Tasks :
Implementation of Monitoring activities as well as Management and Organisation of those activities for international studies.
In charge of controling project data and Documentation
Hands on support to clinical teams
Insure that timelines, budgets and regulatory requirments are respected
Profile :
Fluent in French and in English
Willing to travel
Experienced in Managing CRAs
Experienced on International Studies
Min 4 years experience in Pharma
Excellent knowledge of Regulatory aspects and technical Recommendations
Location : France