CRA II: Oncology Site Monitor (UK)

IQVIA; Reading; On-site; GBP 42,000 - 60,000; Full time

Job summary

IQVIA Biotech is seeking an on-site Monitoring professional to join our fast-paced team in the UK. You will conduct site visits, ensure GCP/ICH compliance, and support recruitment planning across oncology studies.

The role emphasizes collaboration with sites and study teams, documentation, and timely issue resolution, with potential involvement in start-up activities and budget considerations. Visa sponsorship is not available; UK work rights required.

Qualifications

• 1-2 years of on-site monitoring experience.
• Experience monitoring Oncology studies required.
• Bachelor's Degree in scientific discipline or health care preferred.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Basic knowledge of GCP and ICH guidelines.
• Written and verbal communication skills including good command of English language.

Responsibilities

• Perform site monitoring visits per GCP/ICH guidelines.
• Drive and track subject recruitment plans with sites to enhance predictability.
• Administer protocol training to assigned sites and maintain regular communication.
• Evaluate site practices for protocol conduct and regulatory compliance; escalate issues.
• Track regulatory submissions, recruitment, CRF completion, data queries; support start-up phase.
• Maintain TMF and ISF documentation per GCP/ICH and local regs.
• Document site management findings and action plans with regular visit reports.
• Collaborate with study team for project execution support.
• Possibly develop site-specific recruitment plans; may assist site finances/invoicing.

Skills

On-site monitoring experience

Oncology studies monitoring

GCP & ICH guidelines knowledge

Communication skills in English

Education

Bachelor's Degree in scientific discipline or health care

Equivalent combination of education, training and experience may be accepted

Job description

IQVIA Biotech is seeking an on-site Monitoring professional to join our fast-paced team in the UK. You will conduct site visits, ensure GCP/ICH compliance, and support recruitment planning across oncology studies.

The role emphasizes collaboration with sites and study teams, documentation, and timely issue resolution, with potential involvement in start-up activities and budget considerations. Visa sponsorship is not available; UK work rights required.