Experienced Clinical Research Associate — Flexible Work & Growth

IQVIA; Reading; Hybrid; GBP 36,000 - 54,000; Full time

Job summary

IQVIA UK is expanding its cFSP team and seeks experienced Clinical Research Associates to monitor interventional studies on-site in the UK. You will conduct site visits, manage recruitment plans and ensure protocol training and communications with sites are robust.

Role requires at least 2 years of on-site monitoring experience, strong GCP/ICH knowledge, and full UK right to work. The position offers growth within a globally leading clinical research organization.

Qualifications

• Minimum 2 years of on-site monitoring experience for interventional studies.
• Degree in scientific discipline, health care or equivalent industry experience.
• Solid knowledge of GCP/ICH guidelines and regulatory requirements.
• Ability to establish and maintain effective working relationships with colleagues and clients.
• Full UK right to work; visa sponsorship not available.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contract and GCP/ICH.
• Collaborate with sites to drive recruitment plans and improve predictability.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate issues.
• Track regulatory submissions, recruitment, CRF completion and data queries; support start-up phase.
• Ensure site documents are filed in the TMF and ISF maintained.
• Create and maintain documentation on site management, visit findings and action plans.
• Coordinate with study team for project execution support.

Skills

On-site monitoring

Regulatory knowledge

Education

Degree in scientific discipline

Job description

IQVIA UK is expanding its cFSP team and seeks experienced Clinical Research Associates to monitor interventional studies on-site in the UK. You will conduct site visits, manage recruitment plans and ensure protocol training and communications with sites are robust.

Role requires at least 2 years of on-site monitoring experience, strong GCP/ICH knowledge, and full UK right to work. The position offers growth within a globally leading clinical research organization.