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 and employee satisfaction.
- Benefits: Enjoy competitive pay, flexible work options, and opportunities for professional growth.
- Other info: Be part of a dynamic team dedicated to improving patient outcomes globally.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: 1+ year of clinical research experience and strong communication skills 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.
- 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.
Oncology Clinical Research Associate II – Field-Based in Manchester employer: IQVIA Argentina
IQVIA is an exceptional employer, recognised as a 2026 'Glassdoor Best Place to Work in the UK' and #1 in its category on the Fortune® World’s Most Admired Companies™ list. With a strong commitment to employee growth, innovative work culture, and a focus on meaningful contributions to healthcare, employees enjoy a supportive environment that fosters continuous learning and professional development, all while making a significant impact in the field of oncology research.
StudySmarter Expert Advice🤫
We think this is how you could land Oncology Clinical Research Associate II – Field-Based in Manchester
✨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. Show us you know your stuff and can hit the ground running in the oncology space!
✨Tip Number 3
Don’t just wait for the job to come to you! Apply through our website and follow up with a quick email to express your enthusiasm. It shows initiative and keeps you on our radar.
✨Tip Number 4
Be ready to discuss your previous monitoring experiences. We want to hear how you've tackled challenges and contributed to successful studies. Bring those stories to life!
We think you need these skills to ace Oncology Clinical Research Associate II – Field-Based in Manchester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Oncology Clinical Research Associate role. Highlight relevant experience, especially any independent on-site monitoring 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. 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 know their stuff and can apply it effectively.
Apply Through Our Website:Don't forget to apply through our website! It’s the best way to ensure your application gets into the right hands. Plus, it shows us you're serious about joining our team at IQVIA.
How to prepare for a job interview at IQVIA Argentina
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. These are crucial for the role, and being able to discuss them confidently will show that you're well-prepared and knowledgeable.
✨Demonstrate 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 to showcase your hands-on expertise.
✨Showcase Your Communication Skills
Effective communication is key in this role. Prepare to discuss how you've established and maintained relationships with study sites and team members. Use examples that illustrate your ability to manage expectations and resolve issues collaboratively.
✨Prepare Questions About the Role
At the end of the interview, you'll likely have the chance to ask questions. Prepare thoughtful ones about the company's approach to clinical trials or how they support their Clinical Research Associates. This shows your genuine interest in the position and the company.
