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- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, travel opportunities, and contribute to meaningful health outcomes.
- Why this job: Make a real impact on patient health while advancing your career in a dynamic field.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.
- Other info: Flexible travel and excellent growth opportunities in a supportive environment.
The predicted salary is between 35000 - 45000 £ per year.
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK. 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 Good Clinical Practice.
- 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 of Oncology therapeutic area for unblinded studies.
- 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 as required.
Please note - this role is not eligible for visa sponsorship.
Clinical Research Associate in Oxford employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Oxford
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for your interviews by brushing up on GCP and ICH guidelines. Show us you know your stuff! We love candidates who can discuss these topics confidently and relate them to real-world scenarios.
✨Tip Number 3
Don’t forget to follow up after your interviews! A quick thank-you email can keep you fresh in our minds and shows your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. We want to see your application come through our system, so make sure you hit that 'apply' button and showcase your passion for making a difference in clinical research!
We think you need these skills to ace Clinical Research Associate in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
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 background aligns with our mission at IQVIA. Keep it engaging and personal, so we get to know the real you.
Showcase Your GCP Knowledge: Since Good Clinical Practice (GCP) is crucial for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality in our studies.
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 shows you’re serious about joining our team!
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. Being able to discuss these in detail will show that you’re not just familiar with them, but that you truly understand their importance in clinical research.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experiences where you’ve conducted independent on-site monitoring, especially in Oncology studies. Highlight any challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and adaptability.
✨Understand the Recruitment Process
Familiarise yourself with strategies for subject recruitment and how they align with project needs. Be ready to discuss how you would adapt and drive recruitment plans, as this is crucial for enhancing predictability in study outcomes.
✨Communicate Effectively
Since the role involves establishing regular lines of communication with sites, practice articulating how you would manage ongoing project expectations and issues. Think about how you can convey complex information clearly and maintain strong relationships with site staff.