SAS Guru Jobs

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Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Boulder, Colorado, USA

Full-time

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submission
Posted 6 days ago | Updated 4 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

•

Edison, New Jersey, USA

Full-time

Responsibilities: Provide support for all aspects of reporting including report development, maintenance, and documentation. Develop, test, debug, and deploy the SAS programs. Develop statistical analysis using standard reporting, ad hoc reporting, and data statistics. Develop SAS and SQL queries to pull the data translated from a database diagram and report requirements, Work with large data sets and cleanse data to integrity. Deliver timely and accurate output in a variety of different fo
Posted 60+ days ago | Updated 4 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Chicago, Illinois, USA

Full-time

Responsibilities: Lead the design, development, and maintenance of the MHN Analytic Platform. Manage, mentor, and ensure technical and analytical development of a team of analysts. Work with teams to operationalize analytic and reporting innovations. Evaluate BI and machine learning solutions. Identify opportunities for process improvement. Requirements: 6 + years of experience using Base SAS, SAS/Macros, and SQL required. Subject matter expert in healthcare data, with 5 + years
Posted 60+ days ago | Updated 4 hours ago

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

•

Albany, New York, USA

Full-time

Responsibilities: Design, code, and test SAS programs used to generate CDISC SDTM & ADaM domains and tables, listings & figures outputs. Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested. Validate CDISC SDTM and ADaM data sets by using Open-CDISC Validation Tool. Design, code and test SAS macro libraries to be used for development standardization. Create data definition documents for CDISC SDTM and ADaM datasets and other electronic submission
Posted 20 days ago | Updated 4 hours ago

SAS Programmer III

Katalyst Healthcares and Lifesciences

•

Fremont, California, USA

Full-time

Responsibilities: Review and ensure accurate and high-quality statistical programming deliverables from CRO. Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents. Create and maintain specifications as per SDTM/ADaM standard and study SAP. Define and create ad-hoc reports and listings for clinical teams. Develop, implement and maintain SAS programming standards. Builds/tests programs for Data Validation, Derivation, and
Posted 25 days ago | Updated 4 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Indianapolis, Indiana, USA

Full-time

Responsibilities: Perform data manipulation, analysis, and reporting of clinical trial data. Develop and maintain department/system-level macros. Create and review SDTM and Adam specifications. Create and validate SDTM data sets. Create and validate analysis data sets. Create and validate patient profiles. Program and generate tables, figures, and listings (TFLs). Validate and document SAS programs and outputs. Fulfil ad-hoc analysis requests. Provide other services. Requirements: Bachelor's deg
Posted 60+ days ago | Updated 4 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

•

Marlborough, Massachusetts, USA

Full-time

Responsibilities: Subjects who discontinue within 7 days of dose reduction/interruption after experiencing a list of AEs. This listing might require data to be merged from AE, EX and DS domains. nalyse/tour data across multiple compounds and clinical studies from different phases to answer research questions. Requirements: 4+ years' experience as data analyst or SAS programmer in the pharmaceutical industry. Experience developing and validating specification file for SDTM and ADaM datasets.
Posted 60+ days ago | Updated 4 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Irving, Texas, USA

Full-time

Responsibilities: Performing data manipulation, analysis, and reporting of clinical trial data for both safety and efficacy (ISS/Client) utilizing SAS programming. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures ( TLFs). Production and QC / validation programming. Ability to program from scratch and able to handle complicated domains and TLF's. Ability to read and apply protocol and SAP. Demonstrate good understanding of the endpoints and d
Posted 60+ days ago | Updated 4 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Boulder, Colorado, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 40 days ago | Updated 4 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Lake Success, New York, USA

Full-time

Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming activities and deliverables for study projects. Perform acquisition and curation of data, including full Clinical Data Interchange Standards Consortium (CDISC) standardization and Pseudo-CDISC Standardization. Document and implement p
Posted 44 days ago | Updated 4 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I- clinical studies. Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS. Create and review annotated CRF to STDM datasets. Produce and maintain technical programming specification documents. Lead and actively participate in client and project review meetings.
Posted 60+ days ago | Updated 4 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 4 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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
Posted 60+ days ago | Updated 4 hours ago

SAS LEAD

Ekcel Technologies Inc

•

Irving, Texas, USA

Full-time

Job Description Responsibilities: Analyze SAS programs to understand sources, dependencies, data flow. Sanitize SAS programs in preparation for conversion. Optimize SAS programs in preparation for conversion. Incorporate changes in accelerator to ensure generated code aligns to required standards Utilize accelerator to convert SAS programs to PySpark programs. Demonstrate and document code lineage. Unit Test generated PySpark programs Incorporate feedback from PySpark EAP integration, SIT and pa
Easy Apply
Posted 6 days ago

SAS Admin 100% remote

Apex 2000

•

Remote

Third Party, Contract

Job Title - SAS Admin 100% Remote Skill: SAS Admin activities involving Downloading SAS Depot to VMCopy Depot to Linux VM and create SAS Software DepotPerform SAS Installation, Log Review, Root Cause Analysis in case of issues. Verify installation components. Start SAS ServicesInvoke SAS Foundation by using ./sas -nodmsCheck for the status of SAS services by ./sas.servers statusCheck for SAS Management Console to validateVerify that License is valid and not expired.Give proc setinit; run;Perform
Easy Apply
Posted 60+ days ago | Updated 1 day ago

SAS Analyst with PySpark/Python

Newt Global

•

Irving, Texas, USA

Contract

Role: SAS Analyst with PySpark/Python Location: Irving, Texas Work from office, 3days a week Must have 8+ years of work experience largely in the Data Management and Risk modelling space.Must have expertise working with Unix, SQL.Must have expertise working with either PySpark/Python or SAS for data extraction and deep dive activities.Prior lead experience in the banking industry.Good to have working experience on MS Office Package (Excel, Outlook, PowerPoint, etc with VBA) and/or BI Visualiza
Easy Apply
Posted 60+ days ago | Updated 1 day ago

SAS Developers with AML.- Chalotte,NC or Jersey,City,NJ (Hybrid Onsite)

Apetan Consulting

•

US

Contract, Third Party

Hybrid SAS Developers with AML. Chalotte,NC Jersey,City,NJ
Easy Apply
Posted 60+ days ago | Updated 15 days ago