sas programmer Jobs

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Senior SAS Programmer

Innova Solutions, Inc

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Okemos, Michigan, USA

Contract

Innova Solutions has a client that is immediately hiring for a Senior SAS Programmer Position Type: Full-time Contract Duration: Contract to hire Location: Okemos MI Hybrid (minimum of 3 days a week in Okemos office), subject to change in the futureAs a Senior SAS Programmer , you will: We are looking for a Senior SAS Programmer to join our Data Insights Team. Will work to support several reporting platforms. Programmer will create Excel and PDF reports using Base SAS as described by busines
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Posted 15 days ago

Sr SAS Programmer

Apex Systems

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Okemos, Michigan, USA

Full-time

Job#: 2078512 Job Description: Job Title: Senior SAS Programmer Department: Data Insights Team Job Summary: We are seeking a highly skilled Senior SAS Programmer to join our Data Insights Team. This role involves supporting multiple reporting platforms by developing Excel and PDF reports using Base SAS, based on business requirements. The ideal candidate will also contribute to system testing and participate in the full software development lifecycle. Key Responsibilities: Collaborate in req
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Posted 15 days ago | Updated 10 hours ago

SAS Programmer with Healthcare exp

SYSTEM SOFT TECHNOLOGIES LLC

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Okemos, Michigan, USA

Contract, Third Party

System Soft Technologies is widely recognized for its professionalism, strong corporate morals, customer satisfaction, and effective business practices. We provide a full spectrum of business and IT services and solutions, including custom application development, enterprise solutions, systems integration, mobility solutions, and business information management. System Soft Technologies combines business domain knowledge with industry-specific practices and methodologies to offer unique solution
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Posted 15 days ago

Senior SAS Programmer Analyst

GreyCell Labs, Inc

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Albany, New York, USA

Contract, Third Party

70 months of experience in the development of study design for research and evaluation, with the ability to perform complex statistical analysis using SAS, R, Tableau and other statistical and graphical software packages. 60 months of experience in the development of SAS programming code for data requests, reports and analysis in a health department setting after receiving a Bachelor's degree Bachelor's Degree in Statistics or Epidemiology, or any related field of science 24 months of experience
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Posted 2 days ago | Updated 1 day ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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
Posted 13 days ago | Updated 10 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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 20 days ago | Updated 10 hours ago

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

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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 23 days ago | Updated 10 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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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 5 days ago | Updated 10 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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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 9 days ago | Updated 10 hours ago

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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Boston, Massachusetts, USA

Full-time

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases. Perf
Posted 44 days ago | Updated 10 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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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 49 days ago | Updated 10 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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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 49 days ago | Updated 10 hours ago

Sr. Clinical SAS programmer

Katalyst Healthcares and Lifesciences

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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 36 days ago | Updated 10 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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 49 days ago | Updated 10 hours ago

SAS Programmer

Katalyst Healthcares and Lifesciences

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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 40 days ago | Updated 10 hours ago

IT Business Sr Analyst/SAS Programmer

Citi

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Remote or Irving, Texas, USA

Full-time

Job Description Overview of the Role Citi, the leading global bank, has approximately 200 million customer accounts and does business in more than 160 countries and jurisdictions. Citi provides consumers, corporations, governments, and institutions with a broad range of financial products and services, including consumer banking and credit, corporate and investment banking, securities brokerage, transaction services, and wealth management. As a bank with a brain and a soul, Citi creates econom
Posted 31 days ago | Updated 10 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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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 49 days ago | Updated 10 hours ago

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

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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
Posted 49 days ago | Updated 10 hours 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 49 days ago | Updated 10 hours 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
Posted 49 days ago | Updated 10 hours ago