Director, Statistical Programming

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.

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. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually) $165,900.00 - $270,700.00

Permanent