sas engineer Jobs

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Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

•

Charlotte, North Carolina, USA

Full-time

Responsibilities: Lead the development and implementation of submission-ready SDTM datasets in accordance with regulatory requirements (e.g., FDA, EMA, PMDA). Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards. Perform thorough quality control checks to validate the accuracy and completeness of submission datasets. Coordinate the preparation and documentation of submission packages, including data specifications and v
Posted 48 days ago | Updated 7 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 7 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Omaha, Nebraska, 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 9 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

North Chicago, Illinois, USA

Full-time

Responsibilities: Liaise with stakeholders to understand clinical study data aggregation requirements. Use the analytics platform to set up the study for the processing of data from source and/or systems. Load data from EDC, and extract into the analytics platform map to SDTM and/or other custom data formats. Understand the protocol and eCRF document and prepare the SDTM specification. Interact with the study team to understand the study requirements. Understand and identify data loading options
Posted 45 days ago | Updated 7 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Los Angeles, California, USA

Full-time

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes' SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate.
Posted 6 days ago | Updated 7 hours ago

IS Technical Specialist I : Junior

Judge Group, Inc.

•

Columbus, Ohio, USA

Contract

Location: Columbus, OH Salary: $40.00 USD Hourly - $45.00 USD Hourly Description: Job Title: SAS Grid/SAS VIYA Admin Type: 12+ Months Contract Location: Columbus or Minneapolis (REMOTE) Job Summary We are seeking a highly experienced SAS Platform Engineer with deep expertise in migrating from SAS 9.4 M7 Grid (RHEL Linux) to SAS Viya 4 (cloud-based or on-prem). This role demands strong hands-on experience in both environments, with a focus on end-to-end migration planning, infrastructure set
Posted 50 days ago | Updated 4 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Dallas, Texas, 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 14 days ago | Updated 7 hours ago

SAS ADMIN/ARCHIECT

3B Staffing LLC

•

Remote

Contract

MUST HAVES: 5+ years of experience supporting complex SAS environments in federal or regulated sectorsStrong troubleshooting and system tuning capabilitiesExperience with upgrades and SAS software lifecycle planningSAS Certified Platform Administrator for SAS 9SAS Certified Professional: Advanced Programming Using SAS 9.4SAS Certified Data Integration Developer for SAS 9SAS Certified Specialist: Administration of SAS Viya Familiarity with TIGTA or IRS operational environmentsKnowledge of federa
Easy Apply
Posted 1 day ago

SAS Teradata Developer

Innova Solutions, Inc

•

Charlotte, North Carolina, USA

Contract

A client of Innova Solutions is immediately hiring for a SAS Teradata Developer Position: SAS Teradata Developer Position Type: W2-Contract Locations: Charlotte, NC and Plano, TX Hybrid: 3 days Onsite and 2 days remote The ideal candidate will have: SAS, Teradata, Python,SQL and Hadoop Required Qualifications 7+ years of software development experienceStrong experience in complex SQL query, PL/SQL programming,Strong software design, build, test and documentation skills * Proven track record in p
Easy Apply
Posted 38 days ago | Updated 24 days ago

SAS Advisor / Architect (VISA INDEPENDENT CANDIDATES ONLY)

SumasEdge Corporation

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Remote

Contract, Third Party

Job Summary: Seeking a highly qualified SAS Professional Services Consultant to provide expert-level support to the client Treasury department. The ideal candidate will serve as a trusted advisor and technical expert, supporting client s internal SAS administration teams with advanced troubleshooting, upgrade planning, optimization efforts, and general advisory services across a wide suite of SAS products. Job Responsibilities Provide remote, real-time over-the-shoulder technical assistance vi
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Posted 4 days ago | Updated 1 day ago

Senior SAS Consultant

BMR Infotek

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Remote

Contract

Senior SAS ConsultantDuration: 1 - 3 YearsLocation: Remote Visa: or OverviewSenior SAS Professional Services Consultant to provide expert-level support to the Treasury Inspector General for Tax Administration (TIGTA).Serve as a Trusted Advisor and Technical expert, supporting client s internal SAS Administration teams with advanced troubleshooting, upgrade planning, optimization efforts, and Advisory services across a wide suite of SAS products. ResponsibilitiesProvide remote, real-time ov
Easy Apply
Posted 2 days ago

Business Analyst (SAS/Campaign)

AgreeYa Solutions

•

Plano, Texas, USA

Full-time, Third Party

Title- Business Analyst (SAS/Campaign) Location- Chicago, IL, Plano, TX, Atlanta, GA, Overland Park, KS- 3 Days Onsite/Week Type- Contract Duration- 18+ Months Description: Analyst, Campaign Operations & Analytics: Deploy campaigns in SAS Direct as per campaign design specifications. Maintain and enhance existing SAS Direct campaign configurations and ensure timely campaign execution. Maintain and enhance SAS RTDM (Real-Time Decision Manager) workflows for decisioning logic and customer treatmen
Easy Apply
Posted 6 days 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 7 hours ago

Senior SAS Developer

Barclays

•

Hanover, New Jersey, USA

Full-time

Job Description Purpose of the role To design, develop and improve software, utilising various engineering methodologies, that provides business, platform, and technology capabilities for our customers and colleagues. Accountabilities Development and delivery of high-quality software solutions by using industry aligned programming languages, frameworks, and tools. Ensuring that code is scalable, maintainable, and optimized for performance.Cross-functional collaboration with product managers, d
Posted 3 days ago | Updated 7 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

Athens, Georgia, 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 23 days ago | Updated 7 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 7 hours ago

Senior SAS Consultant

Connexions Data Inc

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Remote

Contract

Title: Senior SAS Consultant Start: Immediately Duration: 1 - 3 Years Location: Remote s / Holder Overview Senior SAS Professional Services Consultant to provide expert-level support to the Treasury Inspector General for Tax Administration (TIGTA).Serve as a Trusted Advisor and Technical expert, supporting client s internal SAS Administration teams with advanced troubleshooting, upgrade planning, optimization efforts, and Advisory services across a wide suite of SAS products. Responsibiliti
Easy Apply
Posted 5 days ago | Updated 2 days 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 7 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 30 days ago | Updated 7 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 34 days ago | Updated 7 hours ago