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Biostatistician
£43K – £72K a year
Full–time
Job description
PCD320189
Duration: Up to 2 years
UK, Israel and Ireland Based candidates Only.
Shift Schedule: 8-5 pm local hour in country of candidate.
Core Essential Skill sets:
• 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 Evidence (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.
Position Summary:
• Provide statistical support in protocol development for observational studies and/or clinical trials.
• Author and review of statistical analysis plans, analysis dataset specifications, and the organisation 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.
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