Global CRA: Site Monitoring Expert for Multi-Therapy Trials

An established industry player is seeking skilled Clinical Research Associates (CRAs) to join their expanding team for a global study. This role focuses on ensuring high-quality site monitoring activities in line with the Site Monitoring Plan. Ideal candidates will have a scientific background and experience in clinical research, with a strong understanding of ICH GCP standards. Join a dynamic organization that values quality and timely execution, contributing to the success of clinical trials across various therapeutic areas. If you're ready to enhance your skills and make an impact, this opportunity is for you.