16 of 16 Remote SAS Jobs in the East Midlands

customers that supports decision making and shapes our customer strategy. The core part of the role will involve analysing large volumes of customer data using tools such as Teradata, SAS Enterprise Guide, Python and Power BI. You'll make your insight deeper through the use of predictive analytical techniques and by combining your analysis with understanding from customer research … customer segmentation models using appropriate data manipulation, data science and analytical techniques. Technically robust and comfortable with all elements of the data science lifecycle using tools such as Teradata, SAS Enterprise Guide, Cloud Platforms (ideally Data Bricks), Python and Power BI. Have excellent knowledge of Excel and PowerPoint. Possess excellent communication and influencing skills, with the ability to present More ❯

customers that supports decision making and shapes our customer strategy. The core part of the role will involve analysing large volumes of customer data using tools such as Teradata, SAS Enterprise Guide, Python and Power BI. You’ll make your insight deeper through the use of predictive analytical techniques and by combining your analysis with understanding from customer research … customer segmentation models using appropriate data manipulation, data science and analytical techniques. Technically robust and comfortable with all elements of the data science lifecycle using tools such as Teradata, SAS Enterprise Guide, Cloud Platforms (ideally Data Bricks), Python and Power BI. Have excellent knowledge of Excel and PowerPoint. Possess excellent communication and influencing skills, with the ability to present 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 ❯

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 ❯

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 ❯

the pharmaceutical industry or a clinical research organisation. Ability to understand clinical data structures and present data for data management/clinical review according to user requirements. Experience with SAS Macros and/or similar scripting languages. Experience in debugging SAS programs and/or similar scripting languages. Excellent written and verbal communication skills in fluent English. Strong 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 ❯

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 ❯

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 ❯

will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you More ❯

will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you More ❯

will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you More ❯

will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you More ❯

will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. What in it for you 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 ❯

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 ❯