Vacancy expired!
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.
- 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
- Knowledge of clinical reporting tools (e.g. Cognos, J-Review, SAS, SQL, etc.)
- Strong Project Management skills
- Ability to work with diverse user groups, lead discussions on and creation of User Requirements and Design documentation.
- Support creation and maintenance of standard report libraries.
- Strong knowledge of industry specific data standards e.g., CDASH, CDISC ODM/SDTM.
- Tibco ,Spotfire, CDASH, CDISC,R program, Cognos, clinical
Vacancy expired!