Teams at ClinChoice

Manage 2-3 clinical trials with site start-up, on-site and remote monitoring, SDV, CRF review, safety reporting, investigational product and trial material management, study closeout, site training, and supervision/mentoring of junior CRAs. Support submissions, CRF design, and quality control for oncology and complex trials.

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.

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.