At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: Join IQVIA, a top-rated company recognised for its innovative approach in healthcare.
- Benefits: Enjoy a competitive salary, growth opportunities, and a collaborative work environment.
- Other info: Flexible travel required; this role is not eligible for UK visa sponsorship.
- Why this job: Make a real impact on patient outcomes while working with a passionate team.
- Qualifications: Experience in clinical trial monitoring and knowledge of GCP and ICH guidelines required.
The predicted salary is between 40000 - 50000 £ 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.
Why IQVIA?
- 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.
Awards:
- IQVIA is a 2026 "Glassdoor Best Place to Work in the UK".
- IQVIA is recognised as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list.
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.
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.
Senior Clinical Research Associate - On-site Monitoring in Reading employer: IQVIA
At IQVIA, we are dedicated to fostering a collaborative and innovative work environment that empowers our employees to thrive. As a Senior Clinical Research Associate, you will benefit from our commitment to professional growth, with access to continuous learning opportunities and the chance to make a meaningful impact on healthcare. Our recognition as a top employer reflects our supportive culture and dedication to excellence in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate - On-site Monitoring in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly to hiring managers.
✨Tip Number 2
Prepare for interviews by researching IQVIA and understanding their mission. Familiarise yourself with their projects and values so you can show how your experience aligns with their goals. This will help you stand out as a candidate who truly gets what they’re about.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to site monitoring and GCP guidelines. We recommend doing mock interviews with friends or using online resources to boost your confidence and refine your answers.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in leaving a positive impression. Plus, it shows your enthusiasm for the role and keeps you on their radar.
We think you need these skills to ace Senior Clinical Research Associate - On-site Monitoring in Reading
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Clinical Research Associate role. Highlight your experience with on-site monitoring and any specific clinical trial protocols you've managed. 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 innovative team. Don’t forget to mention why you’re excited about working with IQVIA specifically.
Showcase Your Knowledge:Demonstrate your understanding of GCP and ICH guidelines in your application. We love candidates who are not just experienced but also knowledgeable about the regulations that guide our work in clinical trials.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re proactive and keen to join our team!
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 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 during site monitoring visits and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills.
✨Communicate Effectively
Since the role involves liaising with various stakeholders, practice articulating your thoughts clearly and concisely. You might even want to role-play common scenarios with a friend to get comfortable with discussing project expectations and managing issues.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their approach to site management or how they support their Clinical Research Associates in their professional development. This shows you’re genuinely interested in being part of their team.
