At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Flexible working, career development, well-being support, and recognition as a top workplace.
- Other info: Opportunities for mentorship and professional growth in a dynamic team.
- Why this job: Make a real impact on healthcare while advancing your career in a supportive environment.
- Qualifications: 12 months of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 35000 - 45000 £ 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 South West England.
Why IQVIA?
- Career development opportunities to grow as we grow
- AI-powered career advancement through our internal talent marketplace, Career Connections
- Mentorship opportunities across the organisation via Employee Resource Groups
- Flexible working to assist work–life balance and professional success
- Well-being support covering your physical, mental, and financial health
- Awards 2026 "Glassdoor Best Place to Work in the UK"
- 1 in category - 2026 Fortune World’s Most Admired Companies list (for the FIFTH consecutive year!)
- Brandon Hall Excellence Award for Learning & 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:
- Requires at least 12 months independent on-site monitoring experience of interventional studies
- Experience across start-up, enrolment, maintenance, close-out
- Digital literacy, including confidence using AI tools in a professional setting
- Degree in scientific discipline / health care or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Ability to establish and maintain effective working relationships with coworkers and clients
- Full UK right to work required, this position is not eligible for visa sponsorship
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Clinical Research Associate II, South West England employer: IQVIA
At IQVIA, we are dedicated to fostering a supportive and innovative work environment that prioritises your professional growth and well-being. As a Clinical Research Associate II in South West England, you will benefit from flexible working arrangements, comprehensive well-being support, and access to mentorship opportunities, all while contributing to our mission of advancing healthcare solutions. Join us and be part of a team recognised as one of the best places to work in the UK, where your contributions truly make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, South West England
✨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 you align 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 regulatory compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and demonstrate your experience effectively.
✨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 ready to make an impact in the clinical research world.
We think you need these skills to ace Clinical Research Associate II, South West England
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your relevant experience, especially any independent on-site monitoring you've done. We want to see how your skills align with 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 clinical research and how you can contribute to our mission at IQVIA. Keep it concise but impactful – we love a good story!
Showcase Your Digital Skills:Since we're all about innovation, don’t forget to mention your digital literacy. If you’ve used AI tools or other tech in your previous roles, let us know! It’s a big plus for us at StudySmarter.
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 shows us you’re serious about joining 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 regulations confidently will show that you understand the core of clinical research and can apply them in real-world scenarios.
✨Showcase Your Monitoring Experience
Prepare specific examples from your previous monitoring experiences, especially those involving interventional studies. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will demonstrate your hands-on experience and problem-solving skills.
✨Emphasise Communication Skills
As a Clinical Research Associate, effective communication is key. Be ready to discuss how you've established and maintained relationships with study sites and team members. Share instances where your communication helped resolve issues or improve project outcomes.
✨Familiarise Yourself with AI Tools
Since digital literacy and confidence in using AI tools are important for this role, make sure you can talk about any relevant experience you have with technology in clinical research. Whether it's data management software or AI-driven analytics, showing your tech-savviness will set you apart.
