Teams at ClinChoice

Leads and supports statistical programming for clinical studies within a CRO environment. Implements protocol and clinical development programming, prepares specifications and documentation, ensures quality and regulatory compliance, supports standards and automation, coordinates team activities, escalates risks, and collaborates with statisticians, programmers, data managers, and study leaders.

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.