At a Glance
- Tasks: Monitor clinical sites and ensure compliance with protocols and regulations.
- Company: Join IQVIA, a top-rated company in healthcare innovation.
- Benefits: World-class training, career development, and the chance to impact patient outcomes.
- Other info: Flexible travel opportunities and a dynamic work environment.
- Why this job: Be at the forefront of new medicines and make a real difference in healthcare.
- Qualifications: 18 months of monitoring experience and a life science degree or equivalent.
The predicted salary is between 37000 - 44000 € per year.
Join Us on Our Mission to Drive Healthcare Forward. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.
Why IQVIA? IQVIA is recognized as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list for the fifth 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
- A minimum of 18 months 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!
*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.
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 Calcot employer: IQVIA
At IQVIA, we are dedicated to driving healthcare forward, offering our Clinical Monitoring Associates unparalleled access to world-class training and professional development. Our collaborative work culture fosters genuine career growth opportunities, allowing you to make a meaningful impact on cutting-edge medicines while benefiting from significant data resources that enhance site performance. Join us in a dynamic environment where your contributions are valued, and your career aspirations can flourish.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Monitoring Associate in Calcot
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, join online forums, or even reach out to current Clinical Monitoring Associates on LinkedIn. Building relationships can open doors that a CV just can't.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with GCP and ICH guidelines. Share specific examples of how you've managed clinical trials successfully – it’ll show you know your stuff!
✨Be Ready for the Interview
Prepare for common interview questions related to site monitoring and project management. Think about how you can demonstrate your problem-solving skills and adaptability, especially when it comes to recruitment challenges.
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're genuinely interested in joining our mission to drive healthcare forward.
We think you need these skills to ace Clinical Monitoring Associate in Calcot
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 driving healthcare forward and how your background makes you a great fit for IQVIA. Keep it engaging and personal – we love a good story!
Showcase Your Knowledge of GCP and ICH:Since this role involves adhering to Good Clinical Practice and ICH guidelines, make sure to mention your knowledge and experience with these standards in your application. We appreciate candidates who understand the importance of compliance!
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, 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 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 understand their importance in clinical monitoring.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experience where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced and how you overcame them. This will demonstrate your ability to handle the responsibilities of the Clinical Monitoring Associate role.
✨Understand the Recruitment Process
Since the role involves adapting and driving subject recruitment plans, be ready to discuss strategies you've used in the past. Think about how you can enhance predictability in recruitment and what methods have worked for you at previous sites.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to site management and monitoring. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your career goals. Plus, it gives you a chance to engage with the interviewers!
