Sr Statistical Programmer

Tarrytown, NY, United States
Apr 20, 2019
Required Education
Masters Degree/MBA
Position Type
Full time
Regeneron Pharmaceuticals, Inc. is seeking a Senior Statistical Programmer for our Basking Ridge, NJ location. Responsible for providing timely support to the study team on all programming matters according to the project strategies. Provide programming support for processing data from clinical studies. Assist in providing guidance in implementing and executing the programming and project standards. Work independently to design and test program logic, coding programs, program documentation and preparation of programs. Assist with projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Provide documentation and consistent maintenance of code, logs, and output in a regulated environment. Provide support for programming and QC of analysis datasets, TFL's or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.

Qualified applicants will have a Master's degree in biomedical engineering, statistics, computer science, mathematics, engineering, life sciences, or a related field, and 2 years of pre- or post-Master's programming experience in processing clinical trial data in a biotechnology, pharmaceutical, or health-related industry. In the alternative, employer will accept a Bachelor's degree in stated fields, and 5 years of programming experience in processing clinical trial data in a biotechnology, pharmaceutical, or health-related industry. Must have one year of experience with: relational database structure; reporting systems utilizing multiple data delivery applications; implementing standardization methodology; pharmaceutical clinical development including adhering to safety deliverables and performing efficacy analysis; providing programming support needs for BLA and other regulatory submissions; project management; development and execution of user requirements, validation plans, and operational and performance protocols; and creation of current CDISC data structures, including SAS, Base, Stat, Macro, and graph.

To apply for this position, please submit your resume, indicating Requisition Code 16390BR to:
Lisa Rose
Regeneron Pharmaceuticals, Inc.
777 Old Saw Mill River Road
Tarrytown, New York 10591