Clinical SAS Programmer

VR IT Technosoft Pvt Ltd.

● Good Knowledge of Clinical Trials and Clinical Terminology. Proficient in Understanding of Study Protocol, and Crf-

annotation (case Report Form) Having Excellent Knowledge in Sas/base, Sas/macros, Sas/sql and Sas/ods (rtf, Pdf, Html) Procedures. Good Knowledge On Cdisc- Sdtm rehensive Prepared Reports Using Sas Report Generating Procedures like Proc Print, Proc Means, Proc Report, Proc Freq and Proc Transpose. Good Knowledge in Sas Base Procedures for Data Processing like Format, Sort, Transpose and Sql.

● Data Management Skills like Merging, Handling Missing Values, Reading Raw Data Files, Handling Programming Errors.

● Excellent Knowledge in Sas Functions and Sas Formats/informats.

● Thoroughly Understand Trial Related Documents such as Protocol and acting Data from Excel Sheet to Sas Datasets Using Proc Import Procedure , Develop Statistical Analysis Plans, Including Table, Listing and Graph Specifications.

specify the General Structure of the Analysis Database, Provide Programming Support for Its Development and Validation.

produce Statistical Analyses and Statistical Appendices, with Appropriate Documentation.

validate Statistical Analyses and Statistical Appendices, with Appropriate Documentation.

prepare Statistical Reports, Integrated Summaries of Safety, Integrated Summaries of Efficacy and other Documents, as Required. Contribute Statistical Methods Section for Integrated Clinical Statistical Reports. Review Integrated Clinical Statistical Reports.

• Experience

  2 - 3 Years

• No. of Openings

  30

• Education

  B.Pharma

• Role

  Clinical SAS Programmer

• Industry Type

  IT-Hardware & Networking / IT-Software / Software Services

• Gender

  [ Male / Female ]

• Job Country

  India

• Type of Job

  Full Time

• Work Location Type

  Work from Office