Biostatistician

• Consultant should have excellent working experience with study design analysis, development plan. • This role will involve work in phase I-IV but mainly in phase I later will move to phase II & III. • Been a Trial statistician at the study (any phase) • Written statistical analysis plans (SAPs) including the development of mock shells. • Reviewed CRFs • Performed stat review for clinical trial datasets and their specification, TFLs (tables, figures, and listings), and CSRs Validated key analysis datasets and statistical outputs (TFLs) • Performed statistical analyses and data checks using SAS • Performed sample size calculations for studies.