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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 a relevant Bachelor's degree.
- Other info: Join a team dedicated to advancing healthcare through innovative research.
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) in London 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) in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical trials field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Senior Regulatory Lead role.
✨Tip Number 2
Prepare for interviews by brushing up on your regulatory knowledge and recent developments in oncology and rare diseases. We recommend practising common interview questions with a friend to boost your confidence and ensure you shine during the real deal.
✨Tip Number 3
Showcase your interpersonal skills! During interviews, share examples of how you've effectively communicated with teams or stakeholders in past roles. We want to see how you can bring that collaborative spirit to our dynamic environment.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Senior Regulatory Lead – Clinical Trials (Remote UK) in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights 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 connect their personal motivations to our mission.
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 the past.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and we’ll be able to review your application more efficiently. Don’t miss out on this opportunity!
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 in 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.
✨Interpersonal Skills Matter
Since this role requires strong interpersonal skills, think of examples where you've successfully collaborated with cross-functional teams. Be ready to share how you’ve built relationships with stakeholders and navigated differing opinions to achieve regulatory goals.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to regulatory strategy and their focus on oncology and rare diseases. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.
