At a Glance
- Tasks: Lead regulatory strategies for innovative pharmaceutical products across EMEA.
- Company: Global pharmaceutical leader focused on eye health and patient outcomes.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and patient-centric solutions.
- Why this job: Make a real impact in healthcare by shaping regulatory strategies.
- Qualifications: 8+ years in regulatory affairs with strong EU/UK knowledge.
The predicted salary is between 70000 - 90000 £ per year.
The Company is a global, science-led pharmaceutical organization with a long-established heritage and a focused commitment to eye health. The company operates across multiple global regions and is dedicated to developing innovative ophthalmic therapies that improve patient outcomes. Its mission is to deliver meaningful value to patients and healthcare systems through scientific expertise and a patient-centric approach.
We are seeking an experienced EMEA Regional Regulatory Lead to define and execute regulatory strategies supporting the development and registration of pharmaceutical pipeline products across Europe, the Middle East, and Africa. You will act as a key regional regulatory expert, partnering with global, regional, and local stakeholders to ensure regulatory compliance, anticipate evolving regulatory landscapes, and enable successful development and approvals across the EMEA region. You will also support affiliate-level regulatory activities for selected countries within the region.
- Lead EMEA regulatory strategy development for pipeline development programmes, aligned with global regulatory plans
- Represent the EMEA region in global regulatory teams, providing strategic and regional input
- Own regional regulatory strategy across the product lifecycle
- Oversee selected affiliate regulatory activities, including authority interactions and country-specific submission strategies
- Build and maintain relationships with regulatory authorities across EMEA
- Conduct regulatory intelligence and competitor/landscape monitoring to support risk and opportunity planning
- Monitor changes in regulatory frameworks and assess impact on development and lifecycle strategies
- Review promotional and packaging materials for regulatory compliance
- Support regulatory SOPs, lifecycle management, and cross-functional regulatory deliverables
Requirements:
- 8+ years of experience in medicinal regulatory affairs in Europe/UK
- Proven experience in regulatory strategy, submissions, and lifecycle management
- Experience in Marketing Authorization Applications and clinical development support
- Strong understanding of EU/UK regulatory frameworks and legislation
- Strong stakeholder management and cross-functional collaboration skills
- Excellent written and verbal English
Associate Planning Director in London employer: Barrington James
As a global leader in the pharmaceutical industry, our company offers an exceptional work environment that prioritises innovation and patient-centric solutions. Employees benefit from a collaborative culture that fosters professional growth through continuous learning opportunities and engagement with diverse teams across the EMEA region. With a strong commitment to eye health and a focus on regulatory excellence, we provide a unique platform for individuals to make a meaningful impact in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Planning Director in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those with experience in regulatory affairs. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU/UK regulatory frameworks. Be ready to discuss how your experience aligns with the company's mission and values. Show them you're not just a fit on paper but also in spirit!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email expressing your appreciation for the opportunity. It’s a great way to keep your name fresh in their minds and show your enthusiasm for the role.
✨Tip Number 4
Apply directly through our website! We love seeing candidates who take the initiative. Plus, it gives you a better chance of being noticed by our hiring team. So, don’t wait—get your application in today!
We think you need these skills to ace Associate Planning Director in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Planning Director role. Highlight your experience in regulatory affairs and any specific achievements 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 passionate about eye health and how your skills can contribute to our mission. Keep it engaging and relevant to the role, showing us your personality and enthusiasm.
Showcase Your Regulatory Expertise:In your application, be sure to highlight your experience with regulatory strategies and submissions. We’re keen to see examples of how you've navigated complex regulatory landscapes and built relationships with authorities across EMEA.
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 serious about joining our team!
How to prepare for a job interview at Barrington James
✨Know Your Regulatory Stuff
Make sure you brush up on the latest EU/UK regulatory frameworks and legislation. Being able to discuss recent changes and how they might impact the company's pipeline will show that you're not just knowledgeable but also proactive.
✨Showcase Your Stakeholder Skills
Prepare examples of how you've successfully managed relationships with regulatory authorities or cross-functional teams in the past. This role requires strong collaboration, so demonstrating your experience in this area will be key.
✨Be Ready for Scenario Questions
Expect questions that ask how you would handle specific regulatory challenges or changes in the landscape. Think through potential scenarios beforehand and have a structured approach ready to share during the interview.
✨Communicate Clearly and Confidently
Since excellent written and verbal English is crucial, practice articulating your thoughts clearly. You might even want to rehearse explaining complex regulatory concepts in simple terms, as this will demonstrate your communication skills effectively.
