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.