Clinical Research Associate - Site Monitoring (CRA2)

IQVIA; Reading; On-site; GBP 32,000 - 52,000; Full time

Job summary

IQVIA UK is seeking junior and experienced Clinical Research Associates for its Site Management team. You will perform site monitoring visits, ensure GCP/ICH compliance, and support site communication and data integrity across multiple Sponsor projects.

The role requires travel to sites, strong attention to detail, and the ability to manage protocol execution and regulatory submissions. Competitive salary and career development in a global CRO.

Qualifications

• Experience in on-site monitoring of clinical trials.
• Strong knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Willingness to travel to site locations.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements.
• Work with sites to drive and track subject recruitment plans to enhance predictability.
• Administer protocol and study training to assigned sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate issues as needed.
• Track regulatory submissions, recruitment, CRF completion, data queries; support startup as needed.
• Ensure TMF and ISF documentation is maintained in compliance with GCP and local regs.
• Create and maintain documentation from site visits, including reports and follow-up letters.
• Collaborate with study team members for project execution support.

Skills

GCP & ICH knowledge

Independent on-site monitoring

Travel to sites

Multiple protocol management

Education

Life science degree

Job description

IQVIA UK is seeking junior and experienced Clinical Research Associates for its Site Management team. You will perform site monitoring visits, ensure GCP/ICH compliance, and support site communication and data integrity across multiple Sponsor projects.

The role requires travel to sites, strong attention to detail, and the ability to manage protocol execution and regulatory submissions. Competitive salary and career development in a global CRO.