Clinical SAS Programmer Jobs in Massachusetts

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Senior Clinical SAS Programmer

Sharp Infotech Inc.

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Remote

Contract, Third Party

Psotion: Senior Clinical SAS Programmer Location: REMOTE Duration: 6 Months + Description: - Experience on the Gastroenterology studies. - Review Protocols, Mapping Documents, and Statistical Analysis plan. - Program and Validate SDTM datasets in SAS according to SDTM specifications. - Program and Validate ADAM datasets in SAS according to ADAM specifications. - Produce tables and listings required for various studies. - Efficacy and safety tables for efficacy and safety analysis. - Standard Ma
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Posted 3 days ago

Senior Clinical SAS programmer with Pharma experience -Remonte-W2 -Contract

Biogensys

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Remote

Contract

Biogensys is currently hiring a Senior SAS programmer with Pharma experience for 6 to 12 months contract on w2. This is a remote position, no corp to corp, or 1099. No sponsorship is available. Statistical Programmer II: Pharma experience/Remote At least 7-8 years of experience in ADaM/TLF.Create, validate, and maintain SAS programs for data analysis, reporting, and submission deliverablesDevelop analysis datasets (ADaM) and tables, listings, and figures (TLFs) to support statistical analysis in
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Posted 10 days ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Cambridge, Massachusetts, USA

Full-time

Responsibilities: Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal al study data as tables, listings, and graphs for electronic submission to regulatory agencies. Attending multi-disciplinary team meetings, representing the programmi
Posted 8 days ago | Updated 1 hour ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Boston, Massachusetts, USA

Full-time

Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.). Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies. Develop software systems to generate displays of clinal all stu