4 of 4 Permanent SAS Jobs in East London

analysis, and experimental design . Experience analyzing clinical trials, observational studies, or real-world healthcare data . Proficiency in statistical software such as R, SAS, Python, SPSS, or Stata . Strong understanding of clinical research methodologies, data interpretation, and statistical reporting . Excellent analytical, problem-solving, written, and verbal ...

communication skills are what matter most. Responsibilities Clean, preprocess, validate, and structure complex or messy datasets using statistical tools such as R, Python, SAS, or Stata . Identify and address missing values, inconsistencies, outliers, formatting issues, and other data-quality problems. Apply appropriate descriptive and inferential statistical techniques … Science, Mathematics, Biostatistics, or a related quantitative field . Strong experience cleaning and preparing complex, messy, noisy, or incomplete datasets. Proficiency with R, Python, SAS, or Stata . Strong programming skills for statistical analysis, data manipulation, and visualization. Experience applying descriptive and inferential methods, including hypothesis testing and regression ...

Study design activities, including sample size calculations, ad‐hoc and exploratory analyses Additional statistical support as required across client projects Confident coding in R, SAS, or other non‐SAS languages (or a willingness to learn) Experience & Skills Essential: Senior to Principal level experience in statistics within a clinical ...

skills and advance their careers within a supportive, specialist CRO We have multiple exciting opportunities for Principal and Senior level Statistical Programmers skilled in SAS and R, to join us on a permanent basis. We can offer fully remote, hybrid or office-based working, training and a very supportive … Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities Technical • Previous experience with SAS and some R experience/knowledge. • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs • Author, review and approve study TFL shells ...