Senior Oncology CRA - Site Monitoring & Study Leadership

IQVIA LLC; Sefton; On-site; GBP 45,000 - 65,000; Full time

Job summary

IQVIA Biotech is seeking an experienced Clinical Research Associate to perform site monitoring visits, drive patient recruitment plans and ensure regulatory compliance for oncology studies. The role involves authoring visit reports, coordinating with sites and internal teams, and maintaining TMF/ISF documentation.

Strong English communication and timely issue escalation are essential. Minimum 3–4 years of on-site monitoring experience and a Bachelor’s degree in a scientific field or healthcare

Qualifications

• Minimum 3–4 years of on-site monitoring experience.
• Experience monitoring Oncology studies is a must.
• Basic knowledge of GCP/ICH regulatory requirements.
• Written and verbal communication skills in English.

Responsibilities

• Perform site monitoring visits in accordance with GCP/ICH guidelines.
• Track recruitment and study progress, CRFs, data queries and regulatory submissions.
• Ensure TMF/ISF are maintained and site documents are filed.
• Create visit reports and follow-up letters; liaise with study team for execution.

Skills

On-site monitoring

Oncology experience

GCP/ICH knowledge

English communication

Time management

Regulatory knowledge

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

IQVIA Biotech is seeking an experienced Clinical Research Associate to perform site monitoring visits, drive patient recruitment plans and ensure regulatory compliance for oncology studies. The role involves authoring visit reports, coordinating with sites and internal teams, and maintaining TMF/ISF documentation.

Strong English communication and timely issue escalation are essential. Minimum 3–4 years of on-site monitoring experience and a Bachelor’s degree in a scientific field or healthcare