IQVIA Biotech in Livingston, United Kingdom, is seeking a Clinical Monitor to support on-site visits, ensure adherence to GCP/ICH guidelines, and manage site communications across oncology studies. You will conduct site monitoring visits, support recruitment plans, and help establish strong relationships with study sites to drive trial progress.
The role requires at least 1 year of on-site monitoring experience, a biomedical or health-care degree, and solid knowledge of regulatory requirements.
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CRA 2: Oncology Site Monitoring Expert in Livingston 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.
