13 of 13 SAS Jobs in Cambridge

a quantitative field (e.g., Statistics, Data Science, Mathematics, Economics, Engineering, or Computer Science). A proven track record in consumer products, digital media, or entertainment industries. Proficiency in SQL, SAS, R, Python, or other programming languages for querying and analyzing data. Hands-on expertise with visualization tools such as Tableau or Looker. A proactive approach to problem-solving, with More ❯

field (e.g., Statistics, Business Analytics, Data Science, Mathematics, Economics, Engineering or Computer Science) 5+ years of experience across search, consumer product, digital media or entertainment industries Expertise in SQL, SAS, R, Python or other programming language to query data and perform analysis Hands on experience with visualization tools like Tableau or Looker Have a bias towards action in resolving More ❯

strong quantitative element and analytic focus (or equivalent work experience), you will be adept at managing and analysing large and complex data using computational statistical software (e.g. R, Python, SAS). As our next Senior Data Scientist, you will have demonstrable success in building data pipelines and in developing and operationalising user-friendly data science solutions, such as automated More ❯

direction. BASIC QUALIFICATIONS 2+ years of data scientist experience and 3+ years of data querying languages (e.g., SQL), scripting languages (e.g., Python), or statistical/mathematical software (e.g., R, SAS, Matlab, etc.) experience. 3+ years of machine learning/statistical modeling data analysis tools and techniques experience. Experience applying theoretical models in an applied environment. Bachelor's degree in More ❯

strong quantitative element and analytic focus (or equivalent work experience), you will be adept at managing and analysing large and complex data using computational statistical software (e.g. R, Python, SAS). As our next Senior Data Scientist, you will have demonstrable success in building data pipelines and in developing and operationalising user-friendly data science solutions, such as automated More ❯

Social network you want to login/join with: Specialist, Computational Pharmaceutics, cambridge col-narrow-left Client: Spherical Search Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Views: 4 Posted: 31.05.2025 Expiry Date: 15.07.2025 col 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 ❯

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 ❯

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 ❯

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 Relational 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 principles. More ❯

documents (protocols, SAPs, CRFs, CSRs) Author and review study TFL shells and dataset standards Conduct data checks and exploration (e.g., frequencies, histograms) Program and QC datasets and TFLs in SAS following specifications Review CDISC Validation reports Ensure standards compliance Familiarity with basic statistical techniques (t-test, ANOVA, regression, survival analysis) Review project management documents Maintain audit-ready study documents 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 ❯