Senior CRA: On-Site Monitoring & Study Leadership

IQVIA LLC; Manchester; On-site; GBP 32,000 - 48,000; Full time

Job summary

IQVIA UK’s Site Management team is expanding to include experienced Clinical Research Associates. The role focuses on on-site monitoring visits, site management, and collaboration with study teams to ensure protocol compliance and safe, efficient trial conduct.

Ideal candidates will have proven independent monitoring experience, familiarity with GCP/ICH, and a life science degree. Travel to sites will be required, and visa sponsorship is not available for this position.

Qualifications

• Experience of independent on-site monitoring.
• Managed multiple clinical trial protocols across diverse investigative sites.
• In-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Life science degree or equivalent industry experience.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contract scope and GCP/ICH requirements.
• Drive and track subject recruitment plans to enhance predictability.
• Administer protocol training to sites and maintain regular communication on project expectations and issues.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate issues as needed.
• Manage study progress: regulatory submissions, recruitment, CRF completion, data queries.

Skills

On-site monitoring

Study coordination

GCP/ICH knowledge

Life science degree

Education

Bachelor’s in Life Sciences

Job description

IQVIA UK’s Site Management team is expanding to include experienced Clinical Research Associates. The role focuses on on-site monitoring visits, site management, and collaboration with study teams to ensure protocol compliance and safe, efficient trial conduct.

Ideal candidates will have proven independent monitoring experience, familiarity with GCP/ICH, and a life science degree. Travel to sites will be required, and visa sponsorship is not available for this position.