10 of 10 SAS Macro Jobs in the UK excluding London

support flexible working – click here for more information on flexible working options Flexible Working Options Hybrid Working, Job Share Job Description Summary . Job Description JOB TITLE: Data Engineer (SAS) Salary: £47,790 - £55,000 LOCATION: Halifax HOURS: Full time WORKING PATTERN: Hybrid, 40% (or two days) in our Halifax office. About this opportunity... Exciting opportunity for a Data … Engineer to join the Consumer Risk Data Labs to focus on assisting in the design, development, and maintenance of the Le Mans analytical SAS application, gaining practical experience whilst working under the guidance of senior data engineers. They will help to provide a critical service to enable the effective management and operations of the Le Mans data infrastructure. Le … our 26 million customers. We’re growing with purpose. Join us on our journey and you will too... What you’ll do... Supports the management and operations of the SAS Data Warehouse (Le Mans) which supports 1100+ colleagues across Risk. Collaborates across technology and business teams to deliver the required level of service and data capabilities. Delivers support and More ❯

JOB TITLE: Data Engineer (SAS) Salary: £47,790 - £55,000 LOCATION: Halifax HOURS: Full time WORKING PATTERN: Hybrid, 40% (or two days) in our Halifax office. About this opportunity Exciting opportunity for a Data Engineer to join the Consumer Risk Data Labs to focus on assisting in the design, development, and maintenance of the Le Mans analytical SAS … our 26 million customers. We're growing with purpose. Join us on our journey and you will too What you'll do... Supports the management and operations of the SAS Data Warehouse (Le Mans) which supports 1100+ colleagues across Risk. Collaborates across technology and business teams to deliver the required level of service and data capabilities. Delivers support and … resolves issues on the production scheduled batch on Le Mans. This requires experience of SAS DI Studio. Supports oversight, process execution and customer engagement for compliance and governance (ITEC, UAM, Cyber, SOX, Deloitte, Audit, etc). This requires experience of SAS Management Console. Work closely with customers to understand requirements and specifications, collaborate with team to identify and More ❯

phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests. In this role, you will develop and validate SAS programs for data presentations and analyses and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative new benchmark … on the development of complex TFL shells from a programming perspective Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs Produce/define XML/PDFs, Analysis Results Metadata (ARM), aCRFs …/or equivalent professional experience in statistical programming for clinical trials Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs Solid knowledge of More ❯

talk with your recruiter to learn more. Base pay range Working as a Senior Statistical Programmer in our Lausanne, Paris, or Cambridge UK office, you will use your advanced SAS programming expertise and in-depth knowledge of industry-wide standards to lead and support clinical studies across all phases of development. Reporting to the Director of Biostatistics, you will … support key aspects of the programming effort, ensuring the successful delivery of data and reporting components for various projects. Responsibilities include, but are not limited to, the following: Advanced SAS Programming Expertise Proficient in Base SAS, SAS/Macro, SAS/SQL; experience with SAS/Graph is a plus Demonstrated ability to develop … maintain, and troubleshoot SAS macro libraries Strong Knowledge of CDISC Standards Hands-on experience with the implementation of SDTM and ADaM datasets Experience in Define-XML creation and CDISC validation tools such as Pinnacle 21 Regulatory Reporting Experience Direct involvement in generating outputs for periodic regulatory submissions (e.g., DSURs, PSURs, Annual Safety Reports) Working knowledge of FDA and More ❯

leading programming efforts and representing Clinical and Statistical Programming in meetings with internal and external clients. As a mentor to other Statistical Programmers, you'll integrate statistical concepts with SAS Programming efficiently and optimally. Accountabilities: Develop and validate technical programming specifications for analysis datasets using Alexion or ADaM standards. Independently develop and validate programs that generate analysis datasets based … safety and efficacy analysis datasets, tables, listings, and figures/graphs. Independently and collaboratively resolve problems Clearly communicate processes and standards with management and team members Expertise in using SAS/Base, SAS/Macro, SAS/STAT. Knowledge of SAS/Graph, and SAS/SQL Desirable Skills/Experience: SDTM and ADaM More ❯

You'll also have the opportunity to mentor fellow programmers and represent Statistical Programming in meetings with internal and external clients. Are you prepared to integrate statistical concepts with SAS Programming efficiently and effectively? Accountabilities: Support development of technical programming specifications for SDTM, ADS, or ADaM standards. Independently develop and/or validate programs that generate SDTM and analysis … and efficacy analysis datasets, tables, listings, and figures/graphs. Independently and collaboratively resolve problems. Clearly communicate processes and standards with management and team members. High competence in using SAS/Base, SAS/Macro, SAS/STAT. Knowledge of SAS/Graph, and SAS/SQL. Knowledge and implementation of: SDTM and ADaM More ❯

experience within the Life Science Industry Strong Efficacy experience Advanced knowledge of statistics, programming and/or clinical drug development process Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills More ❯

role is considered Hybrid. Principal Statistical Programmer The Principal Statistical Programmer will provide expert-level hands-on principal programming support and technical leadership to develop, maintain, validate and run SAS computer programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. The ability to work independently and … expert SAS/GRAPH programming experience is required. Summary of Key Responsibilities Write SAS programs that produce or validate tables, listings, figures and analysis datasets, in support of clinical studies or complex integrated analyses for submission; Develop and follow good programming practices, including adequately documenting SAS code; Perform, plan and coordinate project work to ensure timely, quality … delivery across multiple projects; Use, modify, and maintain existing SAS code; Write specifications to describe programming needs; Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency; Keep abreast of current and new statistical programming techniques and other applicable technical advancements while assisting in their implementation; Provide input into, or lead general standardization efforts More ❯

experience within the Life Science Industry • Strong Efficacy experience • Advanced knowledge of statistics, programming and/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills More ❯

experience within the Life Science Industry • Strong Efficacy experience • Advanced knowledge of statistics, programming and/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills More ❯