A global clinical research organization is seeking a full-time Statistical Analyst in Belgium. This role focuses on statistical programming for clinical trials, requiring a Master's Degree and 2-3 years of SAS programming experience. The position offers the chance to work in a flexible environment with competitive compensation and benefits. If you're passionate about making a difference in the pharmaceutical industry, this is the opportunity for you.
Qualifications
2-3 years of industry working experience with SAS programming or SAS certificate.
Knowledge of databases and data management process.
Knowledge of statistical methods commonly used in pharmaceutical clinical trials.
Responsibilities
Write statistical programs for analysis datasets, tables, listings, and figures.
Review analysis plans for appropriate methods.
Program study analyses and review study results.
Communicate project requirements for data cleanup and capture.
Skills
SAS programming
Statistical methods
Data management
Education
Master's Degree
Job description
A global clinical research organization is seeking a full-time Statistical Analyst in Belgium. This role focuses on statistical programming for clinical trials, requiring a Master's Degree and 2-3 years of SAS programming experience. The position offers the chance to work in a flexible environment with competitive compensation and benefits. If you're passionate about making a difference in the pharmaceutical industry, this is the opportunity for you.