Clinical Research Associate II: Flexible Work & Growth

Iqvia; Manchester; On-site; GBP 32,000 - 42,000; Full time

Job summary

IQVIA is seeking experienced Clinical Research Associates to join our Site Management team in the UK. The role involves performing site monitoring visits, ensuring regulatory compliance and data integrity, and coordinating with investigative sites to support study timelines.

You will administer protocol training, track submissions and recruitment, and maintain essential TMF/ISF records while collaborating with the study team to manage expectations and issues.

Qualifications

• Requires at least 2 years on-site monitoring experience of interventional studies.
• Good knowledge of GCP/ICH guidelines and regulatory requirements.
• Ability to establish professional relationships with sites and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope and GCP/ICH.
• Coordinate recruitment plans with sites to support study timelines.
• Provide protocol-related training to sites and maintain clear communication on expectations.
• Assess site conduct and data quality; escalate issues as needed.
• Track regulatory submissions, approvals, recruitment, CRF completion, and data queries.
• Maintain TMF/ISF documentation per regulatory requirements.
• Document visit findings and action plans with timely reports.

Skills

On-site monitoring

GCP/ICH knowledge

Education

Degree in scientific discipline

Job description

IQVIA is seeking experienced Clinical Research Associates to join our Site Management team in the UK. The role involves performing site monitoring visits, ensuring regulatory compliance and data integrity, and coordinating with investigative sites to support study timelines.

You will administer protocol training, track submissions and recruitment, and maintain essential TMF/ISF records while collaborating with the study team to manage expectations and issues.