Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Candidates must be UK based Key Responsibilities: Provide statistical support in protocol development for observational studies and/or clinical trials. Author and review of statistical analysis plans, analysis dataset specifications, and TFL shells. Work with programming and other cross-functional teams in Phase-4 non-interventional study to develop CRF, validate and review the datasets and results. Conduct programming and analysis for Medical Affairs, RWE studies. Support develop abstract, poster and manuscript as deliverables. Education & Qualifications: Education: PhD or MS in Biostatistics or Statistics Experience in pharmaceutical industry to provide statistical input into the study design, statistical analysis, and reporting of interventional and observational studies. Min 4 yrs experience with Phase-4 study, Medical Affairs study, Real World Evience (RWE) or HEOR study. Min 4 yrs experience in statistical software, SAS and R. Min 4 yrs experience with SDTM and ADaM data standards. Min 4 yrs experience with Real World Data (RWD) and RWE methodologies, such as propensity score analysis, causal inference. Min 4 yrs experience with advanced statistical models such as mixed effect model approaches for repeated measures, Machine Learning (ML) methods.