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- Tasks: Monitor clinical trial sites and ensure compliance with regulations while enhancing patient recruitment.
- Company: Join IQVIA, a top-rated workplace recognised for innovation in healthcare.
- Benefits: Competitive salary, opportunities for growth, and a chance to make a real impact.
- Why this job: Be part of a mission to accelerate medical innovation and improve patient outcomes.
- Qualifications: Experience in clinical trials and knowledge of GCP and ICH guidelines required.
- Other info: Flexible travel opportunities and a dynamic work environment await you.
The predicted salary is between 36000 - 60000 £ 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.
- 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.
CRA II, Oncology in Manchester employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CRA II, Oncology in Manchester
✨Tip Number 1
Network like a pro! Reach out to current or former employees at IQVIA through LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research IQVIA’s recent projects and their impact on healthcare. This shows you're genuinely interested and ready to contribute to their mission.
✨Tip Number 3
Practice common interview questions, especially those related to site monitoring and GCP guidelines. We all know interviews can be nerve-wracking, so being prepared will help you feel more confident.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the team at IQVIA.
We think you need these skills to ace CRA II, Oncology in Manchester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CRA II role. Highlight your experience with site monitoring and any relevant clinical trial protocols you've managed. 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 a good story!
Showcase Your GCP Knowledge: Since GCP and ICH guidelines are crucial for this role, make sure to mention your understanding and experience with these regulations in your application. We’re looking for candidates who know their stuff!
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’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 in detail will show that you’re not just familiar with them, but that you understand their importance in clinical trials.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experiences where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and adaptability.
✨Understand the Recruitment Process
Since the role involves enhancing subject recruitment plans, be ready to discuss strategies you've used in the past to drive recruitment. This could include how you’ve worked with sites to adapt plans based on project needs, so have a few examples at the ready.
✨Communicate Effectively
Effective communication is key in this role. Think about how you’ve established lines of communication with study sites in previous roles. Be prepared to share how you manage ongoing project expectations and resolve issues, as this will highlight your collaborative skills.