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 and impact.
- Benefits: Competitive salary, career growth, and a chance to make a difference in healthcare.
- Other info: Dynamic team environment with opportunities for continuous learning.
- Why this job: Be part of a mission to accelerate innovation for a healthier world.
- Qualifications: 1 year of clinical research monitoring experience and strong regulatory knowledge.
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.
Qualifications
- 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 Ottershaw employer: IQVIA
At IQVIA, we pride ourselves on being a leading employer in the clinical research field, offering our Research Associates a dynamic work environment that fosters innovation and professional growth. With recognition as a 'Glassdoor Best Place to Work' and a commitment to employee development, we provide comprehensive training, collaborative culture, and opportunities to make a meaningful impact on global health. Join us in our mission to accelerate innovation for a healthier world, where your contributions truly matter.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Ottershaw
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by researching IQVIA and understanding their mission. We want to see your passion for innovation and how you can contribute to a healthier world. Tailor your answers to show you’re the perfect fit for their team!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We love seeing candidates who are proactive and genuinely interested in the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we’ve got loads of resources to help you ace the process and land that Research Associate role!
We think you need these skills to ace Research Associate in Ottershaw
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 our mission!
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 team. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Knowledge:Demonstrate your understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines in your application. We’re looking for candidates who are not just qualified but also genuinely interested in the field.
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 mission at IQVIA!
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’re not just familiar with them, but that you can apply them in real-world scenarios.
✨Showcase Your Monitoring Experience
Since the role requires at least a year of independent on-site monitoring experience, be ready to share specific examples from your past work. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will demonstrate your hands-on expertise and problem-solving skills.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about their site management processes or how they support ongoing training for Clinical Research Associates. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
✨Emphasise Team Collaboration
The job involves liaising with study team members, so be ready to discuss your experience working in teams. Share examples of how you’ve effectively communicated with colleagues and clients to manage project expectations. This will highlight your ability to build strong working relationships, which is crucial for success in this role.
