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- Tasks: Monitor clinical sites and ensure compliance with study protocols.
- Company: Global leader in clinical research with a focus on innovation.
- Benefits: Full-time hours, competitive salary, and opportunities for professional growth.
- Why this job: Join a dynamic team making a difference in healthcare research.
- Qualifications: 2+ years of monitoring experience and a degree in science or healthcare.
- Other info: Based in Reading, Berkshire with a supportive work environment.
The predicted salary is between 36000 - 60000 £ per year.
A global clinical research provider is seeking experienced Senior Clinical Research Associates in the UK. This role involves performing monitoring and site management to ensure compliance with study protocols.
Candidates should have at least 2 years of on-site monitoring experience and a Bachelor's degree in a scientific discipline or healthcare. Proficiency in GCP and ICH guidelines, alongside strong communication skills, is essential.
The position offers full-time hours and is based in Reading, Berkshire.
Senior CRA - UK Site Monitoring & Study Oversight in London employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior CRA - UK Site Monitoring & Study Oversight 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 a Senior CRA role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how you've applied these in your previous roles. We want to see you shine and show that you’re the perfect fit for ensuring compliance with study protocols!
✨Tip Number 3
Practice your communication skills! As a Senior CRA, you'll need to convey complex information clearly. Try mock interviews with friends or colleagues to get comfortable discussing your experience and how it relates to site monitoring.
✨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. Let’s get you that Senior CRA position!
We think you need these skills to ace Senior CRA - UK Site Monitoring & Study Oversight in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in on-site monitoring and site management. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills in GCP and ICH guidelines!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your experience makes you the perfect fit for our team. Keep it concise but impactful!
Showcase Your Communication Skills: Strong communication is key in this role. In your application, give examples of how you've effectively communicated with teams or stakeholders in past projects. We love seeing real-life examples!
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’s super easy to do!
How to prepare for a job interview at IQVIA LLC
✨Know Your Stuff
Make sure you brush up on your knowledge of GCP and ICH guidelines. Being able to discuss these in detail will show that you’re not just familiar with them, but that you truly understand their importance in clinical research.
✨Showcase Your Experience
Prepare specific examples from your past monitoring experiences. Think about challenges you faced and how you overcame them. This will help demonstrate your problem-solving skills and your ability to ensure compliance with study protocols.
✨Communicate Clearly
Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and qualifications.
✨Research the Company
Take some time to learn about the global clinical research provider you’re interviewing with. Understanding their values, mission, and recent projects can help you tailor your responses and show genuine interest in the role.
