Career Opportunities
Join our team of regulatory experts and help accelerate the development of life-changing medicines. Build your career with industry leaders in an innovative and supportive environment.
Current Openings
Explore exciting opportunities to advance your regulatory affairs career with leading pharmaceutical and biotechnology projects.
Join Our Team
Shape the future of medicine
Regulatory Affairs Consultant - Contract (UK)
Exciting opportunity for an experienced regulatory affairs consultant to join our team on a contract basis. This is a prospective role offering flexibility in working arrangements and the chance to work on cutting-edge pharmaceutical projects. Successful applicants will be contacted when projects become available.
Requirements
- Regulatory submissions, authoring and strategy
- Experience in clinical trials submissions, MAAs, BLAs, NDAs and/or variations
- 10+ years regulatory affairs experience
- Right to work in the UK
- General regulatory affairs expertise required
- Technical skills flexible based on candidate background
- Strong communication and client management skills
Benefits
- Competitive contract rates
- Flexible full-time or part-time arrangements
- Remote working opportunity
- Work on innovative pharmaceutical projects
- Professional development opportunities
- Collaboration with industry experts
Regulatory Affairs Consultant - Contract (Global)
Exciting opportunity for an experienced regulatory affairs consultant to join our team on a contract basis. This is a prospective role offering flexibility in working arrangements and the chance to work on cutting-edge pharmaceutical projects. Successful applicants will be contacted when projects become available.
Requirements
- 10+ years regulatory affairs experience
- General regulatory affairs expertise required
- Technical skills flexible based on candidate background
- Strong communication and client management skills
- Global regulatory market experience preferred
Benefits
- Competitive contract rates
- Flexible full-time or part-time arrangements
- Remote working opportunity
- Work on innovative pharmaceutical projects
- Professional development opportunities
- Collaboration with industry experts
Business Development Manager
Drive business growth through strategic partnerships, client acquisition, and market expansion. Build relationships with pharmaceutical and biotech companies seeking regulatory consulting services.
Requirements
- 3+ years business development experience
- Pharmaceutical or life sciences background preferred
- Strong relationship building and networking skills
- Proven track record in sales and client acquisition
- Excellent communication and presentation skills
Benefits
- Competitive salary plus commission structure
- Remote working with global travel opportunities
- Professional development opportunities
- Performance bonuses
- Be part of a rapidly growing consultancy
- Shape your career and make a significant impact
Regulatory Affairs Internship (Remote)
Entry-level, part-time remote internship designed to provide hands-on experience in regulatory affairs. Gain practical experience in EU variations, US clinical trial IND authoring, marketing authorization applications, and regulatory strategy development across EU, UK, and US markets.
Requirements
- Bachelor's degree in Life Sciences, Engineering, Pharmacy, or related field
- Strong interest in regulatory affairs
- Ability to work independently and as part of a team
- Self-motivated with remote work capabilities
- Proficiency in Microsoft Office applications
Benefits
- Valuable hands-on regulatory experience
- Direct supervision from experienced professionals
- Professional reference upon completion
- Association with Introduction to Regulatory Affairs Course
- Flexible remote working arrangements
- Foundation for regulatory affairs career
Regulatory Affairs Associate (Remote)
Entry-level, part-time remote position managing various regulatory activities including regulatory intelligence projects, comprehensive documentation across EU, UK, and US markets, and ensuring compliance throughout the entire product lifecycle from clinical trials through marketing authorization applications.
Requirements
- Bachelor's degree in Life Sciences, Engineering, Pharmacy, or related field
- Strong interest in regulatory affairs and pharmaceutical industry
- Ability to work independently and collaboratively
- Self-motivated with strong remote work capabilities
- Exceptional attention to detail and problem-solving abilities
Benefits
- Remote work flexibility
- Part-time schedule for work-life balance
- Mentoring by experienced regulatory professionals
- Global accessibility
- Professional development opportunities
Senior Regulatory Affairs Manager - Gene Therapy
Lead regulatory strategy and submissions for innovative gene therapy products across EU and UK markets. Work directly with former MHRA and EMA reviewers.
Requirements
- 8+ years regulatory affairs experience
- Gene therapy or ATMP experience required
- EU and UK regulatory expertise
- Strong scientific writing skills
- PhD in Life Sciences preferred
Benefits
- Competitive salary + bonus
- Flexible working arrangements
- Professional development budget
- Health insurance
- 25 days holiday + bank holidays
CMC Regulatory Specialist
Support CMC regulatory activities for biologics and cell & gene therapies. Collaborate with manufacturing and quality teams to ensure regulatory compliance.
Requirements
- 5+ years CMC regulatory experience
- Biologics manufacturing knowledge
- Quality systems experience
- Master's degree in Chemistry or related field
- Regulatory submission experience
Benefits
- Hybrid working model
- Performance bonuses
- Training and certification support
- Pension scheme
- Career progression opportunities
Regulatory Medical Writer
Create high-quality regulatory documents for pharmaceutical and biotech clients. Focus on clinical study reports, regulatory dossiers, and scientific publications.
Requirements
- 5+ years regulatory medical writing
- Clinical research experience
- Excellent scientific writing skills
- Advanced degree in Life Sciences
- Portfolio of regulatory documents
Benefits
- Competitive daily rates
- Flexible contract terms
- Remote working
- Professional development
- Variety of exciting projects
Don't See the Right Role?
We're always looking for talented regulatory professionals. Send us your CV and we'll keep you in mind for future opportunities.
Send Your CVWhy Work With Us?
Join a team where your expertise is valued, your growth is supported, and your work makes a real difference in bringing life-changing treatments to patients.
Work with Industry Experts
Collaborate directly with former MHRA, EMA, and FDA reviewers
Cutting-Edge Projects
Work on innovative therapies including cell & gene therapy and biologics
Professional Development
Continuous learning opportunities and certification support
Flexible Working
Hybrid and remote working options to support work-life balance
Career Progression
Clear advancement pathways with mentorship and support
Competitive Rewards
Excellent compensation packages with performance bonuses
Application Process
Our recruitment process is designed to be thorough yet efficient, ensuring the right fit for both candidates and our team.
Apply Online
Submit your CV and cover letter through our application portal
Initial Screening
HR review and initial phone/video screening with our team
Skills Assessment
Complete a practical test to evaluate your knowledge and skills
Technical Interview
In-depth discussion with hiring manager
Offer & Onboarding
Receive offer and begin comprehensive onboarding program
Our Culture & Values
We foster an environment of collaboration, innovation, and continuous learning where every team member can thrive and make meaningful contributions.
Collaboration
Working together across disciplines to achieve exceptional results for our clients
Excellence
Striving for the highest standards in everything we do, from client service to professional development
Innovation
Embracing new approaches and technologies to advance regulatory science
Integrity
Maintaining the highest ethical standards in all our professional relationships
Ready to Advance Your Career?
Take the next step in your regulatory affairs career and join a team that's shaping the future of pharmaceutical development.