Tasks

- Processing of SAE's
- Support of feasibility assessments, protocol design, CRF design, site selection & generation of clinical study reports
- Risk management & definition of mitigation strategies
- Participate in the preparation, review and revision of SOPs
- Close interactions with Project Scientists and Operations

Qualifications

- MD with Industry exposure supporting the development of oncological compounds
- Some medical practice exposure desirable
- Familiar of ICH GCP in place
- Excellent communication skills, expereinced working with internal as well as with external stakeholders
- Business fluent in English, German is of advantage