Manager Regulatory Affairs

Posted 10 Days Ago
Be an Early Applicant
2 Locations
In-Office
Junior
Biotech • Pharmaceutical
The Role
Develops EU regulatory strategies for clinical development programs, leads clinical study submissions and regulatory agency interactions, supports study start-up and compliance, monitors EU legislation, and collaborates with clinical, development, business, CRO, and regulatory teams. The role also manages relationships with European and national agencies and contributes to early- and late-stage regulatory planning.
Summary Generated by Built In

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, Regulatory Affairs to join our regulatory function, supporting our European development programmes in a hybrid work model. In this role, you will shape EU regulatory strategy and support timely clinical development while collaborating with development teams, clinical teams, business partners, contract research organisations, and regulatory agencies. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.


When & where:

Multiple locations are being considered for this position (Hybrid)


Discover your role:

  • Develop EU-appropriate regulatory strategies with development teams and regulatory management.
  • Lead clinical study submissions, agency queries, compliance, start-up, and maintenance activities.
  • Represent Regeneron with contract research organisations across complex late-stage clinical studies.
  • Support business partners in aligning EU regulatory strategy with business objectives.
  • Monitor emerging EU legislation and guidance, supporting company awareness and compliance.
  • Build relationships with the European Medicines Agency, national agencies, and alliance partners.
  • Lead early and late-stage regulatory strategy for timely end-to-end study conduct.
  • You champion innovative EU pathways and share expertise across global regulatory and development teams.

This role requires:

  • Advanced degree in a scientific discipline.
  • At least two years’ regulatory experience across clinical development and post-approval activities.
  • Proven experience supporting EU Clinical Trial Applications through approval and study start-up.
  • Direct experience with national regulatory agencies and leading face-to-face agency meetings.
  • Clear stakeholder negotiation and excellent written and verbal communication skills.
  • European Medicines Agency experience, including scientific advice, orphan designation, or paediatric investigation plans, is advantageous.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.  If you have any questions, please speak with your recruiter. 


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. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

€74,000.00 - €120,700.00

Skills Required

  • Advanced degree in a scientific discipline
  • At least two years of regulatory experience across clinical development and post-approval activities
  • Experience supporting EU Clinical Trial Applications through approval and study start-up
  • Direct experience with national regulatory agencies and leading face-to-face agency meetings
  • Clear stakeholder negotiation skills
  • Excellent written and verbal communication skills
  • European Medicines Agency experience, including scientific advice, orphan designation, or paediatric investigation plans

Regeneron Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Regeneron and has not been reviewed or approved by Regeneron.

  • Healthcare Strength — Health coverage is consistently characterized as strong and competitive, forming a core pillar of the total rewards package. Mentions of robust medical benefits appear alongside broader praise for the overall benefits offering.
  • Retirement Support — Retirement contributions and pension support are repeatedly noted as meaningful components that enhance long‑term financial security. These elements are cited alongside other financial benefits as differentiators.
  • Strong & Reliable Incentives — Bonuses and overtime or shift premiums for eligible roles materially boost total compensation beyond base salary. These incentives are commonly highlighted as positives, particularly in manufacturing and shift-based roles.

Regeneron Insights

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The Company
HQ: Tarrytown, NY
15,000 Employees
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in. Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media. An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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