At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research protocols.
- Company: Join IQVIA, a top-rated workplace recognised for innovation in healthcare.
- Benefits: Competitive salary, professional development, and a chance to make a real impact.
- Other info: Dynamic environment with opportunities for growth and learning.
- Why this job: Be part of a mission to accelerate innovation for a healthier world.
- Qualifications: 1 year of independent monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 37000 - 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 Bradley 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 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 Bradley
✨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 role.
✨Tip Number 2
Prepare for the interview by brushing up on GCP and ICH guidelines. We want you to show off your knowledge and confidence, so practice answering common questions related to site monitoring and study management.
✨Tip Number 3
Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression and shows that you’re genuinely interested in the position.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. We love seeing candidates who take the initiative to engage directly with us!
We think you need these skills to ace Clinical Research Associate Ii, Oncology in Bradley
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience, especially any monitoring visits you've conducted and your knowledge of GCP and ICH guidelines. We want to see how you fit into 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 your skills align with our needs. Keep it concise but impactful – we love a good story!
Be Honest and Clear:Remember, honesty is key in our hiring process. Ensure all the information you provide is truthful and complete. We appreciate transparency, so don’t hesitate to showcase your genuine self!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
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.
✨Showcase Your Communication Skills
Since this 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 with sites, as this will demonstrate your ability to collaborate effectively.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the team dynamics, ongoing projects, or how success is measured in the role. This shows your genuine interest in the position and helps you assess if the company culture aligns with your values.
