Clinical SAS Programmer Jobs in California

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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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South San Francisco, California, USA

Full-time

Responsibilities: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes performed are conducted according to sponsor requirements. Works closely with the Biostatistics and Data Management departments on various clinical projects. Designs and/or reviews database structure. Writes edit checks from the Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses specified in the Statistical Anal
Posted 60+ days ago | Updated moments ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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San Diego, California, USA

Full-time

Responsibilities: Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant. Act as a Programming SME for assigned studies, including authoring/reviewing programming specifications, such as SDTM/ADaM specifications, TFLs creation and QC for reporting events, ESUB packages, and documenting production and validation programs. Apply programming skills to support statistical analysis, clinical reporting, regulatory submission