Senior Clinical Research Associate

IQVIA LLC; Maidenhead; On-site; GBP 42,000 - 62,000; Full time

Job summary

IQVIA in Maidenhead, UK, seeks a Senior Clinical Research Associate to conduct on-site monitoring across studies in the UK. You will support site initiation, conduct ongoing monitoring visits and ensure quality and compliance with GCP/ICH guidelines.

The role requires 18 months of independent monitoring experience, strong knowledge of GCP/ICH, and willingness to travel to diverse investigative sites. Visa sponsorship is not available for this position.

Qualifications

• Minimum 18 months of independent on-site monitoring.
• Experience managing multiple clinical trial protocols across diverse sites.
• Strong knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Willingness to travel to study sites.
• Not eligible for UK visa sponsorship.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH guidelines.
• Work with sites to recruit subjects and track recruitment plans.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol compliance and quality issues.
• Track regulatory submissions, recruitment, CRF completion, data queries and resolutions; may support start-up.

Skills

On-site monitoring

GCP knowledge

ICH guidelines

Travel flexibility

Education

Life science degree

Job description

Senior Clinical Research Associate

2026-09-24T00:00:00

Maidenhead

Berkshire

GB

SL6 1

Any

2026-12-23T11:01:04.427

Job Description

Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we'll give you the tools you need to create the career you want.

Why IQVIA?

• IQVIA is recognized as #1 in its category on the 2026 Fortune® World's Most Admired Companies list for the fifth 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

• A minimum of 18 months 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.
• 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.