Senior Statistical Programmer
United Kingdom
princeps technologies
clinical teams to provide high-quality programming support for the design, analysis, and reporting of interventional and observational studies within the pharmaceutical industry. Key Responsibilities: Develop, validate, and maintain SAS programs to generate datasets, tables, listings, and figures (TLFs) for clinical and observational studies. Support programming deliverables across Phase IV, Medical Affairs, RWE, and HEOR studies. Ensure adherence to … support for clinical or observational studies. Experience working on Phase IV, Medical Affairs, Real World Evidence (RWE), or Health Economics and Outcomes Research (HEOR) studies. Hands-on experience in SAS programming; experience in R is an advantage. Experience with CDISC standards, including SDTM and ADaM datasets. Experience with Real World Data (RWD) and RWE methodologies, including propensity score analysis More ❯
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