Katalyst CRO
Overview
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Clinical SAS Programmer
role at
Katalyst CRO . This position involves reviewing CDISC CDASH and SDTM conformant elements, writing and managing SAS code for data mapping to SDTM structures, creating DEFINE specifications, and supporting CDISC standards across projects. Location details and compensation may be referenced in the job posting; this description retains the responsibilities and qualifications as provided. Responsibilities
Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emme\'s SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate. Provide CDISC training and serve as a subject matter support to project staff. Maintain and coordinate CDISC standards efforts, ensure maximum reuse of applied standards, involvement in ongoing process improvement efforts and working with teams to provide technical and process guidance. Stay current with the evolution of all CDISC standards and be involved in creation and maintenance of process documentation. Thorough knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents and regulations. Good understanding of the statistical programming domain and related processes. Assist with developing, monitoring, and enforcing productivity and quality standards along with related documentations. Coordinate with the project management in meeting the timeline and defining/capturing the metrics for monitoring and maintaining the quality and productivity. Requirements
Bachelor\'s or master\'s degree in computer science, Management Information Systems, or a related field. Minimum of 5 years of experience in using SAS to process and analyse large datasets. Experience in conducting data quality reviews including clinical data, tables, graphs, and reports. Experience in developing technical documentation. SAS Certified Base Programmer certification required. Experience with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards. Details
Seniority level: Associate Employment type: Contract Job function: Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x. Get notified about new SAS Developer jobs in Worcester, MA.
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Join to apply for the
Clinical SAS Programmer
role at
Katalyst CRO . This position involves reviewing CDISC CDASH and SDTM conformant elements, writing and managing SAS code for data mapping to SDTM structures, creating DEFINE specifications, and supporting CDISC standards across projects. Location details and compensation may be referenced in the job posting; this description retains the responsibilities and qualifications as provided. Responsibilities
Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emme\'s SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate. Provide CDISC training and serve as a subject matter support to project staff. Maintain and coordinate CDISC standards efforts, ensure maximum reuse of applied standards, involvement in ongoing process improvement efforts and working with teams to provide technical and process guidance. Stay current with the evolution of all CDISC standards and be involved in creation and maintenance of process documentation. Thorough knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents and regulations. Good understanding of the statistical programming domain and related processes. Assist with developing, monitoring, and enforcing productivity and quality standards along with related documentations. Coordinate with the project management in meeting the timeline and defining/capturing the metrics for monitoring and maintaining the quality and productivity. Requirements
Bachelor\'s or master\'s degree in computer science, Management Information Systems, or a related field. Minimum of 5 years of experience in using SAS to process and analyse large datasets. Experience in conducting data quality reviews including clinical data, tables, graphs, and reports. Experience in developing technical documentation. SAS Certified Base Programmer certification required. Experience with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards. Details
Seniority level: Associate Employment type: Contract Job function: Information Technology Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x. Get notified about new SAS Developer jobs in Worcester, MA.
#J-18808-Ljbffr