Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead and oversee global regulatory strategies for innovative pharmaceutical products.
- Company: Join a cutting-edge global pharmaceutical business making waves in the biotech industry.
- Benefits: Enjoy a competitive salary and a comprehensive benefits package.
- Why this job: Be at the forefront of drug development, impacting lives while collaborating with health authorities.
- Qualifications: Extensive experience in regulatory affairs within biotech/biopharma is essential.
- Other info: Connect with Freddie Hill at pharma-partners for more details.
The predicted salary is between 54000 - 84000 £ per year.
Job title: Director Global Regulatory Affairs
An Innovative global pharmaceutical business is seeking a Director, Global Regulatory affairs to join their team. In this role you will provide strategic leadership and oversight to the Regulatory Affairs organisation, and responsible for developing and directing regulatory strategy.
Responsibilities:
- Directs the development of submission of Neurology clinical trial applications, product registration dossiers, supplements, amendments.
- Build and nurture relationships with Health Authorities for successful interactions, such as scientific advice meetings, and outcomes.
- Serves as a regulatory liaison on the project team throughout the product lifecycle.
- Maintain all regulatory aspects of clinical trial activities for products in compliance with the EU Clinical Trial Regulation.
Requirements:
- Extensive industry experience with demonstrated experience in direct Regulatory Affairs in the biotech/biopharmaceutical industry.
- A Demonstrated track record of interfacing effectively with global regulatory agencies, such as the EMA.
- Experience operating at a senior strategic and decision making level.
- Experience Clinical Trial Applications, including submission and maintenance.
Salary and benefits:
A highly competitive salary and wider benefits scheme is on offer.
To apply for this position or hear further details then please contact Freddie Hill via Freddie.hill@pharma-partners.co.uk
Director of Regulatory Affairs employer: Pharma Partners Recruitment Ltd
Contact Detail:
Pharma Partners Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director of Regulatory Affairs
✨Tip Number 1
Make sure to highlight your experience with global regulatory agencies like the EMA. This is crucial for the Director of Regulatory Affairs role, as you'll need to demonstrate your ability to navigate complex regulatory landscapes.
✨Tip Number 2
Network with professionals in the biotech and biopharmaceutical industries. Building relationships can provide you with insights and potential referrals that may help you stand out in the application process.
✨Tip Number 3
Stay updated on the latest trends and changes in EU Clinical Trial Regulations. Showing that you are knowledgeable about current regulations will demonstrate your commitment and expertise in the field.
✨Tip Number 4
Prepare to discuss specific examples of your past experiences in leading regulatory strategies and successful submissions. Being able to articulate your achievements will set you apart during interviews.
We think you need these skills to ace Director of Regulatory Affairs
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Director of Global Regulatory Affairs. Understand the key responsibilities and requirements, especially the importance of strategic leadership and regulatory strategy development.
Highlight Relevant Experience: In your CV and cover letter, emphasize your extensive industry experience in Regulatory Affairs, particularly in the biotech or biopharmaceutical sectors. Provide specific examples of your interactions with global regulatory agencies like the EMA.
Showcase Leadership Skills: Demonstrate your ability to lead and direct teams effectively. Include examples of how you have successfully managed regulatory submissions and built relationships with Health Authorities.
Tailor Your Application: Customize your application materials to reflect the specific requirements of the position. Use keywords from the job description to align your experience with what the company is looking for.
How to prepare for a job interview at Pharma Partners Recruitment Ltd
✨Showcase Your Regulatory Expertise
Be prepared to discuss your extensive experience in regulatory affairs, particularly within the biotech and biopharmaceutical sectors. Highlight specific examples of successful interactions with global regulatory agencies like the EMA.
✨Demonstrate Strategic Leadership
Since this role requires strategic oversight, be ready to share instances where you have led teams or projects. Discuss how you developed and directed regulatory strategies that aligned with business goals.
✨Build Relationships with Health Authorities
Emphasize your ability to build and nurture relationships with health authorities. Prepare to talk about past experiences where you successfully navigated scientific advice meetings or other regulatory interactions.
✨Understand Clinical Trial Regulations
Familiarize yourself with the EU Clinical Trial Regulation and be ready to discuss how you have maintained compliance in clinical trial activities. This will demonstrate your knowledge and commitment to regulatory standards.
