IQVIA Biotech in Leeds is seeking an experienced Clinical Research Associate to perform on-site monitoring visits for oncology trials, ensuring GCP/ICH compliance and proper trial conduct. You will manage site communications, training, and documentation, while supporting recruitment plans and study start-up activities.
The role requires 1 year of on-site monitoring experience, strong English communication, and solid organizational and financial management skills.
Oncology CRA II: Frontline Site Monitoring in Biotech in Leeds 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.
