Senior Statistical Programmer/Analyst Consultant

📋 Description

• Lead and/or support programming for CVRM studies
• Deliver SAS programs for data analysis and reporting
• Create datasets, tables, listings, and figures per study specs
• Collaborate with Biostatistics, Data Management, Clinical teams
• Ensure programming deliverables meet quality standards and timelines
• Participate in study planning and submission support

🎯 Requirements

• Strong SAS programming in pharma/CRO
• CVRM studies experience
• SDTM/ADaM/TLFs generation and validation
• CDISC standards and clinical trial processes
• Respiratory/Immunology experience; ICH/GCP familiarity
• Degree: BS in CS/statistics (5 yrs CDISC) or MS (6 yrs CDISC)

🎁 Benefits

• Global full-service CRO with 28+ years
• Career development and global opportunities
• Client-facing role with strong collaboration
• Equal opportunity employer and inclusive culture