Senior Statistical Programmer Consultant

Working closely with a single sponsor, the full-time Senior Statistical Programmer Consultant will support programming deliveries for clinical studies, ensuring high-quality outputs and compliance while collaborating with cross-functional teams in a remote environment. Key responsibilities: Support programming deliveries of clinical studies or projects Implement statistical programming aspects of protocols and clinical development programs Communicate and escalate risks within assigned studies and projects Required qualifications: Bachelor's degree in computer science, statistics, or related field with 5 years of clinical programming experience; Master's degree with 6 years of experience Oncology therapeutic area experience is required Working knowledge of ICH and Good Clinical Practices, clinical research, and regulatory requirements Strong understanding of the clinical drug development process Proficient ability to influence stakeholders on programming-related items