6 of 6 SAS Jobs in Reading

theories and PRO/COA validation to program analytics Support integration of PRO clinical trial results into value dossier and regulatory submission packages Lead development of statistical programs using SAS for regulatory and non-regulatory submissions (pre-defined and post-hoc) Implement CDISC standards as required for project deliverables Conduct QC programming for descriptive and complex studies in RWD … in psychometrics with 1-year relevant experience Knowledge/experience with PRO/COA methodologies, statistics, programming, and HEOR studies Formal training and demonstrated proficiency in statistical programming using SAS and R, including macros and basic SQL required Knowledge of PRO endpoint psychometric analysis using clinical trial data required Strong written and verbal communication skills including technical writing skills More ❯

theories and PRO/COA validation to program analytics Support integration of PRO clinical trial results into value dossier and regulatory submission packages Lead development of statistical programs using SAS for regulatory and non-regulatory submissions (pre-defined and post-hoc) Implement CDISC standards as required for project deliverables Conduct QC programming for descriptive and complex studies in RWD … in psychometrics with 1-year relevant experience Knowledge/experience with PRO/COA methodologies, statistics, programming, and HEOR studies Formal training and demonstrated proficiency in statistical programming using SAS and R, including macros and basic SQL required Knowledge of PRO endpoint psychometric analysis using clinical trial data required Strong written and verbal communication skills including technical writing skills More ❯

theories and PRO/COA validation to program analytics Support integration of PRO clinical trial results into value dossier and regulatory submission packages Lead development of statistical programs using SAS for regulatory and non-regulatory submissions (pre-defined and post-hoc) Implement CDISC standards as required for project deliverables Conduct QC programming for descriptive and complex studies in RWD … in psychometrics with 1-year relevant experience Knowledge/experience with PRO/COA methodologies, statistics, programming, and HEOR studies Formal training and demonstrated proficiency in statistical programming using SAS and R, including macros and basic SQL required Knowledge of PRO endpoint psychometric analysis using clinical trial data required Strong written and verbal communication skills including technical writing skills More ❯

and implement new decision strategies. Create and maintaining MI to support and evaluate system performance. YOUR SKILLS AND EXPERIENCE Previous experience with decision systems, Lending Metrics would be preferred. SAS or SQL needed. Python or Power BI would be desirable. Degree in a STEM subject. THE BENEFITS Discretionary bonus. 25 days holiday (+ bank holidays). Life insurance. Private More ❯

diverse therapeutic areas will be key to success in this role. What you will be doing: Program and validate SDTMs, ADaMs, and complex efficacy/lab datasets. Proficient in SAS (Base, Macros, Graphs); experience with R or Python is advantageous. Must have hands-on experience with Disclosure tables, especially Basic Results tables. Develop/debug complex macros and program More ❯

Prior programming experience using Flatiron Health data required . Prior experience programming oncology-specific methodologies, including deriving lines of therapy and conducting survival analyses. Intermediate to advanced knowledge of SAS preferred, R acceptable. Good organizational, interpersonal, and communication skills Ability to effectively manage and prioritize multiple tasks and projects. #J-18808-Ljbffr More ❯

or PhD with 2 years of relevant experience required. Knowledge of statistics, programming, and real-world studies Prior programming experience using Flatiron Health data required . Intermediate knowledge of SAS preferred; R acceptable. Good organizational, interpersonal, and communication skills Ability to effectively manage and prioritize multiple tasks and projects. Excellent accuracy and attention to detail. IQVIA is a leading More ❯

or PhD with 2 years of relevant experience required. Knowledge of statistics, programming, and real-world studies Prior programming experience using Flatiron Health data required . Intermediate knowledge of SAS preferred; R acceptable. Good organizational, interpersonal, and communication skills Ability to effectively manage and prioritize multiple tasks and projects. Excellent accuracy and attention to detail. #LI-Remote IQVIA is More ❯

