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Principal Regulatory Consultant

Barrington James

London

Hybrid

GBP 60,000 - 100,000

Full time

30+ days ago

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Job summary

An innovative global consultancy is seeking a Principal/Senior Consultant (CMC) to lead in shaping CMC strategies. This hybrid role offers the chance to provide strategic regulatory advice, oversee submissions, and mentor junior professionals. If you have a passion for navigating complex regulatory landscapes and a proven track record in drug development, this position provides a unique opportunity to influence and guide clients while contributing to business growth. Join a dynamic team where your expertise will shape the future of regulatory affairs and make a significant impact in the industry.

Qualifications

  • Minimum of 8-10 years in drug development and regulatory affairs.
  • Proven experience with FDA, EMA, and/or MHRA processes.

Responsibilities

  • Develop innovative CMC regulatory strategies and drug development plans.
  • Lead the preparation and review of regulatory documents.

Skills

Regulatory Affairs
Project Management
Leadership
Strategic Planning

Education

Advanced degree in life sciences (MSc or PhD preferred)

Job description

Are you an experienced regulatory professional ready to take the lead in shaping innovative CMC strategies? Barrington James is recruiting for a Principal/Senior Consultant (CMC) to join a dynamic and growing global consultancy. This is a hybrid role based in London, United Kingdom, with a flexible schedule and monthly office visits. If you're passionate about guiding clients through complex regulatory landscapes while mentoring the next generation of experts, we want to hear from you!


Minimum of 8 years experience required


In this role, you'll provide strategic and technical regulatory advice to clients, focusing on CMC (Chemistry, Manufacturing, and Controls) aspects of product development. You'll also oversee regulatory submissions, guide multi-jurisdictional projects, and manage client relationships. Additionally, you'll play a key role in mentoring junior team members and contributing to business development efforts.


Responsibilities
  • Develop innovative CMC regulatory strategies, gap analyses, and drug development plans.
  • Lead the preparation, authoring, and review of regulatory documents (INDs, IMPDs, MAAs, etc.).
  • Represent clients in regulatory agency interactions, addressing objections and negotiating outcomes.
  • Oversee project timelines, budgets, and deliverables, ensuring high-quality outcomes.
  • Mentor and manage team members, providing training and technical leadership.
  • Contribute to business development through client relationships and identifying new opportunities.
  • Stay ahead of regulatory trends and ensure compliance with evolving standards.

Requirements
  • Senior Consultant: 8+ years in drug development and regulatory affairs.
  • Principal Consultant: 10+ years in drug development and regulatory affairs.
  • Proven experience with FDA, EMA, and/or MHRA processes, including submissions and negotiations.
  • Expertise in biologics, ATMPs, vaccines, or small molecules.
  • Advanced degree in life sciences (MSc or PhD preferred).
  • Strong leadership, organizational, and time management skills.
  • Willingness to travel occasionally and work flexible hours.

To apply, please contact:
kwilson@barringtonjames.com
Direct line: +44 1293 223 951

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