Clinical Research Associate

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies, mainly observational, and clinical investigations under the supervision by the Project Manager.

Requirements

• Degree in a scientific field
• 0-12 Months of experience as CRA
• Knowledge of ICH-GCP and ISO14155 and techniques for the monitoring of clinical studies and clinical investigations
• Obtain requirements as per local regulation (e.g., for CRA working in Italy, of Ministerial Decree 15.11.2011 in order to conduct interventional clinical trials)
• Able to carry out all the activities related to the monitoring of clinical trials/clinical investigations, guaranteeing the security of information
• Good knowledge of Office Suite
• Good knowledge of English language
• Able to work independently under the supervision of the Project Managers and Clinical Operations Managers
• Able to interact with the personnel of clinical studies and clinical investigations

Benefits

• Competitive salary
• Other benefits/bonuses