Clinical Programmer

Clinical Programmer
Company:

Software Guidance & Assistance


Place:

New York


Clinical Programmer

Details of the offer

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

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.

Skills Required

Tibco ,Spotfire, CDASH, CDISC,R program, Cognos, clinical

Requirements


Knowledges:

  • TIBCO

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