to solve complex problems Your experience and qualifications Bachelor s Degree/ Master s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience. Bachelor s + 5 years or Master s + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.