sas programmer analyst Jobs

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Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Nityo Infotech CorporationCompany Name - Nityo Infotech Corporation

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Raleigh, North Carolina, USA

Full-time

Job Role: Clinical SAS Programmer Job Location: Raleigh, NC/ Bridgewater, NJ/Hartford, CT Job Type: Full Time Job Description: Clinical SAS Programmer Required Skills & Experience: 5+ years of combined experience in SAS and R programming in the clinical research or pharmaceutical domain. Strong expertise in SAS programming for clinical data analysis, including SDTM, ADaM, and TLF programming. Proficiency in R programming for clinical data processing and visualization. Hands-on experience wit

SAS Data AnalystJob Title - SAS Data Analyst

Tektend llcCompany Name - Tektend llc

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Minneapolis, Minnesota, USA

Contract

Job title: SAS Data Analyst Location: Charlotte, NC /Chandler, AZ/ Minneapolis, MN/ Des Moines, IA/ Phoenix, AZ Duration: 12+ months Tax terms: W2 Job Description: 3+ years of SQL, SAS and Excel, Understanding if the code they have is accurate and then interact heavily with the Developers - so prefers more of an Analytics Generalist vs. a hardcore developer/programmer here/ They won't be building the actual tool like the developers will. Will work with BA's and Developers to understand th

SAS Developer/Sr. Data Analyst(SAS Pricing)Job Title - SAS Developer/Sr. Data Analyst(SAS Pricing)

Factspan IncCompany Name - Factspan Inc

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Remote

Full-time

Senior Data Analyst (SAS Pricing)/SAS Developer The Senior Data Analyst/SAS Developer is responsible for supporting internal and external clients through planned strategic analyses of pharmacy claims data. This position will utilize analytic tools to provide insight that allows the company and our clients to make better informed decisions in various areas such as pharmacy benefit plan performance, claims forecasting, pricing savings analyses, member disruption, key initiatives and auditing. The

IT Business Sr Analyst/SAS ProgrammerJob Title - IT Business Sr Analyst/SAS Programmer

CitiCompany Name - 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

Sr. SAS ProgrammerJob Title - Sr. SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS programmerJob Title - Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Sr. Clinical SAS programmerJob Title - Sr. Clinical SAS programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

SAS ProgrammerJob Title - SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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.

SAS ProgrammerJob Title - SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

SAS Clinical Trails ProgrammerJob Title - SAS Clinical Trails Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Cary, North Carolina, USA

Full-time

Responsibilities: The consultant will provide programming/analytical support utilizing client as the primary programming language to create and manage the production of analysis reports. summary tables/listings and graphs for clinical trials submitted to various regulatory bodies worldwide. The consultant must have excellent communication skills and must be able to communicate about the techniques developed and results of analysis both to executives and other analysts in the organization. Pe

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

SAS ProgrammerJob Title - SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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.

SAS ProgrammerJob Title - SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Pleasanton, California, USA

Full-time

Responsibilities: We are seeking experienced SAS programmer analysts to join a Biostatistical Consulting Unit to provide programming and biostatistical support to research studies in all fields of medicine led by clinicians (including medical residents). Description of position: The programmer will support internally funded retrospective research studies, from development of research question, study design and methods, Institutional Review Board (IRB) proposal development and approval; through

Senior SAS ProgrammerJob Title - Senior SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

Clinical SAS ProgrammerJob Title - Clinical SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - 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

SAS AdministratorJob Title - SAS Administrator

LogiX-GuruCompany Name - LogiX-Guru

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Remote

Contract

Job Description : Required Skills and Experience 5+ years of SAS platform administration experience Hands-on experience with SAS 9.4 M7 Grid on RHEL Linux Proven expertise with SAS Viya 4 administration and architecture Deep understanding of SAS compute, CAS server configuration, and Viya services Familiarity with tools like Ansible, Terraform, or shell scripting for automation (a plus) Experience with cloud-based deployments (e.g., AWS) is strongly preferred Strong understanding of SAS licensin