Clinical Research Associate

As a Clinical Research Associate (CRA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. For one of our sponsors, we are looking for a Clinical Research Associate based in the Netherlands. Key responsibilities include performing site qualification, site initiation, and closeout visits, ensuring regulatory and protocol compliance. Visits may be on-site or remote. Generate queries and manage resolutions with site personnel. Document activities via confirmation letters, follow-up letters, trip reports, communication logs and other required study documents as per SOPs and Study Monitoring Plan. Perform investigational product accountability as per the protocol and Study Monitoring Plan. Ensure to set up proper recruitment/maintenance plan based on appropriate analysis of capability of sites selected. Act as primary liaison with site personnel. Management and collection of site's study regulatory documents. Enter data into tracking systems as required. Assist and support audit preparation and CAPA implementation. AE/SAE and expedited reporting and management.