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- Tasks: Lead regulatory activities for oncology clinical trials across Europe.
- Company: Global CRO dedicated to advancing cancer research.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Why this job: Make a real difference in cancer research while working from anywhere.
- Qualifications: 4+ years of EU regulatory experience in the pharmaceutical industry.
- Other info: Join a passionate team committed to clinical trial advancements.
The predicted salary is between 36000 - 60000 £ per year.
A global CRO is seeking a Regulatory Affairs Manager for a remote role based in the UK or Sweden. This full-time position involves leading regulatory activities for oncology clinical trials across Europe. Candidates must have substantial EU regulatory experience, ideally with 4+ years in the pharmaceutical industry. The newly appointed manager will handle CTA submissions and provide expert guidance on evolving regulations. This is an opportunity to contribute significantly to cancer research and clinical trial advancements.
Remote EU Regulatory Affairs Manager – Oncology Trials employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Remote EU Regulatory Affairs Manager – Oncology Trials
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs space, especially those working in oncology. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on the latest EU regulations related to oncology trials. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and confidence during the interview.
✨Tip Number 3
Don’t just apply anywhere—focus on companies that align with your values and career goals. Check out our website for openings that match your skills, and tailor your approach to each company’s mission in cancer research.
✨Tip Number 4
Follow up after interviews! A simple thank-you email can go a long way in keeping you top of mind. Share a brief insight or idea related to the discussion to show your enthusiasm and commitment to the role.
We think you need these skills to ace Remote EU Regulatory Affairs Manager – Oncology Trials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in EU regulatory affairs, especially in oncology. We want to see how your background aligns with the role, so don’t be shy about showcasing your 4+ years in the pharmaceutical industry!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs in oncology and how you can contribute to our mission. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Knowledge of Regulations: Since this role involves navigating evolving regulations, make sure to mention any specific regulations or guidelines you’re familiar with. We’re looking for someone who can hit the ground running, so let us know how you stay updated on changes in the field.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at RBW Consulting
✨Know Your Regulations
Make sure you brush up on the latest EU regulations related to oncology trials. Being able to discuss specific guidelines and how they impact clinical trial applications will show that you're not just familiar with the basics, but that you’re genuinely engaged with the field.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles where you successfully managed CTA submissions or navigated complex regulatory landscapes. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your achievements.
✨Stay Updated on Industry Trends
Familiarise yourself with current trends in oncology research and regulatory changes. Mentioning recent developments during your interview can demonstrate your proactive approach and passion for the industry, making you a more attractive candidate.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to regulatory affairs and their vision for oncology trials. This not only shows your interest in the role but also helps you gauge if the company aligns with your career goals.
