1166# Principal Statistical Programmer Consultant Remote -Oncology

Bachelor’s degree in CS, statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience Oncology TA experience Working knowledge of ICH and Good Clinical Practices Working knowledge of Clinical research, Clinical trial process, and related regulatory requirements and terminology Good understanding of the clinical drug development process Strong communication skills and coordination skills Current knowledge of technical and regulatory requirements Ability to proactively manage concurrent activities Proficient ability to influence relevant stakeholders on programming-related items

Support Programming deliveries of a clinical study or project. Implement statistical programming aspects of the protocol. Ensure high quality in own and team's deliverables. Program independently with high efficiency and quality. Write and/or implement specifications and oversee documentation. Contribute to the development of best practices. Ensure compliance with standards and automation usage. Plan and support team activities. Communicate and escalate risks. Work proactively with study team members.