At M&G, our purpose is to give everyone real confidence to put their money to work. As an international savings and investments business with roots stretching back more than 170 years, we offer a range of financial products and 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 ❯

supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Overview of the role: As a Senior SAS Programmer I, you will assist the US or EU Early Phase Statistical Programming teams by developing SAS programs for analysis datasets. Responsibilities will also include: listing and safety … summary tables, provide project tracking information to the team, address any validation comments, document programming activities, act as a subject matter expert (SME) within the SAS Programming team, and mentor/train other team members. Lead and manage the assigned programming team's deliverables at the study and program level Serve in a client-facing capacity that demonstrates the … Management) Create and maintain analysis dataset specifications to a high standard of quality and accuracy To be successful, you will need: Relevant experience with successfully performing the role of SAS/Statistical Programmer Experience in the clinical research (preferably in a CRO setting) Experience leading studies while managing timelines, resources, and overall quality in a client-facing capacity Working More ❯

statistical programs for listings, safety, efficacy outputs, and ADaM/TLF specifications. Oversee multi-disciplinary teams, ensuring seamless execution of assigned projects. Design, develop, validate, and execute high-quality SAS programming outputs, including listings, tables, figures, and analysis datasets. Deliver high-quality ADaM programming and specification development for analysis and reporting. Mentor and train junior staff to cultivate the More ❯

Senior SAS Programmer I - EMEA Remote or Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. UK or Europe, Office or Homebased. At ICON, it … and brightest in the industry! Are you one of them? As a Sr. Statistical Programmer you will assist the US or EU Early Phase statistical programming teams by developing SAS programs for analysis datasets. Listing and safety summary tables; provide project tracking information to the team, address any validation comments and document programming activities; work on more advanced, complex … SAS requirements, across multiple studies, and act as a subject matter expert within the SAS programming team; mentor and help train other team members from juniors to Programmer II. The role Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and More ❯

Senior SAS Programmer I - EMEA Remote or Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. UK or Europe, Office or Homebased. At ICON, it … and brightest in the industry! Are you one of them? As a Sr. Statistical Programmer you will assist the US or EU Early Phase statistical programming teams by developing SAS programs for analysis datasets. Listing and safety summary tables; provide project tracking information to the team, address any validation comments and document programming activities; work on more advanced, complex … SAS requirements, across multiple studies, and act as a subject matter expert within the SAS programming team; mentor and help train other team members from juniors to Programmer II. The role Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and More ❯

Senior SAS Programmer I - EMEA Remote or Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. UK or Europe, Office or Homebased. At ICON, it … and brightest in the industry! Are you one of them? As a Sr. Statistical Programmer you will assist the US or EU Early Phase statistical programming teams by developing SAS programs for analysis datasets, listing and safety summary tables; provide project tracking information to the team, address any validation comments and document programming activities; work on more advanced, complex … SAS requirements, across multiple studies, and act as a subject matter expert within the SAS programming team; mentor and help train other team members from juniors to Programmer II. The role Lead and manage the assigned programming team's deliverables at the study and program level to ensure project objectives are met within budget, to agreed timelines and More ❯

efficacy outputs (analysis datasets, tables, figures) Create, review, and finalize analysis dataset specifications Create, use, and modify project or department level macros Lead team(s) to produce high quality SAS programming outputs for all deliverables Serve as a mentor and help to train junior staff Provide analysis programming (ADaM/TLF) and ADaM specification development and support for or … research industry Experience leading Phase II and/or Phase III studies Experience creating and validating analysis datasets (CDISC ADaM standard preferred), and Tables, Listings, and Figures (TLF) Strong SAS programming experience Pinnacle 21 experience is strongly preferred Professional leadership skills coupled with exceptional communication skills Bachelor's degree required (Statistics, Mathematics, Computer Science, or related scientific discipline); Master More ❯

Author and review simple and complex dataset standards • Perform data checks and data exploration (e.g. using frequencies, histograms) • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice • Complete and review CDISC Validation tool reports • Ensure the appropriate standards are being applied and adhered to • Familiarisation with simple statistical techniques (e.g. More ❯