Clinical Research Associate II

IQVIA; Reading; On-site; GBP 35,000 - 52,000; Full time

Job summary

IQVIA UK is seeking an experienced Clinical Research Associate for the cFSP sponsor-dedicated team. You will perform site monitoring visits, manage recruitment plans, and ensure regulatory compliance while maintaining regular communication with sites.

The role requires at least 2 years of on-site monitoring experience in interventional studies, a degree in a scientific discipline or healthcare, and full UK work entitlement. Visa sponsorship is not offered.

Qualifications

• 2+ years on-site monitoring experience of interventional studies.
• Knowledge of GCP and ICH guidelines.
• Ability to establish effective working relationships with coworkers and clients.
• Full UK right to work (visa sponsorship not available).

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) per contract and GCP/ICH.
• Drive and track subject recruitment plans to enhance predictability.
• Train sites on protocol and provide regular communication to manage expectations.
• Evaluate site practices for protocol adherence and regulatory compliance; escalate issues as needed.
• Track regulatory submissions, recruitment, CRF completion, data queries; support start-up phase.
• Ensure TMF and ISF documentation is complete and properly filed.
• Create and maintain site management records and visit reports with action plans.
• Collaborate with study team members to support project execution.

Skills

On-site monitoring

Regulatory knowledge (GCP/ICH)

Site management communication

Degree in science/healthcare

Education

Degree in scientific discipline or health care

Job description

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates.

Why IQVIA?

• Career development opportunities to grow as we grow
• AI‑powered career advancement through our internal talent marketplace, Career Connections
• Mentorship opportunities across the organisation via Employee Resource Groups
• Flexible working to assist work–life balance and professional success
• Well‑being support covering your physical, mental, and financial health

Awards

• 2026 "Glassdoor Best Place to Work in the UK"
• #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
• Brandon Hall Excellence Award for Learning & 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

• Requires at least 2 years on-site monitoring experience of interventional studies
• Degree in scientific discipline or health care or equivalent industry experience
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Ability to establish and maintain effective working relationships with coworkers and clients
• Full UK right to work required, this position is not eligible for 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.

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.