Clinical Trials SAS Programmer — Data Integrity & Reporting

Excelya is seeking a Statistical Programmer to join our innovative team dedicated to advancing clinical research. We pride ourselves on our core values of Audacity, Care, and Energy , and we believe that your expertise can help us make a significant impact in the healthcare domain.

As a Statistical Programmer, you will play a critical role in processing and analyzing clinical trial data. Utilizing your programming skills, you will ensure the accuracy and integrity of statistical outputs, contributing to the development of high-quality study reports.

Key Responsibilities:

• Develop, validate, and maintain SAS programs for clinical data analysis and reporting
• Generate statistical tables, listings, and graphics in accordance with study specifications
• Collaborate with biostatisticians and data management teams to clarify deliverables and timelines
• Conduct quality control checks on programming outputs to ensure data consistency and compliance with regulatory standards
• Provide documentation and support for all programming activities, including maintaining version control
• Assist in the preparation of statistical analysis plans and regulatory submissions as needed

Excelya is seeking a Statistical Programmer to join our innovative team dedicated to advancing clinical research. We pride ourselves on our core values of Audacity, Care, and Energy , and we believe that your expertise can help us make a significant impact in the healthcare domain.

As a Statistical Programmer, you will play a critical role in processing and analyzing clinical trial data. Utilizing your programming skills, you will ensure the accuracy and integrity of statistical outputs, contributing to the development of high-quality study reports.

Key Responsibilities:

• Develop, validate, and maintain SAS programs for clinical data analysis and reporting
• Generate statistical tables, listings, and graphics in accordance with study specifications
• Collaborate with biostatisticians and data management teams to clarify deliverables and timelines
• Conduct quality control checks on programming outputs to ensure data consistency and compliance with regulatory standards
• Provide documentation and support for all programming activities, including maintaining version control
• Assist in the preparation of statistical analysis plans and regulatory submissions as needed

Qualifications

To thrive in this role, you should possess a unique combination of technical skills and statistical knowledge.

• Experience: At least 2 years of experience in statistical programming, ideally within clinical trials
• Technical Skills: Strong proficiency in SAS; knowledge of R or Python is advantageous
• Education: Bachelor's degree in Statistics, Mathematics, Computer Science, or a related discipline
• Language Skills: Fluent in English, both written and spoken
• Soft Skills: Detail-oriented, strong analytical thinking, effective teamwork, and communication skills are essential

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here's what makes us unique—

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe'sleading mid-size CRO with thebest employee experience . Ourone-stop provider service model —offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.