Job Details

• Provide sound experimental design and data analysis expertise.
• Author the protocol statistical sections and generate statistical analysis plans and study randomization.
• Review and sign-off on relevant study documents and data management and programming deliverables.
• Prepare mockup tables, figures and listings.
• Determine analysis and data presentations specifications.
• Provide verification reviews on final tables, figures and listings.
• Perform analysis, interpret study results, and collaborate with study team to produce safety monitoring reports, interim and final reports, and publications.
• Represent the biostatistics function on project teams and in cross-functional meetings.

Requirements:

• Ph.D in computer science, statistics, or math with 3-5 years of relevant experience.
• Preferably as a study statistician in oncology and pulmonary.
• Experience in the support of clinical studies in a pharmaceutical or biotech industry setting.
• Understanding of statistical experimental design and analysis, clinical trial requirements.
• Understanding of regulatory guidelines that affect statistical deliverables.
• Excellent organizational and analytical skills.
• Excellent communication skills, both written and verbal.
• Flexible team player with ability to balance multiple projects and instructions often with competing deadlines.
• Creative self-starter with strong organizational, prioritization and interpersonal skills.