JOB ROLE:

• Monitoring of international clinical studies according to national and international standards

• In charge of cross-border, project-related supervision of clinical studies mainly in Italy, Germany and the U.K.

• Communication, support and close collaboration with trial centres, clinical project managers as well as authorities and ethics commissions

• The job will be Zurich-based, however, involving regular travelling within the frame of on-site visits

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:

• Previous CRA experience in either Pharma or CRO

• Profound knowledge of ICH-GCP Guidelines

• Work experience in oncology an asset

• Proficiency in German and English, good working knowledge of Italian

• Should enjoy a fair amount of travelling

To apply please email your fully documented CV to: info@philochem.ch