Director Quantitative Pharmacology
Company: Regeneron Pharmaceuticals, Inc.
Location: Tarrytown
Posted on: February 22, 2026
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Job Description:
As a Director in Pharmacometrics (Quantitative Pharmacology),
this individual is accountable for the delivery of support for one
or more research & development programs, within their
pharmacometrics discipline. In this capacity the Director is
accountable for the timely and accurate delivery of needed
quantitative analyses, interpretation, and messaging to PMx
management, as well as the timely delivery of well-constructed and
well-messaged reports for PMx review. A day in the life of a
Director may look like: Manages and is accountable for the PK/PD
evaluation of a small portfolio of products or projects. Works
independently, with guidance in only the most complex situations.
Informs PMx management of important program and regulatory
developments in a timely manner. Ensures analyses and documentation
are of the highest quality and accuracy. Ensures that reports and
other documents have the appropriate messaging and that a
meaningful story-line is developed. Ensures that study reports and
other documents have an appropriate functional review and are
suitable for review by senior management. Solves complex problems;
takes a broad perspective to identify solutions. Has a strong
publication record and actively publishes work in scientific
literature Makes contributions to multi-disciplinary meetings by
sharing cross-functional skills and knowledge. Has excellent
interpersonal and communication skills, both written and oral, and
has ability to communicate complex information succinctly. This may
be the right role for you if you: Are fully knowledgeable of
pharmacokinetic /pharmacodynamic principles, pharmacology, biology,
and quantitative aspects of drug development as well as having an
advanced knowledge of pharmaceutical drug development. Possess a
deep understanding of scientific literature and technical skills in
a number of PK/PD methods and techniques. Has extensive knowledge
base of the work in overall scientific community in own discipline.
Recognized as an expert in own area within the organization. Have
extensive regulatory experience through authoring of regulatory
briefing books, CTD summaries, contribution at HA meetings, HA
negotiations through regulatory reviews and approvals of BLA or
equivalent. Decisions are guided by policies, procedures and
business plan; receives guidance from head of function. In order to
be considered qualified for this role, you must have a PhD 8 years
with a degree in Quantitative Pharmacology (pharmacometrics) or
related field. Hands on usage of a broad range of quantitative
tools and systems is required, as is a strong publication record in
the field. A proven track record of displaying excellent
interpersonal and communication skills both written and oral and
ability to communicate complex information succinctly. Proven
experience developing QP elements of regulatory strategy and
interacting with regulatory agencies without supervision. PMx 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) $205,000.00
- $341,600.00
Keywords: Regeneron Pharmaceuticals, Inc., West Orange , Director Quantitative Pharmacology, Science, Research & Development , Tarrytown, New Jersey