Teams at ClinChoice

Lead statistical activities for clinical studies, including protocol development, sample size calculations, randomization, statistical analysis plans, data quality oversight, and reporting. Ensure the validity, accuracy, consistency, and timeliness of analyses, tables, figures, listings, and statistical methods sections. Provide statistical guidance, mentor junior statisticians, coordinate assignments, review work, and support high-quality delivery across pharmaceutical, biotechnology, medical device, and consumer health projects.

Leads statistical activities for clinical trials across pharmaceutical, biotech, medical device, and consumer health projects. Acts as lead statistician, overseeing statistical strategy, SAPs, analysis database specifications, clinical study report sections, output interpretation, quality, and regulatory compliance. Collaborates with clinical, programming, data management, and regulatory teams; guides statistical programmers; communicates results and risks to technical and non-technical stakeholders; and ensures adherence to FDA, ICH, GCP, and company SOPs.

Leads and supports statistical programming deliverables for oncology clinical studies, implementing protocol and clinical development requirements. Independently programs high-quality outputs, develops specifications, oversees documentation, ensures standards and automation compliance, supports team activities, manages risks, and collaborates with statisticians, lead programmers, data managers, and study leaders. The role also contributes to programming best practices and requires strong knowledge of clinical research, drug development, ICH, Good Clinical Practices, and regulatory requirements.