At a Glance
- Tasks: Monitor clinical sites and ensure compliance with research protocols and 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 medical innovation and improve patient outcomes.
- Qualifications: 1 year of monitoring experience and knowledge of clinical research regulations required.
The predicted salary is between 35000 - 45000 € 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.
Clinical Research Associate II, Oncology in Stafford 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 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 in the healthcare sector. Join us in our mission to accelerate innovation for a healthier world, and enjoy the unique advantages of working in a dynamic environment dedicated to improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Stafford
✨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 about the role.
✨Tip Number 2
Prepare for the interview by brushing up on GCP and ICH guidelines. We want to see that you know your stuff! Practise common interview questions and think of examples from your experience that showcase your skills.
✨Tip Number 3
Show your passion for oncology! Research current trends and breakthroughs in the field. This will not only impress your interviewers but also help you connect your experiences to 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, it shows you’re serious about joining our mission to make a healthier world.
We think you need these skills to ace Clinical Research Associate II, Oncology in Stafford
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 in site monitoring and your understanding of GCP and ICH guidelines. We want to see how your skills match 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 oncology and how your background makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Achievements:When detailing your experience, focus on specific achievements rather than just duties. Did you improve recruitment rates or streamline processes? We want to know how you've made an impact in your previous roles!
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, 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 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 previous monitoring experiences, especially those related to interventional studies. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will help illustrate your hands-on experience and problem-solving skills.
✨Showcase Your Communication Skills
Since this role involves liaising with various stakeholders, be ready to discuss how you've established effective communication lines in past projects. Share instances where you adapted your communication style to suit different audiences, whether they were site staff or team members.
✨Prepare Questions About the Role
Have a few thoughtful questions ready about the role and the company culture at IQVIA. This shows your genuine interest in the position and helps you assess if it’s the right fit for you. Ask about their approach to site management or how they support ongoing training for Clinical Research Associates.
