IQVIA UK is seeking junior and experienced Clinical Research Associates to join its Site Management team. The role involves performing on-site monitoring visits in accordance with GCP/ICH, supporting site recruitment plans, and administering protocol training to assigned sites.
You will evaluate site conduct, manage regulatory submissions, and maintain TMF/ISF documentation while collaborating with the study team to ensure project success. Some travel to sites will be required.
#J-18808-LjbffrClinical Research Associate - Multi-Sponsor Site Monitoring in Reading 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.
