About this role
Role Overview
- Responsible for defining, developing and delivering the global study start up project strategy
- Manage and coordinate study start up activities globally
- Lead start up sub team for the study, region(s) or countries assigned
- Deliver site activations to plan for studies across high operational complexity
- Accountable for quality and completeness of start up timeline plans at study, country and site level
Requirements
- 5+ years global start up clinical trial/study management experience
- Comprehensive working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations
- Extensive knowledge of clinical trial methodology
- Fluency in English is required
Benefits
- Manageable sites, manageable protocols
- Exciting professional challenges in inspiring studies
- Enormous security and long-term prospects