Planet Pharma
Regulatory Affairs Manager
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Regulatory Affairs Manager – Drive Innovation and Make an Impact
Join a global leader committed to serving patients and transforming lives as a Regulatory Affairs Manager. In this pivotal role, you will oversee vital regulatory processes to support clinical trials and the launch of innovative medicinal products across Europe, making a tangible difference for millions of patients worldwide. If you thrive in a collaborative environment and are passionate about shaping the future of biopharmaceutical development, this is your opportunity to excel.
What You Will Do
- Manage regulatory submissions including clinical trial and marketing applications, ensuring compliance with global and local requirements.
- Implement and execute regional regulatory strategies, providing guidance on document preparation, meetings, and approval processes.
- Support product development by advising on regulatory mechanisms such as Fast Track, Orphan Drug, and compassionate use programs.
- Lead label negotiations and contribute to regional product strategies under supervision.
- Perform regulatory research to stay ahead of legislative changes, assessing impacts on product development.
- Collaborate with the European General Medicine Regulatory team, supporting a diverse portfolio in metabolic, cardiology, inflammation, endocrine, and bone disease areas.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Required Skills
- Scientific degree with proven experience in regulatory affairs or a similar role.
- Sound knowledge of legislation, policies, SOPs, and regulations related to medicinal products.
- Familiarity with registration procedures for clinical trials, marketing authorizations, post-approval changes, and renewals.
- Strong understanding of drug development processes and regional regulatory environments.
- Excellent communication skills—both verbal and written—with the ability to articulate complex scientific and clinical information.
- Proactive problem-solving skills and the ability to anticipate issues and develop strategic solutions.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Nice To Have Skills
- Experience with biosimilars or advanced therapy medicinal products.
- Knowledge of European and global regulatory agencies’ processes.
- Fluency in additional languages.
Preferred Education And Experience
- Advanced degree in a relevant scientific discipline.
- Several years of experience in pharmaceutical or biotech regulatory affairs within a European context.
Other Requirements
- Ability to adapt to evolving regulatory landscapes and maintain awareness of new legislation and policies.
- No travel obligations beyond occasional team meetings.
Embrace an opportunity to be part of something bigger—apply today to join a dynamic team dedicated to innovation and excellence in healthcare. Your expertise can help shape the future of medicine and improve lives around the world.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills