Bio statistic Statistician to join an existing team working on clinical trials, producing high quality statistical outputs, and collaborating with internal and external teams to ensure the successful delivery of clinical trial results.



The ideal candidate will have experience in clinical trials, statistical analysis, and working with pharmaceutical or biotech clients.



Skills
PhD and undergrad or MSc in Biostatistics, Statistics, or a related subject.
Experience in the pharmaceutical or clinical research industry, including clinical trial design, implementation, and statistical analysis.
Good Clinical Practice and regulatory requirements for clinical trials knowledge.
Creation and validation of efficacy datasets
Statistical programming languages SAS, R and Python.
Statistical simulations, randomization schemes and sample size calculation.

Role
Program and validate primary efficacy datasets, summary tables, listings, and complex figures in line with the Statistical Analysis Plan and study documentation.
Develop and validate macros for statistical analyses and figures.

Perform stage 3 quality control.
Write, review, and QC SAPs, statistical sections of protocols, and clinical study reports).