IQVIA UK’s Site Management team is expanding to welcome junior and experienced Clinical Research Associates. Engage in site monitoring visits, support subject recruitment plans, and ensure protocol training and ongoing site communication. The role emphasizes GCP/ICH compliance and thorough documentation across diverse sites.
You will manage regulatory submissions, ISF/TMF maintenance, and collaborate with the study team to drive project execution and quality outcomes.
#J-18808-LjbffrTravel-Ready CRA2: Global Site Monitoring & Impact in Leeds 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.
