Senior CRA - UK Site Monitoring & Study Oversight
Senior CRA - UK Site Monitoring & Study Oversight

Senior CRA - UK Site Monitoring & Study Oversight

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Monitor clinical sites and ensure compliance with study protocols.
  • Company: Global leader in clinical research with a commitment to innovation.
  • Benefits: Full-time hours, competitive salary, and opportunities for professional growth.
  • Why this job: Join a dynamic team making a real difference in healthcare research.
  • Qualifications: 2+ years of monitoring experience and a degree in a scientific or healthcare field.
  • 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 employer: IQVIA LLC

As a leading global clinical research provider, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. Located in the vibrant town of Reading, Berkshire, we offer competitive benefits, ongoing professional development opportunities, and a commitment to work-life balance, making us an exceptional employer for those seeking a meaningful career in clinical research.
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Contact Detail:

IQVIA LLC Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior CRA - UK Site Monitoring & Study Oversight

✨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 Senior CRA roles. 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 site monitoring and study oversight!

✨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 aligns with the job requirements.

✨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

On-site Monitoring Experience
Bachelor's Degree in a Scientific Discipline or Healthcare
GCP Proficiency
ICH Guidelines Knowledge
Site Management Skills
Compliance with Study Protocols
Strong Communication Skills
Attention to Detail

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 communication skills can benefit our team. Keep it concise but impactful – we love a good story!

Showcase Your Experience: When detailing your experience, focus on specific examples that demonstrate your compliance with study protocols. We’re looking for candidates who can clearly articulate their contributions and successes in previous roles.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. 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 LLC

✨Know Your GCP and ICH Guidelines

Make sure you brush up on Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines before the interview. 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 Monitoring Experience

Prepare specific examples from your past monitoring experiences that highlight your skills and successes. Think about challenges you faced and how you overcame them, as well as any improvements you made to site management processes. This will demonstrate your hands-on expertise.

✨Communicate Clearly and Confidently

Strong communication skills are essential for this role, so practice articulating your thoughts clearly. You might want to do a mock interview with a friend or colleague to get comfortable discussing your experience and answering common interview questions.

✨Research the Company

Take some time to learn about the global clinical research provider you’re interviewing with. Understanding their mission, values, and recent projects can help you tailor your responses and show genuine interest in the role and the company.

Senior CRA - UK Site Monitoring & Study Oversight
IQVIA LLC

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