IQVIA LLC in the United Kingdom is seeking an experienced Clinical Research Associate to monitor Phase I–IV trials. You will perform site evaluations, initiation visits, and ongoing monitoring in line with Good Clinical Practices and IQVIA Biotech procedures, coordinating with the CTM or Lead CRA to ensure study requirements are met.
Responsibilities include investigator recruitment visits, training on eCRF/EDC, data quality reviews, and timely preparation of monitoring reports.
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Oncology Freelance CRA — Field Monitoring Expert in East Boldon employer: IQVIA LLC
At IQVIA, we pride ourselves on being an exceptional employer, particularly for those in the field of Pharmaceutical Development. Our Cambridge location fosters a collaborative and innovative work culture, where you will have the opportunity to influence scientific direction, mentor junior scientists, and engage directly with clients. With a strong focus on employee growth and the integration of cutting-edge AI-enabled approaches, we are committed to supporting your professional development while making a meaningful impact in the pharmaceutical industry.
