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- Tasks: Monitor clinical trial sites and ensure compliance with regulations while supporting innovative medical research.
- Company: Join IQVIA, a top-rated company driving healthcare forward with cutting-edge solutions.
- Benefits: World-class training, career development, and the chance to work on groundbreaking medicines.
- Why this job: Make a real impact in healthcare and grow your career in a dynamic environment.
- Qualifications: Experience in clinical monitoring and a life sciences degree or equivalent experience.
- Other info: Flexible travel opportunities and a commitment to continuous learning.
The predicted salary is between 28800 - 48000 £ 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
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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Clinical Research Associate employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities that aren’t even advertised!
✨Tip Number 2
Prepare for interviews by researching IQVIA and understanding their mission. We want you to show genuine interest in their work and how you can contribute to driving healthcare forward. Tailor your answers to reflect their values!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your responses. We all know that confidence is key, so the more you practice, the more comfortable you’ll feel when it’s time to shine.
✨Tip Number 4
Don’t forget to follow up after your interview! A simple thank-you email can go a long way in leaving a positive impression. We recommend mentioning something specific from your conversation to make it personal.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience with site monitoring and knowledge of GCP and ICH guidelines. We want to see how your background aligns 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 at IQVIA. Keep it concise but impactful – we love a good story!
Showcase Relevant Experience: When filling out your application, make sure to showcase any relevant experience managing clinical trial protocols. We’re keen on seeing how you've handled diverse investigative sites and your ability to adapt to different project needs.
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
✨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 truly understand their importance in clinical research.
✨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 in the field.
✨Understand the Company’s Mission
Take some time to research IQVIA and its mission to drive healthcare forward. Being able to articulate how your values align with theirs will make a strong impression and show that you’re genuinely interested in contributing to their goals.
✨Prepare Questions for Them
Have a few thoughtful questions ready to ask at the end of your interview. This could be about their approach to site selection or how they support career development. It shows that you’re engaged and eager to learn more about the role and the company.