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Principal Statistical Programmer

Job in Clifton, Passaic County, New Jersey, 07015, USA
Listing for: BioSpace
Full Time position
Listed on 2026-06-14
Job specializations:
  • IT/Tech
    Data Analyst, Data Scientist, Data Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Overview

This is an onsite opportunity and is NOT eligible remote.

A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards.

The evaluation and development of study requirements and validation plan are also in the scope of this position. The incumbent works independently to design and test program logic, code programs, program documentation, and prepare programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical ad‑hoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.

Responsibilities
  • Support and/or lead programmer for programming and QC of analysis datasets, TFLs 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.
  • Support creation and validation of submission requirements (i.e., annotated CRF, data export files, define documents).
  • Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch, and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.
  • Provide programming support for simple presentations and basic statistical ad‑hoc requests. Assist in more complex data presentations.
  • Participate in department working groups; provide input in development of tools and improvement of processes.
Qualifications
  • Master's Degree.
  • Proficiency in SAS (Base, Stat, Macro, graph).
  • 3+ Years of experience as a statistical programmer.
Salary Range (annually)

$ - $

EEO Statement

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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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