Clinical Research Associate - Cra
CurrentManaging multiple Clinical Trials:- Oncological- Infection and Infectious Diseases- Neurological- Performing Site Initiation Visits (web and on-site), Monitoring Visits (on-site, remote and centralized) and Close-Out Visits- Being responsible for documenting adherence to Protocol and compliance to GCP of the assigned Sites- Being responsible for the quality of collected data- Verifying correct IP/Device management and storing- Coordinating clinical and non-clinical staff involved in the trials- Knowledge of Standard Operating Procedures (SOPs)- Continuous training on European Regulations- Supporting Project Leaders with the preparation and submission of regulatory documents- Maintaining good relationship and collaboration with Sponsor and Site Study Staff