Clinical Research Associate II

IQVIA Argentina; Reading; On-site; GBP 36,000 - 48,000; Full time

Job summary

IQVIA UK seeks experienced Clinical Research Associates to join our cFSP sponsor-dedicated team in Reading. You will perform site monitoring visits and ensure GCP/ICH compliance while maintaining strong site relationships.

With at least 2 years of on-site monitoring, you will drive subject recruitment plans, deliver protocol training, and coordinate regulatory submissions. This full-time role offers cross-functional collaboration in a fast-paced environment.

Qualifications

• Requires at least 2 years on-site monitoring experience of interventional studies.
• Good knowledge of applicable clinical research regulatory requirements (GCP and ICH).

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH and contract.
• Drive and track subject recruitment plans with sites to improve predictability.
• Administer protocol training to sites and maintain regular communication on project expectations and issues.
• Evaluate site practices for protocol conduct and regulatory compliance; escalate issues as needed.
• Track regulatory submissions, recruitment, CRF completion and data query resolution; may support start-up phase.
• Maintain TMF/ISF documentation and ensure filing per regulatory requirements.
• Create and maintain visit reports, follow-up letters and other study documentation.
• Collaborate with study team members to support project execution.

Skills

On-site monitoring experience

GCP/ICH knowledge

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. 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.