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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

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

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

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

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.

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

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

SAS Advisor / Architect (VISA INDEPENDENT CANDIDATES ONLY)

SumasEdge Corporation

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

Senior SAS Consultant

BMR Infotek

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

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

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

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.

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

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

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.

Senior SAS Consultant

Connexions Data Inc

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

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

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

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

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

Edison, New Jersey, USA

Full-time

Responsibilities: Serve as the statistical programming lead on internal project teams and coordinate programming, verification, and documentation of statistical programs for use in creating analysis datasets, tables, listings, and figures. Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department. Assist in ensuring the optimum performance of