1 of 1 SAS Macro Jobs in the UK

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 ❯

data sources to drive business value. Proactively develop ideas, concepts, and relationships to support department data initiatives that inform the strategic direction of the business. Support ongoing migration to SAS Viya and utilize new technology to enhance ETL processes. Review data processing methods regularly to improve efficiency and processing times. Promote data governance activities, policies, and procedures. Drive continuous … risks and report accordingly. Ensure daily data processing completes on time with no failures. Previous experience in a DW or BI role is required. Essential experience with coding in SAS and SAS Macros, SAS DI Studio, and Enterprise Guide. Experience with data modelling, ETL, data warehousing, and data quality management concepts. Advanced Excel skills. Strong problem-solving … technical audiences. Ability to operate effectively in a fast-changing environment and handle issues proactively. Confidence in judgment and decision-making, viewing challenges as opportunities for development. Experience with SAS Viya, SAS Visual Analytics, SQL Server, Apache Airflow, and MS DevOps for workflows and CI/CD pipelines. #J-18808-Ljbffr 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 ❯

Senior Statistical SAS Programmer - home- or office-based, EMEA Pay Competitive Employment type Full-Time Job Description Req#: 2260641 As an experienced Statistical SAS Programmer in our Clinical Development Services (CDS) business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. Oftentimes you will have … 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 presentation, analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative new benchmark drugs … 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 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 ❯

to agreed timelines and quality. This will be a hands-on role in which you will be expected to produce both datasets and outputs. Key responsibilities will include: · Writing SAS programs to create analysis datasets, tables, listings, and figures. · Adhere to CDISC standards for data management and analysis, including SDTM (Study Data Tabulation Model) and ADaM (ADAM Data Model … statistical analysis plans). · Oversight of statistical programming tasks outsourced to CROs, ensuring that their performance meets the agreed quality. Required Knowledge · 3+ years of experience in clinical trial SAS programming. · Demonstrated knowledge of and experience in applying CDISC standards. · Self-starter with the ability to work within a Biostatistics team. Skills and Abilities · Proficiency with SAS programming … and SAS macro code development required along with a good understanding of SAS GRAPH and SAS ODS. · Understanding of clinical trial data and terminology. · Strong attention to detail and accuracy. · Excellent written and verbal communication skills. · Experience working with cross-functional groups. · Ability to manage multiple priorities and work effectively under pressure. · Knowledge of R would More ❯

to agreed timelines and quality. This will be a hands-on role in which you will be expected to produce both datasets and outputs. Key Responsibilities Will Include Writing SAS programs to create analysis datasets, tables, listings, and figures. Adhere to CDISC standards for data management and analysis, including SDTM (Study Data Tabulation Model) and ADaM (ADAM Data Model … analysis plans). Oversight of statistical programming tasks outsourced to CROs, ensuring that their performance meets the agreed quality. Requirements Required Knowledge 3+ years of experience in clinical trial SAS programming. Demonstrated knowledge of and experience in applying CDISC standards. Self-starter with the ability to work within a Biostatistics team. Skills And Abilities Proficiency with SAS programming … and SAS macro code development required along with a good understanding of SAS GRAPH and SAS ODS. Understanding of clinical trial data and terminology. Strong attention to detail and accuracy. Excellent written and verbal communication skills. Experience working with cross-functional groups. Ability to manage multiple priorities and work effectively under pressure. Knowledge of R would 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 ❯

analytical skills and ability to both program and understand/interpret data are the keys to success, and you will have the opportunity to continually grow your knowledge in SAS and CDISC across all phases and multiple therapy areas. What you will do Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets … and change. It is essential that the job holder possesses strong analytical skills and attentiveness to detail. Your experience Educated to degree level or equivalent. The jobholder has advanced SAS programming skills with expert knowledge in SAS/Macro, Proc Report and ODS. Good working knowledge in SAS/Graph, Proc SQL, SAS/STAT. 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 ❯

programming projects, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. Your expertise will guide and mentor junior programmers, while your ability to integrate statistical concepts with SAS Programming will drive efficiency and effectiveness. Are you prepared to take on this challenge? Accountabilities: Support development of technical programming specifications for SDTM, ADS or ADaM standards. Independently develop … 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 ❯

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 ❯

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 ❯

for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure … specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format. Leads and oversees the development of global tools that will increase the efficiency … or related area with relevant experience Experience • At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. • Indepth understanding of clinical programming and/or statistical programming processes and standards. • Indepth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). • Extensive experience More ❯

for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities: Collaborates with the study teams to design data structure … specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format. Leads and oversees the development of global tools that will increase the efficiency … or related area with relevant experience Experience • At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. • Indepth understanding of clinical programming and/or statistical programming processes and standards. • Indepth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). • Extensive experience More ❯