Manager Clinical Supply Operations
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Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
The Manager Clinical Supply Operations is a key member of the team responsible for leading clinical supply activities that support the development and operation of clinical supply logistics processes. Partnering with crossfunctional teams and external vendors you will provide operational oversight identify and implement improvements and drive continuous optimization using datadriven insights.
A Typical Day
Coordinate Clinical Logistics Vendors in the execution of distribution; supervise performance drive improvements and resolve issues to meet study timelines and quality expectations.
Collaborate with crossfunctional partners (e.g. Clinical Operations CMC Quality Regulatory Finance) to develop and improve Clinical Supply operational processes that ensure timely infull delivery of clinical trial materials.
Lead crossfunctional improvement initiatives to optimize operational efficiencies streamline handoffs and support strategic decisionmaking and problemsolving.
Represent the needs of the team in crossfunctional forums and initiatives; champion organisational change and adoption of new or improved processes and tools.
Create and lead performance metrics and dashboards to provide clarity into operational performance trends and opportunities; translate insights into action plans.
Act as an advisor to team members on operational tasks process issues projects and initiatives; mentor and train others to achieve highquality results.
Maintain standardized SOPs work instructions playbooks and templates; drive continuous improvement in planning processes and vendor management.
Identify and mitigate supply risks and dependencies early; propose pragmatic solutions and secure alignment on course corrections across collaborators.
Partner with digital/data and systems teams to harness IRT/RTSM ERP/WMS and analytics tools for planning and tracking; ensure data integrity and audit readiness.
May directly supervise staff; set priorities coach performance and support development.
This Role Might Be for You If You Have
Handson experience leading clinical trial supply operations and distribution including oversight of thirdparty logistics providers and pack/label/ship activities.
Strong project management skills with the ability to lead multiple concurrent workstreams deadlines and collaborators in a matrixed environment.
Proven vendor management expertise including service level oversight performance management and continuous improvement.
Excellent communication and relationshipbuilding skills; adept at influencing across functions and levels.
High attention to detail with creative datadriven problemsolving.
Proficiency with clinical supply and data tools (e.g. IRT/RTSM ERP WMS) and Microsoft Excel PowerPoint and Word.
Familiarity with GxP/GDP requirements and best practices for clinical supply distribution and documentation.
To Be Considered
Bachelors degree in supply chain life sciences engineering or a related field with 6 years of professional experience. Experience supporting global or multiregion clinical studies is advantageous; . Fluency in English; additional languages are a plus.
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 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 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 Companys 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.
Required Experience:
Manager
Key Skills
About Company
Discover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.
