Senior Clinical Research Associate – Oncology Trials Lead

IQVIA is seeking an on-site Clinical Research Monitor with 3–4 years of experience to oversee oncology studies across trial sites. You will conduct monitoring visits, ensure protocol compliance, and support site training and communication with project teams.

The role requires familiarity with GCP/ICH guidelines, strong organizational skills, and proficiency in MS Office tools. Bachelor’s degree in a scientific or healthcare field is preferred, with a focus on accuracy and timelines.

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