Clinical Research Associate II

IQVIA LLC; Reading; Hybrid; GBP 35,000 - 50,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Associate II to support clinical trials through on-site monitoring. Candidates should have over 2 years of independent monitoring experience and strong project management skills. The role requires flexibility for nationwide travel and focuses on ensuring compliance with regulatory guidelines. This position combines on-site and remote work to enhance work-life balance.

Benefits

Career development opportunities

Working at the forefront of new medicines development

Qualifications

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

Responsibilities

• Perform site monitoring visits per regulatory guidelines.
• Work with sites to adapt and track subject recruitment plans.
• Evaluate site practices to ensure compliance with protocols.

Skills

On-site monitoring

GCP compliance

Project management

Oncology experience

Nationwide travel

Job description

Clinical Research Associate II page is loaded

Clinical Research Associate II

Apply locations Reading, Berkshire, United Kingdom Leeds, West Yorkshire, United Kingdom Bath, United Kingdom Tunbridge Wells, United Kingdom Cambridge, United Kingdom time type Full time posted on Posted Yesterday time left to apply End Date: August 21, 2025 (19 days left to apply) job requisition id R1493628

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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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.