knowledge and master all clinical trial database systems Ability to successfully complete the organizations clinical training... of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical...
knowledge and master all clinical trial database systems Ability to successfully complete the organizations clinical training... of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical...
, come and join us - IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 20 hours a week for a period... and tracking visits and procedures completed against budget in the clinical trial management system (CTMS) Preparing...
, come and join us - IQVIA are looking Clinical Research Coordinator. This role has an immediate start working 20 hours a week for a period... into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial...