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 in healthcare.
- Benefits: Gain valuable experience, competitive salary, and opportunities for continuous learning.
- Other info: Dynamic team environment with a focus on professional growth and integrity.
- Why this job: Make a real impact on patient outcomes while advancing your career in clinical research.
- Qualifications: 1 year of independent monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 € 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.
Qualifications
- 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.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Clinical Monitoring Associate in Royal Tunbridge Wells employer: IQVIA
At IQVIA, we pride ourselves on being a top employer, 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. Our collaborative work culture fosters continuous learning and professional growth, while our commitment to innovation in clinical research allows you to make a meaningful impact on global health outcomes. Join us in our mission to accelerate innovation for a healthier world and enjoy the unique advantages of working in a dynamic, supportive environment.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Monitoring Associate in Royal Tunbridge Wells
✨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 hunt for a Clinical Monitoring Associate role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how you've applied these in your previous roles. We want to see that you’re not just familiar with the terms, but that you can bring real-world experience to the table.
✨Tip Number 3
Showcase your communication skills! During interviews, highlight examples of how you've effectively managed relationships with sites and team members. This is key in clinical monitoring, so make sure we see your ability to keep everyone on the same page.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining IQVIA and making an impact in the clinical research world.
We think you need these skills to ace Clinical Monitoring Associate in Royal Tunbridge Wells
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Monitoring Associate role. Highlight your relevant experience, especially any independent on-site monitoring you've done. We want to see how your skills align 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 Knowledge:Demonstrate your understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines in your application. We appreciate candidates who are well-versed in the regulatory landscape!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at IQVIA
✨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 regulations confidently will show that you understand the core of clinical research and can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your past experience where you've performed site monitoring visits. Highlight how you managed recruitment plans, tracked regulatory submissions, or resolved data queries. This will help the interviewers see your practical knowledge in action.
✨Showcase Your Communication Skills
Since this role involves liaising with various stakeholders, be ready to discuss how you've established effective communication lines in previous roles. Share instances where you successfully managed project expectations or resolved issues with sites, as this will demonstrate your ability to collaborate effectively.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's projects, culture, or future goals. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career aspirations. Plus, it makes for a more engaging conversation!
