At a Glance
- Tasks: Lead regulatory strategies for innovative pharmaceutical products across EMEA.
- Company: Dynamic pharmaceutical company backed by top industry investors.
- Benefits: Join a pioneering team with opportunities for career growth and impactful projects.
- Other info: Exciting opportunity with a collaborative culture and ambitious goals.
- Why this job: Be at the forefront of groundbreaking studies in the pharmaceutical industry.
- Qualifications: 8+ years in Regulatory Affairs, preferably with EMEA experience.
The predicted salary is between 80000 - 100000 € per year.
Barrington James are excited to post a fantastic opportunity for one of our close clients. This company is a big Pharmaceutical in the UK, backed by serious investors in the industry and looking for future support within their Regulatory Affairs team. This opportunity is perfect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects.
Key Responsibilities
- Lead regional filing strategies for pharmaceutical products across Europe, the Middle East, and Africa (EMEA).
- Establish and optimise regulatory structures across the region, managing relationships with key regulatory agencies directly.
- Oversee affiliate-level Regulatory Affairs activities across the UK & Ireland cluster, managing approximately 12–13 marketing authorisations in both places.
- Develop regulatory strategy throughout the product lifecycle, from clinical development through to commercialisation.
- Collaborate cross-functionally with internal stakeholders to ensure alignment on regulatory objectives and successful execution of submission plans.
Candidate Requirements
- Minimum 8 years of Regulatory Affairs experience within the pharmaceutical industry.
- Strong experience supporting drug development programmes from clinical phase through to commercial launch.
- Prior experience as an EMEA Regulatory Lead is strongly preferred.
- Ophthalmology experience would be an advantage, but is not essential.
- Background within innovative pharmaceutical organisations such as Alcon, Novartis, AbbVie, or similar is highly desirable.
- Fluent in English, both written and spoken.
- Proactive, self-motivated, and able to work independently while contributing as a strong collaborative team player.
This truly is an exciting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies. The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking "apply" you will be sending your CV to Isobella at Barrington James. Isobella is an RA/QA Recruitment specialist and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
EMEA, UK and IE Regional Regulatory Lead employer: Barrington James
This leading pharmaceutical company in the UK offers an exceptional work environment that fosters innovation and ambition. With a strong focus on employee growth, they provide opportunities for professional development and collaboration on groundbreaking projects within the Regulatory Affairs team. The supportive culture, backed by significant industry investors, ensures that employees are empowered to make impactful contributions while enjoying a dynamic and rewarding workplace.
StudySmarter Expert Advice🤫
We think this is how you could land EMEA, UK and IE Regional Regulatory Lead
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience in Regulatory Affairs. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show them you’re not just another candidate; you’re genuinely interested in their innovative work and how you can contribute to their success.
✨Tip Number 3
Practice your pitch! Be ready to explain your experience and how it aligns with the role of EMEA Regulatory Lead. Highlight your past successes in managing regulatory strategies and working with agencies.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re here to support you throughout the process, so let’s get you that dream job!
We think you need these skills to ace EMEA, UK and IE Regional Regulatory Lead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of EMEA, UK and IE Regional Regulatory Lead. Highlight your relevant experience in Regulatory Affairs and any specific projects that align with the job description. We want to see how your background fits perfectly with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share your passion for regulatory affairs and how your skills can contribute to our innovative projects. Remember, we love a good story!
Showcase Your Achievements:When detailing your experience, focus on your achievements rather than just responsibilities. Quantify your successes where possible, like the number of marketing authorisations you've managed or successful submissions you've led. We want to see the impact you've made!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for this exciting opportunity. Don’t miss out – hit that 'apply' button now!
How to prepare for a job interview at Barrington James
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of regulatory affairs, especially within the pharmaceutical industry. Familiarise yourself with the latest regulations and guidelines in EMEA, as well as any specific requirements for the UK and Ireland. This will show that you're not just a candidate, but a knowledgeable expert ready to lead.
✨Showcase Your Experience
Prepare to discuss your past experiences in detail, particularly those that align with the responsibilities of the role. Highlight your experience in managing marketing authorisations and leading regulatory strategies. Use specific examples to demonstrate how you've successfully navigated complex regulatory environments.
✨Collaborate Like a Pro
Since this role involves cross-functional collaboration, be ready to talk about how you've worked with different teams in the past. Share examples of how you’ve aligned regulatory objectives with other departments, ensuring everyone is on the same page. This will illustrate your ability to work independently while still being a team player.
✨Ask Insightful Questions
Prepare some thoughtful questions to ask during the interview. Inquire about the company's current projects, their approach to regulatory challenges, or how they envision the role evolving. This shows your genuine interest in the position and helps you assess if the company is the right fit for you.
