Manager Regulatory Affairs
Regeneron Pharmaceuticals, Inc., Uxbridge, Greater London
Manager Regulatory Affairs
Salary not available. View on company website.
Regeneron Pharmaceuticals, Inc., Uxbridge, Greater London
- Full time
- Permanent
- Onsite working
Posted today, 5 Nov | Get your application in now to be one of the first to apply.
Closing date: Closing date not specified
Job ref: e6040cc0857742a3bde6cdec3d200fc2
Location ref: Uxbridge, Greater London
Full Job Description
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 you have any questions, please speak with your recruiter.