Elevate your career as a Senior Statistical Programmer in clinical trials with extensive SAS experience. Contribute to TFL programming and enhance submission processes using CDISC standards.

In this role, you will leverage over six years of statistical programming experience to support clinical trial projects. Your expertise in TFL programming and operational knowledge of CDISC (SDTM, ADaM) will enhance data quality and submission readiness. You may also lead project management functions including timelines and resource allocation.

Key Responsibilities:
• Prepare clinical data for submission using CDISC standards
• Develop and verify SAS programs for data conversion and analysis
• Train and mentor other statistical programming team members
• Create programming specification documents for various data types
• Ensure adherence to Standard Operating Procedures (SOPs)

Requirements:
• Minimum 6 years of experience in...