Manager, Biostatistics - Hematology

Discover Your Role
- Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
- Develop protocols and statistical analysis plans; determine statistical methodology for data analysis.
- Collaborate with Statistical Programming on tables, figures, and listings for decision making and regulatory reporting.
- Evaluate software for planned analyses; identify needs for novel statistical methods/tools.
- Analyze and interpret clinical trial and non-trial data to support program-level decisions.
- Prepare presentations and written reports for project teams, management, and regulatory agencies; co-present findings to management.
- Support research in innovative statistical methods and provide training to non-statisticians.

This Role Requires
- PhD (or equivalent) in statistics/biostatistics with >2 years’ pharmaceutical industry experience, or MS with >7 years.
- Knowledge of drug discovery and development; ability to integrate statistical concepts into strategy.
- Strong influence/leadership; proven cross-functional collaboration.
- Critical thinking, time management, and effective communication.
- Solid knowledge of statistical analysis methodologies, experimental and clinical trial design.
- Expertise in R or SAS.

When & Where
- Work location: Tarrytown, NY or Warren, NJ; 4 days/week on site; up to 25% travel.

Application
- Apply now.