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- Tasks: Monitor clinical trial sites and ensure compliance with regulations while driving patient recruitment.
- Company: Join IQVIA, a top-rated company in healthcare innovation and research.
- Benefits: Career development opportunities, competitive salary, and a chance to work on groundbreaking medicines.
- Why this job: Make a real impact in healthcare by working on cutting-edge clinical trials.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines required.
- Other info: Dynamic role with opportunities for travel and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
locations: Reading, Berkshire, United Kingdom
time type: Full time
posted on: Posted Today
job requisition id: R1524544
Join Us on Our Mission to Drive Healthcare Forward
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
* 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. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
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
- Experience of independent on-site monitoring (minimum 6 months).
- 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 CRA - Single Sponsor Dedicated employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced CRA - Single Sponsor Dedicated
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. The more people you know, the better your chances of landing that CRA role.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show them you’re not just another candidate; you’re genuinely interested in their mission to drive healthcare forward. Tailor your answers to reflect how your experience aligns with their goals.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your responses. Focus on articulating your experience with GCP and ICH guidelines, as these are crucial for the CRA role.
✨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 innovative medical treatments.
We think you need these skills to ace Experienced CRA - Single Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the role of Experienced CRA. Highlight your relevant experience, especially in site monitoring and adherence to GCP and ICH guidelines. 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. Be genuine and let your personality come through – we love that!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've successfully managed clinical trial protocols or improved site performance. Numbers and outcomes speak volumes!
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 shows you’re keen on joining our mission to drive 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 trials.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past roles where you successfully managed multiple clinical trial protocols. Highlight your independent on-site monitoring experience and how it contributed to the success of the studies. This will demonstrate your capability and readiness for the role.
✨Understand the Company’s Mission
Take some time to research IQVIA and their mission to drive healthcare forward. Be ready to discuss how your values align with theirs and how you can contribute to their goal of improving patient outcomes. This shows genuine interest and commitment.
✨Prepare Questions for Them
Have a few thoughtful questions ready to ask at the end of your interview. This could be about their approach to site selection or how they support their CRAs in managing study challenges. It shows you’re engaged and thinking critically about the role.
