Position Overview
Responsibilities:
Convert specifications into SAS code to generate datasets and Tables, Listings, and Figures outputs.
Be responsible for overall project delivery, including clinical trial reports and other regulatory submission deliverables.
Create statistical analysis outputs to be used in support of final reports, abstracts, posters, Manu scripts and other clinical publications; support systems to produce electronic regulatory submissions.
Assist in establishing standardized programming procedures and work instructions.
Develop, enhance, evaluate, and validate standardized macros and utility programs to ensure that regulatory requirements are met through validation/compliance activities.
Develop and maintain clinical processing workflow systems.
Assist in the development of client proposal documents.
Provide leadership, project specific training, stakeholder managemen...