Senior Clinical Research Associate - Site Monitoring

IQVIA; Reading; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading global provider of clinical research services is seeking an experienced Clinical Research Associate in Reading, UK. The role involves performing site monitoring visits, managing study progress, and ensuring compliance with regulatory requirements. Ideal candidates will have a life science degree, experience in on-site monitoring, and a strong understanding of GCP and ICH guidelines. This position offers a career with purpose and impact.

Qualifications

• Experience of independent on-site monitoring.
• Successfully managed multiple clinical trial protocols across diverse sites.
• In-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.

Responsibilities

• Perform site monitoring visits according to GCP and ICH guidelines.
• Adapt and track subject recruitment plans with sites.
• Administer protocol training and manage communications.
• Evaluate quality and integrity of study site practices.
• Manage study progress and regulatory submissions.
• Ensure site documents are properly filed.
• Document site management and monitoring visit findings.
• Collaborate with study team members for project execution.

Skills

Independent on-site monitoring

Management of clinical trial protocols

Knowledge of Good Clinical Practice (GCP)

Knowledge of ICH guidelines

Flexibility to travel

Education

Life science degree or equivalent experience

Job description

A leading global provider of clinical research services is seeking an experienced Clinical Research Associate in Reading, UK. The role involves performing site monitoring visits, managing study progress, and ensuring compliance with regulatory requirements. Ideal candidates will have a life science degree, experience in on-site monitoring, and a strong understanding of GCP and ICH guidelines. This position offers a career with purpose and impact.