entry level sas programer Jobs

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Senior SAS Programmer Analyst

GreyCell Labs, Inc

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Albany, New York, USA

Third Party, Contract

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 3 days ago | Updated 8 hours ago

Senior Full Stack Developer SAS and Informatica

Mindlance

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McLean, Virginia, USA

Third Party, Contract

Position Title: Senior Full Stack Developer Location: Full Time on-site in McLean, VA Duration: 3 months assignment Must Have Skills: SAS and Informatica are Primary Skills & AWS, Kubernetes, PySpark, Python, Node.JS, Microservices, Postgres Behave/Cucumber for automation, and Pytest are Secondary Skills Qualification: Development of microservices based on Python, Pyspark, AWS EKS, AWS Postgres for a data-oriented modernization project.New System: Python and PySpark, AWS Postgres DB, Behave/Cucu
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Posted 14 days ago | Updated 14 days ago

SAS Developer

Factspan Inc

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Remote

Full-time

Job Title: SAS Developer Job Type: Full Time Job Location: Remote The 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
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Posted 35 days ago | Updated 21 days ago

Placement Role - Python Developer with SAS/ Informatica/AWS exp - Onsite - McLean VA

Infinity Tech Group Inc

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McLean, Virginia, USA

Contract

Role: Python Developer with SAS/ Informatica/AWS exp (Day1 Onsite) Financial Client Location: McLean, VA Duration: 6+ Months No OP ts & H Ones for this Role Job Description: Seeking a Senior Informatica, Python, SAS developer for a 3 month contract position with a mortgage loan corporation located in McLean, VA. This position is fully onsite. 5 days a week on site Summary: Development of microservices based on Python, Pyspark, AWS EKS, AWS Postgres for a data-oriented modernization projectNew
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Posted 15 days ago | Updated 15 days ago

SAS Developer

Expedite Technology Solutions

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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.
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Posted 60+ days ago | Updated moments ago

Python Developer with SAS (Healthcare Exp)

ConglomerateIT

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Texas, USA

Contract

Job Title: Python Developer with SAS (Healthcare Exp) Tax Term: W2/1099 Only Location: 100% Remote Employment Type: Contract About us Conglomerate IT is a certified and a pioneer in providing premium end-to-end Global Workforce Solutions and IT Services to diverse clients across various domains. Visit us at Our mission is to establish global cross culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power o
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Posted 22 days ago | Updated 16 hours 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 14 days ago | Updated 2 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 24 days ago | Updated 2 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 21 days ago | Updated 2 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 45 days ago | Updated 2 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 32 days ago | Updated 2 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 50 days ago | Updated 2 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 50 days ago | Updated 2 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 37 days ago | Updated 2 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 50 days ago | Updated 2 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 6 days ago | Updated 2 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 50 days ago | Updated 2 hours ago

SAS Clinical Trails Programmer

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
Posted 50 days ago | Updated 2 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 10 days ago | Updated 2 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 41 days ago | Updated 2 hours ago