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- Tasks: Oversee global clinical trials and manage project team activities.
- Company: Leading clinical research organisation in the UK with a focus on innovation.
- Benefits: Work-life balance, competitive salary, and opportunities for professional growth.
- Why this job: Take on exciting challenges while making a real impact in clinical research.
- Qualifications: 5+ years in clinical research with leadership experience in trials.
- Other info: Dynamic work environment with a strong emphasis on collaboration.
The predicted salary is between 42000 - 84000 £ per year.
A leading clinical research organization in the United Kingdom is seeking a Clinical Trial Manager (CTM) to oversee study-level activities for global clinical trials. The ideal candidate will have over 5 years of experience in clinical research, with at least 2-3 years leading clinical trials.
Responsibilities include:
- Integrating project team activities
- Managing vendor relationships
- Ensuring regulatory compliance
The position offers exciting challenges while maintaining work-life balance.
Senior UK CTM: CRO Oversight & Global Study Delivery in London employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior UK CTM: CRO Oversight & Global Study Delivery in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. This shows you're genuinely interested and helps you tailor your answers to what they value most in a CTM.
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. Structure your responses around Situation, Task, Action, and Result to clearly demonstrate your experience and problem-solving skills.
✨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 take that extra step to connect with us directly.
We think you need these skills to ace Senior UK CTM: CRO Oversight & Global Study Delivery in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in clinical research and project management. We want to see how your background aligns with the role of a Senior CTM, so don’t be shy about showcasing your leadership skills and relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your experience makes you the perfect fit for our team. We love hearing personal stories that connect your journey to the role.
Showcase Your Regulatory Knowledge: Since regulatory compliance is key in this role, make sure to mention any specific experiences or certifications you have related to regulations in clinical research. We appreciate candidates who understand the importance of compliance in delivering successful trials.
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 gives you a chance to explore more about our company culture and values!
How to prepare for a job interview at Parexel International
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your knowledge of clinical trials, especially the ones you've led. Be ready to discuss specific challenges you faced and how you overcame them. This shows your depth of experience and problem-solving skills.
✨Vendor Relationships Matter
Since managing vendor relationships is key for this role, prepare examples of how you've successfully collaborated with vendors in the past. Highlight any strategies you used to ensure compliance and efficiency in your projects.
✨Regulatory Compliance is Key
Familiarise yourself with the latest regulations in clinical research. Be prepared to discuss how you've ensured compliance in previous roles. This will demonstrate your commitment to maintaining high standards in clinical trials.
✨Balance is Essential
The job description mentions work-life balance, so be ready to talk about how you manage your time and priorities. Share examples of how you've maintained a healthy balance while delivering successful projects.
