Senior CRA – UK Onsite Monitoring in London
Senior CRA – UK Onsite Monitoring

Senior CRA – UK Onsite Monitoring in London

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

  • Tasks: Conduct site monitoring visits and boost recruitment for clinical trials.
  • Company: Leading global clinical research provider in the UK.
  • Benefits: Full-time role with opportunities for personal and professional growth.
  • Why this job: Join an innovative environment and make a real difference in clinical research.
  • Qualifications: 6 months of independent monitoring experience and a life science degree.
  • Other info: Ideal for those passionate about advancing healthcare through research.

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

A leading global clinical research provider in the UK is seeking an Experienced Clinical Research Associate to perform site monitoring visits and enhance recruitment efforts for clinical trials.

Ideal candidates will have:

  • At least 6 months of independent monitoring experience
  • A deep understanding of Good Clinical Practice (GCP)
  • A life science degree

This full-time role offers significant opportunities for personal and professional growth in an innovative environment.

Senior CRA – UK Onsite Monitoring in London employer: IQVIA LLC

As a leading global clinical research provider, we pride ourselves on fostering a dynamic and supportive work culture that prioritises employee development and innovation. Our team members benefit from comprehensive training programmes, opportunities for career advancement, and the chance to make a meaningful impact in the field of clinical research, all while working in the vibrant UK healthcare landscape.
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Contact Detail:

IQVIA LLC Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior CRA – UK Onsite Monitoring 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 opportunities. You never know who might have a lead on a Senior CRA position or can refer you directly.

Tip Number 2

Prepare for those interviews! Brush up on your GCP knowledge and be ready to discuss your independent monitoring experiences. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.

Tip Number 3

Showcase your passion for clinical trials! During interviews, share specific examples of how you've contributed to recruitment efforts or improved site monitoring processes. This will help you stand out as a candidate who truly cares about the work.

Tip Number 4

Don't forget to apply through our website! We make it super easy for you to find and apply for roles like the Senior CRA position. Plus, it shows you're serious about joining our innovative team!

We think you need these skills to ace Senior CRA – UK Onsite Monitoring in London

Site Monitoring
Clinical Trials
Good Clinical Practice (GCP)
Independent Monitoring Experience
Life Science Degree
Recruitment Strategies
Regulatory Compliance
Data Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your independent monitoring experience and understanding of Good Clinical Practice (GCP). We want to see how your background aligns with the role, so don’t be shy about showcasing your life science degree and relevant 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. We love seeing candidates who are genuinely excited about the role and our mission.

Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just listing duties. We want to know how you’ve made an impact in your previous roles, especially in enhancing recruitment efforts for clinical trials.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you’re considered for this exciting opportunity with us!

How to prepare for a job interview at IQVIA LLC

Know Your GCP Inside Out

Make sure you brush up on Good Clinical Practice (GCP) guidelines before the interview. Be ready to discuss how you've applied these principles in your previous roles, as this will show your depth of understanding and commitment to quality in clinical research.

Showcase Your Monitoring Experience

Prepare specific examples from your past independent monitoring experiences. Highlight challenges you faced, how you overcame them, and the impact of your work on recruitment efforts for clinical trials. This will demonstrate your hands-on expertise and problem-solving skills.

Research the Company

Take some time to learn about the clinical research provider you're interviewing with. Understand their mission, recent projects, and any innovative practices they employ. This knowledge will help you tailor your answers and show genuine interest in the role.

Ask Insightful Questions

Prepare thoughtful questions to ask at the end of the interview. Inquire about the company's approach to site monitoring or how they support professional growth. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.

Senior CRA – UK Onsite Monitoring in London
IQVIA LLC
Location: London

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