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