Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage and monitor clinical sites, ensuring effective recruitment and training.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Opportunity to make a real impact and continuous learning.
- Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
- Qualifications: Experience in on-site monitoring and knowledge of GCP and ICH guidelines.
- Other info: Flexible travel required; not eligible for UK visa sponsorship.
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. 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
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!
#LI-ADAMTHOMPSON
*Please note – this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com
#J-18808-Ljbffr
Experienced Clinical Research Associate employer: IQVIA
Contact Detail:
IQVIA 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, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Familiarise yourself with their recent studies and be ready to discuss how your experience aligns with their goals. This shows you're genuinely interested and invested in their mission.
✨Tip Number 3
Don’t just wait for job postings! Reach out directly to hiring managers or recruiters at IQVIA. A friendly email expressing your interest can set you apart from the crowd and might just land you an interview.
✨Tip Number 4
Keep your LinkedIn profile updated and engaging. Share relevant articles, comment on industry trends, and showcase your achievements. This not only boosts your visibility but also positions you as a knowledgeable candidate in the clinical research space.
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 management and monitoring, as well as your knowledge of 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 goal of creating a healthier world. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to showcase your skills in your application. Whether it's your ability to adapt recruitment plans or mentor junior team members, make sure we know what you bring to the table. We’re looking for someone who can hit the ground running!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. 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 Site Management Experience
Prepare specific examples from your past roles where you've successfully managed sites. Talk about your experience with site selection, initiation, and monitoring. This will help demonstrate your hands-on experience and how you can contribute to the team.
✨Be Ready to Discuss Recruitment Strategies
Since driving and tracking subject recruitment is a key responsibility, think about strategies you've used in the past. Be prepared to share how you adapted plans to meet recruitment goals, as this will highlight your problem-solving skills and adaptability.
✨Mentoring and Teamwork
If you've had experience mentoring junior members, be ready to discuss it. Share how you approach training and supporting others, as this shows your leadership potential and commitment to team success, which is crucial in a collaborative environment.
