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