At a Glance
- Tasks: Lead regulatory strategies for innovative pharmaceutical products across EMEA.
- Company: Global science-led pharmaceutical organisation focused on eye health.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to innovation and patient-centric solutions.
- Why this job: Make a real impact in patient outcomes through regulatory expertise.
- Qualifications: 8+ years in medicinal regulatory affairs with strong stakeholder management skills.
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 - Contract 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 meaningful platform for those looking to make a significant impact in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Planning Director - Contract in London
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend relevant events. Building connections can open doors and give you insider info about job opportunities.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory landscape. Show them you know their mission and how your experience aligns with their goals. Confidence is key!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can leave a lasting impression. It shows your enthusiasm and keeps you on their radar.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities, and applying directly can sometimes give you an edge. Plus, it’s super easy!
We think you need these skills to ace Associate Planning Director - Contract 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 with our mission in eye health!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory strategy and how you can contribute to our team. Keep it concise but impactful, showing us your personality and expertise.
Showcase Your Experience:When detailing your experience, focus on your 8+ years in medicinal regulatory affairs. Be specific about your roles in submissions and lifecycle management, as this will resonate with what we’re looking for in a candidate.
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’re considered for the role. Plus, it shows us you’re keen to join our team!
How to prepare for a job interview at Barrington James
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of EU/UK regulatory frameworks and legislation. Be ready to discuss specific examples from your past experience that demonstrate your understanding of regulatory strategies and submissions.
✨Showcase Your Stakeholder Skills
Prepare to talk about how you've successfully managed relationships with regulatory authorities and cross-functional teams. Think of concrete examples where your collaboration led to successful outcomes, as this will highlight your stakeholder management skills.
✨Stay Updated on Industry Changes
Familiarise yourself with recent changes in the regulatory landscape that could impact the pharmaceutical industry. Being able to discuss these changes and their implications during the interview will show that you're proactive and well-informed.
✨Practice Your Communication
Since excellent written and verbal English is crucial for this role, practice articulating your thoughts clearly and concisely. Consider doing mock interviews with a friend or using online resources to refine your communication skills.
