CRA II

As a CRA sponsor dedicated, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas, assisting other CRAs with co-monitoring activities both remote and on-site. You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators. You'll review source to CRF/eCRF, ensuring patient safety and data integrity aspect of the study. Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct.