ClinChoice

Consultant

• Provide statistical expertise and hands-on support for Phase III oncology clinical trials
• Contribute to study design, statistical analysis, interpretation of results, and clinical study deliverables
• Apply censoring and time-to-event analyses
• Apply and interpret Kaplan-Meier analysis, Cox Proportional Hazards models, and stratified log-rank tests
• Author, review, and provide input into TFL and ADaM specifications with Statistical Programming
• Review statistical programming outputs, identify discrepancies, and collaborate with programmers to resolve issues
• Use SAS to review outputs and perform data and analysis checks
• Manage deliverables across multiple concurrent clinical studies
• Collaborate with Biostatistics, Statistical Programming, Data Management, Clinical, Regulatory, and other cross-functional teams
• Support interim analyses and IDMC/DMC activities, including preparation and review of DMC outputs

Senior/Principal Statistician Consultant – Phase III Oncology