Evidence synthesis
Systematic review to Cochrane standards, including protocol development and registration. Meta-analysis, including aggregate-data methods with time-to-event outcomes. Trial sequential analysis. Critical appraisal and registration of hepatobiliary trials at editorial level.
Trial design and conduct
Randomised controlled trial design, including double-blind sham-controlled design. Multicentre trial delivery as site principal investigator. Prospective diagnostic accuracy studies with parallel health economic analysis.
Observational study design
Long-term prospective cohort studies. Case-control design. Cross-sectional studies. Multicentre audit methodology.
Statistics and data
Survival analysis. Univariate and multivariate prognostic modelling. Development and validation of predictive models. Database design. Direct collaboration with medical statisticians, including publication in a statistics journal.
Laboratory methods
Immunohistochemical expression analysis. Molecular genetic analysis including allelotyping. Physiological measurement — hepatic venous pressure and portal blood flow.