Location: Irvine, CA Bill : $93.82 HR Responsible:
NO SAS Programmers Needed
This individual will lead the design, development, validation, rollout of reports/dashboards using business intelligence tools (e.g., Spotfire, J-Review) and programs (e.g., SQL, PL-SQL, SAS) used in Clinical Research and Development studies.
Additionally, the (PCSP) will analyze Clinical Study design requirements against third party system specifications to support the implementation of electronic systems (e.g., electronic diaries) used in Clinical studies.
The candidate will act in a project management role managing various study-related projects and initiatives.
This individual will lead the design, development, validation, rollout of reports/dashboards using business intelligence tools (e.g., Spotfire, J-Review) and programs (e.g., SQL, PL-SQL, SAS) used in Clinical Research and Development studies.
Additionally, the (PCSP) will analyze Clinical Study design requirements against third party system specifications to support the implementation of electronic systems (e.g., electronic diaries) used in Clinical studies.
Education and Experience:
BA/BS degree or equivalent experience in Computer Science, Life Science or related field required.
Knowledge of Oracle databases and structure
Knowledge of visualization tools, such as TIBCO Spotfire with R programming experience