Job Description
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry and delivering exemplary customer service.
Office-based in Vienna
You will:
- Conduct and report all types of onsite monitoring visits as well as remote visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be involved in site identification process
- Assist in training of less expert CRAs, depending on your level of experience
*Senior CRA can be assigned as Lead Monitor in some projects, while still partially monitoring.