Clinical Research Associate (CRA)
Duties include investigator recruitment for national and international clinical studies and the performance of pre-study, initiation, routine and final monitoring visits to the investigational sites, as well as the coordination of all necessary regulatory and associated activities. Willingness to travel extensively in France and occasionally to other European countries is a must.

You are a life science graduate and have at least 3 years experience as a CRA, as well as perfect knowledge of ICH-GCP and the regulatory environment in France. You have the ability to work independently under the supervision of the project manager and to communicate appropriately with your team. You have excellent knowledge of both written and spoken English and French. Proficient use of MS-Office applications is essential.

Clinical Operations

Paris, France