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- Tasks: Lead regulatory operations for cancer trials, ensuring compliance and improving processes.
- Company: A top cancer trials centre dedicated to innovative research.
- Benefits: Competitive salary, hybrid working, and opportunities for professional growth.
- Why this job: Make a real difference in cancer research while leading a passionate team.
- Qualifications: Extensive knowledge of clinical trials regulations and leadership experience.
The predicted salary is between 48000 - 72000 £ per year.
A leading cancer trials center is seeking an experienced Clinical Trials Operations Manager (Regulatory) to provide strategic operational leadership across its regulatory-critical functions. This senior role involves ensuring compliance with GCP, MHRA, and HRA requirements while improving systems and processes.
The ideal candidate will have high-level knowledge of clinical trials regulations, experience in leading teams, and a pragmatic approach to operational challenges. Competitive salary and hybrid working conditions are offered.
Senior Regulatory Trials Operations Leader employer: UCL
Contact Detail:
UCL Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Trials Operations Leader
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trials field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP, MHRA, and HRA requirements. We want you to be able to discuss these topics confidently, showing that you’re not just familiar but also passionate about compliance and operational excellence.
✨Tip Number 3
Showcase your leadership skills! When chatting with potential employers, share specific examples of how you've led teams through regulatory challenges. This will highlight your experience and pragmatic approach to problem-solving.
✨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 and engaged with our platform.
We think you need these skills to ace Senior Regulatory Trials Operations Leader
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical trials operations and regulatory compliance. We want to see how your background aligns with the specific requirements mentioned in the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've led teams and tackled operational challenges in the past.
Showcase Your Knowledge: Demonstrate your understanding of GCP, MHRA, and HRA requirements in your application. We’re looking for someone who knows their stuff and can navigate the regulatory landscape with ease.
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 during the process!
How to prepare for a job interview at UCL
✨Know Your Regulations
Make sure you brush up on GCP, MHRA, and HRA requirements before the interview. Being able to discuss these regulations confidently will show that you’re not just familiar with them but can also apply them in a practical setting.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led teams in previous roles. Think about specific challenges you faced and how you overcame them. This will demonstrate your ability to provide strategic operational leadership.
✨Be Process-Oriented
Since the role involves improving systems and processes, come ready with ideas or examples of how you've enhanced operational efficiency in past positions. This shows that you have a proactive mindset and are focused on continuous improvement.
✨Ask Insightful Questions
Prepare thoughtful questions about the centre's current regulatory challenges or their approach to compliance. This not only shows your interest in the role but also your understanding of the complexities involved in clinical trials operations.
