Vice President, Regulatory in London

Vice President, Regulatory in London

London Full-Time 120000 - 150000 £ / year (est.) Home office (partial)
BioTalent

At a Glance

  • Tasks: Lead innovative clinical programmes in a fast-paced biotech environment.
  • Company: Dynamic biotechnology company focused on cell-based therapies.
  • Benefits: Competitive salary, hybrid work model, and opportunities for professional growth.
  • Other info: Join a collaborative team dedicated to innovation and excellence.
  • Why this job: Shape the future of healthcare with cutting-edge science and impactful therapies.
  • Qualifications: Medical degree and significant drug development experience required.

The predicted salary is between 120000 - 150000 £ per year.

This is a senior leadership opportunity within a well-funded, clinical-stage biotechnology company advancing innovative cell-based therapies. The organisation is developing a differentiated pipeline across areas of high unmet medical need, with a focus on translating cutting-edge science into clinically meaningful outcomes.

You will play a central role in shaping and delivering a key clinical programme, working in a highly collaborative and fast-paced environment at the intersection of research, clinical development, and manufacturing.

As Executive Director, Clinical Development, you will be responsible for the strategic leadership and execution of a clinical-stage programme, guiding it from early development through to late-stage planning. This position requires a strong scientific foundation, strategic thinking, and the ability to operate effectively across cross-functional teams. You will contribute to defining the development pathway, ensuring alignment with regulatory expectations and broader business objectives.

Key Responsibilities
  • Lead the development strategy for a novel cell therapy programme across clinical stages
  • Drive programme planning, prioritisation, and execution to optimise development timelines and value
  • Design and oversee clinical studies, including protocols, endpoints, and operational delivery
  • Provide medical and scientific oversight of clinical data, including safety and efficacy interpretation
  • Contribute to longer-term development planning, supporting future regulatory submissions
  • Collaborate closely with cross-functional teams including research, regulatory, CMC, and commercial functions
  • Ensure integration of clinical and translational insights into development strategy
  • Maintain awareness of the external scientific and competitive landscape
  • Engage with external experts, investigators, and key stakeholders to inform programme development
  • Represent the organisation in interactions with regulatory authorities and at scientific forums
  • Build and lead a high-performing clinical development team
  • Promote a culture of innovation, accountability, and collaboration
Key Requirements
  • Medical degree (MD or equivalent)
  • Significant experience in drug development within biotech or pharmaceutical settings
  • Demonstrated leadership in advancing therapies through clinical development
  • Experience in complex disease areas is advantageous but not essential
  • Strong understanding of clinical trial design, regulatory considerations, and translational science
  • Ability to balance scientific innovation with strategic and commercial considerations
  • Excellent communication, leadership, and stakeholder management skills

If you are interested and would like to find out more details, please submit your application or reach out to.

Vice President, Regulatory in London employer: BioTalent

Join a pioneering biotechnology company in London, where innovation meets collaboration in the development of cutting-edge cell-based therapies. As a Vice President, Regulatory, you will thrive in a dynamic work culture that prioritises employee growth and fosters a spirit of accountability and teamwork. With a strong focus on advancing medical science, this role offers unique opportunities to shape impactful clinical programmes while enjoying the benefits of a hybrid working environment.

BioTalent

Contact Details:

BioTalent Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Vice President, Regulatory in London

Tip Number 1

Network like a pro! Reach out to industry contacts on LinkedIn or attend relevant events. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream role.

Tip Number 2

Prepare for interviews by researching the company and its pipeline. We want you to be able to discuss how your experience aligns with their goals, especially in innovative cell-based therapies. Show them you’re not just another candidate!

Tip Number 3

Practice your pitch! You’ll want to clearly articulate your leadership experience and how you’ve driven clinical programmes in the past. We suggest rehearsing with a friend or in front of a mirror to boost your confidence.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Vice President, Regulatory in London

Strategic Leadership
Clinical Development
Drug Development
Clinical Trial Design
Regulatory Considerations
Translational Science
Stakeholder Management

Some tips for your application 🫡

Tailor Your CV:Make sure your CV reflects the specific skills and experiences that align with the role of Executive Director, Clinical Development. Highlight your leadership in drug development and any relevant clinical trial experience to catch our eye!

Craft a Compelling Cover Letter:Your cover letter is your chance to tell us why you're the perfect fit for this role. Share your passion for innovative therapies and how your background in biotech can contribute to our mission. Keep it engaging and personal!

Showcase Your Collaborative Spirit:Since this role involves working closely with cross-functional teams, make sure to highlight examples of successful collaboration in your application. We love seeing how you’ve worked with others to achieve common goals!

Apply Through Our Website:We encourage you to submit your application through our website for the best chance of being noticed. It’s straightforward and ensures your application goes directly to our hiring team. Don’t miss out on this opportunity!

How to prepare for a job interview at BioTalent

Know Your Science

Make sure you have a solid grasp of the scientific principles behind cell-based therapies. Brush up on recent advancements in the field and be ready to discuss how they relate to the company's pipeline. This will show your passion and expertise.

Demonstrate Strategic Thinking

Prepare examples that showcase your ability to think strategically about clinical development. Think about how you've previously led programmes from early development to late-stage planning, and be ready to share these experiences during the interview.

Showcase Leadership Skills

As a senior role, they’ll want to see your leadership style. Be prepared to discuss how you've built and led high-performing teams in the past. Highlight your approach to fostering collaboration and innovation within cross-functional teams.

Engage with Regulatory Insights

Familiarise yourself with the regulatory landscape relevant to the company’s work. Be ready to discuss how you’ve navigated regulatory challenges in previous roles and how you plan to engage with regulatory authorities effectively.