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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Senior Clinical Research Associate - Oncology Trials Lead employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
