Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Shape regulatory strategies and ensure compliance in the UK pharmaceutical market.
- Company: Join a global leader in pharmaceuticals committed to innovation.
- Benefits: Competitive salary, flexible working options, and career development opportunities.
- Why this job: Make a real impact on patient access to life-changing medicines.
- Qualifications: Degree in Life Sciences and extensive UK Regulatory Affairs experience required.
- Other info: Collaborative environment with strong mentorship and growth potential.
The predicted salary is between 43200 - 72000 £ per year.
Are you a seasoned Regulatory Affairs professional looking for a strategic role where your expertise directly impacts patient access to life-changing medicines? This is your chance to join a global pharmaceutical leader committed to innovation and improving lives.
Your new role:
- As a Regulatory Affairs Partner, you will play a pivotal role in shaping regulatory strategies and ensuring compliance within the UK market.
- You’ll work at the heart of a collaborative regulatory team, partnering with cross-functional stakeholders to navigate the evolving UK regulatory landscape post-Brexit.
- Your work will influence clinical trial applications, national licensing, early access programs, and UK components of centralised European procedures.
- You’ll also act as the primary liaison with the MHRA, driving negotiations and building strong external relationships.
- Lead UK regulatory submissions and provide strategic guidance across therapeutic areas.
- Develop and implement regulatory strategies aligned with business objectives.
- Ensure compliance with UK and EU regulatory requirements.
- Act as a Subject Matter Expert (SME) and mentor within the regulatory chapter.
- Collaborate globally to support product lifecycle management and market access.
What you’ll need to succeed:
- Degree in Life Sciences or related discipline.
- Extensive experience in UK Regulatory Affairs, including post-Brexit submissions.
- Strong knowledge of UK and EU regulatory frameworks.
- Proven ability to develop and communicate regulatory strategies.
- Excellent documentation and stakeholder management skills.
What you’ll get in return:
Flexible working options available.
Senior Regulatory Affairs Manager UK and Ire employer: hays-gcj-v4-pd-online
Contact Detail:
hays-gcj-v4-pd-online Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Affairs Manager UK and Ire
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend relevant events. Building connections can open doors to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory strategies. Show them you’re not just another candidate; you’re someone who understands their mission and can contribute to it.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the role of Senior Regulatory Affairs Manager. Highlight your knowledge of UK and EU frameworks and your ability to navigate post-Brexit challenges.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior Regulatory Affairs Manager UK and Ire
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Senior Regulatory Affairs Manager. Highlight your experience in UK regulatory affairs and any specific achievements that align with the job description. We want to see how your background makes you the perfect fit for this strategic position!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs and how your expertise can impact patient access to medicines. We love seeing genuine enthusiasm, so let your personality come through while keeping it professional.
Showcase Your Stakeholder Management Skills: Since this role involves collaborating with cross-functional teams, make sure to highlight your stakeholder management skills. Share examples of how you've successfully navigated complex relationships in previous roles. We’re looking for someone who can build strong connections!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows us you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at hays-gcj-v4-pd-online
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of UK and EU regulatory frameworks. Be ready to discuss specific post-Brexit changes and how they impact submissions. This shows you’re not just familiar with the basics but are also on top of current developments.
✨Showcase Your Strategic Thinking
Prepare examples of how you've developed and communicated regulatory strategies in the past. Think about times when your strategic input led to successful outcomes, especially in clinical trial applications or licensing negotiations. This will highlight your ability to think critically and act decisively.
✨Demonstrate Collaboration Skills
Since this role involves working with cross-functional teams, be ready to share experiences where you’ve successfully collaborated with other departments. Discuss how you’ve built relationships and navigated challenges to achieve common goals, particularly in a regulatory context.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s regulatory strategies and how they plan to adapt to future changes. This not only shows your interest in the role but also your proactive approach to understanding the company's position in the market.
