CRA2: Multi-Sponsor Site Monitoring Specialist

IQVIA; Reading; Hybrid; GBP 30,000 - 50,000; Full time

Job summary

IQVIA UK’s Site Management team is seeking junior and experienced Clinical Research Associates to support multi-sponsor studies in Reading and across the UK. The role focuses on on-site monitoring, site qualification, initiation, monitoring and close-out visits in line with GCP and ICH.

You will liaise with sites to support recruitment plans, ensure protocol training, maintain essential documentation, and collaborate with the study team to drive project timelines.

Qualifications

• Experience of independent on-site monitoring.
• In-depth knowledge of GCP and ICH guidelines.
• Life science degree educated or equivalent industry experience.
• Willingness to travel to sites.

Responsibilities

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements (GCP/ICH).
• Work with sites to adapt, drive, and track subject recruitment plan to enhance predictability.
• Administer protocol and related study 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; may support start-up.
• Maintain TMF/ISF and document submission; prepare visit reports and follow-up letters.
• Collaborate with study team members for project execution support.

Skills

On-site monitoring

GCP & ICH

Site management

Travel flexibility

Education

Life science degree

Job description

IQVIA UK’s Site Management team is seeking junior and experienced Clinical Research Associates to support multi-sponsor studies in Reading and across the UK. The role focuses on on-site monitoring, site qualification, initiation, monitoring and close-out visits in line with GCP and ICH.

You will liaise with sites to support recruitment plans, ensure protocol training, maintain essential documentation, and collaborate with the study team to drive project timelines.