At a Glance
- Tasks: Lead regulatory strategy and ensure successful outcomes for pharmaceutical products across Europe.
- Company: Join a leading pharmaceutical company with a focus on innovation and collaboration.
- Benefits: Competitive hourly rate, flexible hybrid working, and opportunities for professional growth.
- Other info: Work in a dynamic environment with a focus on leadership and independence.
- Why this job: Make a real impact in the pharmaceutical industry while shaping regulatory strategies.
- Qualifications: Degree in life sciences and strong experience in European Regulatory Affairs required.
Location: Maidenhead/Remote (hybrid)
Duration: 12 months initial (FOUR days per week / 0.8 FTE)
Rate: £70-85 per hour (based on experience)
We are working with a leading pharmaceutical company who are seeking an experienced Senior Manager, Regulatory Affairs to shape and drive regulatory strategy across the Europe Area. This high-impact role will work across development and marketed products, partnering closely with global teams, affiliates and health authorities to ensure successful regulatory outcomes.
Key Responsibilities- Lead the development and implementation of regulatory strategies and risk assessments for assigned products across the Europe Area
- Represent regional regulatory requirements within global regulatory project teams to ensure appropriate consideration in global strategy
- Collaborate with affiliate Regulatory Affairs teams to guide submissions, health authority interactions and life-cycle management activities
- Assess scientific data for regulatory submissions, identify gaps, and develop mitigation strategies to support approvals
- Monitor evolving European legislation and lead the development of regulatory responses and policy implementation
- Degree in pharmacy, biology, chemistry, pharmacology, or related life sciences discipline
- Strong experience in European Regulatory Affairs, including centralised, MRP/DCP and national procedures
- Proven track record leading regulatory activities for development products (e.g., scientific advice, PIP)
- Effective communicator able to work across complex international and matrixed environments
- Strong leadership, organisational skills and ability to work independently with minimal supervision
To apply: SRG would be delighted to discuss this opportunity further with you. Please click to apply or contact Theo Charles for more details.
Senior) Manager, Regulatory Affairs in Maidenhead employer: Carbon 60
Join a leading pharmaceutical company that prioritises employee growth and development, offering a dynamic work culture that fosters collaboration and innovation. With the flexibility of a hybrid working model in Maidenhead, you will have the opportunity to shape regulatory strategies while enjoying competitive rates and a supportive environment that values your expertise and contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Senior) Manager, Regulatory Affairs in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those 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 regulatory achievements. We want you to show off your knowledge and passion for the role, so be ready to discuss how you can contribute to their success.
✨Tip Number 3
Practice your pitch! You never know when you'll meet someone who could help you land that Senior Manager role. Have a concise summary of your experience and what you bring to the table ready to go.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take the initiative to connect with us directly.
We think you need these skills to ace Senior) Manager, Regulatory Affairs in Maidenhead
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Manager, Regulatory Affairs role. Highlight your experience in European Regulatory Affairs and any relevant projects you've led. We want to see how your background aligns with the key responsibilities mentioned in the job description.
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. Mention specific experiences that demonstrate your ability to lead regulatory strategies and collaborate with global teams. We love a good story!
Showcase Your Communication Skills:As an effective communicator, it's crucial to showcase this in your application. Use clear and concise language in your CV and cover letter. We want to see how you can convey complex information simply, just like you would in a regulatory environment.
Apply Through Our Website:Don't forget to apply through our website! It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re proactive and keen to join our team at StudySmarter!
How to prepare for a job interview at Carbon 60
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of European regulatory affairs. Familiarise yourself with centralised, MRP/DCP, and national procedures. Being able to discuss these confidently will show that you're the right fit for the role.
✨Showcase Your Leadership Skills
Prepare examples of how you've led regulatory activities in the past. Think about specific projects where you guided teams or made significant decisions. This will demonstrate your ability to work independently and lead in a complex environment.
✨Communicate Effectively
Practice articulating your thoughts clearly and concisely. Since this role involves collaboration with global teams and health authorities, being an effective communicator is key. Consider doing mock interviews to refine your delivery.
✨Stay Updated on Legislation
Keep yourself informed about the latest changes in European legislation. Being able to discuss recent developments and their implications during the interview will show your commitment to the field and your proactive approach.
