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- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Competitive salary, growth opportunities, and a collaborative work environment.
- Why this job: Make a real impact on patient outcomes while advancing your career.
- Qualifications: Experience in clinical trials and knowledge of GCP and ICH guidelines.
- Other info: Dynamic team culture focused on innovation and continuous learning.
The predicted salary is between 36000 - 60000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in the UK.
- We share a passion for the work we do, and the impact it has on customers and patients.
- We are innovative, curious, and feel empowered to explore new ideas and ways of working.
- We collaborate to bring out the best in each other and get the most out of our different skills, perspectives, and expertise.
- We are committed to growth, always learning, and making the most of agile career opportunities.
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.
Please note - this role is not eligible for UK visa sponsorship. Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Experienced Clinical Research Associate in London employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate 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 or can refer you to someone at IQVIA.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and ICH guidelines. Be ready to discuss your previous experiences managing clinical trials and how you tackled challenges. Show them you’re the perfect fit!
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on their radar.
✨Tip Number 4
Stay curious and keep learning! Engage with online courses or webinars related to clinical research. This not only boosts your skills but also shows potential employers that you’re committed to growth.
We think you need these skills to ace Experienced Clinical Research Associate in London
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 adherence to GCP and ICH guidelines. We want to see how your skills align with our mission!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for clinical research and how you can contribute to our team. Be sure to mention any specific projects or experiences that showcase your expertise.
Showcase Your Soft Skills: While technical skills are crucial, don’t forget to highlight your soft skills too! Collaboration, communication, and adaptability are key in our fast-paced environment. Let us know how you’ve demonstrated these in your previous roles.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows you’re serious about joining our innovative team at IQVIA!
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 from your past roles where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for the role.
✨Communicate Effectively
Since collaboration is key in this role, practice articulating how you’ve established communication lines with study sites in the past. Be ready to discuss how you handle ongoing project expectations and resolve issues, as this will reflect your ability to work well within a team.
✨Be Ready to Discuss Recruitment Strategies
Think about how you’ve adapted and driven subject recruitment plans in previous projects. Be prepared to share your insights on what worked, what didn’t, and how you can apply those lessons to enhance predictability in future studies.
