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- Tasks: Monitor clinical trial sites, ensuring compliance and quality throughout the research process.
- Company: IQVIA is a top global provider of clinical research services, recognised for its 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 in healthcare while working with cutting-edge medicines and technologies.
- Qualifications: Must have over 12 months of independent monitoring experience and knowledge of GCP guidelines.
- Other info: This role requires flexibility for nationwide travel and is not eligible for UK Visa Sponsorship.
The predicted salary is between 28800 - 43200 £ 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 12 months 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**
#LI-AdamThompson
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 I employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate I
✨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 be invaluable during your application process.
✨Tip Number 3
Highlight any hands-on experience you have in the Oncology therapeutic area. This specific knowledge can set you apart from other candidates and show that you are well-prepared for the responsibilities of the role.
✨Tip Number 4
Be ready to discuss your experience managing multiple clinical trial protocols. Prepare examples that showcase your organisational skills and ability to handle the complexities of site management, as this is a key aspect of the CRA role.
We think you need these skills to ace Clinical Research Associate I
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Clinical Research Associate I at IQVIA. Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, as these are crucial for the role.
Tailor Your CV: Highlight your relevant experience in clinical trials, especially any independent on-site monitoring experience. Emphasise your hands-on experience in the Oncology therapeutic area and any specific achievements that demonstrate your ability to manage multiple clinical trial protocols.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for advancing healthcare and your commitment to improving patient outcomes. Mention why you want to work at IQVIA specifically and how your skills align with their mission and values.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential in clinical research.
How to prepare for a job interview at IQVIA
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Clinical Research Associate. Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, as these are crucial for the role.
✨Showcase Your Experience
Be prepared to discuss your previous experience in clinical trials, especially any hands-on monitoring you've done. Highlight specific examples where you successfully managed multiple protocols or dealt with challenges at investigative sites.
✨Demonstrate Communication Skills
Since the role involves liaising with various stakeholders, practice articulating how you would establish and maintain communication with study sites. Share examples of how you've effectively communicated project expectations and resolved issues in the past.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical trials and their use of data for site selection and recruitment. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.