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- Tasks: Lead regulatory strategy for clinical trials and ensure compliance with regulations.
- Company: Top clinical research organisation in the UK, focused on oncology and rare diseases.
- Benefits: Remote work flexibility, competitive salary, and opportunities for travel.
- Why this job: Make a difference in clinical trials while working in a dynamic and impactful environment.
- Qualifications: 5-7 years of regulatory experience and strong interpersonal skills.
- Other info: Exciting career growth opportunities in a fast-paced industry.
The predicted salary is between 48000 - 72000 £ per year.
A leading clinical research organization in the UK is seeking a Regulatory Manager / Senior Regulatory Manager. The role focuses on providing regulatory strategy and guidance for clinical trials, ensuring compliance with applicable regulations, and preparing high-quality regulatory submissions.
Ideal candidates will have at least 5 to 7 years of regulatory experience, a relevant Bachelor's degree, and strong interpersonal skills. This is a remote position with potential travel involved, in a dynamic environment focused on oncology and rare diseases.
Senior Regulatory Lead – Clinical Trials (Remote UK) employer: Precision For Medicine
Contact Detail:
Precision For Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Lead – Clinical Trials (Remote UK)
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical trials space on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for those interviews! Research the company and its recent projects, especially in oncology and rare diseases. We want you to show them you’re not just another candidate, but someone who’s genuinely interested in their mission.
✨Tip Number 3
Practice your pitch! You’ll want to clearly articulate your regulatory experience and how it aligns with the role. We suggest rehearsing with a friend or in front of a mirror to boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace Senior Regulatory Lead – Clinical Trials (Remote UK)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your regulatory experience, especially in clinical trials. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills and achievements!
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 rare diseases. We love seeing candidates who can convey their enthusiasm and fit for our dynamic environment.
Showcase Your Interpersonal Skills: Since this role involves collaboration, make sure to highlight your interpersonal skills in your application. We value teamwork and communication, so share examples of how you've successfully worked with others in past roles.
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’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Precision For Medicine
✨Know Your Regulations
Make sure you brush up on the latest regulations related to clinical trials, especially those relevant to oncology and rare diseases. Being able to discuss specific guidelines and how they apply to your previous experiences will show that you're not just familiar with the rules but can also navigate them effectively.
✨Showcase Your Experience
Prepare to discuss your past regulatory submissions in detail. Highlight any challenges you faced and how you overcame them. This will demonstrate your problem-solving skills and your ability to ensure compliance under pressure, which is crucial for this role.
✨Emphasise Interpersonal Skills
Since this role requires strong interpersonal skills, think of examples where you've successfully collaborated with cross-functional teams or communicated complex regulatory information to non-experts. This will help illustrate your ability to work in a dynamic environment and build relationships.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to regulatory strategy and their current projects in oncology and rare diseases. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.
