CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston
CRA II: Sponsor-Dedicated Site Monitoring (UK)

CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston

Livingston Full-Time 28800 - 43200 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Conduct monitoring visits and manage site communications to improve patient outcomes.
  • Company: Leading global provider of clinical research services with a dynamic team.
  • Benefits: Opportunity to enhance healthcare delivery and make a real difference.
  • Why this job: Join a passionate team dedicated to improving patient care worldwide.
  • Qualifications: Bachelor’s Degree in a scientific discipline and 1 year of monitoring experience.
  • Other info: Not eligible for UK visa sponsorship.

The predicted salary is between 28800 - 43200 £ per year.

A leading global provider of clinical research services is seeking experienced Clinical Research Associates in the UK.

Responsibilities include conducting monitoring visits and managing site communications.

Requires a Bachelor’s Degree in a scientific discipline, at least 1 year of on-site monitoring experience, and knowledge of clinical research regulations.

This role offers an opportunity to work within a dynamic team that aims to improve patient outcomes and enhance healthcare delivery worldwide.

Note, this position is not eligible for UK visa sponsorship.

CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston 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 Clinical Research Associates to make a real impact in healthcare. Our UK team benefits from comprehensive professional development opportunities, competitive remuneration, and a supportive environment that values work-life balance, making it an excellent place for those looking to grow their careers while contributing to meaningful patient outcomes.
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Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston

✨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 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 those interviews! Brush up on your knowledge of clinical research regulations and be ready to discuss your monitoring experience. 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 improving patient outcomes! During interviews, share specific examples of how you've contributed to enhancing healthcare delivery in your previous roles. This will help you stand out as a candidate who truly cares about the impact of their work.

✨Tip Number 4

Don't forget to apply through our website! We make it super easy for you to find and apply for CRA positions. Plus, it shows that you're genuinely interested in joining our dynamic team dedicated to making a difference in clinical research.

We think you need these skills to ace CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston

Clinical Research Knowledge
On-Site Monitoring Experience
Bachelor’s Degree in a Scientific Discipline
Site Communication Management
Knowledge of Clinical Research Regulations
Team Collaboration
Patient Outcome Improvement
Healthcare Delivery Enhancement

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 responsibilities of 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 improving patient outcomes and how your experience makes you a great fit for our dynamic team. Keep it engaging and personal!

Showcase Your Knowledge: Since this role requires knowledge of clinical research regulations, make sure to mention any relevant training or certifications you have. We love candidates who are up-to-date with industry standards and practices!

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 follow the prompts!

How to prepare for a job interview at IQVIA

✨Know Your Stuff

Make sure you brush up on your clinical research regulations and monitoring experience. Be ready to discuss specific examples from your past roles that highlight your skills and knowledge in these areas.

✨Show Your Passion

This role is all about improving patient outcomes, so let your enthusiasm for clinical research shine through. Share why you’re passionate about this field and how you can contribute to the team’s goals.

✨Prepare Questions

Have a few thoughtful questions ready to ask at the end of the interview. This shows your interest in the role and helps you gauge if the company culture aligns with your values.

✨Practice Makes Perfect

Consider doing mock interviews with a friend or using online resources. Practising your responses will help you feel more confident and articulate during the actual interview.

CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston
IQVIA
Location: Livingston
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  • CRA II: Sponsor-Dedicated Site Monitoring (UK) in Livingston

    Livingston
    Full-Time
    28800 - 43200 £ / year (est.)
  • I

    IQVIA

    10000+
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