IQVIA Biotech is seeking an experienced Clinical Site Monitor to conduct on-site visits for oncology studies in strict accordance with GCP/ICH guidelines, ensuring data integrity and regulatory compliance.
You will collaborate with study teams to adapt recruitment plans, administer protocol training, manage documentation and communicate effectively with sites. The role may involve site financial oversight and TMF/ISF management.
Senior Oncology CRA - Site Monitoring & Oversight 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.
