Principal Statistical Programmer

About the role

A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. In This Role, a Typical Day Might Include:

• Project leadership and programming support for processing data from clinical studies.
• Assists in providing guidance in implementing and executing the programming and project standards.
• Evaluation and development of study requirements and validation plan.
• Designs and tests program logic, codes programs, documents programs, and prepares programs.
• Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses.
• Maintains documentation and consistent maintenance of code, logs, and output in a regulated environment.

Responsibilities

Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.

Requirements

• Masters Degree
• SAS, (Base, Stat, Macro, graph)
• 3 + Years experience

Qualifications

• 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).
• Provide programming support for simple presentations and basic statistical ad-hoc requests.
• Assist in the more complex data presentations.
• Participate in department working groups; provide input in development of tools and improvement of processes.

Skills

• Experience in SAS programming, including Base, Stat, Macro, and Graph.
• Experience in supporting clinical trial data analysis and reporting.
• Ability to work independently and as part of a multidisciplinary team.
• Strong communication and documentation skills.
• Knowledge of regulatory standards and compliance.

Benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

• Annual bonuses or other incentive plans
• Equity awards
• Pension or retirement benefits
• 401(k) company match
• Health and wellness programs
• Fitness centers
• Insurance benefits (e.g. medical, dental, vision, life and disability)
• Paid time off
• Family support benefits

Pay

$109,900.00 - $179,300.00 annually

Schedule

Onsite