What are the responsibilities and job description for the Clinical SAS Programmer position at Katalyst Healthcares & Life Sciences?
Responsibilities
Maintain programmatic data quality checks.
Create submission ready data and analysis elements, such as ADaM, TLFs, DEFINE.xml, etc.
Provide oversight of vendor activities to ensure the quality of vendor deliverables, such as SDTM, ADaM, and analysis outputs.
Support study team needs as ad-hoc analysis and analysis for publications.
Work cross-functionally across the study team to support other functions programming needs, such as cross-domain data check, safety monitoring outputs, etc.
Help to improve and innovate internal tools and processes.
Requirements:
Bachelor's degree in Statistics, Mathematics, Computer Science, Computer Information Systems, or Public Health (Master's degree is preferred).
5 years of SAS programming experience in pharmaceutical or CRO environments.
Strong knowledge of CDISC SDTM, ADaM, Define.xml, CFR 21 Part 11 compliance, ICH, and FDA standards.
Understanding data and system dependencies, validation techniques, and integration of studies for ISS/Client.
A thorough knowledge of SAS and working knowledge of different SAS environment (i.e., SAS EG in UNIX and Windows) is required.
Truly enjoy programming and innovation.
Strong writing and communication skills.
Requires good understanding of data standards (i.e., CDISC SDTM, ADAM, and Define.xml), as well as ICH and regulatory guidelines on data, and reporting standards.
Maintain programmatic data quality checks.
Create submission ready data and analysis elements, such as ADaM, TLFs, DEFINE.xml, etc.
Provide oversight of vendor activities to ensure the quality of vendor deliverables, such as SDTM, ADaM, and analysis outputs.
Support study team needs as ad-hoc analysis and analysis for publications.
Work cross-functionally across the study team to support other functions programming needs, such as cross-domain data check, safety monitoring outputs, etc.
Help to improve and innovate internal tools and processes.
Requirements:
Bachelor's degree in Statistics, Mathematics, Computer Science, Computer Information Systems, or Public Health (Master's degree is preferred).
5 years of SAS programming experience in pharmaceutical or CRO environments.
Strong knowledge of CDISC SDTM, ADaM, Define.xml, CFR 21 Part 11 compliance, ICH, and FDA standards.
Understanding data and system dependencies, validation techniques, and integration of studies for ISS/Client.
A thorough knowledge of SAS and working knowledge of different SAS environment (i.e., SAS EG in UNIX and Windows) is required.
Truly enjoy programming and innovation.
Strong writing and communication skills.
Requires good understanding of data standards (i.e., CDISC SDTM, ADAM, and Define.xml), as well as ICH and regulatory guidelines on data, and reporting standards.
SAS Programming
Integrated Resources INC -
Madison, NJ
SAS Administrator
E*Pro Inc -
Hoboken, NJ
