Manager Clinical Supply Operations

Company: Regeneron Pharmaceuticals, Inc.
Location: Warren
Posted on: January 25, 2026

Job Description:

The Manager of Clinical Supply Operations is a key member of the Clinical Supply Operations Team, whose primary responsibility is leading Clinical Supply activities that support the development and operation of Clinical Supply Logistics processes. This position plays a key role in the operational oversight of Clinical Supply processes, identifying areas of improvement, and driving continuous improvements, while leveraging data driven insights. NOTE: this role is NOT eligible remote and must be in office 4-days a week with 1-day from home. A typical day in this role looks like: Support the oversight of Clinical Logistics Vendors in the operational execution of Clinical Supply Distribution. Includes monitoring performance, driving improvements, and issue resolution. Collaborate with cross functional partners to develop and enhance Clinical Supply Operational processes to ensure delivery of Clinical Trail Supply Lead cross functional improvement initiatives to optimize operational efficiencies and support strategic decision-making/problem-solving. Represent the needs of Clinical Supply Operations at cross functional discussions/initiatives and be a champion of change management. Create and manage performance metrics to provide visibility to operational performance, insights, trends, and identify areas of opportunity. Act as advisor to Clinical Supply Operations team members on operational tasks, process issues, projects, and initiatives. Mentors and trains others to obtain quality results. May directly supervise staff. This role may be for you if you have: Ability to effectively communicate across an organization. Experience working with external vendors. Experience leading cross functional projects/initiatives. Effective stakeholder management, influence and negotiation skills. Ability to effectively multi-task and adapt to changing priorities. Experiencing coaching and mentoring others. Working knowledge of clinical trial methodology. Working knowledge of GCP and ICH Guidelines. To be considered for this opportunity, a minimum of a BS/BA and at least 6 years of relevant experience in the biotechnology/pharmaceutical industry. 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) $114,800.00 - $187,400.00

Keywords: Regeneron Pharmaceuticals, Inc., Vineland , Manager Clinical Supply Operations, Science, Research & Development , Warren, New Jersey