Clinical Research Associate II

IQVIA; England; Hybrid; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization in the United Kingdom is seeking a Clinical Research Associate to perform site monitoring and ensure compliance with regulatory guidelines. The ideal candidate will have over 2 years of independent monitoring experience and expertise in the Oncology therapeutic area. This role involves nationwide travel and the opportunity to contribute to advanced clinical trials.

Qualifications

• Over 2 years of independent on-site monitoring experience.
• Experience managing multiple clinical trial protocols.
• Hands-on experience in the Oncology therapeutic area.

Responsibilities

• Perform site monitoring visits in accordance with GCP and ICH guidelines.
• Adapt and track subject recruitment plans.
• Administer protocol training to assigned sites.
• Evaluate study site practices and escalate quality issues.
• Manage progress of assigned studies.
• Ensure site documents are available for filing.
• Create documentation regarding site management.
• Collaborate with study team members.

Skills

Site monitoring

Regulatory compliance

Oncology experience

Job description

Overview

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

Qualifications

• 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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