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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 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 30000 - 42000 £ per year.
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Clinical Research Associate I, Cambridge
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Client:
IQVIA
Location:
Cambridge, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
524ae94c3e13
Job Views:
2
Posted:
12.07.2025
Expiry Date:
26.08.2025
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Job Description:
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
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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
Network with professionals in the clinical research field, especially those who work at IQVIA or similar companies. Attend industry conferences, webinars, and local meetups to make connections that could lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in oncology clinical trials. Being knowledgeable about current research can help you stand out during interviews and discussions with potential colleagues.
✨Tip Number 3
Consider reaching out to current or former Clinical Research Associates at IQVIA via LinkedIn. Ask them about their experiences and any tips they might have for succeeding in the application process.
✨Tip Number 4
Prepare for the interview by practising common CRA interview questions and scenarios. Focus on demonstrating your problem-solving skills and ability to manage multiple projects effectively, as these are crucial for the 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: Customise your CV to highlight relevant experience, especially any independent on-site monitoring experience and work in the Oncology therapeutic area. Use specific examples that demonstrate your ability to manage clinical trial protocols effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your commitment to improving patient outcomes. Mention why you want to work at IQVIA specifically and how your skills align with their mission.
Proofread Your Application: Before submitting, carefully proofread your application materials 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 Relevant Experience
Highlight your previous experience in clinical trials, especially any hands-on work in the Oncology therapeutic area. Be prepared to discuss specific protocols you've managed and how you ensured compliance with regulations.
✨Demonstrate Communication Skills
As a CRA, you'll need to communicate effectively with various stakeholders. Prepare examples of how you've established lines of communication with sites and managed project expectations in the past.
✨Prepare for Travel Questions
Since the role requires nationwide travel, be ready to discuss your flexibility and commitment to travel. Share any previous experiences that demonstrate your ability to manage travel while maintaining work-life balance.
