Experienced Clinical Research Associate

IQVIA LLC; Reading; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical research organization is seeking an Experienced Clinical Research Associate in Reading, UK. The role involves conducting site monitoring visits, managing clinical trial protocols, and ensuring compliance with regulatory standards. Ideal candidates will have a life science degree and experience in clinical research. This position offers genuine opportunities for career development in a dynamic environment.

Qualifications

• Experience of independent on-site monitoring.
• Successfully managed multiple clinical trial protocols across diverse investigative sites.
• In-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Flexibility to travel to sites.

Responsibilities

• Perform site monitoring visits in accordance with regulatory requirements.
• Work with sites to drive and track subject recruitment.
• Administer protocol training to assigned sites.
• Evaluate quality of study site practices.
• Manage the progress of assigned studies.
• Ensure documentation is available for filing in the TMF.
• Create and maintain appropriate documentation regarding site management.

Skills

Independent on-site monitoring

Management of multiple clinical trial protocols

Knowledge of GCP and ICH guidelines

Life science degree or equivalent

Flexibility to travel

Education

Life science degree

Job description

Experienced Clinical Research Associate page is loaded

Experienced Clinical Research Associate

Apply locations Reading, Berkshire, United Kingdom time type Full time posted on Posted Yesterday job requisition id R1482675

Join Us on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

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

Requirements

• Experience of independent on-site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

#LI-ADAMTHOMPSON

*Please note - this role is not eligible for UK visa sponsorship*

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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About Us

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.