- Alimos, Attica, Greece
- Hybrid
- 8–10 years
Manage a team of CRAs, ensuring strong monitoring in clinical trials and compliance with regulations.
Compensation
We offer an attractive compensation package, outstanding benefits, and an exciting work environment with varied tasks in an international environment.
Responsibilities
- Work allocation, staff development and performance appraisal
- Provides input for capacity planning
- Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country
- Interacts with sites to resolve operational issues
- Attend local Investigator Meetings if requested
Requirements
- Bachelor’s degree in Science required; advanced degree in a relevant scientific or healthcare field preferred