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Clinical SAS Consultant (W-2 Only)

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Clinical SAS Consultant (W-2 only)

Qualifications:

Minimum Education: B.S. or equivalent in computer science, mathematics, or life science.

Required Experience:

A minimum of 5 years of relevant clinical research programming experience, 3 years specifically in the pharmaceutical industry.

Demonstrable experience/expertise in analysis and reporting of phase I-IV clinical trial data.

Demonstrable experience/expertise using SAS/Base and SAS/Stat.

Demonstrable experience/expertise using CDISC standards: CDASH, SDTM, ADaM, DEFINE-XML, Controlled Terminology.

Demonstrable proficiency in MS Office (Outlook, Word, Excel, PowerPoint).

Provide programming support for study deliverables as assigned, ensuring that timelines are met and expected quality is attained.

Liaise with Data Management and Biostatistics for database and dataset specifications, timelines, and quality requirements.

Create and validate SDTM and ADaM datasets and associated submission deliverables in compliance with published industry standards and project/study specific requirements.

Create and validate TFL output in compliance with study specific requirements.

Receive, import, and verify the structure of external data.

Create and maintain supporting documentation.

Maintain professional currency through:

Demonstrable expertise in SAS analysis and reporting programming.

Demonstrable expertise with CDISC CDASH, SDTM, ADaM, DEFINE-XML, and/or controlled terminology.

Perform other duties as assigned.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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