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: Competitive salary, career growth, and a chance to make a real impact.
- Other info: Dynamic team environment with opportunities for continuous learning and development.
- Why this job: Be part of a mission to accelerate healthcare innovation and improve patient outcomes.
- Qualifications: 1 year of clinical research 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.
- 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.
Research Associate in Town Row 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 Research Associate in Town Row
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend 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 the company and its culture. Understand their mission and values, especially since IQVIA is all about innovation for a healthier world. Tailor your answers to show how you align with their goals.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online platforms to refine your responses. Focus on articulating your experience in clinical research and how it relates to the role of a Research Associate.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining IQVIA and being part of their mission.
We think you need these skills to ace Research Associate in Town Row
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your relevant experience, especially any site monitoring or clinical research work 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 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 of clinical research.
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 shows 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 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 illustrate your hands-on experience and problem-solving skills.
✨Show Your Communication Skills
Since the 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 through clear communication.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the team dynamics, ongoing projects, or how they measure success in this role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
