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.
This opportunity is for the CRA II:
Oncology Site Monitor (UK) role at IQVIA.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the CRA II:
Oncology Site Monitor (UK) role in the description above.
We appreciate your interest in this position.
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Take a moment to read everything above and see whether this role is right for you.
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