Senior Oncology CRA — Advanced Site Monitoring Lead

IQVIA Biotech is seeking an experienced Clinical Trial Monitor focused on on-site activities and Oncology studies. You will conduct site visits, ensure protocol compliance and regulatory adherence, and support site recruitment and data integrity across multiple sites.

The role requires 3–4 years of on-site monitoring experience, strong English communication, and solid knowledge of GCP/ICH guidelines. This position is not visa-sponsored and offers a dynamic, fast-paced environment within IQVIA

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