Clinical Research Associate I

IQVIA LLC; Reading; On-site; GBP 30,000 - 45,000; Full time

Job summary

A global clinical research organization is seeking a Clinical Research Associate I in Reading, UK. This role involves performing site monitoring visits, ensuring compliance with regulatory requirements, and managing multiple clinical trial protocols. Applicants must have over a year of on-site monitoring experience and flexibility for travel. Join an innovative team dedicated to improving patient outcomes.

Qualifications

• Over 12 months of independent on-site monitoring experience, ensuring compliance with GCP and regulatory guidelines.
• Successfully managed multiple clinical trial protocols across diverse investigative sites.
• Flexibility and commitment to nationwide travel.

Responsibilities

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements.
• Work with sites to adapt, drive, and track subject recruitment plans.
• Evaluate the quality and integrity of study site practices.

Skills

On-site monitoring experience

Knowledge of GCP

Flexibility for nationwide travel

Job description

Clinical Research Associate I page is loaded

Clinical Research Associate I

Apply locations Reading, Berkshire, United Kingdom Northamptonshire, England, United Kingdom Nottinghamshire, England, United Kingdom Somerset, England, United Kingdom Oxfordshire, England, United Kingdom time type Full time posted on Posted Yesterday job requisition id R1495114

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 sponsor-dedicated team and looking for passionate CRAs who are ready to make a difference.

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..
• 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.