Clinical Trial Coordinator 50-100%

In this exciting role, you will ensure the independent project management of clinical trials as the interface to sponsors / CRO (Contract Research Organisation) and internal coordination. Additionally, you are responsible for planning study-specific examinations, coordinating patient visits, and managing study-specific correspondence. Maintaining various databases, assisting with the implementation of sponsor studies including contract and budget review within the studies, further expand this exciting range of tasks. Your activities are rounded off by assisting in the creation and management of documents for quality management within the studies as well as preparing and accompanying monitoring visits, audits, and inspections.

Start date immediate or by arrangement.

• Completed training as a nursing professional HF / FH, health specialist, medical practice assistant and/or experience in conducting clinical studies, as well as scientific interest
• Good German and English skills, spoken and written
• Independent, structured, and proactive working style
• Eager to learn, team-oriented, and flexible personality
• Very good IT skills

• A motivated team
• High degree of independence
• A varied, exciting field of activity
• Collaboration with many internal departments
• A quiet, pleasant workplace in the chalet of the Thun hospital
• Regular working hours (home office by arrangement)
• Flexible choice of vacation and pension fund model

If you have any questions, Dr. med. Christoph Ackermann, Deputy Chief Physician Oncology and Head of Study Coordination, is available at phone +41 (0) 58 636 26 45.

A job with prospects: At the Thun hospital, in addition to the state-of-the-art infrastructure and a versatile activity in a family environment, you will also find the opportunity for flexible leisure activities in the surrounding nature and lake region. Are you looking for meaningfulness but also fairness? Then you are in the right place.