IQVIA in the United Kingdom seeks experienced Clinical Research Associates to monitor and manage study sites in accordance with protocol, regulations and sponsor requirements. You will perform initiation, monitoring and close-out visits, drive recruitment plans, and ensure high-quality data and site documentation.
Applicants should have at least 1 year of on-site monitoring experience, strong knowledge of GCP/ICH, and excellent communication.
#J-18808-LjbffrCRA II: On‑Site Monitoring & Site Management (UK) employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
