Teams at ClinChoice

Leads and supports statistical programming deliveries for oncology clinical studies, implementing protocol and clinical development programming, producing compliant documentation, ensuring quality and standards adherence, managing concurrent activities, and coordinating with statisticians, programmers, data managers, and study leaders. The role independently delivers high-quality programming, escalates risks, supports team planning, and contributes to process improvements within a CRO client-facing environment.

Lead and support statistical programming for oncology clinical studies, implementing CDISC-related deliverables, writing/implementing specifications, ensuring high-quality outputs, coordinating with statisticians, data managers and study leads, and driving best practices and compliance with regulatory and technical standards.

Leads statistical activities for oncology clinical trials, serving as lead statistician for study strategy and deliverables. Authors and reviews Statistical Analysis Plans, Analysis Database Specifications, and statistical sections of clinical study reports. Interprets analysis outputs, ensures regulatory compliance, collaborates with clinical, programming, data management, and regulatory teams, and guides statistical programmers. Communicates statistical results and risks to technical and non-technical stakeholders.