Karin Almasan

Managing site activities remotely from study start to termination. Performing all clinical monitoring tasks remotely for designated projects in accordance with relevant regulations. Ensuring patient safety and data integrity.

Supporting Clinical Leads and Study Managers in their day to day duties. Coordination of clinical team. Monitoring study timelines and patient recruitment. Compiling monthly study reports. Maintaining the international trial master file. Performing quality checks and communication of findings.

Assisting Director's in their business. Making travel arrangements, organization of meetings. Role model for junior Assistants. Handling of correspondence. Filing of project documentation. Designing presentations. Preparation of sales documentation and calculation of projects.