IQVIA Biotech in the United Kingdom seeks an experienced Clinical Research Associate to perform on-site monitoring visits per GCP/ICH, with a focus on oncology studies.
You will drive recruitment planning with sites, administer protocol training, manage TMF/ISF, and collaborate with study teams to ensure data quality and regulatory compliance throughout the trial lifecycle.
Bachelor's degree in a scientific discipline or healthcare is preferred; 1 year of on-site monitoring experience is required.
Oncology CRA II - Site Monitoring & Study Oversight in Salford 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.
