Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Monitor clinical trial sites and ensure compliance with regulations while driving recruitment plans.
- Company: Join IQVIA, a top-rated workplace recognised for innovation in healthcare.
- Benefits: Competitive salary, career growth, and the chance to make a real impact.
- Other info: Flexible travel opportunities and a dynamic work environment await you.
- Why this job: Be part of a mission to improve patient outcomes and accelerate medical innovation.
- Qualifications: Experience in clinical trials 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 Site Management (multi-sponsor) team is growing and 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!
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.
Senior Clinical Research Associate, Oncology employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate, Oncology
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at IQVIA. A friendly chat can open doors and give you insider info on the company culture and what they’re really looking for.
✨Tip Number 2
Prepare for the interview by brushing up on GCP and ICH guidelines. We all know that knowledge is power, so being able to discuss these topics confidently will show you’re serious about the role and ready to hit the ground running.
✨Tip Number 3
Showcase your experience with site monitoring visits. Be ready to share specific examples of how you’ve managed multiple clinical trial protocols. This will demonstrate your hands-on expertise and make you stand out from the crowd.
✨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 to improve patient outcomes.
We think you need these skills to ace Senior Clinical Research Associate, Oncology
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 site monitoring and managing clinical trial protocols, as these are key aspects of the job. We want to see how your background aligns 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 oncology and how your skills can contribute to our team. Keep it engaging and personal – we love to see your personality come through!
Showcase Relevant Experience: When filling out your application, be sure to showcase your independent on-site monitoring experience and knowledge of GCP and ICH guidelines. We’re looking for candidates who can hit the ground running, so make this stand out!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way to ensure your application gets to us directly. Plus, you’ll find all the details you need about the role and our company culture there!
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 can apply them in real-world scenarios.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past roles where you successfully managed multiple clinical trial protocols. Highlight your independent on-site monitoring experience and how you tackled challenges at diverse investigative sites. This will demonstrate your capability and confidence in the role.
✨Understand the Recruitment Process
Familiarise yourself with strategies for enhancing subject recruitment plans. Be ready to discuss how you’ve adapted and driven recruitment efforts in previous studies, as this is crucial for the role. Showing that you can think strategically about recruitment will set you apart.
✨Communicate Effectively
Since the role involves regular communication with sites, practice articulating your thoughts clearly and concisely. Think of examples where you established strong lines of communication with study teams or sites, and be prepared to discuss how you manage ongoing project expectations and issues.