Dir Statistical Programming

Basking Ridge, New Jersey, United States of America
Jul 14, 2021
Required Education
Associate Degree
Position Type
Full time
Job Title: Dir Statistical Programming

Department: 1412-Statistical Programming

Location: Tarrytown or Basking Ridge

Date Created: 04May2009


The Director manages the statistical programming group, oversees and manages all activities, both internally and externally by CROs, related to statistical and non-statistical analysis related to ongoing clinical program(s), and ensures standardization across therapeutic areas. The incumbent develops an overall strategy for the programming group and coordinates the effort across therapeutic areas to identify, develop and implement departmental standards, applications, processes and training. The incumbent is responsible for addressing all administrative functions required for project management such as compilation of resource requirements and milestones, identifying and communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies. The incumbent provides timely support to the project teams on all statistical programming matters according to the project strategies.

  • Overseeing all management functions as head of statistical programming. Coordinate the standardization of Regeneron data models across global therapeutic areas.
  • Coordinate the implementation of standard tools and technology to facilitate analysis dataset creation and analysis results following the Regeneron standard data models a standard data displays.
  • Demonstrate company values and act as a role model through respect of others, performing collaboratively within and across departments and teams, taking ownership of assignments and striving to deliver quality products in expected timelines.
  • Define roles and responsibilities of the statistical/system programming function with input from other department functions.
  • Work with project team to ensure members are committed to their roles and responsibilities. Communicate the need for each member embracing their roles and responsibilities.
  • Review and select resumes, screen and interview candidates for contractor and permanent positions.
  • Prepare yearly performance appraisals, define career path for associates and identify areas for improvements.


  • Prepare yearly performance appraisals, define career path for associates and identify areas for improvements
  • Master's Degree.
  • Also acceptable - MS. in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 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 multiple therapeutic areas. SAS Certification desirable.
  • SAS, (Base, Stat, Macro, graph) and S-Plus/R.

  • 10 + Years.