Principal Statistical Programmer /Analyst Consultant -CVRM

📋 Description

• Leading statistical programming activities for clinical trials
• Developing/reviewing SAS programs, datasets, tables, listings, and figures
• Providing technical guidance to Statistical Programmers
• Reviewing programming specifications and outputs
• Supporting SDTM/ADaM and regulatory submissions
• Working closely with statisticians, data managers, and clinical teams

🎯 Requirements

• Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5
• Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process
• Good understanding of the clinical drug development process.
• Strong communication skills and coordination skills.
• Current knowledge of technical and regulatory requirements relevant for the role
• Ability to proactively manage concurrent activities within a project