Senior Scientist, Statistical Programming

Senior Scientist, Statistical Programming role supporting late-stage clinical development and regulatory submissions for drugs and vaccines. Responsible for developing statistical analysis datasets, tables, and figures while collaborating with cross-functional teams throughout the product lifecycle.

Responsibilities

• Develop and execute statistical analysis and reporting deliverables for clinical trials and regulatory submissions
• Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation
• Collaborate with statistics teams and stakeholders to ensure efficient execution and timely quality deliverables
• Lead one or more projects and serve as statistical programming point of contact throughout product lifecycle
• Apply scientific methodologies and tools to support drug and vaccine discovery, development, and regulatory approval

Requirements

• Expertise in SAS including data steps, procedures, macros, and graphics for clinical trial programming
• Experience with CDISC and ADaM standards
• Knowledge of statistical databases, data management concepts, and analysis plan comprehension
• Demonstrated ability to design complex programming algorithms and ensure process compliance
• Strong interpersonal, presentation, and written communication skills
• Project leadership capability and ability to work independently

Compensation: $117,000-$184,200 base