Statistical Programmer I

What You Will Be Doing:

• Assisting in the development, validation, and maintenance of statistical programs (SAS, R, or similar) for data manipulation and analysis in clinical trials.
• Collaborating with senior statistical programmers and biostatisticians to understand project requirements and contribute to statistical analysis plans (SAPs).
• Performing data cleaning and preparation tasks to ensure data integrity and accuracy prior to analysis.
• Participating in the preparation of reports and documentation to support regulatory submissions and clinical study reports.
• Learning and applying industry standards, including ICH/GCP guidelines, to programming tasks to ensure compliance.

Your Profile:

• Bachelor s degree in statistics, mathematics, computer science, or a related field.
• Basic knowledge of statistical programming languages such as SAS or R; coursework or internships in programming is a plus.
• Strong analytical and problem-solving skills, with attention to detail and a willingness to learn.
• Ability to work collaboratively in a team environment and communicate effectively with team members.
• Familiarity with clinical trials and data management processes is an advantage but not required.