Experienced CRA - Single Sponsor Dedicated

IQVIA Inc; Reading; On-site; GBP 32,000 - 46,000; Full time

Job summary

IQVIA is seeking experienced Clinical Research Associates in the UK to perform on-site monitoring, ensure GCP/ICH compliance, and drive site recruitment plans. The role involves regular site visits, training, and close collaboration with the study team across diverse sites.

Candidates should have independent monitoring experience, strong GCP/ICH knowledge, and flexibility to travel. This is a sponsor-dedicated CRA position based in the UK.

Qualifications

• Experience of independent on-site monitoring (minimum 6 months).
• Manage multiple clinical trial protocols across diverse sites.
• In-depth knowledge of GCP and ICH guidelines.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH guidelines.
• Work with sites to drive and track recruitment plans to align with project needs.
• Administer protocol training to sites and establish regular communication.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Track submissions, recruitment, CRF completion and data queries; may support start-up.
• Maintain TMF/ISF documents and ensure regulatory filing readiness.
• Create and maintain site management documentation and visit reports.
• Collaborate with study team members for project execution support.

Skills

On-site monitoring

Clinical trial management

GCP & ICH knowledge

Travel flexibility

Education

Life science degree

Job description

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 (minimum 6 months).
• 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

*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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.