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Clinical SAS Programmer

This job posting is for a senior SAS programmer to work remotely. The programmer will be responsible for developing and validating SAS programs to generate statistical tables, listings, figures and datasets from clinical trial data according to specifications. Qualifications include a degree in statistics, computer science or related field, at least 3 years of SAS programming experience including 2 years in a CRO or pharmaceutical company, strong SAS and data manipulation skills, and experience mapping SDTM datasets.

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noafkhalid09
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47 views2 pages

Clinical SAS Programmer

This job posting is for a senior SAS programmer to work remotely. The programmer will be responsible for developing and validating SAS programs to generate statistical tables, listings, figures and datasets from clinical trial data according to specifications. Qualifications include a degree in statistics, computer science or related field, at least 3 years of SAS programming experience including 2 years in a CRO or pharmaceutical company, strong SAS and data manipulation skills, and experience mapping SDTM datasets.

Uploaded by

noafkhalid09
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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Clinical SAS Programmer

Remote
Easy Apply
The Senior SAS Programmer / Statistical SAS Programmer is responsible for providing programming support
for clinical trials and contributing to the development of departmental standards. This includes developing and
validating SAS programs for statistical tables, data listings, figures, and derived datasets according to
specifications.
Responsibilities

 Follow Standard Operating Procedures (SOPs)


 Understand and implement CDISC and other regulatory standards.
 Develop and implement internal SAS programming standards.
 Create and maintain specifications for CDISC SDTM and ADaM datasets and other derived datasets.
 Apply knowledge of SAS programming to develop and validate statistical tables, data listings, figures,
and derived datasets (including STDM and ADaM datasets) for clinical trials data and for integrated
summaries according to SAP and other specifications.
 Review annotated case report forms and database structures.
 Perform ad hoc analyses of current and legacy databases.
 Work closely with other programmers, statisticians, data managers, and database programmers to
ensure accurate and high-quality deliverables.
 Support the efforts of others and share knowledge and skills.

Qualifications
The ideal candidate should have a degree in Statistics, Computer Science or a closely related field, with a
minimum of 3 years of experience as a SAS programmer, and a minimum of 2 years of experience in a CRO or
pharmaceutical company. The candidate should have knowledge of basic statistical concepts, must have strong
SAS programming skills, including data manipulation and statistical analysis procedures, and must have
experience with Word, Excel, and PowerPoint. Experience in mapping SDTM datasets is a strong plus.
Excellent communication skills (both oral and written) and organizational skills are required. Candidate must
be detail-oriented, team-oriented, and self-motivated, and must work well under pressure.
Job Types: Full-time, Fixed term contract
Contract length: 18 months
Salary: $70,000.00-$90,000.00 per year
Schedule:

 8 hour shift

Job Type: Full-time


Pay: $90.00 - $100.00 per hour
Schedule:

 8 hour shift
Experience:

 SAS Programming: 8 years (Required)

Work Location: Remote

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