Manager, Product & Pipeline Communications

Regeneron Pharmaceuticals, Inc.; United States; On-site; USD 130,000 - 180,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Manager, Product & Pipeline Communications to join the Corporate Affairs team in Sleepy Hollow, NY.

This on-site role supports the commercialized portfolio and investigational pipeline with cross-functional collaboration across Commercial, Clinical, Medical Affairs, Legal and Regulatory. You will lead science-driven communications, deliver strategic messaging, manage media relations, and ensure regulatory compliance while driving impactful campaigns

Qualifications

• Experience translating complex science into clear messages.
• Ability to manage multi-stakeholder communications programs.
• Knowledge of biotech/pharmaceutical regulatory landscapes a plus.

Responsibilities

• Lead multi-channel communications for U.S. and global audiences.
• Develop media materials, manage media relations and events.
• Implement plans for milestones, approvals, and post‑approval engagement.
• Deliver disease awareness and thought leadership initiatives.
• Partner with Commercial, Clinical, Medical Affairs, Legal and Regulatory.

Skills

Stakeholder engagement

Written communication

Editing and storytelling

Cross-functional collaboration

Strategic thinking

Education

Bachelor's degree

Job description

Build our future together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Product & Pipeline Communications to join our Corporate Affairs team, supporting our commercialized portfolio and investigational pipeline in an onsite work model at our Sleepy Hollow, NY location. In this role, you will lead high-impact, science-driven communications that protect and strengthen Regeneron's reputation while collaborating with Commercial, Clinical, Medical Affairs, Legal, Regulatory and other cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where

• Location: Sleepy Hollow, NY
• Work model/flexibility: Onsite a minimum of four days per week; not open to fully remote or hybrid arrangements

Discover your role

• Manage multi-channel U.S. and global communications programs that engage key stakeholders
• Develop media materials, manage media relations and events, and support medical congresses
• Implement communications plans for data and regulatory milestones, product approvals, and post-approval stakeholder engagement
• Deliver disease awareness, branded campaigns, and thought leadership initiatives
• Partner with Commercial, Clinical, Medical Affairs, Legal, and Regulatory to align communications with business priorities
• Anticipate and respond to potential issues
• Contribute strategic ideas and support Corporate Affairs reputation-building efforts
• Ensure all communications meet regulatory, legal, and compliance guidelines

This role might be for you

• You are passionate about science and patient impact, and stay curious about news, trends, and audience insights
• You are results-oriented and collaborative, with a talent for influencing and building trusted relationships
• You write, edit, and design with precision, turning complex clinical data into clear, compelling stories
• You bring executive presence and sound judgment to advise senior leaders on sensitive matters
• You use digital and social strategies to deliver measurable communications impact
• You thrive in a fast-paced, start-up style environment and juggle multiple priorities with agility
• You manage agencies and vendors effectively to deliver cohesive, high-quality work

This role requires

• Bachelor's degree with a minimum of 7 years of relevant experience
• Majority of experience in product and/or pipeline communications (in-house or agency)
• Understanding of the regulatory, commercial, and legal landscape for pre- and post-approval product communications
• Preferred: Experience with biotechnology/pharmaceutical therapies at leading biopharmaceutical companies

We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site.