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Clinical SAS Programmer

$25/hr Starting at $100

- Good Exposure in SAS Application development in Clinical Domain in MS-Windows Environment. -Experience in SAS programming with reference to Base, Access, Sql, Macros and knowledge on SAS EG and Advance Excel. ? Hands on Experience on all the SAS Functions, Statements, Dataset Options and System Options including the ones introduced in SAS Version 9.2 ? Excellent knowledge and work experience in data manipulation, data cleaning, sorting. ? Good at study documentation and understanding and implementation of client standards ? Ability to meet the study timelines and deliver the study deliverables on time and capable to work simultaneously on different projects ? Good at study documentation and understanding and implementation of client standards ? Customizing Applications by the Macro Facility. Strong knowledge involving all phases (I-IV) of clinical trials. ? Experience in implementing CDISC SDTM for intervention, event, findings, and special purpose domain models. ? Worked with clinical data management team for creating annotated CRF. Created new analysis data sets from raw data sets for clinical trials. ? Good Comprehension of FDA and CDISC guidelines, Good Clinical Practice (GCP), International Conference of Harmonization (ICH). ? Good Experience in understanding the PROTOCOLS, CDISC Process, SOP’s and SAP’S.

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$25/hr Ongoing

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- Good Exposure in SAS Application development in Clinical Domain in MS-Windows Environment. -Experience in SAS programming with reference to Base, Access, Sql, Macros and knowledge on SAS EG and Advance Excel. ? Hands on Experience on all the SAS Functions, Statements, Dataset Options and System Options including the ones introduced in SAS Version 9.2 ? Excellent knowledge and work experience in data manipulation, data cleaning, sorting. ? Good at study documentation and understanding and implementation of client standards ? Ability to meet the study timelines and deliver the study deliverables on time and capable to work simultaneously on different projects ? Good at study documentation and understanding and implementation of client standards ? Customizing Applications by the Macro Facility. Strong knowledge involving all phases (I-IV) of clinical trials. ? Experience in implementing CDISC SDTM for intervention, event, findings, and special purpose domain models. ? Worked with clinical data management team for creating annotated CRF. Created new analysis data sets from raw data sets for clinical trials. ? Good Comprehension of FDA and CDISC guidelines, Good Clinical Practice (GCP), International Conference of Harmonization (ICH). ? Good Experience in understanding the PROTOCOLS, CDISC Process, SOP’s and SAP’S.

Skills & Expertise

AnalyticsMacroManagementProgrammingRawSAS

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