Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Monitor clinical trial sites and ensure compliance with regulations while driving patient recruitment.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Career growth opportunities, competitive salary, and the chance to work on innovative medicines.
- Why this job: Make a real impact in healthcare by working on cutting-edge medical treatments.
- Qualifications: Experience in clinical trials, knowledge of GCP/ICH guidelines, and a life sciences degree.
- Other info: Dynamic role with travel opportunities and a focus on continuous learning.
The predicted salary is between 36000 - 60000 £ per year.
Join Us on Our Mission to Drive Healthcare Forward. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
- IQVIA is recognized as #1 in its category on the 2025 Fortune World’s Most Admired Companies list for the FOURTH consecutive year!
- We offer genuine career development opportunities for those who want to grow as part of the organization.
- The chance to work on cutting edge medicines at the forefront of new medicines development.
- IQVIA has access to significant data pools allowing better site selection and recruitment, driving performance of sites and making the CRA role more efficient.
Responsibilities:
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Requirements:
- Experience of independent on-site monitoring.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Please note - this role is not eligible for UK visa sponsorship.
Experienced Clinical Research Associate employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate
✨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 researching the company and its projects. Show genuine interest in their work and be ready to discuss how your experience aligns with their mission. This will help you stand out as a candidate who truly cares.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to site monitoring and GCP guidelines. Being articulate about your experience will boost your confidence and make a great impression.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining our team and contributing to our mission in healthcare.
We think you need these skills to ace Experienced Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience, especially in site monitoring and managing clinical trial protocols. We want to see how your background aligns with our mission!
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 Knowledge of GCP and ICH: Since this role requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, make sure to mention any relevant training or experience. We appreciate candidates who are well-versed in these standards!
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be one step closer to joining us in driving healthcare forward!
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 Conference on Harmonization (ICH) guidelines before your 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 of your previous site monitoring visits. Talk about how you managed multiple clinical trial protocols and the challenges you faced. This will demonstrate your hands-on experience and ability to handle the responsibilities of the role.
✨Communicate Effectively
Since the role involves liaising with various stakeholders, practice articulating your thoughts clearly. You might be asked how you would establish communication lines with sites or manage ongoing project expectations, so have a strategy ready to share.
✨Demonstrate Flexibility and Adaptability
Be prepared to discuss how you’ve adapted to changing project needs in the past. Highlight any experiences where you had to adjust recruitment plans or manage unexpected issues at sites, as this will show your ability to thrive in a dynamic environment.
