Senior Statistical Programmer/Analyst Consultant- CVRM

📋 Description Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables and the quality delivered by other programmers. Programs independently with high efficiency and quality. Writes and/or implements specifications and oversees completeness of relevant documentation. Contribute to the development of best practices to improve quality, efficiency, and effectiveness 🎯 Requirements Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 Need to have Oncology TA experience. 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