At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Join IQVIA, a top-rated workplace recognised for innovation and employee satisfaction.
- Benefits: Enjoy competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Be part of a dynamic team dedicated to improving patient outcomes globally.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: 1+ year of clinical research experience and strong communication skills required.
The predicted salary is between 35000 - 45000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.
We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and #1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!). Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Essential Functions- 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.
- 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.
- Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please note - this role is not eligible for UK visa sponsorship.
Oncology Clinical Research Associate II | Field-Based UK in Reading employer: IQVIA Argentina
At IQVIA, we pride ourselves on being a leading employer in the clinical research field, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through our numerous awards for leadership development and learning opportunities, ensuring that you can forge a meaningful career while making a significant impact on global health outcomes. Join us in Reading, where you'll be part of a team recognised as one of the best places to work in the UK, dedicated to advancing healthcare solutions.
StudySmarter Expert Advice🤫
We think this is how you could land Oncology Clinical Research Associate II | Field-Based UK in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at IQVIA. A friendly chat can open doors and give you insider info about the role.
✨Tip Number 2
Prepare for the interview by brushing up on GCP and ICH guidelines. Show us you know your stuff! We love candidates who can discuss these topics confidently and relate them to real-world scenarios.
✨Tip Number 3
Be ready to showcase your monitoring experience. Think of specific examples where you’ve tackled challenges or improved site practices. We want to see how you can make an impact right from the start!
✨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 us you’re genuinely interested in joining our mission to accelerate innovation.
We think you need these skills to ace Oncology Clinical Research Associate II | Field-Based UK in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Clinical Research Associate II. Highlight your relevant experience in site monitoring and knowledge of GCP and ICH guidelines. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology research and how you can contribute to our mission. Keep it concise but impactful – we love a good story!
Showcase Your Communication Skills:As a Clinical Research Associate, you'll need to communicate effectively with various stakeholders. In your application, give examples of how you've successfully managed relationships or resolved issues in past roles. We value strong communicators!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way to ensure your application gets to us directly. Plus, it shows you're serious about joining our team at IQVIA. We can't wait to hear from you!
How to prepare for a job interview at IQVIA Argentina
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. These are crucial for the role, and being able to discuss them confidently will show that you're well-prepared and knowledgeable.
✨Demonstrate Your Monitoring Experience
Since the role requires at least a year of independent on-site monitoring experience, be ready to share specific examples from your past work. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries to showcase your hands-on expertise.
✨Showcase Your Communication Skills
Effective communication is key in this role. Prepare to discuss how you've established and maintained relationships with study sites and team members. Use examples that illustrate your ability to manage expectations and resolve issues collaboratively.
✨Prepare Questions About the Role
At the end of the interview, have a few thoughtful questions ready about the company's projects or team dynamics. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
