Senior Clinical Research Associate - Site Monitoring in Reading
Senior Clinical Research Associate - Site Monitoring

Senior Clinical Research Associate - Site Monitoring in Reading

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

  • Tasks: Conduct site monitoring visits and manage study progress for clinical research.
  • Company: Leading global provider of clinical research services based in Reading, UK.
  • Benefits: Career with purpose, impact, and opportunities for professional growth.
  • Why this job: Make a difference in healthcare while ensuring compliance and quality.
  • Qualifications: Life science degree and experience in on-site monitoring required.
  • Other info: Join a dynamic team dedicated to advancing clinical research.

The predicted salary is between 36000 - 60000 £ per year.

A leading global provider of clinical research services is seeking an experienced Clinical Research Associate in Reading, UK. The role involves performing site monitoring visits, managing study progress, and ensuring compliance with regulatory requirements.

Ideal candidates will have:

  • a life science degree,
  • experience in on-site monitoring,
  • a strong understanding of GCP and ICH guidelines.

This position offers a career with purpose and impact.

Senior Clinical Research Associate - Site Monitoring in Reading employer: IQVIA

As a leading global provider of clinical research services, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in the healthcare sector. Located in Reading, UK, we offer competitive benefits, continuous professional development opportunities, and a supportive environment that values work-life balance, making us an excellent employer for those looking to advance their careers in clinical research.
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Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Clinical Research Associate - Site Monitoring in Reading

✨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 a lead 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 that you’re not just familiar with the rules, but that you live and breathe them!

✨Tip Number 3

Showcase your site monitoring experience! Be ready to share specific examples of how you've managed study progress and ensured compliance during your visits. This is your chance to shine and demonstrate your impact in previous roles.

✨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 directly with us.

We think you need these skills to ace Senior Clinical Research Associate - Site Monitoring in Reading

Site Monitoring
Regulatory Compliance
GCP (Good Clinical Practice)
ICH Guidelines
Life Science Degree
Study Management
Attention to Detail
Communication Skills
Problem-Solving Skills
Project Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in site monitoring and your understanding of GCP and ICH guidelines. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!

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

Showcase Your Life Science Degree: Since a life science degree is essential for this role, make sure to mention it prominently in your application. We’re looking for candidates who have a solid foundation in the sciences, so let us know how your education has prepared you for this position.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates from us. Plus, it’s super easy!

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 Council for Harmonisation (ICH) guidelines. Be ready to discuss how you've applied these in your previous roles, as this will show your understanding and commitment to compliance.

✨Showcase Your Monitoring Experience

Prepare specific examples from your past site monitoring visits. Highlight challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for the role.

✨Understand the Company’s Impact

Research the company’s mission and recent projects. Being able to articulate how their work aligns with your values and career goals will set you apart. It shows that you’re not just looking for a job, but a purpose-driven career.

✨Ask Insightful Questions

Prepare thoughtful questions about the role and the company’s future projects. This not only shows your interest but also helps you gauge if the company is the right fit for you. Think about what you want to know regarding study progress management and team dynamics.

Senior Clinical Research Associate - Site Monitoring in Reading
IQVIA
Location: Reading
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  • Senior Clinical Research Associate - Site Monitoring in Reading

    Reading
    Full-Time
    36000 - 60000 £ / year (est.)
  • I

    IQVIA

    10000+
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