Experienced CRA - Single Sponsor Dedicated

IQVIA LLC; Chieveley; On-site; GBP 35,000 - 55,000; Full time

Benefits offered by this job

Career development opportunities

Work on cutting-edge medicines

Access to large data pools

Job summary

IQVIA is seeking experienced Clinical Research Associates in the UK for single sponsor dedicated roles. You will perform on-site monitoring visits, manage site communications, ensure GCP/ICH compliance, and support recruitment plans across diverse sites.

Join IQVIA to work on cutting-edge medicines, access large data pools for site performance, and develop your clinical research career with global opportunities. This role requires travel and is not visa-sponsored in the UK.

Qualifications

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

Responsibilities

• Perform site monitoring visits in accordance with contract scope and regulatory requirements (GCP/ICH).
• Drive and track subject recruitment plans to meet project needs.

Skills

Site monitoring

GCP/ICH knowledge

Travel flexibility

Education

Life science degree or equivalent

Job description

Experienced CRA - Single Sponsor Dedicated

Date posted: 2026-09-26T00:00:00

Location: Berkshire, GB, RG20 8TY

Application deadline: 2026-12-26T03:03:13.663

Join Us on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) is 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, driving site performance and making the CRA role more efficient.
• 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 plans in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular 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, CRF completion and submission, and data query resolution; may support start-up phase.
• Ensure 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 documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, follow-up letters, and other study documentation.
• Collaborate with study team members for project execution support as appropriate.

Requirements

• Experience of independent on-site monitoring (minimum 6 months).
• Successfully managed multiple clinical trial protocols across diverse investigative sites.
• In-depth knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Flexibility to travel to sites.

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

About IQVIA

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.

Our Commitment

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.

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!

• 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 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.