Supports the Global Clinical Study Manager in global study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget. Supports study vendor management in addition to other study management activities assigned.
Requirements
- Bachelor or higher degree in a scientific or healthcare discipline
- 3 or more years of experience in clinical research within Biotech, Pharma or CRO industry
- Proficiency in MS Office Suite, including Excel, PowerPoint, and Project
Benefits
- Market competitive compensation package including performance-based annual bonus scheme
- Company shares (generous welcome grant!)
- In-house and external learning and development opportunities
- Fantastic benefits program
