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- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a top-rated global leader in clinical research services.
- Benefits: Competitive salary, career growth, and a supportive learning environment.
- Why this job: Make a real impact on patient outcomes while working with innovative teams.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines.
- Other info: Flexible travel opportunities and a commitment to continuous learning.
The predicted salary is between 35000 - 45000 £ per year.
Locations: Bath, United Kingdom; Reading, Berkshire, United Kingdom
Time type: Full time
Posted on: Posted Today
Job requisition id: R
Join IQVIA on our mission to accelerate innovation for a healthier world!
IQVIA are seeking experienced Clinical Research Associates in South West England to strengthen our cFSP sponsor-dedicated team.
- 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(R) World’s Most Admired Companies(TM) list (for the FIFTH consecutive year!).
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.
- 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.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Experienced Clinical Research Associate in Bath employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate in Bath
✨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 lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching IQVIA's values and recent projects. Show them you’re not just another candidate; you’re genuinely interested in their mission to improve patient outcomes.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to GCP and ICH guidelines. Being well-prepared will help you feel more confident and articulate during the interview.
✨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 our team at IQVIA.
We think you need these skills to ace Experienced Clinical Research Associate in Bath
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight relevant experience, especially in site monitoring and GCP compliance. 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 team. Be genuine and let us know why you’re excited about this opportunity.
Showcase Your Knowledge: Demonstrate your understanding of GCP and ICH guidelines in your application. We appreciate candidates who are knowledgeable and can articulate their expertise clearly. It shows us you’re serious about the role!
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 makes the process smoother for both you and us!
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 research.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experiences where you performed site monitoring visits. Highlight how you managed the progress of studies and dealt with any challenges. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for the role.
✨Communicate Effectively
Since collaboration is key in this role, practice articulating how you’ve established communication lines with study sites in the past. Be ready to discuss how you’ve handled ongoing project expectations and resolved issues, as this will reflect your ability to work well within a team.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to clinical trials and how they support their teams. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your values, especially their commitment to innovation and growth.