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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: Join a dynamic team and make a real difference in clinical research.
- Qualifications: 5+ years in clinical research with leadership experience in trials.
- Other info: Exciting challenges await in a supportive work environment.
The predicted salary is between 48000 - 72000 £ 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 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
✨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 the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of global study delivery and regulatory compliance. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your leadership skills! When discussing your experience, highlight specific examples where you’ve successfully led clinical trials or managed vendor relationships. This will help you stand out as a strong candidate.
✨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 UK CTM: CRO Oversight & Global Study Delivery
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Senior UK CTM. Highlight your experience in clinical research and any leadership roles you've had in managing clinical trials. We want to see how your background aligns with the responsibilities listed 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 integrated project team activities or managed vendor relationships in your previous roles. We love a good story!
Showcase Your Regulatory Knowledge: Since regulatory compliance is key in this role, make sure to highlight your knowledge and experience in this area. We want to know how you've navigated regulations in past projects and how you can bring that expertise to our team.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates. Plus, it’s super easy!
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 Management is Key
Since managing vendor relationships is a big part of the 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 Matters
Familiarise yourself with the latest regulations in clinical research. Be prepared to discuss how you've ensured compliance in your previous roles. This will demonstrate your commitment to maintaining high standards in clinical trials.
✨Work-Life Balance is a Priority
The job description mentions work-life balance, so be ready to talk about how you manage your time effectively. Share your strategies for maintaining productivity while ensuring you have time for personal commitments. This shows you're a well-rounded candidate.
