sas senior credit risk analyst Jobs

Refine Results
21 - 40 of 51 Jobs

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

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

SAS Programmer III

Katalyst Healthcares and Lifesciences

Fremont, California, USA

Full-time

Responsibilities: Review and ensure accurate and high-quality statistical programming deliverables from CRO. Perform generation, validation and QC/QA of SDTM, ADam and TFL output in accordance with SOPs, SOIs, and guidance documents. Create and maintain specifications as per SDTM/ADaM standard and study SAP. Define and create ad-hoc reports and listings for clinical teams. Develop, implement and maintain SAS programming standards. Builds/tests programs for Data Validation, Derivation, and

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

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

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

Albany, New York, USA

Full-time

Responsibilities: Design, code, and test SAS programs used to generate CDISC SDTM & ADaM domains and tables, listings & figures outputs. Perform analyses defined in the statistical analysis plan as well as ad hoc analyses as requested. Validate CDISC SDTM and ADaM data sets by using Open-CDISC Validation Tool. Design, code and test SAS macro libraries to be used for development standardization. Create data definition documents for CDISC SDTM and ADaM datasets and other electronic submission

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

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

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

SAS Marketing Analyst-SAS Direct SAS RTDM-Marketing Campaigns-Hybrid

Elite Technical

Chicago, Illinois, USA

Contract

Our client, a multinational telecommunications technology company, has an urgent and immediate need for a SAS Marketing Analyst to deploy campaigns in SAS Direct as per campaign design specifications. Required skills are BS Degree in a STEM field Minimum 5 years of BA exp. Strong SAS experience including SAS Direct and SAS RTDM This will be a long-term contract and requires you to be onsite at least 3-days per week. The position can be staffed at one of our client's locations in Plano, TX / Alp

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

SAS Allowance for Credit Loss

Princeton IT Services

CA

Contract, Third Party

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

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Dallas, Texas, 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

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

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

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