151 to 157 of 157 SAS Jobs in England

subsidiary of SAS, is committed to empowering scientists and engineers via our world-class family of statistical software products. For over 35 years, JMP has enabled customers to speed new drugs to market, to design better products and processes, and to figure out how to restore ecosystems. Advancements … monitor progress toward goals; tenaciously working to meet or exceed goals while deriving satisfaction from that achievement and continuous improvement. You are welcome here.At SAS and JMP, it’s not about fitting into our culture – it’s about adding to it. We believe our people make the difference. ...

subsidiary of SAS, is committed to empowering scientists and engineers via our world-class family of statistical software products. For over 35 years, JMP has enabled customers to speed new drugs to market, to design better products and processes, and to figure out how to restore ecosystems. Advancements … monitor progress toward goals; tenaciously working to meet or exceed goals while deriving satisfaction from that achievement and continuous improvement. You are welcome here.At SAS and JMP, it’s not about fitting into our culture – it’s about adding to it. We believe our people make the difference. ...

your energy exactly where it matters most: delivering high-quality, high-impact programming work. Day to day, that looks like: Writing and validating SAS programs to generate derived analysis datasets and clinical Tables, Figures, and Listings (TFLs) – work that feeds directly into regulatory decision‐making Contributing to electronic submission … degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences Demonstrated industry experience in statistical programming Core Skills & Knowledge Strong, proven proficiency in SAS for producing derived analysis datasets and TFLs In‐depth understanding of clinical data structures, including CDISC standards (SDTM, ADaM) and relational databases Hands‐on experience ...

Title:Sr. Manager, Statistical ProgrammingCompany:Ipsen Innovation (SAS)About Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France … Ensures the quality of Statistical Programming deliverables, including tables, listings, figures, datasets, and associated documentation, e.g. DEFINE.XML. Participate in the development and implementation of SAS programming standards, SOPs and work instructions, including program validation and documentation;Ensures their study related documentation according to Ipsen processes and in a ready ...

technically minded person with strong communication skills and SDTM knowledge. Having experience in Study Design, CRF annotation, CDISC standards, Vendor management with SAS programming skills will be key for this position. The role can be based remotely from anywhere in Europe or in South Africa.This role is part … specifications• Review of log files for errors and warnings• Resolving/trouble shooting errors• Experience with data mapping and SDTM Controlled Terminology• Experience with SAS programming and SDTM deliveries• Prior experience in a clinical or pharmaceutical related field is required.• Prior experience in a Data Management related field ...

OverviewThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of ...

activities across phase 1–4 trials, collaborating with sponsors and cross‐functional teams to deliver high‐quality analyses in line with regulatory expectations. Strong SAS programming and CDISC SDTM/ADaM expertise are essential, as is the ability to manage projects and communicate clearly with clients and stakeholders. #J ...