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- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: IQVIA is a top global provider of clinical research services, recognised for innovation in healthcare.
- Benefits: Enjoy a mix of remote and on-site work, plus genuine career development opportunities.
- Why this job: Make a real impact on patient outcomes while working with cutting-edge medicines.
- Qualifications: Over 2 years of independent monitoring experience and hands-on oncology expertise required.
- Other info: This role requires flexibility for nationwide travel and is not eligible for UK Visa Sponsorship.
The predicted salary is between 36000 - 60000 £ per year.
Join Us on Our Mission to Drive Healthcare Forward
As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. We’re expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
Why IQVIA?
- IQVIA is recognized as #1 in its category on the 2025 Fortune World’s Most Admired Companies list for the FOURTH consecutive year!
- We offer genuine career development opportunities for those who want to grow as part of the organization.
- The chance to work on cutting edge medicines at the forefront of new medicines development.
- IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
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
Profile
- Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- Hands-on experience in the Oncology therapeutic area.
- Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
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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
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Clinical Research Associate II employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have experience as Clinical Research Associates. Attend industry conferences or webinars to make connections and gain insights into the role, which can give you an edge during the application process.
✨Tip Number 3
Highlight your hands-on experience in the Oncology therapeutic area during discussions. This specific knowledge is highly valued, so be prepared to discuss relevant projects or trials you've worked on that relate to this field.
✨Tip Number 4
Be ready to discuss your flexibility and commitment to travel. Since the role involves nationwide travel, showcasing your willingness and past experiences with travel can reassure employers of your suitability for the position.
We think you need these skills to ace Clinical Research Associate II
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Associate II position. Familiarise yourself with the key tasks such as site monitoring visits and compliance with GCP guidelines.
Tailor Your CV: Customise your CV to highlight relevant experience, especially your independent on-site monitoring experience and any work in the Oncology therapeutic area. Use specific examples that demonstrate your ability to manage clinical trial protocols.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for advancing clinical research and improving patient outcomes. Mention why you want to work at IQVIA and how your skills align with their mission and values.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is accurate and presented professionally.
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
As a Clinical Research Associate, it's crucial to have a solid understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Brush up on these regulations before your interview, as you may be asked to discuss how you've applied them in your previous roles.
✨Showcase Your Monitoring Experience
Highlight your independent on-site monitoring experience during the interview. Be prepared to share specific examples of how you've managed multiple clinical trial protocols and ensured compliance with regulatory requirements. This will demonstrate your capability and confidence in the role.
✨Discuss Your Flexibility and Travel Commitment
Since this role requires nationwide travel, be ready to discuss your flexibility and willingness to travel for site visits. Share any past experiences where you successfully managed travel logistics while maintaining project timelines, as this will show your commitment to the role.
✨Prepare Questions About Site Management
Prepare thoughtful questions about the site management processes at IQVIA. Inquire about their approach to subject recruitment and how they support CRAs in managing ongoing project expectations. This shows your genuine interest in the company and the role, making you a more appealing candidate.