Senior/Principal Statistical Programmer

Key Responsibilities The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs. Technical: Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs Author and review simple and complex study TFL shells 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. t-test, ANOVA, regression, standard survival) Review of project management related documents Maintain study master file documents and any other documents that are required to be audit ready.

Required: Oncology experience. R programming skills (Upskilling to Proficient) ADaM/TLF programming Preferred: R programming skills (Advanced to Expert) ISS/ISE/Submissions/RTQs . Familiarity with agile ways of working Prior experience with GSK tools