Explore exciting opportunities to advance your regulatory affairs career with leading pharmaceutical and biotechnology projects.
Shape the future of medicine
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.
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
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
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.
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
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
Drive business growth through strategic partnerships, client acquisition, and market expansion. Build relationships with pharmaceutical and biotech companies seeking regulatory consulting services.
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
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
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.
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
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
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.
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
Remote work flexibility
Part-time schedule for work-life balance
Mentoring by experienced regulatory professionals
Global accessibility
Professional development opportunities
Lead regulatory strategy and submissions for innovative gene therapy products across EU and UK markets. Work directly with former MHRA and EMA reviewers
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
Competitive salary + bonus
Flexible working arrangements
Professional development budget
Health insurance
25 days holiday + bank holidays
Support CMC regulatory activities for biologics and cell & gene therapies. Collaborate with manufacturing and quality teams to ensure regulatory compliance.
5+ years CMC regulatory experience
Biologics manufacturing knowledge
Quality systems experience
Master's degree in Chemistry or related field
Regulatory submission experience
Hybrid working model
Performance bonuses
Training and certification support
Pension scheme
Career progression opportunities
Create high-quality regulatory documents for pharmaceutical and biotech clients. Focus on clinical study reports, regulatory dossiers, and scientific publications.
5+ years regulatory medical writing
Clinical research experience
Excellent scientific writing skills
Advanced degree in Life Sciences
Portfolio of regulatory documents
Competitive daily rates
Flexible contract terms
Remote working
Professional development
Variety of exciting projects
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.
Collaborate directly with former MHRA, EMA, and FDA reviewers
Work on innovative therapies including cell & gene therapy and biologics
Continuous learning opportunities and certification support
Hybrid and remote working options to support work-life balance
Clear advancement pathways with mentorship and support
Excellent compensation packages with performance bonuses
Submit your CV and cover letter through our application portal
HR review and initial phone/video screening with our team
Complete a practical test to evaluate your knowledge and skills
In-depth discussion with hiring manager
Receive offer and begin comprehensive onboarding program
We foster an environment of collaboration, innovation, and continuous learning where every team member can thrive and make meaningful contributions.
Working together across disciplines to achieve exceptional results for our clients
Striving for the highest standards in everything we do, from client service to professional development
Embracing new approaches and technologies to advance regulatory science
Maintaining the highest ethical standards in all our professional relationships
Expert Regulatory Consulting
Accelerating Innovation | Delivering for Patients
Leading regulatory affairs consultancy specializing in EU and UK regulatory support for pharmaceutical and biotechnology companies
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