Clinical Research Associate

Duties to include:
Initiating, managing and reporting international clinical phase I IV studies
Study conduct
CRO management
Interface for data management and data resolution.

Skills/experience required:
Life sciences degree
Experience of working in clinical research (as CRA) in CRO, pharmaceutical or biotechnology company
Experience in direct monitoring
A team-oriented approach and good negotiating skills
Advanced computer skills (Internet, Microsoft Office)
Excellent English and German (written and spoken)
Willingness to travel

Personal strengths:
Strong operational, organisational, presentation, documentation and interpersonal skills
Self starter requiring minimal supervision
Excellent in communication

There is an excellent salary and benefits package available for the right candidate.