Biostatistician

Contact: Neisha Camacho/Terra Parsons -
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.