Opportunity Description
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 ...
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