Global Study Manager - Coordination of clinical studies (VAC/87)

Reference: VAC/87
Region: International
Sector: Pharmaceutical Industry
Type of contract: Permanent - Full Time
Category: Clinical trials

For a leading pharmaceutical company. 

Description

The Global Study Manager (GSM) is responsible for the operational aspects of clinical trials and ensures that studies are conducted according to the GCP/ICH guidelines and SOP’s for world wide studies.

• World wide study co-ordination;
• Monitoring world wide and in countries where no local monitor is available (if needed);
• Study co-ordination with different functions and other departments. 

Profile

• Medical, paramedical or scientific study background;
• Excellent oral and written communication skills in English and French & good Dutch speaking skills;
• Very well organized and able to follow-up complex projects;
• Proactivity, integrity and a strong feeling for ethics;
• Flexible and open to travel internationally;
• Computer literate. 

Experience

Minimum 2 years of experience as CRA .

Languages

English: Very Good
Dutch: Good
French: Very Good
German: Not applicable