IQVIA UK is seeking freelance Clinical Research Associates to participate in site evaluation, initiation visits, and ongoing monitoring. The role involves ensuring adherence to GCP/ICH guidelines, training site staff on eCRF/EDC, and collaborating with the CTM and Lead CRA to meet study requirements.
The candidate should have oncology experience and at least 2 years as a CRA, with strong communication skills and the ability to manage multiple trials simultaneously.
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London Freelance CRA - Oncology Field Monitor 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.
