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At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director to lead our Biostatistics Immunology & Inflammation therapeutic area.

The incumbent will have responsibility for strategic and operational activities and for assisting the Head, Biostatistics in the development and implementation of departmental scientific policies, operational guidelines, and administrative structure. The incumbent could also serve as senior research expert, with demonstrated ability to be a leader within Global Development and within the field for specific statistical methodology or application. The successful candidate should have a track record in leading teams and the ability to effectively structure a function to manage the anticipated growth in the product pipeline. They must also possess excellent communication skills to interface with senior leadership on behalf of the department and work closely with medical study directors to provide and receive direction on clinical programs and have the ability to influence the medical and clinical teams.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Work Location: Tarrytown, NY, Cambridge, MA or Warren, NJ

• 4 days per week on site

• 25% Travel may be required

Discover your role:

• Determining Department goals and resource allocation in conjunction with the Department Executive Director.

• Ensure project teams have high quality statistical support for creation of clinical development plans, study design, and operational aspects.

• Work with senior management to ensure statistical representation in key project decisions and regulatory meetings. Serve as departmental representative on corporatewise teams.

• Oversee process for statistical reporting. Review critical documents, such as SAP, analysis results presentations, CSR, and integrated summaries. Ensure compliance with data submission guidelines.

• Plan and track project activities, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization across projects or areas. Effect longrange planning.

• Ensure technical direction and mentoring for staff. Encourage personal development in the context of project work. Learn and apply techniques to promote teamwork, quality, and motivation. Recruit, develop, and retain high quality staff.

• Maintain awareness of industry standards and regulatory requirements. Alert staff to new or changing standards. Within area of control, harmonize policies with departmental guidelines SOPs and with industry standards. Develop polices promoting application of corporate values in work practices.

This role requires:

• Ph.D. in statistics or related discipline with 10+ years of experience (or MS in statistics or related discipline with 15+ years) in the biotechnology, pharmaceutical or health related industry, including significant interaction with both FDA and EMEA, history of successful project and people management (6+ years), and expertise in multiple therapeutic areas.

• Active research interests in area related to clinical trial.

• Demonstrated ability to work in a changing and busy environment and to exercise judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks.

• Ability to work independently - selfdirected, high energy and strong work ethic. High degree of creativity, latitude and attention to detail required.

• Demonstrated strong leadership, project management, teamwork and interpersonal skills.

• Excellent presentation skills.

• Experience and proven ability leading and managing major process and technology initiatives with utilization and impact across multiple functional groups.

• Broad knowledge and superior understanding of advanced statistical concepts and techniques.

• Outstanding ability and skills to effectively represent Biostatistics and Data Management in interactions with senior management or crossfunctional committees.

• Thorough knowledge of pharmaceutical clinical development and life cycle management; ability to innovatively apply technical principles, theories and concepts to clinical drug development leading to regulatory approvals.

• Thorough working knowledge of regulatory guidelines on drug development, regulatory submissions, and statistical practice.

• Understanding of the drug discovery and development process, regionally and globally.

• Strong administrative skills.

• Ability to influence others to achieve results.

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