A company is looking for a Senior Statistical Programmer I to analyze clinical trial data and support statistical analysis processes.
Key Responsibilities
Develop and validate SAS programs for statistical analysis and reporting of clinical trial data
Collaborate with biostatisticians to define analysis plans and statistical methods
Perform quality control checks on statistical outputs and assist in preparing statistical reports for regulatory submissions
Required Qualifications
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field
Experience in statistical programming, preferably in a clinical research or pharmaceutical setting
Strong proficiency in SAS programming with a solid understanding of statistical concepts
Experience in quality control and reporting of statistical outputs
Ability to work collaboratively in a team environment
Senior Programmer • Buffalo, New York, United States