CRA II: Field Monitoring & Study Execution in Reading
CRA II: Field Monitoring & Study Execution

CRA II: Field Monitoring & Study Execution in Reading

Reading Full-Time 35000 - 45000 £ / year (est.) No home office possible
IQVIA

At a Glance

  • Tasks: Conduct site monitoring visits and manage clinical project executions.
  • Company: Join IQVIA, a leader in clinical research and innovation.
  • Benefits: Competitive salary, travel opportunities, and professional growth.
  • Other info: Flexible travel and dynamic work environment await you.
  • Why this job: Make a difference in healthcare by ensuring compliance and quality.
  • Qualifications: Life science degree and independent monitoring experience required.

The predicted salary is between 35000 - 45000 £ per year.

IQVIA is seeking experienced Clinical Research Associates (CRA II and Senior CRA 1) across the UK to strengthen our cFSP sponsor‑dedicated team. The role involves performing site monitoring visits, managing project executions, and ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Candidates should have:

  • Independent monitoring experience
  • A life science degree or equivalent
  • Flexibility to travel

This position is not eligible for UK visa sponsorship.

CRA II: Field Monitoring & Study Execution in Reading employer: IQVIA

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for advancement within the clinical research field. Located across the UK, our teams benefit from a supportive environment that values flexibility and work-life balance, making it an ideal place for professionals seeking meaningful and rewarding careers in clinical research.
IQVIA

Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CRA II: Field Monitoring & Study Execution in Reading

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly.

✨Tip Number 2

Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss your independent monitoring experience confidently. We recommend practising common interview questions with a friend or using mock interview tools to get comfortable.

✨Tip Number 3

Showcase your flexibility! Since travel is part of the gig, be ready to discuss your availability and willingness to go the extra mile. Highlight any previous experiences where you successfully managed travel for site visits.

✨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 the initiative to connect with us directly.

We think you need these skills to ace CRA II: Field Monitoring & Study Execution in Reading

Site Monitoring
Project Management
Good Clinical Practice (GCP)
International Conference on Harmonization (ICH) Guidelines
Independent Monitoring Experience
Life Science Degree or Equivalent
Flexibility to Travel
Attention to Detail

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research and monitoring. We want to see how your background aligns with the CRA II role, so don’t be shy about showcasing your skills!

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 you can contribute to our team. Keep it concise but impactful – we love a good story!

Showcase Your Flexibility: Since this role involves travel, let us know about your flexibility and willingness to adapt. Share any previous experiences where you’ve successfully managed travel for work – it’ll make you stand out!

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 – just a few clicks!

How to prepare for a job interview at IQVIA

✨Know Your GCP and ICH Guidelines

Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these in detail will show that you’re not just familiar with them, but that you understand their importance in clinical research.

✨Highlight Your Monitoring Experience

Prepare specific examples from your previous roles where you successfully conducted site monitoring visits. Discuss challenges you faced and how you overcame them, as this will demonstrate your independent monitoring experience and problem-solving skills.

✨Show Flexibility and Travel Readiness

Since the role requires travel, be ready to discuss your availability and willingness to travel for site visits. Share any past experiences where you managed travel effectively while maintaining project timelines.

✨Ask Insightful Questions

Prepare thoughtful questions about the team dynamics, project expectations, and company culture. This not only shows your interest in the role but also helps you gauge if the company is the right fit for you.

CRA II: Field Monitoring & Study Execution in Reading
IQVIA
Location: Reading

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