Associate Director Clinical Supply Operations
Company: Regeneron Pharmaceuticals, Inc.
Location: Warren
Posted on: January 25, 2026
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Job Description:
The Associate Director of Clinical Supply Operations is
responsible for driving the strategy, optimization and execution of
business processes within the Clinical Supply Operations (CSO)
department. This position plays a key role in translating planning
excellence into operational outcomes, while leveraging data driven
insights, and driving a culture of continual improvement and
responsiveness. The incumbent will be responsible for ensuring
strategic alignment of operational activity in the organization
while providing value-added analytical insights to support the
goals of the CSO team. NOTE: This role requires 4-days onsite and
is NOT eligible remote. A typical day in this role looks like:
Manage and oversee Clinical Logistics Vendors in the strategic and
operational execution of Clinical Supply Distribution. Includes
monitoring performance, driving improvements, issue resolution, and
escalation management. Manage and oversee strategic and operational
Clinical Supply Operations activities, driving standardization,
analytics, and continuous improvement. Lead a team providing
support for Global Clinical Logistics planning & execution,
ensuring compliant and timely shipment and delivery between depots
and investigator sites, working with our Logistics Providers.
Ensure seamless logistical execution through global Inventory
visibility including management of material movements, expiry,
returns, reconciliation & destruction processes, leveraging IRT and
related systems and processes. Ensure appropriate visibility to
priorities for optimization of QP release, Regulatory Release
processes and support for Logistics Vendor and Industrial
Operations activities (e.g. packaging campaign documentation),
including co-ordination of expedited shipments. Define needs for
data analytics capabilities to enable data driven insights on the
worldwide clinical supply chain, collaborating with partner
Clinical Drug Supply & Logistics Teams and the wider Regeneron
Supply Organization (e.g. Industrial Operations). Develop reporting
that drives continuous improvement against key performance measures
both internally and with our logistics vendors. This will be
accomplished by analyzing operational data to inform performance
improvement opportunities with an emphasis on understanding key
operational performance indicators and the impact they have on
supply delivery. Create and manage reporting metrics and determine
how best to provide visibility to operations performance via report
creation, insights and analyzing system dashboards. Ensure team is
in continual state of inspection readiness with robust
documentation workflow and archival of documentation of IP supply
activities provided to clinical trial teams for the Trial Master
File. Lead process improvement opportunities that enable more agile
operations, enhanced strategic insights, and analytical
capabilities. This role may be for you if you have: Must be able to
effectively communicate to all levels of the organization,
including senior management. Experience working with and/or
managing external vendors. Must be able to develop and present
varied and unique ideas. Effective stakeholder management,
influence and negotiation skills. Proven Functional and Line
Management skills. Financial acumen in creating and managing
budgets. Must have broad knowledge and cross-functional
understanding of clinical trial methodology. Working knowledge of
GCP and ICH Guidelines. To be considered for this opportunity, you
should have a BS/BA and at least 10 years of relevant experience in
the biotechnology/pharmaceutical industry, with 5 years line
management experience. This is an opportunity to join our select
team that is already leading the way in the Pharmaceutical/Biotech
industry. Apply today and learn more about Regenerons unwavering
commitment to combining good science & good business. 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) $157,200.00
- $256,600.00
Keywords: Regeneron Pharmaceuticals, Inc., Greenwich , Associate Director Clinical Supply Operations, Healthcare , Warren, Connecticut