Manager, Biostatistics - Hematology

What you'll do

• Formulate statistical approaches and design clinical experiments to address drug development questions.
• Co-author clinical study protocols and detailed statistical analysis plans (SAPs).
• Perform statistical analyses for interim and final reports using R or SAS software.
• Collaborate with programming teams to develop tables, figures, and listings for regulatory reporting.
• Evaluate the appropriateness of existing software and identify needs for novel statistical methodologies.
• Interpret clinical trial data to facilitate program-level decision-making and provide results to management.
• Develop and deliver training on statistical concepts to non-statistical colleagues.
• Participate in professional associations and conferences to influence the pharmaceutical industry and regulatory environment.

What we're looking for

• A PhD in statistics or biostatistics with over 2 years of pharmaceutical industry experience is required.
• An MS degree in statistics or biostatistics with over 7 years of experience is required.
• Knowledge of drug discovery and development to integrate statistical concepts into development strategies is required.
• Solid knowledge of statistical analysis methodologies, experimental design, and clinical trial design is required.
• Expertise in statistical software such as R or SAS is required.
• Excellent influence, leadership, and cross-functional collaboration skills are required.
• Demonstrated critical thinking, time management, and effective communication skills are required.