Sr. Statistical Programmer

📋 Description

• Develop and maintain statistical programming code using SAS or other relevant software to generate
• Perform independent validation programming and quality control activities to ensure the accuracy
• Review and interpret study documentation, including Statistical Analysis Plans, mock shells
• Lead statistical programming activities across assigned clinical projects, coordinating
• Develop programming specifications for datasets and outputs of varying complexity, anticipating
• Maintain accurate, organized, and inspection-ready project documentation, including testing

🎯 Requirements

• Bachelor's degree, preferably in a scientific, statistical, mathematical, or related discipline.
• Extensive hands-on experience in statistical programming using SAS or other relevant programming
• Strong knowledge of clinical trial data, statistical programming methodologies, and the development
• Experience developing, validating, and reviewing complex datasets, tables, listings, and figures in
• Previous experience leading statistical programming activities, coordinating project deliverables
• Familiarity with clinical study documentation, including SAPs, annotated CRFs, mock shells, and

🎁 Benefits

• Remote working opportunities, subject to applicable role and location arrangements.
• Opportunities to collaborate with international clinical research and biopharmaceutical teams.
• Access to technical training, therapeutic-area learning, and continuous professional development.
• Career progression opportunities within a growing global life sciences organization.
• Supportive and engaged management, with opportunities for mentoring and professional growth.
• Recognition programs and comprehensive total rewards offerings.