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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

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

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

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.

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

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

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

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

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 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.

Capacity Accreditation Engineer

NYISO

Rensselaer, New York, USA

Full-time

Job DescriptionThe New York Independent System Operator (NYISO) manages the efficient flow of electricity on more than 11,000 circuit-miles of high-voltage transmission lines, dispatching power from hundreds of generating units across the state. The NYISO's Market Operations department invites applications for a full-time Capacity Accreditation Engineer. The Capacity Accreditation Engineer will support the NYISO's activities related to the Capacity Accreditation process to ensure accurate Capa

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.

PowerBI Developer

Resource Informatics Group

Remote or Irving, Texas, USA

Contract

Solicitation Reference Number: 70125073 Working Title: PowerBI Developer Title/Level: Data Analyst/Report Writer 3 Category: Data/Database Administration I. DESCRIPTION OF SERVICESTexas Education Agency requires the services of 1 Data Analyst/Report Writer 3, hereafter referred to as Candidate(s), who meets the general qualifications of Data Analyst/Report Writer 3, Data/Database Administration and the specifications outlined in this document for the Texas Education Agency.All work products res

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

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

Associate Server Systems Administrator

Vanderbilt University

Nashville, Tennessee, USA

Full-time

Job Description The Associate Server Systems Administrator is part of the Advanced Computing Center for Research and Education (ACCRE) at Vanderbilt University and contributes to the maintenance and availability of virtual and physical server systems. Reporting directly to the Director of Research Computing Operations, the Associate Server System Administrator will be part of ACCRE's Infrastructure Group and collaborate with members of other ACCRE units. The Associate Server Systems Administra

Chronic Disease Data Analyst, Bureau of Chronic Disease Prevention

City of New York

Queens, New York, USA

Full-time

Company Description Job Description The Center for Health Equity & Community Wellness (CHECW) seeks to eliminate racial and other inequities resulting in premature mortality. With an unwavering grounding in history and structural analysis, CHECW works to increase visibility of the harm perpetuated by centuries of racist, socially unjust policy while pushing towards redress for the most impacted NYC communities. CHECW addresses inequity across community and healthcare systems in partnership wit

FSCM Subject Matter Expert (SME) General Ledger

HyperGen, Inc.

Westborough, Massachusetts, USA

Contract

NO C2C-must be authorized to work in the US with no sponsorship We are seeking an experienced FSCM Subject Matter Expert (SME) with deep General Ledger (GL) expertise to support a major ERP Roadmap initiative for a higher education client. This role will ensure the client s financial management needs are clearly defined and fully addressed during solution demonstrations, peer benchmarking, and roadmap development. The SME will bring a deep understanding of ERP financial modules with an emphasis

Data Reporting and Analytics Consultant IV - SAS Programming

Kaiser Permanente

Oakland, California, USA

Full-time

Job Summary: This individual contributor is primarily responsible for driving strategic data-informed decisions, gathering data and information on targeted variables in an established systematic fashion, preparing data for analytic efforts, and interpreting data analyses. This position executes creative data analytic approaches leading to actionable outcomes, develops, implements, and automates business and reporting solutions, and develops analytical and/or statistical models enabling informe