Key skills
Google Cloud PlatformGCPGoogle CloudCommunication
About this role
Role Overview
- Initiate and coordinate activities and essential documents management during startup
- Prepare, validate and submit regulatory documents for internal review
- Manage communication between client and ethics committee for approvals
- Support investigators sites with local IRB workflow
- Maintain trial master files and project compliance
Requirements
- Minimum 2 years relevant experience in clinical site management
- Knowledge of clinical research and development processes
- Understand basic medical terminology and GCP requirements
- Proficient in computer operations and Microsoft Suite
- Experience with Clinical Trial Management Systems (CTMS) and Electronic Trial Master File
Tech Stack
- Google Cloud Platform
Benefits
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development