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- Tasks: Maintain clinical documentation and support trial logistics in a dynamic environment.
- Company: Leading global provider of clinical research services, recognised as a top employer.
- Benefits: Hybrid working model, competitive salary, and opportunities for career advancement.
- Why this job: Join a team making a real difference in clinical research and patient care.
- Qualifications: Prior clinical trials experience and a degree in life sciences required.
- Other info: Exciting opportunity to grow in a supportive and innovative company.
The predicted salary is between 36000 - 60000 £ per year.
A leading global provider of clinical research services is seeking a Senior Clinical Trials Assistant to join their cFSP team. The role involves maintaining clinical documentation, supporting trial logistics, and ensuring compliance with regulatory standards.
Candidates should have prior clinical trials experience and a degree in life sciences. The position offers a hybrid working model based three days a week in Bedfordshire, England. This is an exciting opportunity in a company recognized as a top employer.
Senior Clinical Trials Coordinator (Hybrid UK) in Reading employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Trials Coordinator (Hybrid UK) in Reading
✨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 a lead or can put in a good word for you.
✨Tip Number 2
Prepare for those interviews! Research the company and its cFSP team thoroughly. Be ready to discuss how your previous experience aligns with their needs, especially around maintaining clinical documentation and ensuring compliance.
✨Tip Number 3
Showcase your skills! Bring along examples of your past work in clinical trials to demonstrate your expertise. Whether it’s managing trial logistics or navigating regulatory standards, let your experience shine.
✨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 Clinical Trials Coordinator (Hybrid UK) in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical trials. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about this opportunity and how your experience makes you the perfect fit for our cFSP team. Keep it engaging and personal.
Showcase Your Compliance Knowledge: Since ensuring compliance with regulatory standards is key, make sure to mention any specific experiences or training you have in this area. We love candidates who understand the importance of following the rules!
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 from our team!
How to prepare for a job interview at IQVIA
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your clinical trials knowledge. Familiarise yourself with the latest regulations and compliance standards in the industry. Being able to discuss specific trials you've worked on and how you ensured documentation accuracy will impress the interviewers.
✨Showcase Your Organisational Skills
As a Senior Clinical Trials Coordinator, you'll need to juggle multiple tasks. Prepare examples of how you've successfully managed trial logistics in the past. Highlight any tools or systems you used to keep everything on track, as this will demonstrate your ability to handle the role's demands.
✨Emphasise Team Collaboration
This role involves working closely with various teams. Be ready to share experiences where you collaborated effectively with others, whether it was coordinating with investigators or liaising with regulatory bodies. This shows that you can thrive in a team-oriented environment.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the company’s approach to trial management or how they support their staff in staying compliant with evolving regulations. This not only shows your interest but also your proactive attitude towards the role.
