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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.

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

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 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

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.

SAS Professional Services Advisor/Architect - 3 Years - REMOTE

Montek System

Remote

Contract

Role: SAS Professional Services Advisor/Architect Job Summary: Seeking a highly qualified SAS Professional Services Consultant to provide expert-level support to the Treasury Inspector General for Tax Administration (TIGTA). The ideal candidate will serve as a trusted advisor and technical expert, supporting TIGTA s internal SAS administration teams with advanced troubleshooting, upgrade planning, optimization efforts, and general advisory services across a wide suite of SAS products. Job Respon

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

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.

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

Data Scientist -Python SAS Viya SQL Big Data platforms -Hybrid

Elite Technical

Plano, Texas, USA

Contract

Absolutely no third parties please !! Responsibilities Our Client is seeking a Data Scientist to Analyze complex datasets to uncover patterns, trends, and insights that drive strategic business decisions. Develop predictive models, machine learning algorithms, and statistical analyses to solve business problems and improve campaign or operational performance. Collaborate with business and technical teams to define data science use cases and translate business requirements into analytical solutio

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

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

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

SAS Teradata Consultant

KE Staffing

Plano, Texas, USA

Contract

Must have SAS, Teradata, SQL query, PL/SQL Or Python, Spark and Hadoop its a huge plus Required Skills: Bachelor s in computer science or related field7+ years of software development experienceStrong experience in complex SQL query, PL/SQL programming,

SAS Developer

Expedite Technology Solutions

No location provided

Full-time, Contract

Job Description: Must Have:- Statical Analysis Systems (SAS), Data Pipelines, Data Migration Participate in design and SAS code reviews. Recognize potential system opportunities or issues during data transfer/predictions and collaborates with data scientists or other IT groups as appropriate Collaborate with SAS Technical Support on issue resolution or enhancements Experience with distributed framework platforms, in this case SAS Load Balancer or equivalent middleware's.

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

Seattle, Washington, USA

Full-time

Responsibilities: The senior programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. Candidates must have excellent SAS and SQL programming skills and the ability to implement complex logic. Candidates must be comfortable with creating complex analysis data sets derived from various data sources with a careful eye for outliers and errors. Prior experience building patient cohorts and evalu

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

Bridgewater, New Jersey, USA

Full-time

Responsibilities: Lead and participate in the development and validation of high quality CDISC datasets based on the implementation guides and consultations with sponsors, project leads, systems analysts, other programmers, and end users. Use your expertise in data standards and regulatory requirements to lead discussions with clients about appropriate approaches to database design. Use study protocol, CRF, Data Transfer Agreements from vendors, data sources, CDISC CT, TAUGS, and CDISC implement