CRA II: Oncology Trials Monitoring & Site Oversight
Listed on 2026-11-01
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Research/Development
Clinical Research, Oncology Care, Research Scientist -
Science
Clinical Research, Oncology Care, Research Scientist
IQVIA Biotech in the United Kingdom seeks a site monitor with 1–2 years of on-site monitoring experience, especially in oncology trials. You will ensure quality, compliance with GCP/ICH, and effective collaboration with clinical sites.
Your role includes coordinating site training, tracking recruitment, and maintaining TMF/ISF documentation, with potential involvement in start-up and contract-based financial tasks. English proficiency is essential.
Are you ready to take on the CRA II:
Oncology Trials Monitoring & Site Oversight role at IQVIA?
Full responsibilities and requirements are described in the listing above.
Learn more about the CRA II:
Oncology Trials Monitoring & Site Oversight role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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