Senior Director Regulatory Affairs, null
Senior Director Regulatory Affairs, null

Senior Director Regulatory Affairs, null

Full-Time 54000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory strategy and manage early development projects in a dynamic CRO.
  • Company: Join an exciting, growing CRO with an international and motivated team.
  • Benefits: Enjoy a market-leading salary, work-life balance, and impactful daily contributions.
  • Why this job: This role offers the chance to leverage your expertise in a vibrant, evolving environment.
  • Qualifications: Minimum 8 years of regulatory affairs experience in consulting or pharmaceuticals required.
  • Other info: EU work permit is necessary for this position.

The predicted salary is between 54000 - 84000 £ per year.

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Senior Director Regulatory Affairs

Client:

Location:

United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

3dede2ae3f5d

Job Views:

7

Posted:

03.03.2025

Expiry Date:

17.04.2025

Job Description:

Your new company

This is an exciting and growing CRO. You will be working in an international, energetic, motivated team. A dynamic and growing organisation.

Your new role

They are looking for a minimum of 8 years of regulatory affairs experience in consulting or the pharmaceutical industry. They want this professional to have experience with early development projects, including PIPs, ODDs, authority meetings and MAAs under the centralized procedure. In this role, they would love you to hit the ground running and to be able to bring a wealth of expertise.

What you’ll need to succeed

You will need to be a highly motivated and open-minded personality, able to work in an international environment. This company wants you to be able to lead and execute a consistent regulatory strategy.

What you’ll get in return

Market leading salary, a work-life balance and the opportunity to make a significant daily impact in a growing CRO.

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Senior Director Regulatory Affairs, null employer: TN United Kingdom

Join a dynamic and growing CRO in the United Kingdom, where you will be part of an international and motivated team dedicated to making a significant impact in the regulatory affairs landscape. With a market-leading salary, a strong emphasis on work-life balance, and ample opportunities for professional growth, this company is committed to fostering a supportive work culture that values expertise and innovation.
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Contact Detail:

TN United Kingdom Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Director Regulatory Affairs, null

✨Tip Number 1

Make sure to highlight your extensive experience in regulatory affairs, especially with early development projects. This will show that you can hit the ground running and bring valuable expertise to the team.

✨Tip Number 2

Network with professionals in the CRO and pharmaceutical industry. Engaging with others in your field can provide insights into the company culture and may even lead to referrals.

✨Tip Number 3

Prepare to discuss specific examples of how you've successfully led regulatory strategies in previous roles. This will demonstrate your capability to execute a consistent regulatory strategy effectively.

✨Tip Number 4

Familiarize yourself with the latest trends and regulations in the industry. Showing that you are up-to-date will reflect your motivation and commitment to the role.

We think you need these skills to ace Senior Director Regulatory Affairs, null

Regulatory Affairs Expertise
Pharmaceutical Industry Knowledge
Experience with Early Development Projects
Knowledge of PIPs and ODDs
Authority Meeting Management
MAA Submission Experience
Centralized Procedure Familiarity
Strategic Planning Skills
Leadership Abilities
International Collaboration
Strong Communication Skills
Problem-Solving Skills
Adaptability in Dynamic Environments
Motivational Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your regulatory affairs experience, especially in consulting or the pharmaceutical industry. Emphasize your work on early development projects, PIPs, ODDs, authority meetings, and MAAs.

Craft a Compelling Cover Letter: Write a cover letter that showcases your motivation and open-minded personality. Discuss how your expertise aligns with the company's needs and how you can contribute to their regulatory strategy.

Highlight International Experience: Since the role requires working in an international environment, be sure to mention any relevant international experience or cross-cultural skills that demonstrate your ability to thrive in diverse teams.

Proofread Your Application: Before submitting, carefully proofread your application materials for any errors or inconsistencies. A polished application reflects your attention to detail and professionalism.

How to prepare for a job interview at TN United Kingdom

✨Showcase Your Regulatory Expertise

Make sure to highlight your extensive experience in regulatory affairs, especially with early development projects. Be prepared to discuss specific examples of PIPs, ODDs, and MAAs you've worked on.

✨Demonstrate Leadership Skills

Since the role requires leading a regulatory strategy, be ready to share instances where you've successfully led teams or projects. Emphasize your ability to motivate and guide others in an international setting.

✨Be Open-Minded and Adaptable

The company values open-mindedness, so express your willingness to embrace new ideas and adapt to changing environments. Share experiences that showcase your flexibility and innovative thinking.

✨Prepare for Authority Meetings

Given the importance of authority meetings in this role, prepare to discuss your approach to these interactions. Highlight any successful outcomes from past meetings and how you navigated challenges.

Senior Director Regulatory Affairs, null
TN United Kingdom
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  • Senior Director Regulatory Affairs, null

    Full-Time
    54000 - 84000 £ / year (est.)

    Application deadline: 2027-03-13

  • T

    TN United Kingdom

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