Director Statistical Programming provides leadership and support to the teams on all statistical programming matters according to the project strategies within therapeutic area(s).

In this role, a typical day might include the following:

• Oversee all management functions, including internal team and external functional service providers to ensures timely and high-quality deliverables. Lead the development, dissemination, and implementation of programming standards, applications, processes, and trainings across global therapeutic areas.

• Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability.

• Prioritizes activities across projects and facilitates resolutions to project conflicts between groups or individuals, creating solutions to address business and operational challenges

• Oversee development of direct reports by setting goals, managing performance, evaluating and monitoring training needs, supporting development plans, mentoring, and coaching

• Meets with Statistical Programming management team routinely to evaluate and develop solutions for project resourcing, quality, timelines, budget, standard processes, and training needs. Keeps senior leadership informed of decisions and issues which impact the department.

This role may be for you if you have:

• Extensive experience in SAS programming in a clinical data environment across multiple therapeutic areas.

• Extensive experience in the global development and execution of project user requirements, system design, validation plans, operational and performance protocols, research and development of applications and toolkits for end-users.

• Thorough understanding of pharmaceutical clinical development across multiple therapeutic areas (i.e., understanding of statistical concepts, techniques, and clinical trial principles) and ability to manage and lead regulatory submissions.

• Extensive experience in managing the training material development and training implementation for use of standardized systems in a global environment

• Experienced project manager encompassing resource allocation, management of technical information, administrative information, and project information across multiple therapeutic areas. Ability to manage and prioritize projects and personnel independent of geographic location.

To be considered for this opportunity, you must have the following:

• MS. in Statistics, Computer Science, Mathematics, Engineering, Life Science or related subject area

• 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including history of successful project and people management, and expertise in one or more therapeutic areas.

• SAS Certification desirable.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

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.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$198,000.00 - $330,000.00