Associate Director leading Biostatistics in drug development at Regeneron. Collaborating across teams and representing statistical issues in regulatory meetings in a hybrid environment.
Responsibilities
support Clinical Biostatistics with Global Development
lead efforts of the Biostatistics department with cross-functional teams to articulate drug development questions
assess the feasibility of endpoints and frame statistical approaches to address those questions
design clinical experiments and interventional studies to generate and analyze the resulting data
work with teams to appropriately interpret the results and make decisions
represent statistical issues in regulatory agency meetings
lead the development and delivery of training to non-statistical colleagues
lead the development of new infrastructure and processes
mentor and oversee less experienced statisticians, with the potential to manage full-time staff
Requirements
PhD or equivalent degree in statistics/biostatistics with >6 years’ experience in the pharmaceutical industry, or MS degree in statistics/biostatistics with >11 years’ experience
Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies
Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment
Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills
Solid knowledge of statistical analysis methodologies, experimental and clinical trial design
Expertise in statistical software such as R or SAS is required
Benefits
health and wellness programs (including medical, dental, vision, life, and disability insurance)
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