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Clinical SAS programmer

Katalyst Healthcares and Lifesciences

•

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 42 days ago | Updated 1 hour ago

SAS Developer

Newt Global

•

Irving, Texas, USA

Contract

Must have 8+ years of work experience largely in the Data Management and Risk modelling space.Must have expertise working with Unix, SQL.Must have expertise working with either Pyspark/Python or SAS for data extraction and deep dive activities.Prior lead experience in the banking industry.Good to have working experience on MS Office Package (Excel, Outlook, PowerPoint, etc with VBA) and/or BI Visualization tools like Tableau is a plus
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Posted 10 days ago | Updated 5 days ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 1 hour ago

Senior Full Stack Developer SAS and Informatica

Mindlance

•

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 11 days ago | Updated 11 days ago

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 22 days ago | Updated 1 hour ago

Sr SAS Programmer

Apex Systems

•

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 13 days ago | Updated 2 hours ago

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
Posted 47 days ago | Updated 1 hour ago

Python Developer with SAS (Healthcare Exp)

ConglomerateIT

•

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 19 days ago | Updated 6 hours ago

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
Posted 19 days ago | Updated 1 hour ago

SAS Allowance for Credit Loss

Princeton IT Services

•

CA

Third Party, Contract

Job Description Job Title: SAS Allowance for Credit Loss Location: Remote Job Type: Contract Job Summary: We are seeking a highly skilled SAS Viya ACL (Access Control List) Specialist to support the implementation and administration of fine-grained access control policies within the SAS Viya platform. The ideal candidate will have hands-on experience with SAS Viya security administration, role-based access control (RBAC), and policy enforcement to ensure secure access to data, services, a
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Posted 4 days ago | Updated 2 hours ago

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
Posted 34 days ago | Updated 1 hour ago

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
Posted 47 days ago | Updated 1 hour ago

SAS Viya ACL Specialist

Princeton IT Services

•

IN

Contract, Third Party

Job Title: SAS Viya ACL Specialist Location: Remote Job Type: Contract Job Summary: We are seeking a highly skilled SAS Viya ACL (Access Control List) Specialist to support the implementation and administration of fine-grained access control policies within the SAS Viya platform. The ideal candidate will have hands-on experience with SAS Viya security administration, role-based access control (RBAC), and policy enforcement to ensure secure access to data, services, and applications. Key Resp
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Posted 4 days ago | Updated 2 hours ago

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

Infinity Tech Group Inc

•

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 13 days ago | Updated 12 days ago

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.
Posted 47 days ago | Updated 1 hour ago

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
Posted 4 days ago | Updated 1 hour ago

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
Posted 12 days ago | Updated 1 hour 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 8 days ago | Updated 1 hour ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

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 47 days ago | Updated 1 hour ago

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.
Posted 38 days ago | Updated 1 hour ago