Clinical Monitoring Associate

Iqvia Uk's Cfsp; Sonning; On-site; GBP 30,000 - 48,000; Full time

Benefits offered by this job

Career development opportunities

Flexible working

Job summary

IQVIA UK's cFSP is seeking experienced Clinical Research Associates to perform on-site monitoring visits across interventional studies. The role emphasizes GCP/ICH compliance, site management, and collaboration with study teams in the UK.

The position requires at least 2 years of on-site monitoring experience, a degree in a scientific discipline or health care, and the ability to establish strong working relationships with sites and stakeholders. UK right to work is required.

Qualifications

• GCP and ICH regulatory requirements knowledge and application.
• Minimum 2 years on-site monitoring experience for interventional studies.
• Ability to establish and maintain effective working relationships with coworkers and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contract scope and GCP/ICH guidance.
• Collaborate with sites to drive recruitment plans and enhance study predictability.
• Administer protocol training and maintain regular communication with sites to manage expectations.
• Track regulatory submissions, recruitment, CRF completion, data queries, and support start-up if needed.
• Ensure TMF/ISF documentation is complete and compliant with regulatory requirements.
• Record visit findings and action plans, generate reports and follow-up communications.

Skills

GCP & ICH knowledge

Relationship building

Education

Science/healthcare degree or equivalent

Job description

• 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
  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 UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates.

Why IQVIA?

• Career development opportunities to grow as we grow
• 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, 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.