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Job Description & How to Apply Below
Elevate your career as a Lead Statistical Analyst II, leveraging your SAS programming experience in a pharmaceutical environment. Manage complex data analysis and mentor junior programmers effectively.
In this senior role, you will develop and validate ADaM datasets and TFLs, create efficiency-enhancing macros, and lead programming projects. Your expertise in SAS will support communication with clients and ensure quality compliance with standards like ICH-GCP and CDISC.
Key Responsibilities:
• Develop and validate analysis datasets and TFLs using SAS
• Write and review programming specifications and documentation
• Create standard macros to streamline processes
• Lead programming projects, assigning tasks and managing timelines
• Conduct SAS code reviews and ensure quality standards
Requirements:
• Bachelor's degree in Statistics, Mathematics, or related field
• Over 5 years of SAS programming experience
• Strong knowledge of clinical trials and regulatory standards
• Proven project leadership and mentoring experience
• Excellent communication skills in global team settings
Make a significant impact through your statistical analysis and programming skills.
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