Senior Statistical Programmer

📋 Description

• Support and lead statistical programming activities across clinical research projects, ensuring the
• Specify, develop, program, and validate CDISC-compliant SDTM and ADaM datasets in accordance with
• Develop and validate statistical analysis outputs, including analysis datasets, tables, listings
• Prepare, review, and maintain statistical programming documentation and other relevant CDISC
• Create, validate, and maintain clinical trial randomization lists, ensuring accuracy and compliance
• Ensure that all statistical programming activities comply with internal Standard Operating

🎯 Requirements

• Bachelor's or Master's degree, or equivalent academic and professional experience, preferably in
• At least 3 years of professional experience in statistical programming, preferably within clinical
• Excellent SAS programming skills, with the ability to develop, validate, and troubleshoot complex
• Strong knowledge of CDISC standards, particularly SDTM and ADaM, and their application in clinical
• Good understanding of clinical research principles, statistical programming methodologies, and
• Experience producing and validating statistical analysis datasets, tables, listings, and figures is

🎁 Benefits

• Fully remote working opportunity across Europe, offering flexibility in your working location.
• Full-time professional engagement within an international healthcare and life sciences environment.
• Opportunity to contribute to clinical research projects and support the development of innovative
• Collaboration with a global multidisciplinary team of scientists, statisticians, clinicians, and
• Professional development opportunities, including access to learning initiatives and technical
• Exposure to international clinical research projects and opportunities to collaborate with global