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This position is for a qualified statistician/biostatistician to support Clinical Biostatistics within Global Development. It requires a strong background in biostatistics, exceptional leadership capabilities, and the ability to contribute meaningfully to drug development and regulatory strategies while fostering collaboration and innovation across teams.
Responsibilities
- Lead and/or oversee the efforts of the Biostatistics department with cross‑functional teams to articulate drug development questions, assess feasibility of endpoints, and frame statistical approaches.
- Design clinical experiments and interventional studies to generate and analyze data and work with teams to interpret results and make decisions appropriately.
- Work with Strategic Project Teams on clinical and regulatory strategies for the clinical development strategy, and represent statistical issues in regulatory agency meetings.
- Lead the development and delivery of training to non‑statistical colleagues.
- Develop new infrastructure and processes, and be active in representing the company in professional associations, conferences, and publications.
- Mentor and oversee less experienced statisticians, and where applicable, manage full‑time staff.
- Represent Biostatistics in Global Clinical Subteams, partner with Medical Directors, Clinical Scientists, and other stakeholders to design and analyze clinical trials, ensuring programs are appropriately structured for success.
- Guide staff in preparing materials for regulatory interactions, including analysis plans, tables, figures, and listings for submissions and advisory committee meetings.
- Co‑present findings to regulatory agencies and management.
- Identify gaps in processes and lead working groups to implement improvements, develop and revise SOPs, and contribute to cross‑functional workstreams.
- Lead research teams to establish new statistical methodologies as needed.
- Prepare presentations and reports to communicate statistical findings to project teams, management, and regulatory bodies.
- Deliver training programs to enhance statistical understanding among non‑statistical colleagues.
Qualifications
- Ph.D. in Statistics/Biostatistics with over 8 years of pharmaceutical industry experience (Ph.D. strongly preferred) or M.S. with over 13 years of experience.
- Preferred experience in obesity, cardiovascular, and/or metabolism fields.
- In‑depth knowledge of drug discovery and development, with the ability to integrate statistical concepts into strategic decision‑making.
- Strong leadership and influence skills, with a proven ability to collaborate effectively in cross‑functional teams.
- Demonstrated critical thinking, time management, and communication skills to thrive in a fast‑paced, collaborative environment.
Salary Range (annually)
$202,000.00 – $336,600.00
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.
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