Senior Manager, Statistical Programming
Company: Regeneron Pharmaceuticals, Inc.
Location: Warren
Posted on: February 23, 2026
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Job Description:
A Sr. Manager provides timely support to the project team on all
programming matters according to the project strategies within a
therapeutic area. As an integral part of a project team, the
incumbent provides project leadership and contributes to the
programming support for processing data from clinical studies.
Project requirements will be identified according to a Statistical
Analysis Plan, programming specifications or user
requirements/design documents using internal standards and
guidelines. The incumbent is responsible for leading the
programming aspect of the project, both internally or CROs, for all
programming deliverables and participates in the identification and
development of programming standards and macro development to
facilitate the creation of statistical deliverables from a single
study through to regulatory approval, product launch, and annual
reports. May be asked to oversee special projects / work with
clinical task force. Meets statistical adhoc requests of senior
management. As a Senior Manager, A typical day may include:
Independently coordinate and oversee the preparation, execution,
reporting and documentation of project analysis programming within
a therapeutic area using appropriate tools to track, allocate and
summarize extent of work required, progress and completion of
programming deliverables. Manage and coordinate programming and QC
of analysis datasets and TFLs following Regeneron standard data
models and/o integration of data across studies in support of
CSS/CSE and esub deliverables. Implement and mentor others on the
use of department standardization tools or therapeutic area
standard analysis when programming clinical data or system
application deliverables. Contribute to programming development and
quality control of the programming deliverables utilizing Regeneron
tools and methodologies. Programming representative within a
therapeutic area in a multidisciplinary study team to ensure timely
and quality support for analysis and reporting of clinical trials
up to regulatory approval, product launch and annual reports. If
applicable, programming representative for an application
development to the user audience. Develop data models, programming
standards and code, and training end users in the use of project
standards to support programming deliverables that follow
regulatory submission requirements. Mentor junior level staff in
therapeutic area requirements. Develop collaborative work
environment and be a positive role model. Advises all relevant
employees about the procedures surrounding retention of data,
records, and information for employees in their group. To be
considered for this role, you must meet the following requirements
: Education Masters Degree SAS Certification desirable. Experience
8 10 Years Does this sound like you? Apply now to take your first
step towards living the Regeneron Way! We have an inclusive culture
that provides comprehensive benefits, which vary by location. In
the U.S., benefits may include health and wellness programs
(including medical, dental, vision, life, and disability
insurance), fitness centers, 401(k) company match, family support
benefits, equity awards, annual bonuses, paid time off, and paid
leaves (e.g., military and parental leave) for eligible employees
at all levels! For additional information about Regeneron benefits
in the US, please visit
https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.
For other countries specific benefits, please speak to your
recruiter. Please be advised that at Regeneron, we believe we are
most successful and work best when we are together. For that
reason, many of Regenerons roles are required to be performed
on-site. Please speak with your recruiter and hiring manager for
more information about Regenerons on-site policy and expectations
for your role and your location. 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. The Company
will also provide reasonable accommodation to the known
disabilities or chronic illnesses of an otherwise qualified
applicant for employment, unless the accommodation would impose
undue hardship on the operation of the Company's business. For
roles in which the hired candidate will be working in the U.S., the
salary ranges provided are shown in accordance with U.S. law and
apply to U.S.-based positions. For roles which will be based in
Japan and/or Canada, the salary ranges are shown in accordance with
the applicable local law and currency. If you are outside the U.S,
Japan or Canada, please speak with your recruiter about salaries
and benefits in your location. Please note that certain background
checks will form part of the recruitment process. Background checks
will be conducted in accordance with the law of the country where
the position is based, including the type of background checks
conducted. The purpose of carrying out such checks is for Regeneron
to verify certain information regarding a candidate prior to the
commencement of employment such as identity, right to work,
educational qualifications etc. Salary Range (annually) $150,500.00
- $245,500.00
Keywords: Regeneron Pharmaceuticals, Inc., Danbury , Senior Manager, Statistical Programming, Science, Research & Development , Warren, Connecticut