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.,
- 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.
- 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.
- 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
#J-18808-Ljbffr
Manager Regulatory Affairs in Uxbridge employer: Regeneron Pharmaceuticals, Inc
At Regeneron, we pride ourselves on being a science-driven organisation that is dedicated to making a meaningful difference in patients' lives. As a Director of International Commercialization Immunology based in Uxbridge, UK, you will thrive in a collaborative and inclusive work culture that values innovation and employee growth. With competitive benefits, including health and wellness programmes, and opportunities for professional development, Regeneron is an excellent employer for those looking to contribute to impactful healthcare solutions while enjoying a supportive work environment.
Contact Details:
Regeneron Pharmaceuticals, Inc Recruitment Team