IQVIA UK's Site Management team is seeking junior and experienced Clinical Research Associates to perform on-site monitoring visits across diverse sites, ensuring GCP/ICH compliance and protocol adherence.
The role involves coordinating subject recruitment plans, training sites on the protocol, maintaining regular communication, and managing regulatory submissions, ISF/TMF, and data queries while supporting start-up activities when needed.
#J-18808-Ljbffr
Clinical Research Associate II: Site Monitoring in Eccles 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.
