IQVIA Biotech in the United Kingdom seeks an on-site Clinical Research Associate to monitor oncology studies per GCP/ICH guidelines and contracted scope. You will manage site visits, training, site communications and TMF/ISF filing to ensure data integrity and regulatory compliance.
Responsibilities include tracking recruitment plans, regulatory submissions, data queries and visit reports. The role requires 1 year of on-site monitoring experience and a Bachelor’s degree in a scientific or health
Oncology Clinical Research Associate II — Site Monitoring in Ossett 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.
