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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.
Join Us on Our Mission to Drive Healthcare Forward. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
- 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, helping drive performance of sites 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 (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 in London 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 in London
✨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 genuine interest in their work and be ready to discuss how your experience aligns with their needs. We want to see your passion for driving healthcare forward!
✨Tip Number 3
Practice your interview skills with a friend or mentor. Get comfortable talking about your past experiences and how they relate to the CRA role. Confidence is key, so let’s make sure you shine when it counts!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Experienced CRA - Single Sponsor Dedicated in London
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. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to highlight your skills in managing multiple clinical trial protocols and your ability to adapt to project needs. We’re looking for someone who can drive performance and enhance predictability at sites.
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 us you’re serious about 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 site monitoring visits. Highlight how you adapted to challenges and ensured compliance with protocols. This will demonstrate your hands-on experience and problem-solving skills.
✨Understand the Recruitment Process
Familiarise yourself with strategies for enhancing subject recruitment. Be ready to discuss how you’ve previously tracked and adapted recruitment plans to meet project needs. This shows you can think critically about site performance and patient engagement.
✨Communicate Effectively
Practice articulating your thoughts clearly and confidently. Since the role involves regular communication with sites and team members, being able to convey your ideas effectively will be crucial. Consider doing mock interviews to refine your communication skills.